Tumor Suppressor Proteins
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Subject Areas on Research
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A Genetic Response Score for Hydrochlorothiazide Use: Insights From Genomics and Metabolomics Integration.
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A de novo frame-shift mutation in the tuberin gene.
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A decrease in the dose of the lgl tumor suppressor increases life span of Drosophila in stress and is related to the maternal effect.
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A genome-wide RNAi screen reveals multiple regulators of caspase activation.
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A methylthioadenosine phosphorylase (MTAP) fusion transcript identifies a new gene on chromosome 9p21 that is frequently deleted in cancer.
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A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.
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A multicenter phase I dose escalation trial to evaluate safety and tolerability of intra-arterial temozolomide for patients with advanced extremity melanoma using normothermic isolated limb infusion.
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A network of substrates of the E3 ubiquitin ligases MDM2 and HUWE1 control apoptosis independently of p53.
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A new role for ATM: regulating mitochondrial function and mitophagy.
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A new strategy for studying protein kinase B and its three isoforms. Role of protein kinase B in phosphorylating glycogen synthase kinase-3, tuberin, WNK1, and ATP citrate lyase.
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A novel ATM-dependent pathway regulates protein phosphatase 1 in response to DNA damage.
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A novel functional DEC1 promoter polymorphism -249T>C reduces risk of squamous cell carcinoma of the head and neck.
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A novel role for the cyclin-dependent kinase inhibitor p27(Kip1) in angiotensin II-stimulated vascular smooth muscle cell hypertrophy.
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A novel splice site mutation (156 + 1G-->A) in the TSC2 gene.
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A phase II study of O6-benzylguanine and temozolomide in pediatric patients with recurrent or progressive high-grade gliomas and brainstem gliomas: a Pediatric Brain Tumor Consortium study.
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A randomized phase II trial of veliparib, radiotherapy, and temozolomide in patients with unmethylated MGMT glioblastoma: the VERTU study.
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A sensitized genetic system for the analysis of murine B lymphocyte signal transduction pathways dependent on Bruton's tyrosine kinase.
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A tuberous sclerosis complex signalling node at the peroxisome regulates mTORC1 and autophagy in response to ROS.
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ABCB5 is a limbal stem cell gene required for corneal development and repair.
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ATM activation in normal human tissues and testicular cancer.
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ATM binds to beta-adaptin in cytoplasmic vesicles.
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ATM phosphorylates p95/nbs1 in an S-phase checkpoint pathway.
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ATM polymorphisms predict severe radiation pneumonitis in patients with non-small cell lung cancer treated with definitive radiation therapy.
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ATM regulates a DNA damage response posttranscriptional RNA operon in lymphocytes.
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ATM signals to TSC2 in the cytoplasm to regulate mTORC1 in response to ROS.
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ATM--a key determinant of multiple cellular responses to irradiation.
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ATM-dependent phosphorylation of Mdm2 on serine 395: role in p53 activation by DNA damage.
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ATM-dependent suppression of stress signaling reduces vascular disease in metabolic syndrome.
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ATM: genome stability, neuronal development, and cancer cross paths.
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ATR functions as a gene dosage-dependent tumor suppressor on a mismatch repair-deficient background.
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ATR/ATM-mediated phosphorylation of human Rad17 is required for genotoxic stress responses.
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Absence of PTEN germ-line mutations in men with a potential inherited predisposition to prostate cancer.
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Activation of TLX3 and NKX2-5 in t(5;14)(q35;q32) T-cell acute lymphoblastic leukemia by remote 3'-BCL11B enhancers and coregulation by PU.1 and HMGA1.
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Activation of the ATM kinase by ionizing radiation and phosphorylation of p53.
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Activin induces hepatocyte cell growth arrest through induction of the cyclin-dependent kinase inhibitor p15INK4B and Sp1.
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Adenovirus-mediated intraarterial delivery of PTEN inhibits neointimal hyperplasia.
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Akt requires glucose metabolism to suppress puma expression and prevent apoptosis of leukemic T cells.
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Alveolar rhabdomyosarcoma-associated PAX3-FOXO1 promotes tumorigenesis via Hippo pathway suppression.
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An ATM/Chk2-mediated DNA damage-responsive signaling pathway suppresses Epstein-Barr virus transformation of primary human B cells.
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An essential role for Prox1 in the induction of the lymphatic endothelial cell phenotype.
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An expanded role of the tumor suppressor TSC1 in T cell tolerance.
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An unbiased evaluation of CK2 inhibitors by chemoproteomics: characterization of inhibitor effects on CK2 and identification of novel inhibitor targets.
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Analysis of the gene coding for the BRCA2-interacting protein PALB2 in hereditary prostate cancer.
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Aneuploidy of chromosome 9 and the tumor suppressor genes p16(INK4) and p15(INK4B) detected by in situ hybridization in locally advanced prostate cancer.
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Assessment of autoantibodies to meningioma in a population-based study.
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Association and interactions between DNA repair gene polymorphisms and adult glioma.
