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Subject Areas on Research
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5-[211 At]astato-2'-deoxyuridine, an alpha particle-emitting endoradiotherapeutic agent undergoing DNA incorporation.
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A functional isoform of the human granulocyte/macrophage colony-stimulating factor receptor has an unusual cytoplasmic domain.
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A histologic study (including DNA quantification and Ki-67 labeling index) in uveal melanomas after brachytherapy with ruthenium plaques.
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A map of human cancer signaling.
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A natural history of melanoma: serial gene expression analysis.
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A neural survival factor is a candidate oncogene in breast cancer.
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A phase II study of capecitabine, oxaliplatin, bevacizumab and cetuximab in the treatment of metastatic colorectal cancer.
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A single tube, four-color flow cytometry assay for evaluation of ZAP-70 and CD38 expression in chronic lymphocytic leukemia.
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A statistic for comparing two correlated markers which are prognostic for time to an event.
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A transcriptional repressor of osteopontin expression in the 4T1 murine breast cancer cell line.
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A variant of the DNA repair gene XRCC3 and risk of squamous cell carcinoma of the head and neck: a case-control analysis.
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APC promoter hypermethylation contributes to the loss of APC expression in colorectal cancers with allelic loss on 5q.
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Aberrant expression of cell-cycle regulatory proteins in human mesenchymal neoplasia.
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Aberrant splicing of the TSG101 tumor suppressor gene in human breast and ovarian cancers.
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Abnormal expression of cell cycle regulatory proteins in ductal and lobular carcinomas of the breast.
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Absence of a correlation of androgen receptor gene CAG repeat length and prostate cancer risk in an African-American population.
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Absent ras gene mutations in human adrenal cortical neoplasms and pheochromocytomas.
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Allele loss on chromosome 1p36 in epithelial ovarian cancers.
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Allelotype analysis of uterine leiomyoma: localization of a potential tumor suppressor gene to a 4-cM region of chromosome 7q.
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Alteration of the tumor suppressor gene p53 in a high fraction of hormone refractory prostate cancer.
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Amplification of telomeric DNA directly correlates with metastatic potential of human and murine cancers of various histological origin.
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Amplification of the c-myc gene in human medulloblastoma cell lines and xenografts.
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An efficient multiple-exposure analysis of the toxicity of crisnatol, a DNA intercalator in phase II clinical trials.
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An in vitro assay procedure to test chemotherapeutic drugs on cells from human solid tumors.
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Analysis of genetic alterations in uterine leiomyomas and leiomyosarcomas by comparative genomic hybridization.
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Analysis of homeobox gene HOXA10 mutations in cryptorchidism.
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Androgen receptor mutations in androgen-independent prostate cancer: Cancer and Leukemia Group B Study 9663.
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Aneuploid subpopulations in tumour-invaded lymph nodes from breast cancer patients.
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Antineoplastic activity of a series of boron analogues of alpha-amino acids.
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Antineoplastic activity of boron-containing thymidine nucleosides in Tmolt3 leukemic cells.
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Antineoplastic activity of tetrakis-mu-(trimethylamine-boranecarboxylato)-bis (trimethylamine-carboxyborane)dicopper (II) in Ehrlich ascites carcinoma.
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Array CGH profiling of favourable histology Wilms tumours reveals novel gains and losses associated with relapse.
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Array comparative genomic hybridisation (aCGH) analysis of premenopausal breast cancers from a nuclear fallout area and matched cases from Western New York.
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Array-based comparative genomic hybridization from formalin-fixed, paraffin-embedded breast tumors.
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Assessment of pancreatic duct strictures.
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Association between ratio of matrix metalloproteinase-1 to tissue inhibitor of metalloproteinase-1 and local recurrence, metastasis, and survival in human chondrosarcoma.
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Association of chromosome 11 locus D11S12 with histology, stage, and metastases in lung cancer.
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Association of genomic subtypes of lower-grade gliomas with shape features automatically extracted by a deep learning algorithm.
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AutoCSA, an algorithm for high throughput DNA sequence variant detection in cancer genomes.
