Chromosomes, Human, Pair 11
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Subject Areas on Research
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A 137-kb deletion within the Potocki-Shaffer syndrome interval on chromosome 11p11.2 associated with developmental delay and hypotonia.
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A case of infantile acute lymphoblastic leukemia presenting with rearrangement of MLL at 11q23 and apparent insertion or translocation at 10p12.
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A frequent human CD20 (B1) differentiation antigen DNA polymorphism detected with MspI is located near 11q12-13.
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A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic.
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A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11: distal p13 to proximal p15.1.
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A large set of Finnish affected sibling pair families with type 2 diabetes suggests susceptibility loci on chromosomes 6, 11, and 14.
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A molecular genetic linkage map of mouse chromosome 7.
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A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis.
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A novel chromosomal inversion at 11q23 in infant acute myeloid leukemia fuses MLL to CALM, a gene that encodes a clathrin assembly protein.
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A novel chromosomal rearrangement associated with therapy-related acute leukemia.
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A novel sampling design to explore gene-longevity associations: the ECHA study.
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A pathobiological role of the insulin receptor in chronic lymphocytic leukemia.
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A physical map across chromosome 11q22-q23 containing the major locus for ataxia telangiectasia.
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A proximal mouse chromosome 9 linkage map that further defines linkage groups homologous with segments of human chromosomes 11, 15, and 19.
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A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci.
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Adult patients with de novo acute myeloid leukemia and t(9; 11)(p22; q23) have a superior outcome to patients with other translocations involving band 11q23: a cancer and leukemia group B study.
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An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.
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An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.
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Association of chromosome 11 locus D11S12 with histology, stage, and metastases in lung cancer.
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Association of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.
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Attention deficit/hyperactivity disorder children with a 7-repeat allele of the dopamine receptor D4 gene have extreme behavior but normal performance on critical neuropsychological tests of attention.
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Biphenotypic sarcoma with characteristics of both a Ewing sarcoma and a desmoplastic small round cell tumor.
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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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Chromosomal localization of human glutamate receptor genes.
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Chromosomal localization of two genes underlying late-infantile neuronal ceroid lipofuscinosis.
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Chromosome-specific subsets of human alpha satellite DNA: analysis of sequence divergence within and between chromosomal subsets and evidence for an ancestral pentameric repeat.
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Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization.
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Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia.
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Common genetic determinants of vitamin D insufficiency: a genome-wide association study.
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Common variants conferring risk of schizophrenia.
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Deletion of cyclin-dependent kinase 4 inhibitor genes P15 and P16 in non-Hodgkin's lymphoma.
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Delineation of the critical interval of Bardet-Biedl syndrome 1 (BBS1) to a small region of 11q13, through linkage and haplotype analysis of 91 pedigrees.
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Desmoplastic small round cell tumor masquerading as advanced ovarian cancer.
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Dinucleotide repeat polymorphism at the human gene for the brain-derived neurotrophic factor (BDNF).
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Erythroid transcription factor NF-E2 coordinates hemoglobin synthesis.
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Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1).
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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.
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Genetic changes in human adrenocortical carcinomas.
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Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease.
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Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.
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Genome-wide association analysis identifies a meningioma risk locus at 11p15.5.
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Genome-wide association study identifies three susceptibility loci for laryngeal squamous cell carcinoma in the Chinese population.
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Genomic organization and cloning of the human homologue of murine Sipa-1.
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Growth inhibition of a human lung adenocarcinoma cell line by genetic complementation with chromosome 11.
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Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.
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Inherited variant on chromosome 11q23 increases susceptibility to IDH-mutated but not IDH-normal gliomas regardless of grade or histology.
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Isolated trisomy of chromosomes 8, 11, 13 and 21 is an adverse prognostic factor in adults with de novo acute myeloid leukemia: results from Cancer and Leukemia Group B 8461.
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Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13.
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LDL receptor-related protein 5 (LRP5) affects bone accrual and eye development.
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Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function.
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Linkage of a gene causing familial focal segmental glomerulosclerosis to chromosome 11 and further evidence of genetic heterogeneity.
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Linkage studies in tuberous sclerosis. Chromosome 9?, 11?, or maybe 14!
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Localization of a gene that escapes inactivation to the X chromosome proximal short arm: implications for X inactivation.
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Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM.
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Loss of heterozygosity for genes on 11p and the clinical course of patients with lung carcinoma.
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Lymphoblastic lymphoma and excessive toxicity from chemotherapy: an unusual presentation for Fanconi anemia.
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MEN1 gene mutation analysis of high-grade neuroendocrine lung carcinoma.
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Moderation of breastfeeding effects on the IQ by genetic variation in fatty acid metabolism.
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Molecular characteristics of mantle cell lymphoma presenting with clonal plasma cell component.
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New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndrome.
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Novel imprinted DLK1/GTL2 domain on human chromosome 14 contains motifs that mimic those implicated in IGF2/H19 regulation.
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Oligodontia is caused by mutation in LTBP3, the gene encoding latent TGF-beta binding protein 3.
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Organization and evolution of alpha satellite DNA from human chromosome 11.
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Proliferation indices correlate with diagnosis and metastasis in diagnostically challenging melanocytic tumors.
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Report of the Sixth International Workshop on Human Chromosome 11 Mapping 1998. Nice, France, May 2-5, 1998.
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Rescue of targeted regions of mammalian chromosomes by in vivo recombination in yeast.
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Select high-risk genetic features predict earlier progression following chemoimmunotherapy with fludarabine and rituximab in chronic lymphocytic leukemia: justification for risk-adapted therapy.
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Structural organization of the human MS4A gene cluster on Chromosome 11q12.
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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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The gene that encodes the human CD20 (B1) differentiation antigen is located on chromosome 11 near the t(11;14)(q13;q32) translocation site.
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The generation of ordered sets of cosmid DNA clones from human chromosome region 11p.
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The insulin gene is transcribed in the human thymus and transcription levels correlated with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes.
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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 multiple causes of human SCID.
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Therapy-related acute lymphoblastic leukemia without 11q23 abnormality: report of six cases and a literature review.
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Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer.
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Tumorigenic suppression of a human cutaneous squamous cell carcinoma cell line in the nude mouse skin graft assay.
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Uncoupling protein-2: a novel gene linked to obesity and hyperinsulinemia.
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Variability of the SIRT3 gene, human silent information regulator Sir2 homologue, and survivorship in the elderly.
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Whole genome scanning identifies genotypes associated with recurrence and metastasis in prostate tumors.
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cDNA cloning and chromosomal localization of the human beta-adrenergic receptor kinase.