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Publication Listing for the MeSH term chromosome. Found 17 abstracts

Berger AH, Knudson AG, Pandolfi PP, Venee Wk VP. A continuum model for tumour suppression. Nature. 2011 Aug;476(7359):163-9.   PMCID: PMC3206311
Knudson AG. A personal sixty-year tour of genetics and medicine. Annual Review of Genomics and Human Genetics. 2005 Jan;6:1-14.
Rokman A, Baffoe-Bonnie AB, Gillanders E, Fredriksson H, Autio V, Ikonen T, Gibbs KD, Jones MP, Gildea D, Freas-Lutz D, Markey C, Matikainen MP, Koivisto PA, Tammela TL, Kallioniemi OP, Trent J, Bailey-Wilson JE, Schleutker J. Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus. Human Genetics. 2005 Jan;116(1-2):43-50.
Gillanders EM, Xu JF, Chang BL, Lange EM, Wiklund F, Bailey-Wilson JE, Baffoe-Bonnie A, Jones M, Gildea D, Riedesel E, Albertus J, Isaacs SD, Wiley KE, Mohai CE, Matikainen MP, Tammela TL, Zheng SL, Brown WM, Rokman A, Carpten JD, Meyers DA, Walsh PC, Schleutker J, Gronberg H, Cooney KA, Isaacs WB, Trent JM. Combined genome-wide scan for prostate cancer susceptibility genes. Journal of the National Cancer Institute. 2004 Aug 18;96(16):1240-7.
Aubry MC, Myers JL, Ryu JH, Henske EP, Logginidou H, Jalal SM, Tazelaar HD. Pulmonary lymphangioleiomyomatosis in a man. American Journal of Respiratory and Critical Care Medicine. 2000 Aug;162(2):749-52.
Kaneko Y, Knudson AG. Mechanism and relevance of ploidy in neuroblastoma. Genes Chromosomes & Cancer. 2000 Oct;29(2):89-95.
Koshland DE, Guacci V. Sister chromatid cohesion: the beginning of a long and beautiful relationship. Current opinion in cell biology. 2000 Jun;12(3):297-301.
Royal C, Baffoe-Bonnie A, Kittles R, Powell I, Bennett J, Hoke G, Pettaway C, Weinrich S, Vijayakumar S, Ahaghotu C, Mason T, Johnson E, Obeikwe M, Simpson C, Mejia R, Boykin W, Roberson P, Frost J, Faison-Smith L, Meegan C, Foster N, Furbert-Harris P, Carpten J, Bailey-Wilson J, Trent J, Berg K, Dunston G, Collins F. Recruitment experience in the first phase of the African American Hereditary Prostate Cancer (AAHPC) Study. Annals of Epidemiology. 2000 Nov;10(8):S68-S77.
Bruening W, Prowse AH, Schultz DC, Holgado-Madruga M, Wong A, Godwin AK. Expression of OVCA1, a candidate tumor suppressor, is reduced in tumors and inhibits growth of ovarian cancer cells. Cancer Research. 1999 Oct;59(19):4973-83.
Garay CA, Al-Saleem T, Testa JR, Smith MR. Coexisting myelodysplasia and myeloproliferative features in a single clone containing 5q-, Ph and i(17q). Leukemia Research. 1999 Oct;23(10):965-7.
Jaiswal AK, Bell DW, Radjendirane V, Testa JR. Localization of human NQO1 gene to chromosome 16q22 and NQO2- 6p25 and associated polymorphisms. Pharmacogenetics. 1999 Jun;9(3):413-8.
Basu J, Logarinho E, Herrmann S, Bousbaa H, Li ZX, Chan GK, Yen TJ, Sunkel CE, Goldberg ML. Localization of the Drosophila checkpoint control protein Bub3 to the kinetochore requires Bub1 but not Zw10 or Rod. Chromosoma. 1998 Dec;107(6-7):376-85.
Lehman AL, Nakatsu Y, Ching A, Bronson RT, Oakey RJ, Keiper-Hrynko N, Finger JN, Durham-Pierre D, Horton DB, Newton JM, Lyon MF, Brilliant MH. A very large protein with diverse functional motifs is deficient in rjs (runty, jerky, sterile) mice. Proceedings of the National Academy of Sciences of the United States of America. 1998 Aug 04;95(16):9436-41.
Oetting WS, Brilliant MH, King RA. The clinical spectrum of albinism in humans. Molecular Medicine Today. 1996 Aug;2(8):330-5.
Bell DW, Yeung RS, Bohlander SK, Cheng JQ, Jin F, Testa JR. A Microdissection Library of the Rat Renal-Carcinoma Gene Region. Cytogenetics and Cell Genetics. 1995 Jan;70(1-2):92-4.
Franke TF, Tartof KD, Tsichlis PN. The Sh2-Like Akt Homology (Ah) Domain of C-Akt Is Present in Multiple Copies in the Genome of Vertebrate and Invertebrate Eukaryotes - Cloning and Characterization of the Drosophila- Melanogaster C-Akt Homolog Dakt1. Oncogene. 1994 Jan;9(1):141-8.
Buetow KH, Murray JC, Israel JL, London WT, Smith M, Kew M, Blanquet V, Brechot C, Redeker A, Govindarajah S. Loss of heterozygosity suggests tumor suppressor gene responsible for primary hepatocellular carcinoma. Proceedings of the National Academy of Sciences of the United States of America. 1989 Jan;86(22):8852-6.
The above publications are sorted by year, faculty last name, and first author. Click on any highlighted author listed to find all publications attributed to that individual. Click on the publication title to see the abstract. First authors who are faculty are highlighted like this. Last authors who are faculty are highlighted like this. Other authors who are faculty are highlighted like this.