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BP1, a new homeobox gene, is frequently expressed in acute leukemias.
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BRCA1 expression is induced before DNA synthesis in both normal and tumor-derived breast cells.
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BRCA1 maps proximal to D17S579 on chromosome 17q21 by genetic analysis.
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Bayesian analysis of binary prediction tree models for retrospectively sampled outcomes.
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Benign nodal nevi frequently harbor the activating V600E BRAF mutation.
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Bilateral diffuse uveal melanocytic proliferation associated with pancreatic carcinoma: a case report and literature review of this paraneoplastic syndrome.
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Biphasic malignant meningioma: a comparative genomic hybridization study.
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Both BRAF V600E mutation and older age (≥ 65 years) are associated with recurrent papillary thyroid cancer.
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Breakpoints of the t(11;18)(q21;q21) in mucosa-associated lymphoid tissue (MALT) lymphoma lie within or near the previously undescribed gene MALT1 in chromosome 18.
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Brief report: lymphoma of donor origin occurring in the porta hepatis of a transplanted liver.
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C-reactive protein as a marker of melanoma progression.
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CDKN2 in HPV-positive and HPV-negative cervical-carcinoma cell lines.
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CDKN2A promoter methylation in gastric adenocarcinomas: clinical variables.
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CORRELATION OF GENE EXPRESSION PROFILE STATUS AND AMERICAN JOINT COMMISSION ON CANCER STAGE IN UVEAL MELANOMA.
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Caspase 8 is absent or low in many ex vivo gliomas.
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Caspase-8 levels correlate with the expression of signal transducer and activator of transcription 1 in high-grade but not lower grade neuroblastoma.
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Cell cycle kinetic effects of tamoxifen on human breast cancer cells. Flow cytometric analyses of DNA content, BrdU labeling, Ki-67, PCNA, and statin expression.
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Characterization of the DNase I hypersensitive site 3' of the human beta globin gene domain.
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Characterization of the epidermal growth factor receptor in human glioma cell lines and xenografts.
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Characterization of the mouse FTZ-F1 gene, which encodes a key regulator of steroid hydroxylase gene expression.
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Chemotherapy-induced apoptosis in epithelial ovarian cancers.
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Cholera toxin and cell growth: role of membrane gangliosides.
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Chromosomal aberrations of primary lung adenocarcinomas in nonsmokers.
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Chromosome 3 analysis of uveal melanoma using fine-needle aspiration biopsy at the time of plaque radiotherapy in 140 consecutive cases.
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Chromosome 3 analysis of uveal melanoma using fine-needle aspiration biopsy at the time of plaque radiotherapy in 140 consecutive cases: the Deborah Iverson, MD, Lectureship.
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Circulating mutational portrait of cancer: manifestation of aggressive clonal events in both early and late stages.
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Clinical performance and utility of a DNA methylation urine test for bladder cancer.
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Clinical pharmacodynamics of high-dose methotrexate in acute lymphocytic leukemia. Identification of a relation between concentration and effect.
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Clinical utility of FoundationOne tissue molecular profiling in men with metastatic prostate cancer.
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Clonal origin of epithelial ovarian carcinoma: analysis by loss of heterozygosity, p53 mutation, and X-chromosome inactivation.
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Combining prostate specific antigen with cancer and gland volume to predict more reliably pathological stage: the influence of prostate specific antigen cancer density.
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Common variants within 6p21.31 locus are associated with chronic lymphocytic leukaemia and, potentially, other non-Hodgkin lymphoma subtypes.
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Common variation in Nemo-like kinase is associated with risk of ovarian cancer.
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Comparison of fluorescence in situ hybridization, cytogenetic analysis, and DNA index analysis to detect chromosomes 4 and 10 aneuploidy in pediatric acute lymphoblastic leukemia: a Pediatric Oncology Group study.
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Comprehensive DNA copy number profiling of meningioma using a chromosome 1 tiling path microarray identifies novel candidate tumor suppressor loci.
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Comprehensive, Integrative Genomic Analysis of Diffuse Lower-Grade Gliomas.
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Compromised HOXA5 function can limit p53 expression in human breast tumours.