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Association between the N-terminally truncated (DeltaN) p63alpha (DeltaNp63alpha) isoform and debulking status, VEGF expression and progression-free survival in previously untreated, advanced stage epithelial ovarian cancer: A Gynecologic Oncology Group study.
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Association between the V109G polymorphism of the p27 gene and the risk and progression of oral squamous cell carcinoma.
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Association of a p73 exon 2 G4C14-to-A4T14 polymorphism with risk of squamous cell carcinoma of the head and neck.
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Association of combined p73 and p53 genetic variants with tumor HPV16-positive oropharyngeal cancer.
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Associations between antibiotic exposure during pregnancy, birth weight and aberrant methylation at imprinted genes among offspring.
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Associations between prenatal physical activity, birth weight, and DNA methylation at genomically imprinted domains in a multiethnic newborn cohort.
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Ataxia telangiectasia mutant protein activates c-Abl tyrosine kinase in response to ionizing radiation.
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Ataxia telangiectasia-mutated and p53 are potential mediators of chloroquine-induced resistance to mammary carcinogenesis.
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Atm deficiency affects both apoptosis and proliferation to augment Myc-induced lymphomagenesis.
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Autistic-like behaviour and cerebellar dysfunction in Purkinje cell Tsc1 mutant mice.
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Autophagic activity dictates the cellular response to oncogenic RAS.
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Autophagy-dependent metabolic reprogramming sensitizes TSC2-deficient cells to the antimetabolite 6-aminonicotinamide.
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Aven-dependent activation of ATM following DNA damage.
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Axon guidance pathways served as common targets for human speech/language evolution and related disorders.
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BAP1 Tumor Predisposition Syndrome Presenting as a Recurrent Ovarian Sex Cord-Stromal Tumor.
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BIN1 is reduced and Cav1.2 trafficking is impaired in human failing cardiomyocytes.
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Bevacizumab for patients with metastatic renal cancer: an update.
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Bmp and Fgf signaling are essential for liver specification in zebrafish.
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CTLA-4-Mediated inhibition of early events of T cell proliferation.
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CYLD inhibits melanoma growth and progression through suppression of the JNK/AP-1 and β1-integrin signaling pathways.
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CYLD inhibits tumorigenesis and metastasis by blocking JNK/AP1 signaling at multiple levels.
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Cancer and Leukemia Group B 90206: A randomized phase III trial of interferon-alpha or interferon-alpha plus anti-vascular endothelial growth factor antibody (bevacizumab) in metastatic renal cell carcinoma.
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Carcinogen 7,12-dimethylbenz[a]anthracene-induced mammary tumorigenesis is accelerated in Smad3 heterozygous mice compared to Smad3 wild type mice.
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Carcinogenicity of a nephrotoxic metabolite of the "nongenotoxic" carcinogen hydroquinone.
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Cardiac BIN1 folds T-tubule membrane, controlling ion flux and limiting arrhythmia.
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Cell biology: A BID for the pathway.
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Cell cycle deregulation and xeroderma pigmentosum group C cell transformation.
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Cell cycle. Checking two steps.
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Cell proliferation is insufficient, but loss of tuberin is necessary, for chemically induced nephrocarcinogenicity.
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Cell-Based Therapy Restores Olfactory Function in an Inducible Model of Hyposmia.
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Characterization of interactions between PinX1 and human telomerase subunits hTERT and hTR.
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Characterization of the porcine ATM gene: towards the generation of a novel non-murine animal model for Ataxia-Telangiectasia.
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Chloroquine improves survival and hematopoietic recovery after lethal low-dose-rate radiation.
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Chromium (VI) activates ataxia telangiectasia mutated (ATM) protein. Requirement of ATM for both apoptosis and recovery from terminal growth arrest.
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Cilengitide with metronomic temozolomide, procarbazine, and standard radiotherapy in patients with glioblastoma and unmethylated MGMT gene promoter in ExCentric, an open-label phase II trial.
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Combined effects of the p53 and p73 polymorphisms on lung cancer risk.
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Combined effects of the p53 codon 72 and p73 G4C14-to-A4T14 polymorphisms on the risk of HPV16-associated oral cancer in never-smokers.
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Combined p53-related genetic variants together with HPV infection increase oral cancer risk.
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Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium.
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Common non-synonymous polymorphisms in the BRCA1 Associated RING Domain (BARD1) gene are associated with breast cancer susceptibility: a case-control analysis.
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Completeness of required site-specific factors for brain and CNS tumors in the Surveillance, Epidemiology and End Results (SEER) 18 database (2004-2012, varying).
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Comprehensive Molecular and Pathologic Evaluation of Transitional Mesothelioma Assisted by Deep Learning Approach: A Multi-Institutional Study of the International Mesothelioma Panel from the MESOPATH Reference Center.
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Comprehensive genomic characterization defines human glioblastoma genes and core pathways.
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Congenital cystic hemangioblastomas of the cerebral hemisphere in a neonate without alteration in the VHL gene.
