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Publication Listing for the MeSH term locus. Found 30 abstracts

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Antoniou AC, Kartsonaki C, Sinilnikova OM, Soucy P, McGuffog L, Healey S, Lee A, Peterlongo P, Manoukian S, Peissel B, Zaffaroni D, Cattaneo E, Barile M, Pensotti V, Pasini B, Dolcetti R, Giannini G, Putignano AL, Varesco L, Radice P, Mai PL, Greene MH, Andrulis IL, Glendon G, Ozcelik H, Thomassen M, Gerdes AM, Kruse TA, Jensen UB, Cruger DG, Caligo MA, Laitman Y, Milgrom R, Kaufman B, Paluch-Shimon S, Friedman E, Loman N, Harbst K, Lindblom A, Arver B, Ehrencrona H, Melin B, Nathanson KL, Domchek SM, Rebbeck T, Jakubowska A, Lubinski J, Gronwald J, Huzarski T, Byrski T, Cybulski C, Gorski B, Osorio A, Cajal TR, Fostira F, Andres R, Benitez J, Hamann U, Hogervorst FB, Rookus MA, Hooning MJ, Nelen MR, van der Luijt RB, van Os TA, van Asperen CJ, Devilee P, Meijers-Heijboer HE, Garcia EB, Peock S, Cook M, Frost D, Platte R, Leyland J, Evans DG, Lalloo F, Eeles R, Izatt L, Adlard J, Davidson R, Eccles D, Ong KR, Cook J, Douglas F, Paterson J, Kennedy MJ, Miedzybrodzka Z, Godwin A, Stoppa-Lyonnet D, Buecher B, Belotti M, Tirapo C, Mazoyer S, Barjhoux L, Lasset C, Leroux D, Faivre L, Bronner M, Prieur F, Nogues C, Rouleau E, Pujol P, Coupier I, Frenay M, Hopper JL, Daly MB, Terry MB, John EM, Buys SS, Yassin Y, Miron A, Goldgar D, Singer CF, Tea MK, Pfeiler G, Dressler AC, Hansen TV, Jonson L, Ejlertsen B, Barkardottir RB, Kirchhoff T, Offit K, Piedmonte M, Rodriguez G, Small L, Boggess J, Blank S, Basil J, Azodi M, Toland AE, Montagna M, Tognazzo S, Agata S, Imyanitov E, Janavicius R, Lazaro C, Blanco I, Pharoah PD, Sucheston L, Karlan BY, Walsh CS, Olah E, Bozsik A, Teo SH, Seldon JL, Beattie MS, van Rensburg EJ, Sluiter MD, Diez O, Schmutzler RK, Wappenschmidt B, Engel C, Meindl A, Ruehl I, Varon-Mateeva R, Kast K, Deissler H, Niederacher D, Arnold N, Gadzicki D, Schonbuchner I, Caldes T, de la Hoya M, Nevanlinna H, Aittomaki K, Dumont M, Chiquette J, Tischkowitz M, Chen XQ, Beesley J, Spurdle AB, Neuhausen SL, Ding YC, Fredericksen Z, Wang X, Pankratz VS, Couch F, Simard J, Easton DF, Chenevix-Trench G, Swe-Brca Hebon Embrace Cemo Study Collaborators; Breast Canc Family Registry; kConFab Investigators; CIMBA. Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers. Human molecular genetics. 2011 Aug;20(16):3304-21.   PMCID: NIHMS347818
Kelly DF, Lake RJ, Middelkoop TC, Fan HY, Artavanis-Tsakonas S, Walz T. Molecular Structure and Dimeric Organization of the Notch Extracellular Domain as Revealed by Electron Microscopy. Plos One. 2010 May;5(5).   PMCID: PMC2866536
Larson GP, Ding Y, Cheng LS, Lundberg C, Gagalang V, Rivas G, Geller L, Weitzel J, MacDonald D, Archambeau J, Slater J, Neuberg D, Daly MB, Angel I, Benson AB, Smith K, Kirkwood JM, O'Dwyer PJ, Raskay B, Sutphen R, Drew R, Stewart JA, Werndli J, Johnson D, Ruckdeschel JC, Elston RC, Krontiris TG. Genetic linkage of prostate cancer risk to the chromosome 3 region bearing FHIT. Cancer Research. 2005 Feb;65(3):805-14.