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Constitutively active ESR1 mutations in gynecologic malignancies and clinical response to estrogen-receptor directed therapies.
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Correlation of DNA ploidy and histologic diagnosis from prostate core-needle biopsies: is DNA ploidy more sensitive than histology for the diagnosis of carcinoma in small specimens?
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Cyclin E overexpression relates to ovarian cancer histology but not to risk factors.
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Cytoplasmic and/or nuclear accumulation of the beta-catenin protein is a frequent event in human osteosarcoma.
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Cytotoxicity of alpha-particle-emitting 5-[211At]astato-2'-deoxyuridine in human cancer cells.
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DNA content and chromosomes in permanent cultured cell lines derived from malignant human gliomas.
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DNA hypermethylation within TERT promoter upregulates TERT expression in cancer.
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DNA in radical prostatectomy specimens. Prognostic value of tumor ploidy.
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DNA interstrand crosslinking and strand break repair in human glioma cell lines of varying [1,3-bis(2-chloroethyl)-1-nitrosourea] resistance.
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DNA methylation and ovarian cancer. I. Analysis of CpG island hypermethylation in human ovarian cancer using differential methylation hybridization.
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DNA mismatch repair and O6-alkylguanine-DNA alkyltransferase analysis and response to Temodal in newly diagnosed malignant glioma.
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DNA ploidy in nonseminomatous germ cell testicular tumor.
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DNA ploidy of malignant melanoma determined by image cytometry of fresh frozen and paraffin-embedded tissue.
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DNA repair in lymphoblastoid cell lines from patients with head and neck cancer.
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DNA repair: a double-edged sword.
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DNA-binding agents.
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DNA-binding agents.
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Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein.
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Detection and quantification of mutations in the plasma of patients with colorectal tumors.
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Detection of BRCA1 mutations in women with early-onset ovarian cancer by use of the protein truncation test.
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Detection of DNA damage in transcriptionally active genes by RT-PCR and assessment of repair of cisplatin-induced damage in the glutathione S-transferase-pi gene in human glioblastoma cells.
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Detection of circulating tumor DNA in early- and late-stage human malignancies.
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Detection of clonal lymphoid receptor gene rearrangements in langerhans cell histiocytosis.
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Detection of frequent allelic loss on proximal chromosome 17q in sporadic breast carcinoma using microsatellite length polymorphisms.
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Detection of mutated c-Ki-ras in the bile of patients with pancreatic cancer.
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Detection of stool DNA mutations before and after treatment of colorectal neoplasia.
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Dideoxy fingerprinting assay for BRCA1 mutation analysis.
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Differential gene expression patterns in HER2/neu-positive and -negative breast cancer cell lines and tissues.
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Differential inactivation of CDKN2 and Rb protein in non-small-cell and small-cell lung cancer cell lines.
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Differing molecular pathology of pancreatic adenocarcinoma in Egyptian and United States patients.
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Does phaster mean better?
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Dual role of glutathione in modulating camptothecin activity: depletion potentiates activity, but conjugation enhances the stability of the topoisomerase I-DNA cleavage complex.
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Electric field-mediated transport of plasmid DNA in tumor interstitium in vivo.
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Endogenous expression of transforming growth factor beta1 inhibits growth and tumorigenicity and enhances Fas-mediated apoptosis in a murine high-grade glioma model.
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Epidermal growth factor receptor gene analysis in renal cell carcinoma.
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Epigenetic silencing of genes in human colon cancer.
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Epstein-Barr virus in gastric adenocarcinomas: association with ethnicity and CDKN2A promoter methylation.
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Establishment and characterization of a new human prostatic carcinoma cell line (DuPro-1).
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Estrogen receptor alpha (ESR1) mutant A908G is not a common feature in benign and malignant proliferations of the breast.
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Etiology of the mutational spectrum of ras genes in human carcinomas.
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Evaluation of microsatellite instability, hMLH1 expression and hMLH1 promoter hypermethylation in defining the MSI phenotype of colorectal cancer.
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Expression of MAGE and GAGE in high-grade brain tumors: a potential target for specific immunotherapy and diagnostic markers.