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Contextual tumor suppressor function of T cell death-associated gene 8 (TDAG8) in hematological malignancies.
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Convergence of the fanconi anemia and ataxia telangiectasia signaling pathways.
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Critical role of the tumor suppressor tuberous sclerosis complex 1 in dendritic cell activation of CD4 T cells by promoting MHC class II expression via IRF4 and CIITA.
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DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors.
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DNA damage activates ATM through intermolecular autophosphorylation and dimer dissociation.
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DNA damage responses: mechanisms and roles in human disease: 2007 G.H.A. Clowes Memorial Award Lecture.
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DOK2 inhibits EGFR-mutated lung adenocarcinoma.
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Decrease in the lgl tumor suppressor dose in Drosophila increases survival and longevity in stress conditions.
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Degradation of the tumor suppressor PML by Pin1 contributes to the cancer phenotype of breast cancer MDA-MB-231 cells.
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Deletions and point mutations of p16,p15 gene in primary tumors and tumor cell lines.
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Depression in pregnancy, infant birth weight and DNA methylation of imprint regulatory elements.
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Design of potent thiophene inhibitors of polo-like kinase 1 with improved solubility and reduced protein binding.
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Development of the human female reproductive tract.
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Differential cellular localization of CELSR2 and ING4 and correlations with hormone receptor status in breast cancer.
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Differential expression of p63 isoforms in female reproductive organs.
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Differential responsiveness of MCF-7 human breast cancer cell line stocks to the pineal hormone, melatonin.
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Dinucleotide polymorphism of p73 gene is associated with a reduced risk of lung cancer in a Chinese population.
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Disappearance of the telomere dysfunction-induced stress response in fully senescent cells.
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Distinct IL-2 receptor signaling pattern in CD4+CD25+ regulatory T cells.
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Distinct functional domains of Nbs1 modulate the timing and magnitude of ATM activation after low doses of ionizing radiation.
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Distinct functions of Nijmegen breakage syndrome in ataxia telangiectasia mutated-dependent responses to DNA damage.
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Distinct roles of the co-activators p300 and CBP in retinoic-acid-induced F9-cell differentiation.
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Downregulation of TSLC1 and DAL-1 expression occurs frequently in breast cancer.
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Dysregulation of the mTOR pathway secondary to mutations or a hostile microenvironment contributes to cancer and poor wound healing.
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E2F4-RB and E2F4-p107 complexes suppress gene expression by transforming growth factor beta through E2F binding sites.
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EURACAN/IASLC Proposals for Updating the Histologic Classification of Pleural Mesothelioma: Towards a More Multidisciplinary Approach.
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Effect of Nivolumab vs Bevacizumab in Patients With Recurrent Glioblastoma: The CheckMate 143 Phase 3 Randomized Clinical Trial.
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Endosome and INPP4B.
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Epidermal growth factor regulates hematopoietic regeneration after radiation injury.
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Epigenetic silencing of tumor suppressor Par-4 promotes chemoresistance in recurrent breast cancer.
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Estrogen treatment enhances hereditary renal tumor development in Eker rats.
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Everolimus tablets for patients with subependymal giant cell astrocytoma.
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Evidence from molecular cloning that SPARC, a major product of mouse embryo parietal endoderm, is related to an endothelial cell 'culture shock' glycoprotein of Mr 43,000.
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Exome sequencing identifies distinct mutational patterns in liver fluke-related and non-infection-related bile duct cancers.
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Exome-wide Sequencing Shows Low Mutation Rates and Identifies Novel Mutated Genes in Seminomas.
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Expansion of adult beta-cell mass in response to increased metabolic demand is dependent on HNF-4alpha.
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Expression and assay of recombinant ATM.
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Expression of p27 in residual rectal cancer after preoperative chemoradiation predicts long-term outcome.
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Fatty acid synthase inhibition engages a novel caspase-2 regulatory mechanism to induce ovarian cancer cell death.
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Fine mapping of genetic variants in BIN1, CLU, CR1 and PICALM for association with cerebrospinal fluid biomarkers for Alzheimer's disease.
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Flavopiridol induces apoptosis in chronic lymphocytic leukemia cells via activation of caspase-3 without evidence of bcl-2 modulation or dependence on functional p53.
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Fragments of ATM which have dominant-negative or complementing activity.
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Frequent engagement of the classical and alternative NF-kappaB pathways by diverse genetic abnormalities in multiple myeloma.
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Frequent inactivation of PTEN by promoter hypermethylation in microsatellite instability-high sporadic colorectal cancers.
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Functional assessment of variants in the TSC1 and TSC2 genes identified in individuals with Tuberous Sclerosis Complex.
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Functional variations in the ATM gene and susceptibility to differentiated thyroid carcinoma.
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GPR54 is a target for suppression of metastasis in endometrial cancer.
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Gene expression profiling and genetic markers in glioblastoma survival.
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Gene expression profiling reveals progesterone-mediated cell cycle and immunoregulatory roles of Hoxa-10 in the preimplantation uterus.
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Gene markers in brain tumors: what the epileptologist should know.