MeSH cloud from publications including the MeSH term chromosome

chromosome risk gene germline mutations mutation condensation identification dna budding yeast families locus susceptibility locus saccharomyces- hpc1 malignant-melanoma linked ocular albinism system micronodular pneumocyte hyperplasia amplification oxidoreductase dna-replication mutagenicity 1p human-p-gene epithelial-cells NQO1 two hits cancer-genetic chaos rcc1 intragenic deletion retinoblastoma complex dependent dna polymerase autosomal-dominant inheritance hematopoietic stem-cells somatic gene mapping Oncogenes in-vivo mitosis melanogaster nucleotide sequence reductase dioxin cowden-disease NQO2 genetics 17p133 gene family mutations prevention linkage chronic myelogenous leukemia saccharomyces-cerevisiae pten dt-diaphorase Restriction Fragment Length Polymorphism tsc2 gene allelic loss Genetic Suppression eker rat model neuro-blastoma smc proteins dominantly inherited cancer African American breast-cancer tumors Philadelphia syndrome localization spindle-assembly checkpoint age hamartin angiomyolipomas recessive oncogenesis prader-willi region prognosis protein-kinase-c prader-willi-syndrome quinones tuberous sclerosis conditional loss human-genome-project lymphangiomyomatosis unattached kinetochores cancer tay-sachs-disease populations Human Chromosomes-Pair 4 chromosome 4 acute promyelocytic leukemia chromosome 5 abnormalities genome-wide scan segregation comparative genomic hybridization deletion disease participation human tyrosinase gene susceptibility RFLP linkage analysis nad(p)h fission yeast cerevisiae ubiquitous protein family hermansky-pudlak syndrome Heterozygote tuskegee dilution p locus japan product oncogene liver cell carcinoma primitive neuroectodermal tumors model sequence wild-type finland embryonic-development segregation analysis twins cancer susceptibility 17 abnormalities anaphase mouse eker rat prostate cancer molecular-basis uterine cervix sarcoma blast crisis retinoblastoma gene clinical-trials infants hormonal-control myelodysplasia genetic alterations positive oculocutaneous albinism carcinoma-cells sequence-analysis separation angelman-syndrome
Last updated on Friday, December 06, 2019