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Expression of nucleotide excision repair proteins in lymphocytes as a marker of susceptibility to squamous cell carcinomas of the head and neck.
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Expression of osteocalcin and its transcriptional regulators core-binding factor alpha 1 and MSX2 in osteoid-forming tumours.
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Flow cytometric DNA analysis of interleukin-2 responsive renal cell carcinoma.
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Flow cytometric analysis of comedocarcinoma of the prostate: an uncommon histopathological variant of prostatic adenocarcinoma.
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Flow cytometric and quantitative histological parameters to predict occult disease in clinical stage I nonseminomatous testicular germ cell tumors.
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Flow cytometric assessment of deoxyribonucleic acid content in renal adenocarcinoma: does ploidy status enhance prognostic stratification over stage alone?
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Flow cytometric determination of ploidy in prostatic adenocarcinoma: a comparison with seminal vesicle involvement and histopathological grading as a predictor of clinical recurrence.
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Flow cytometry as a predictive indicator in patients with operable gastric cancer.
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Formation and repair of 1,3-bis-(2-chloroethyl)-1-nitrosourea and cisplatin induced total genomic DNA interstrand crosslinks in human glioma cells.
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Frequency of homozygous deletion at p16/CDKN2 in primary human tumours.
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Frequent BRAF mutations suggest a novel oncogenic driver in colonic neuroendocrine carcinoma.
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Frequent IGF2/H19 domain epigenetic alterations and elevated IGF2 expression in epithelial ovarian cancer.
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Frequent detection of bcl-2/JH translocations in human blood and organ samples by a quantitative polymerase chain reaction assay.
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Frequent detection of codon 877 mutation in the androgen receptor gene in advanced prostate cancers.
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Frequent fusion of the JAZF1 and JJAZ1 genes in endometrial stromal tumors.
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Frequent loss of heterozygosity on chromosome arm 18q in squamous cell carcinomas. Identification of 2 regions of loss--18q11.1-q12.3 and 18q21.1-q23.
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Frequent microsatellite instability in primary small cell lung cancer.
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Functional Analysis and Fine Mapping of the 9p22.2 Ovarian Cancer Susceptibility Locus.
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Functional Variants in Notch Pathway Genes NCOR2, NCSTN, and MAML2 Predict Survival of Patients with Cutaneous Melanoma.
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Genetic And Morphological Evaluation (GAME) score for patients with colorectal liver metastases.
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Genetic Variants in WNT2B and BTRC Predict Melanoma Survival.
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Genetic and phenotypic characteristics of pleomorphic lobular carcinoma in situ of the breast.
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Genetic basis for p53 overexpression in human breast cancer.
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Genetic changes in contralateral bronchioloalveolar carcinomas of the lung.
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Genetic heterogeneity of diffuse large B-cell lymphoma.
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Genetic variations in TERT-CLPTM1L genes and risk of squamous cell carcinoma of the head and neck.
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Genome wide analysis and clinical correlation of chromosomal and transcriptional mutations in cancers of the biliary tract.
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Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
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Genomic Landscape of Cell-Free DNA in Patients with Colorectal Cancer.
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Genomic sweeping for hypermethylated genes.
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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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Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors.
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Global search for chromosomal abnormalities in infiltrating ductal carcinoma of the breast using array-comparative genomic hybridization.
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Glutathione content and glutathione-S-transferase expression in 1,3-bis(2-chloroethyl)-1-nitrosourea-resistant human malignant astrocytoma cell lines.
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Glutathione-associated cis-diamminedichloroplatinum(II) metabolism and ATP-dependent efflux from leukemia cells. Molecular characterization of glutathione-platinum complex and its biological significance.
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Ha-ras polymorphisms in epithelial ovarian cancer.
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Haplotypes of two variants in p16 (CDKN2/MTS-1/INK4a) exon 3 and risk of squamous cell carcinoma of the head and neck: a case-control study.
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High levels of nuclear MYC protein predict the presence of MYC rearrangement in diffuse large B-cell lymphoma.