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Generation of S phase-dependent DNA double-strand breaks by Cr(VI) exposure: involvement of ATM in Cr(VI) induction of gamma-H2AX.
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Genetic Determinants of Outcome in Intrahepatic Cholangiocarcinoma.
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Genetic polymorphisms of ataxia telangiectasia mutated and breast cancer risk.
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Genetic variants in MGMT and risk of lung cancer in Southeastern Chinese: a haplotype-based analysis.
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Genetic variants in p53-related genes confer susceptibility to second primary malignancy in patients with index squamous cell carcinoma of head and neck.
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Genetic variants of the p53 and p73 genes jointly increase risk of second primary malignancies in patients after index squamous cell carcinoma of the head and neck.
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Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer.
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Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians.
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Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.
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Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos.
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Genome-wide linkage scan for prostate cancer susceptibility from the University of Michigan Prostate Cancer Genetics Project: suggestive evidence for linkage at 16q23.
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Genomic analysis demonstrates that histologically-defined astroblastomas are molecularly heterogeneous and that tumors with MN1 rearrangement exhibit the most favorable prognosis.
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Genomic and Molecular Landscape of DNA Damage Repair Deficiency across The Cancer Genome Atlas.
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Genotoxic stress regulates expression of the proto-oncogene Bcl6 in germinal center B cells.
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Genotypic analysis of tumor suppressor genes PTEN/MMAC1 and p53 in head and neck squamous cell carcinomas.
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Germline genetic variants in men with prostate cancer and one or more additional cancers.
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Gli Transcription Factors Mediate the Oncogenic Transformation of Prostate Basal Cells Induced by a Kras-Androgen Receptor Axis.
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Glucose metabolism attenuates p53 and Puma-dependent cell death upon growth factor deprivation.
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HIN-1, a putative cytokine highly expressed in normal but not cancerous mammary epithelial cells.
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HSV-1 amplicon vector-mediated expression of ATM cDNA and correction of the ataxia-telangiectasia cellular phenotype.
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HTS-Compatible CometChip Enables Genetic Screening for Modulators of Apoptosis and DNA Double-Strand Break Repair.
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Hepatic mTORC1 Opposes Impaired Insulin Action to Control Mitochondrial Metabolism in Obesity.
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Hereditary renal cell carcinoma in the Eker rat: a unique animal model for the study of cancer susceptibility.
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Hsp 70/Hsp 90 organizing protein as a nitrosylation target in cystic fibrosis therapy.
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Human T-cell leukemia virus type 1 tax attenuates the ATM-mediated cellular DNA damage response.
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Human adipocyte lipid-binding protein: purification of the protein and cloning of its complementary DNA.
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Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouse.
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Human syngeneic intestinal transplantation: evaluation of enterocyte viability with serum levels of intestinal fatty acid binding protein.
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Ibudilast sensitizes glioblastoma to temozolomide by targeting Macrophage Migration Inhibitory Factor (MIF).
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Identification of cis-suppression of human disease mutations by comparative genomics.
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Immunogenetic Determinants of Susceptibility to Head and Neck Cancer in the Million Veteran Program Cohort.
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Immunohistochemical [corrected] detection of the alternate INK4a-encoded tumor suppressor protein p14(ARF) in archival human cancers and cell lines using commercial antibodies: correlation with p16(INK4a) expression.
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Immunohistochemical localization of netrin-1 in the embryonic chick nervous system.
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Immunologic escape after prolonged progression-free survival with epidermal growth factor receptor variant III peptide vaccination in patients with newly diagnosed glioblastoma.
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In vitro biological activity of a novel small-molecule inhibitor of polo-like kinase 1.
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Influence of ATM function on telomere metabolism.
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Inhibition of vascular smooth muscle cell proliferation, migration, and survival by the tumor suppressor protein PTEN.
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Initial testing (stage 1) of temozolomide by the pediatric preclinical testing program.
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Initial testing (stage 1) of the PARP inhibitor BMN 673 by the pediatric preclinical testing program: PALB2 mutation predicts exceptional in vivo response to BMN 673.
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Inositol diphosphate signaling regulates telomere length.
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Insulin inhibits dexamethasone effect on angiotensinogen gene expression and induction of hypertrophy in rat kidney proximal tubular cells in high glucose.
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Integrated genomic analyses identify ERRFI1 and TACC3 as glioblastoma-targeted genes.
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Integrated genomic profiling of chronic lymphocytic leukemia identifies subtypes of deletion 13q14.
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Integrative Molecular Characterization of Malignant Pleural Mesothelioma.
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Integrin acts upstream of netrin signaling to regulate formation of the anchor cell's invasive membrane in C. elegans.
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Integrin-β1 is required for the renal cystogenesis caused by ciliary defects.
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Interactions of TLC1 (which encodes the RNA subunit of telomerase), TEL1, and MEC1 in regulating telomere length in the yeast Saccharomyces cerevisiae.
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Intracellular lipid metabolism impairs β cell compensation during diet-induced obesity.
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Involvement of the MKK6-p38gamma cascade in gamma-radiation-induced cell cycle arrest.
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Involvement of the cohesin protein, Smc1, in Atm-dependent and independent responses to DNA damage.
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Ionizing radiation activates the ATM kinase throughout the cell cycle.
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Isoform-Specific Effects of Wild-Type Ras Genes on Carcinogen-Induced Lung Tumorigenesis in Mice.
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Isolation of unique STAT5 targets by chromatin immunoprecipitation-based gene identification.
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Knockin mice expressing a chimeric p53 protein reveal mechanistic differences in how p53 triggers apoptosis and senescence.
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Knocking out lca5 in zebrafish causes cone-rod dystrophy due to impaired outer segment protein trafficking.
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LRIG1 is a pleiotropic androgen receptor-regulated feedback tumor suppressor in prostate cancer.
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Lack of cyclin-dependent kinase 4 inhibits c-myc tumorigenic activities in epithelial tissues.
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Lack of utility of intestinal fatty acid binding protein levels in predicting intestinal allograft rejection.
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Large-scale analysis of BAP1 expression reveals novel associations with clinical and molecular features of malignant pleural mesothelioma.
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Lead Exposure during Early Human Development and DNA Methylation of Imprinted Gene Regulatory Elements in Adulthood.
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Loss of G(1)/S checkpoint in human immunodeficiency virus type 1-infected cells is associated with a lack of cyclin-dependent kinase inhibitor p21/Waf1.
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Loss of Nuclear Localized Parathyroid Hormone-Related Protein in Primary Breast Cancer Predicts Poor Clinical Outcome and Correlates with Suppressed Stat5 Signaling.
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Loss of PTEN/MMAC1/TEP in EGF receptor-expressing tumor cells counteracts the antitumor action of EGFR tyrosine kinase inhibitors.
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Loss of atm radiosensitizes multiple p53 null tissues.
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Loss of nuclear localized and tyrosine phosphorylated Stat5 in breast cancer predicts poor clinical outcome and increased risk of antiestrogen therapy failure.
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Loss of the mismatch repair protein MSH6 in human glioblastomas is associated with tumor progression during temozolomide treatment.
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Loss of tumor suppressor IGFBP4 drives epigenetic reprogramming in hepatic carcinogenesis.
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Low-dose genistein induces cyclin-dependent kinase inhibitors and G(1) cell-cycle arrest in human prostate cancer cells.
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MGMT immunoexpression in silent subtype 3 pituitary adenomas: possible therapeutic implications.
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MGMT immunoexpression predicts responsiveness of pituitary tumors to temozolomide therapy.
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MGMT: Immunohistochemical Detection in High-Grade Astrocytomas.
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Macrophage cells secrete factors including LRP1 that orchestrate the rejuvenation of bone repair in mice.
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Malignant Mesothelioma and Its Non-Asbestos Causes.
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Malignant Mesothelioma in Individuals With Nonmesothelial Neoplasms.
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Mammalian target of rapamycin (mTOR) activation increases axonal growth capacity of injured peripheral nerves.
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Maternal B vitamins: effects on offspring weight and DNA methylation at genomically imprinted domains.
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Mechanism of inactivation of CDKN2 and MTS2 in non-small cell lung cancer and association with advanced stage.
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Mechanisms of action of rapamycin in gliomas.
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Metformin, independent of AMPK, inhibits mTORC1 in a rag GTPase-dependent manner.
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Microcell-mediated chromosome transfer identifies EPB41L3 as a functional suppressor of epithelial ovarian cancers.
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Mig-6 modulates uterine steroid hormone responsiveness and exhibits altered expression in endometrial disease.
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Mismatch repair deficiency: a temozolomide resistance factor in medulloblastoma cell lines that is uncommon in primary medulloblastoma tumours.
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Missense Variants in RHOBTB2 Cause a Developmental and Epileptic Encephalopathy in Humans, and Altered Levels Cause Neurological Defects in Drosophila.
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Mitochondrial dysfunction in ataxia-telangiectasia.
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Molecular Analysis of a Patient With Neurofibromatosis 2 (NF2) and Peritoneal Malignant Mesothelioma.
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Molecular alternations in uveal melanoma.
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Molecular analysis of P16(Ink4)/CDKN2 and P15(INK4B)/MTS2 genes in primary human testicular germ cell tumors.
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Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.
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Molecular genetic aspects of oligodendrogliomas including analysis by comparative genomic hybridization.
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Molecular genetic parameters in pathogenesis and prognosis of testicular germ cell tumors.
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Molecular pathogenesis of malignant gliomas.
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Molecular pathways: translational and therapeutic implications of the Notch signaling pathway in cancer.
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Molecular subtypes of diffuse large B-cell lymphoma arise by distinct genetic pathways.
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Multiple Genetically Distinct Uveal Melanomas Arise in the Same Eye of Two Patients with Melanosis Oculi.
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Multiple signaling pathways involving ATM.
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Muscle atrophy in transgenic mice expressing a human TSC1 transgene.