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High-throughput detection of glutathione s-transferase polymorphic alleles in a pediatric cancer population.
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Histologic grade, DNA ploidy, and intraglandular tumor extent as indicators of tumor progression of clinical stage B prostatic carcinoma. A direct comparison.
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Human Dkk-1, a gene encoding a Wnt antagonist, responds to DNA damage and its overexpression sensitizes brain tumor cells to apoptosis following alkylation damage of DNA.
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Hydroxyurea synchronization increases mitotic yield in human glioma cell lines.
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Hypermethylated APC DNA in plasma and prognosis of patients with esophageal adenocarcinoma.
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Hypermethylation of 14-3-3 sigma (stratifin) is an early event in breast cancer.
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Hypermutability and mismatch repair deficiency in RER+ tumor cells.
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IL26, a Noncanonical Mediator of DNA Inflammatory Stimulation, Promotes TNBC Engraftment and Progression in Association with Neutrophils.
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Identification of an amplified, highly expressed gene in a human glioma.
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Identification of an enhancer element in the estrogen receptor upstream region: implications for regulation of ER transcription in breast cancer.
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Identification of candidate genes in ulcerative colitis and Crohn's disease using cDNA array technology.
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Identification of p18 INK4c as a tumor suppressor gene in glioblastoma multiforme.
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Identification of resting cells by dual-parameter flow cytometry of statin expression and DNA content.
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Identification of the breast cancer susceptibility gene BRCA2.
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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 and genetic analysis of non-small cell and small cell gallbladder carcinoma and their precursor lesions.
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Immunohistochemical p16INK4a analysis of archival tumors with deletion, hypermethylation, or mutation of the CDKN2/MTS1 gene. A comparison of four commercial antibodies.
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Immunotherapy of cancer with dendritic cell-based vaccines.
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Impact of Specimen Heterogeneity on Biomarkers in Repository Samples from Patients with Acute Myeloid Leukemia: A SWOG Report.
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In vitro BPDE-induced DNA adducts in peripheral lymphocytes as a risk factor for squamous cell carcinoma of the head and neck.
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In vitro and in vivo molecular evidence of genistein action in augmenting the efficacy of cisplatin in pancreatic cancer.
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In vitro determination of thymidine-3H labeling index in human solid tumors.
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Increased DNA excision-repair as pathogenesis of a human leukemia.
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Individualised multiplexed circulating tumour DNA assays for monitoring of tumour presence in patients after colorectal cancer surgery.
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Induction of apoptosis by diethylstilbestrol in hormone-insensitive prostate cancer cells.
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Induction of transformational changes in normal endothelial cells by cultured human astrocytoma cells.
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Inhibition of DNA replication by tirapazamine.
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Inhibition of DNA synthesis and enhancement of the uptake and action of methotrexate by low-power-density microwave radiation in L1210 leukemia cells.
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Insulin-like growth factor binding protein-3 induces early apoptosis in malignant prostate cancer cells and inhibits tumor formation in vivo.
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Integrated RNA and DNA sequencing reveals early drivers of metastatic breast cancer.
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Intra-tumoral heterogeneity of gemcitabine delivery and mass transport in human pancreatic cancer.
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Intratumoral heterogeneity in primary breast carcinoma: study of concurrent parameters.
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Is Hepatectomy Justified for BRAF Mutant Colorectal Liver Metastases?: A Multi-institutional Analysis of 1497 Patients.
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Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells.
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KRAS2 mutations in human pancreatic acinar-ductal metaplastic lesions are limited to those with PanIN: implications for the human pancreatic cancer cell of origin.
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LIN28B polymorphisms influence susceptibility to epithelial ovarian cancer.
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Localization of the VHR phosphatase gene and its analysis as a candidate for BRCA1.
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Loss of heterozygosity at chromosome segment Xq25-26.1 in advanced human ovarian carcinomas.
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Lymphoproliferative lesions of the ocular adnexa. Analysis of 112 cases.
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M6P/IGF2 receptor: a candidate breast tumor suppressor gene.
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MEN1 gene mutation analysis of high-grade neuroendocrine lung carcinoma.
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MOLECULAR PROGNOSTICS FOR UVEAL MELANOMA.
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MYCC and MYCN oncogene amplification in medulloblastoma. A fluorescence in situ hybridization study on paraffin sections from the Children's Oncology Group.
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Maintenance of DNA content and erbB-2 alterations in intraductal and invasive phases of mammary cancer.
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Mathematical modeling of folate metabolism: predicted effects of genetic polymorphisms on mechanisms and biomarkers relevant to carcinogenesis.
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Mechanism of the anti-tumour effect of biochemotherapy in melanoma: preliminary results.
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Metastatic clear cell renal cell carcinoma: Circulating biomarkers to guide antiangiogenic and immune therapies.
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Methylation and messenger RNA expression of p15INK4b but not p16INK4a are independent risk factors for ovarian cancer.
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Methylation patterns in cell-free plasma DNA reflect removal of the primary tumor and drug treatment of breast cancer patients.
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Microarray sampling-platform fabrication using bubble-jet technology for a biochip system.
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Microsatellite instability in gynecological sarcomas and in hMSH2 mutant uterine sarcoma cell lines defective in mismatch repair activity.
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Mismatch repair, genetic stability and tumour avoidance.
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Mitochondrial C-tract alteration in premalignant lesions of the head and neck: a marker for progression and clonal proliferation.
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Mitochondrial DNA alterations in thyroid cancer.
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Mitochondrial mutations are a late event in the progression of head and neck squamous cell cancer.
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Modulation of cyclophosphamide activity by O6-alkylguanine-DNA alkyltransferase.
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Molecular biologic staging of lung cancer.
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Molecular characteristics of mantle cell lymphoma presenting with clonal plasma cell component.
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Molecular evidence for increased antitumor activity of gemcitabine by genistein in vitro and in vivo using an orthotopic model of pancreatic cancer.
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Molecular profiling of tumors of the brainstem by sequencing of CSF-derived circulating tumor DNA.
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Monoclonal antibodies for brain tumour treatment.
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Monoclonal antibody against human T cell leukemia virus p19 defines a human thymic epithelial antigen acquired during ontogeny.
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Multicolor in vitro translation.
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Multiple DNA repair mechanisms and alkylator resistance in the human medulloblastoma cell line D-283 Med (4-HCR).
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Mutation analysis of the THRA1 gene in breast cancer: deletion/fusion of the gene to a novel sequence on 17q in the BT474 cell line.
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Mutation and overexpression of p53 in early-stage epithelial ovarian cancer.
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Mutation and overexpression of the p53 tumor suppressor gene frequently occurs in uterine and ovarian sarcomas.
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Mutation of MSH3 in endometrial cancer and evidence for its functional role in heteroduplex repair.
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Mutational analysis of the estrogen-receptor gene in endometrial carcinoma.
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Mutational analysis of the p21/WAF1/CIP1/SDI1 coding region in human tumor cell lines.
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Mutations of PIK3CA in anaplastic oligodendrogliomas, high-grade astrocytomas, and medulloblastomas.
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Mutations of the E-cadherin gene in human gynecologic cancers.
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Mutations of the p16 gene product are rare in prostate cancer.
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NCCN Guidelines Insights: Colorectal Cancer Screening, Version 1.2018.
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Nanoscale chromatin profiling of gastric adenocarcinoma reveals cancer-associated cryptic promoters and somatically acquired regulatory elements.
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Needle-in-a-haystack detection and identification of base substitution mutations in human tissues.
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Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk.
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Nuclear DNA content of clear cell adenocarcinoma of the vagina and cervix and its relationship to prognosis.
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Nuclear DNA study of vaginal and cervical squamous cell abnormalities in DES exposed progeny.
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Oncogenic mutations in melanomas and benign melanocytic nevi of the female genital tract.
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Overexpression and mutation of p53 in epithelial ovarian cancer.
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PTEN gene mutations are seen in high-grade but not in low-grade gliomas.
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Participation of p53 protein in the cellular response to DNA damage.
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Performance of amplified DNA in an Illumina GoldenGate BeadArray assay.