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Mutagenicity and carcinogenicity of biological reactive intermediate's derived from a "non-genotoxic" carcinogen.
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Mutation analysis of the TSC2 gene in an African-American family.
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Mutation and polymorphism analysis in the tuberous sclerosis 2 (TSC2) gene.
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Mutation of the PTEN tumor suppressor gene in endometrial hyperplasias.
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Mutation of the PTEN tumor suppressor gene is not a feature of ovarian cancers.
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Mutational analysis of the PTEN gene in human uterine sarcomas.
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Netrin-1 and peripheral nerve regeneration in the adult rat.
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Netrin-1-mediated axon guidance in mouse embryonic stem cells overexpressing neurogenin-1.
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Neurotrophins and netrins require calcineurin/NFAT signaling to stimulate outgrowth of embryonic axons.
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Newborns of obese parents have altered DNA methylation patterns at imprinted genes.
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Novel role for Netrins in regulating epithelial behavior during lung branching morphogenesis.
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O6-Methylguanine DNA Methyltransferase Status Does Not Predict Response or Resistance to Alkylating Agents in Well-Differentiated Pancreatic Neuroendocrine Tumors.
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Our cells get stressed too! Implications for human disease.
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PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS.
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PI3K/Akt and apoptosis: size matters.
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PIN1, the cell cycle and cancer.
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PTEN as an effector in the signaling of antimigratory G protein-coupled receptor.
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PTEN modulates vascular endothelial growth factor-mediated signaling and angiogenic effects.
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PTEN mutation in endometrial cancers is associated with favorable clinical and pathologic characteristics.
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PTEN polymorphism (IVS4) is not associated with risk of prostate cancer.
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Paradoxical role of Id proteins in regulating tumorigenic potential of lymphoid cells.
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Partial denervation of sub-basal axons persists following debridement wounds to the mouse cornea.
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Participation of ATM in insulin signalling through phosphorylation of eIF-4E-binding protein 1.
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Pathogenic Germline Variants in 10,389 Adult Cancers.
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Pathway discovery in mantle cell lymphoma by integrated analysis of high-resolution gene expression and copy number profiling.
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Personalized and targeted therapy of esophageal squamous cell carcinoma: an update.
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Perturbed myoepithelial cell differentiation in BRCA mutation carriers and in ductal carcinoma in situ.
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Phosphoinositide 3-kinase regulates beta2-adrenergic receptor endocytosis by AP-2 recruitment to the receptor/beta-arrestin complex.
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Phosphorylation of FEZ1 by Microtubule Affinity Regulating Kinases regulates its function in presynaptic protein trafficking.
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Phosphorylation of SMC1 is a critical downstream event in the ATM-NBS1-BRCA1 pathway.
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Phosphorylation of serine 1387 in Brca1 is specifically required for the Atm-mediated S-phase checkpoint after ionizing irradiation.
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Pills of PTEN? In and out for tumor suppression.
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Polycystic kidney disease as a result of loss of the tuberous sclerosis 2 tumor suppressor gene during development.
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Polymorphisms of TP53 Arg72Pro, but not p73 G4C14>A4TA4 and p21 Ser31Arg, contribute to risk of cutaneous melanoma.
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Polymorphisms of p16, p27, p73, and MDM2 modulate response and survival of pancreatic cancer patients treated with preoperative chemoradiation.
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Polymorphisms of the DNA repair gene MGMT and risk and progression of head and neck cancer.
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Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery disease.
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Positive selection in noncoding genomic regions of vocal learning birds is associated with genes implicated in vocal learning and speech functions in humans.
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Potential role of PTEN phosphatase in ethanol-impaired survival signaling in the liver.
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Primary cilia attenuate hedgehog signalling in neoplastic chondrocytes.
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Prognostic methylation markers for overall survival in cytogenetically normal patients with acute myeloid leukemia treated on SWOG trials.
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Protein kinase activity of Tel1p and Mec1p, two Saccharomyces cerevisiae proteins related to the human ATM protein kinase.
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Protein patterns and proteins that identify subtypes of glioblastoma multiforme.
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Proteolysis of Rad17 by Cdh1/APC regulates checkpoint termination and recovery from genotoxic stress.
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Quantitative detection of RASSF1A DNA promoter methylation in tumors and serum of patients with serous epithelial ovarian cancer.
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RASSF4 is required for skeletal muscle differentiation.
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Racial disparity in the frequency of PTEN mutations, but not microsatellite instability, in advanced endometrial cancers.
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Radiotherapy combined with nivolumab or temozolomide for newly diagnosed glioblastoma with unmethylated MGMT promoter: An international randomized phase III trial.
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Rapamycin and p53 act on different pathways to induce G1 arrest in mammalian cells.
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RasGRP1 is a potential biomarker to stratify anti-EGFR therapy response in colorectal cancer.
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Re-examination of CD91 function in GRP94 (glycoprotein 96) surface binding, uptake, and peptide cross-presentation.
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Reactivation of PTEN tumor suppressor for cancer treatment through inhibition of a MYC-WWP1 inhibitory pathway.
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Receptor signaling in immune cell development and function.
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Receptor-recognized α₂-macroglobulin binds to cell surface-associated GRP78 and activates mTORC1 and mTORC2 signaling in prostate cancer cells.
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Reciprocal control of Forkhead box O 3a and c-Myc via the phosphatidylinositol 3-kinase pathway coordinately regulates p27Kip1 levels.
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Regulation of T-cell survival and mitochondrial homeostasis by TSC1.
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Regulation of mast cell survival and function by tuberous sclerosis complex 1.
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Renal cell carcinoma development in the rat independent of alterations at the VHL gene locus.
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Replication of genome-wide association signals of type 2 diabetes in Han Chinese in a prospective cohort.
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Requirement of protein phosphatase 5 in DNA-damage-induced ATM activation.
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Role of tumor suppressor TSC1 in regulating antigen-specific primary and memory CD8 T cell responses to bacterial infection.
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Roles of ATM and NBS1 in chromatin structure modulation and DNA double-strand break repair.
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SPOP Promotes Ubiquitination and Degradation of the ERG Oncoprotein to Suppress Prostate Cancer Progression.
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STAT1-induced ASPP2 transcription identifies a link between neuroinflammation, cell polarity, and tumor suppression.
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Sequencing Analysis at 8p23 Identifies Multiple Rare Variants in DLC1 Associated with Sleep-Related Oxyhemoglobin Saturation Level.
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Single nucleotide polymorphisms of RecQ1, RAD54L, and ATM genes are associated with reduced survival of pancreatic cancer.
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Specificity protein 1-modulated superoxide dismutase 2 enhances temozolomide resistance in glioblastoma, which is independent of O6-methylguanine-DNA methyltransferase.
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Structure and regulation of the mouse ing1 gene. Three alternative transcripts encode two phd finger proteins that have opposite effects on p53 function.
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Substrate specificities and identification of putative substrates of ATM kinase family members.
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Subtyping sub-Saharan esophageal squamous cell carcinoma by comprehensive molecular analysis.
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Suppression of PGC-1α Is Critical for Reprogramming Oxidative Metabolism in Renal Cell Carcinoma.
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Suppression of tumorigenesis and induction of p15(ink4b) by Smad4/DPC4 in human pancreatic cancer cells.
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Suppressor and activator functions mediated by a repeated heptad sequence in the liver fatty acid-binding protein gene (Fabpl). Effects on renal, small intestinal, and colonic epithelial cell gene expression in transgenic mice.
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Survival Outcomes of Elderly Patients With Glioblastoma Multiforme in Their 75th Year or Older Treated With Adjuvant Therapy.
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Sustained activation of mTORC1 in macrophages increases AMPKα-dependent autophagy to maintain cellular homeostasis.
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Systemic inflammatory response syndrome after human syngeneic intestinal transplantation: evidence for disruption of enterocyte barrier function.
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TSC1 Promotes B Cell Maturation but Is Dispensable for Germinal Center Formation.
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Targeting lysosomal degradation induces p53-dependent cell death and prevents cancer in mouse models of lymphomagenesis.
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Targeting methylguanine-DNA methyltransferase in the treatment of neuroblastoma.
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Targeting the ATM Kinase to Enhance the Efficacy of Radiotherapy and Outcomes for Cancer Patients.
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Testing hypotheses for the functions of APC family proteins using null and truncation alleles in Drosophila.
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Tetraspanin CD37 protects against the development of B cell lymphoma.
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The 2015 World Health Organization Classification of Tumors of the Pleura: Advances since the 2004 Classification.
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The 2021 WHO Classification of Tumors of the Pleura: Advances Since the 2015 Classification.
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The ATM-dependent DNA damage signaling pathway.
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The BIN1 rs744373 SNP is associated with increased tau-PET levels and impaired memory.
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The Cancer Genome Atlas Comprehensive Molecular Characterization of Renal Cell Carcinoma.
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The FNIP co-chaperones decelerate the Hsp90 chaperone cycle and enhance drug binding.
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The Genetic Basis of Hepatosplenic T-cell Lymphoma.
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The PI 3-kinase/Akt signaling pathway is activated due to aberrant Pten expression and targets transcription factors NF-kappaB and c-Myc in pancreatic cancer cells.
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The Rad50S allele promotes ATM-dependent DNA damage responses and suppresses ATM deficiency: implications for the Mre11 complex as a DNA damage sensor.
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The Role of EBV-Induced Hypermethylation in Gastric Cancer Tumorigenesis.
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The activity of letrozole in patients with advanced or recurrent endometrial cancer and correlation with biological markers--a study of the National Cancer Institute of Canada Clinical Trials Group.
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The amphiphysin-like protein 1 (ALP1) interacts functionally with the cABL tyrosine kinase and may play a role in cytoskeletal regulation.
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The functions and regulation of the PTEN tumour suppressor: new modes and prospects.