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Persistent genetic instability in cancer cells induced by non-DNA-damaging stress exposures.
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Phase I clinical and plasma and cellular pharmacological study of topotecan without and with granulocyte colony-stimulating factor.
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Pilot study of rapid MR pancreas screening for patients with BRCA mutation.
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Placenta-Specific Protein 1 Expression in Human Papillomavirus 16/18-Positive Cervical Cancers Is Associated With Tumor Histology.
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Ploidy analysis of epithelial ovarian cancers using image cytometry.
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Polymorphic repeats in the androgen receptor gene: molecular markers of prostate cancer risk.
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Polymorphisms in hMLH1 and risk of early-onset lung cancer in a southeast Chinese population.
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Polymorphisms of DNA repair gene XRCC3 Thr241Met and risk of gastric cancer in a Chinese population.
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Precise localization of the FHIT gene to the common fragile site at 3p14.2 (FRA3B) and characterization of homozygous deletions within FRA3B that affect FHIT transcription in tumor cell lines.
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Prevalence of HTLV-I-associated T-cell lymphoma.
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Primary intraocular T-cell-rich large B-cell lymphoma.
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Prognostic factors in colorectal cancer. College of American Pathologists Consensus Statement 1999.
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Prognostic factors in renal cancer.
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Prognostic significance of DNA ploidy in carcinoma of prostate.
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Prognostic value of MIB-1 in advanced ovarian carcinoma as determined using automated immunohistochemistry and quantitative image analysis.
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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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RNASEL mutations in hereditary prostate cancer.
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Rare germline mutations in African American men diagnosed with early-onset prostate cancer.
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Recombinant adenovirus vector expressing wild-type p53 is a potent inhibitor of prostate cancer cell proliferation.
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Regulation of tumor necrosis factor cytotoxicity by calcineurin.
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Repair analysis of 4-hydroperoxycyclophosphamide-induced DNA interstrand crosslinking in the c-myc gene in 4-hydroperoxycyclophosphamide-sensitive and -resistant medulloblastoma cell lines.
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Resection of adrenocortical carcinoma liver metastasis: is it justified?
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Risk factors for cancer.
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Risk factors for ovarian cancers with and without microsatellite instability.
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Risk of adverse events in children completing treatment for acute lymphoblastic leukemia: St. Jude Total Therapy studies VIII, IX, and X.
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Sensitive digital quantification of DNA methylation in clinical samples.
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Serine substitution of proline at codon 151 of TP53 confers gain of function activity leading to anoikis resistance and tumor progression of head and neck cancer cells.
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Simultaneous detection of the tumor suppressor FHIT gene and protein using the multi-functional biochip.
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Small changes in expression affect predisposition to tumorigenesis.
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Small choroidal melanoma with chromosome 3 monosomy on fine-needle aspiration biopsy.
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Smoking, DNA repair capacity and risk of nonsmall cell lung cancer.
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Somatic Mutation Allelic Ratio Test Using ddPCR (SMART-ddPCR): An Accurate Method for Assessment of Preferential Allelic Imbalance in Tumor DNA.
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Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis.
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Somatic mutations in the neurofibromatosis 1 gene in gliomas and primitive neuroectodermal tumours.
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Some properties of a DNA-unwinding protein unique to lymphocytes from chronic lymphocytic leukemia.
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Strand-specific mismatch correction in nuclear extracts of human and Drosophila melanogaster cell lines.
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Structure of the human allelic glutathione S-transferase-pi gene variant, hGSTP1 C, cloned from a glioblastoma multiforme cell line.
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Studies on the enhanced interaction of halodeoxyuridine-substituted DNAs with H1 histones and other polypeptides.
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Studies on the mechanism of the synergistic interaction between 2'-deoxy-5-azacytidine and cisplatin.
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Suppression of tumorigenicity of A549 lung adenocarcinoma cells by human chromosomes 3 and 11 introduced via microcell-mediated chromosome transfer.
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Syndrome of inappropriate secretion of antidiuretic hormone in a patient with carcinoma of the nasopharynx.
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Synergistic cytotoxicity using 2'-deoxy-5-azacytidine and cisplatin or 4-hydroperoxycyclophosphamide with human tumor cells.
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Synergistic cytotoxicity with 2'-deoxy-5-azacytidine and topotecan in vitro and in vivo.
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Synergistic interactions between cyclophosphamide or melphalan and VP-16 in a human rhabdomyosarcoma xenograft.
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Tagging single nucleotide polymorphisms in excision repair cross-complementing group 1 (ERCC1) and risk of primary lung cancer in a Chinese population.
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Telomerase activity in normal leukocytes and in hematologic malignancies.
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The DNA-repair gene MGMT and the clinical response of gliomas to alkylating agents.
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The DNA-repair gene MGMT and the clinical response of gliomas to alkylating agents.
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The biology of malignant gliomas--a comprehensive survey.
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The hOGG1 Ser326Cys polymorphism and lung cancer risk: a meta-analysis.
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The isolation and characterization of a novel cDNA demonstrating an altered mRNA level in nontumorigenic Wilms' microcell hybrid cells.
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The nuclear factor-kappa B RelA transcription factor is constitutively activated in human pancreatic adenocarcinoma cells.
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The p53 signal transduction pathway is intact in human neuroblastoma despite cytoplasmic localization.
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The pathology of liver-localized post-transplant lymphoproliferative disease: a report of three cases and a review of the literature.
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The pattern of gene amplification is determined by the chromosomal location of hairpin-capped breaks.
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The synthesis and anti-neoplastic activity of N2-isobutyryl-2'-deoxyguanosine-N7-cyanoborane derivatives.
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Tirapazamine: a hypoxia-activated topoisomerase II poison.
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Toward a Shared Vision for Cancer Genomic Data.
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Transient inhibition of ATM kinase is sufficient to enhance cellular sensitivity to ionizing radiation.
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Transport properties of pancreatic cancer describe gemcitabine delivery and response.
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Two identical triplet sisters carrying a germline BRCA1 gene mutation acquire very similar breast cancer somatic mutations at multiple other sites throughout the genome.
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Type 1 neurofibromatosis gene: identification of a large transcript disrupted in three NF1 patients.
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Use of laser scanning cytometry to study tumor microenvironment.
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Use of single nucleotide polymorphism arrays to identify a novel region of loss on chromosome 6q in squamous cell carcinomas of the oral cavity.
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Whole-epigenome analysis in multiple myeloma reveals DNA hypermethylation of B cell-specific enhancers.
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[A study of epithelial cell kinetics of the odontogenic keratocyst].
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cDNA sequencing confirms HTLV-I expression in adult T-cell leukemia/lymphoma and different sequence variations in vivo and in vitro.
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miR-203, a tumor suppressor frequently down-regulated by promoter hypermethylation in rhabdomyosarcoma.
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p16 Improves interobserver agreement in diagnosis of anal intraepithelial neoplasia.
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p53 gene alterations in human prostate carcinoma.
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p53 gene expression in node-positive breast cancer: relationship to DNA ploidy and prognosis.
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p53 status in spontaneous and dimethylnitrosamine-induced renal cell tumors from rats.
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rac, a novel ras-related family of proteins that are botulinum toxin substrates.
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Keywords of People
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Bennett, Vann,
George Barth Geller Distinguished Professor of Molecular Biology,
Duke Cancer Institute
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Berchuck, Andrew,
James M. Ingram Distinguished Professor of Gynecologic Oncology,
Obstetrics and Gynecology, Gynecologic Oncology
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Halabi, Susan,
Professor of Biostatistics and Bioinformatics,
Biostatistics & Bioinformatics
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Luftig, Micah Alan,
Associate Professor of Molecular Genetics and Microbiology,
Immunology
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McLendon, Roger Edwin,
Professor of Pathology,
Pathology
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Pang, Herbert,
Adjunct Assistant Professor in the Department of Biostatistics and Bioinformatics,
Biostatistics & Bioinformatics
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Yan, Hai,
Henry S. Friedman Distinguished Professor of Neuro-Oncology in the School of Medicine,
Pathology