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The genomic landscape of familial glioma.
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The glucocorticoid receptor interacting protein 1 (GRIP1) localizes in discrete nuclear foci that associate with ND10 bodies and are enriched in components of the 26S proteasome.
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The many substrates and functions of ATM.
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The role and regulation of mTOR in T-lymphocyte function.
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The role of tuberous sclerosis complex 1 in regulating innate immunity.
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The telomeric protein TRF2 binds the ATM kinase and can inhibit the ATM-dependent DNA damage response.
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The tumor suppressor folliculin inhibits lactate dehydrogenase A and regulates the Warburg effect.
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The viral oncoprotein E1A blocks transforming growth factor beta-mediated induction of p21/WAF1/Cip1 and p15/INK4B.
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The von Hippel-Lindau protein, vascular endothelial growth factor, and kidney cancer.
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The von Hippel-Lindau tumor suppressor gene and kidney cancer.
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The von Hippel-Lindau tumor suppressor gene inhibits hepatocyte growth factor/scatter factor-induced invasion and branching morphogenesis in renal carcinoma cells.
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Transforming growth factor beta activates the promoter of cyclin-dependent kinase inhibitor p15INK4B through an Sp1 consensus site.
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Transforming growth factor-beta-mediated p15(INK4B) induction and growth inhibition in astrocytes is SMAD3-dependent and a pathway prominently altered in human glioma cell lines.
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Transient inhibition of ATM kinase is sufficient to enhance cellular sensitivity to ionizing radiation.
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Trefoil factor 1 acts to suppress senescence induced by oncogene activation during the cellular transformation process.
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Tuberin-dependent membrane localization of polycystin-1: a functional link between polycystic kidney disease and the TSC2 tumor suppressor gene.
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Tuberous sclerosis 1 promotes invariant NKT cell anergy and inhibits invariant NKT cell-mediated antitumor immunity.
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Tumor suppressor MMAC/PTEN inhibits cytokine-induced NFkappaB activation without interfering with the IkappaB degradation pathway.
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Tumor suppressor TSC1 is critical for T-cell anergy.
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Twenty-year survival in glioblastoma: a case report and molecular profile.
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Two mammalian longevity assurance gene (LAG1) family members, trh1 and trh4, regulate dihydroceramide synthesis using different fatty acyl-CoA donors.
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Two molecularly distinct G(2)/M checkpoints are induced by ionizing irradiation.
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Two novel TP63 mutations associated with the ankyloblepharon, ectodermal defects, and cleft lip and palate syndrome: a skin fragility phenotype.
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Tyrosine kinase inhibitors in renal cell carcinoma.
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Veliparib in combination with radiotherapy for the treatment of MGMT unmethylated glioblastoma.
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Widespread activation of the DNA damage response in human pancreatic intraepithelial neoplasia.
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[Cowden disease].
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iNKT cells require TSC1 for terminal maturation and effector lineage fate decisions.
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miR-203, a tumor suppressor frequently down-regulated by promoter hypermethylation in rhabdomyosarcoma.
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p27 and cyclin D1 abnormalities in uterine papillary serous carcinoma.
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p53 and ATM: cell cycle, cell death, and cancer.
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p53: a two-faced cancer gene.
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p63 expression confers significantly better survival outcomes in high-risk diffuse large B-cell lymphoma and demonstrates p53-like and p53-independent tumor suppressor function.
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p63 expression profile in normal and malignant prostate epithelial cells.
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p63, a p53 homolog at 3q27-29, encodes multiple products with transactivating, death-inducing, and dominant-negative activities.
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p73 G4C14-to-A4T14 gene polymorphism and interaction with p53 exon 4 Arg72Pro on cancer susceptibility: a meta-analysis of the literature.
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p73 G4C14-to-A4T14 polymorphism and risk of human papillomavirus-associated squamous cell carcinoma of the oropharynx in never smokers and never drinkers.
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p73 G4C14-to-A4T14 polymorphism and risk of lung cancer.
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p73 G4C14-to-A4T14 polymorphism and risk of second primary malignancy after index squamous cell carcinoma of head and neck.
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Keywords of People
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Bejsovec, Amy,
Associate Professor of Biology,
Biology
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Berchuck, Andrew,
James M. Ingram Distinguished Professor of Gynecologic Oncology,
Obstetrics and Gynecology, Gynecologic Oncology
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Chen, Ming,
Associate Professor in Pathology,
Cell Biology
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Gunn, Michael Dee,
Professor of Medicine,
Integrative Immunobiology
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Hogan, Brigid L. M.,
Research Professor of Cell Biology,
Cell Biology
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Luftig, Micah Alan,
Professor of Molecular Genetics and Microbiology,
Cell Biology
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McLendon, Roger Edwin,
Professor of Pathology,
Pathology
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Sampson, John Howard,
Robert H., M.D. and Gloria Wilkins Professor of Neurosurgery, in the School of Medicine,
Biomedical Engineering
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Zhong, Xiaoping,
Professor of Pediatrics,
Integrative Immunobiology