Wang LQ, Chen XL, Tang BQ, Hua X, Klein-Szanto A, Kruger WD. Expression of mutant human cystathionine beta-synthase rescues neonatal lethality but not homocystinuria in a mouse model. Human molecular genetics. 2005 Aug;14(15):2201-8.
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.
Hou L, Pavan WJ, Shin MK, Arnheiter H. Cell-autonomous and cell non-autonomous signaling through endothelin receptor B during melanocyte development. Development. 2004 Jul;131(14):3239-47.
Louzoun Y, Friedman R, Prak EL, Litwin S, Weigert M. Analysis of B cell receptor production and rearrangement Part 1. Light chain rearrangement. Seminars in immunology. 2002 Jun;14(3):169-90.
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.
Juo SH, Pugh EW, Baffoe-Bonnie A, Kingman A, Sorant AJ, Klein AP, O'Neill J, Mathias RA, Wilson AF, Bailey-Wilson JE. Possible linkage of alcoholism, monoamine oxidase activity and p300 amplitude to markers on chromosome 12q24. Genetic epidemiology. 1999 Jan;17:S193-S198.
Mehr R, Shannon M, Litwin S. Models for antigen receptor gene rearrangement. I. Biased receptor editing in B cells: Implications for allelic exclusion. Journal of Immunology. 1999 Aug 15;163(4):1793-8.
El-Shanti H, Murray JC, Semina EV, Beutow KH, Scherpbier T, Al-Alami J. Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene. European Journal of Human Genetics. 1998 May;6(3):251-6.
Randhawa GS, Bell DW, Testa JR, Feinberg AP. Identification and mapping of human histone acetylation modifier gene homologues. Genomics. 1998 Jul 15;51(2):262-9.
Homanics GE, DeLorey TM, Firestone LL, Quinlan JJ, Handforth A, Harrison NL, Krasowski MD, Rick CE, Korpi ER, Makela R, Brilliant MH, Hagiwara N, Ferguson C, Snyder K, Olsen RW. Mice devoid of gamma-aminobutyrate type A receptor beta 3 subunit have epilepsy, cleft palate, and hypersensitive behavior. Proceedings of the National Academy of Sciences of the United States of America. 1997 Apr 15;94(8):4143-8.
Lidral AC, Murray JC, Buetow KH, Basart AM, Schearer H, Shiang R, Naval A, Layda E, Magee K, Magee W. Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines. Cleft Palate-Craniofacial Journal. 1997 Jan;34(1):1-6.
Lund PM, Puri N, DurhamPierre D, King RA, Brilliant MH. Oculocutaneous albinism in an isolated Tonga community in Zimbabwe. Journal of Medical Genetics. 1997 Sep;34(9):733-5.
DurhamPierre D, King RA, Naber JM, Laken S, Brilliant MH. Estimation of carrier frequency of a 2.7 kb deletion allele of the P gene associated with OCA2 in African-Americans. Human Mutation. 1996 Jan;7(4):370-3.
LeFur N, Kelsall SR, Mintz B. Base substitution at different alternative splice donor sites of the tyrosinase gene in murine albinism. Genomics. 1996 Oct 15;37(2):245-8.
Gahl WA, Potterf B, DurhamPierre D, Brilliant MH, Hearing VJ. Melanosomal tyrosine transport in normal and pink-eyed dilution murine melanocytes. Pigment Cell Research. 1995 Oct;8(5):229-33.
Orlow SJ, Hearing VJ, Sakai C, Urabe K, Zhou BK, Silvers WK, Mintz B. Changes in Expression of Putative Antigens Encoded by Pigment Genes in Mouse Melanomas at Different Stages of Malignant Progression. Proceedings of the National Academy of Sciences of the United States of America. 1995 Oct 24;92(22):10152-6.
Brilliant MH, Ching A, Nakatsu Y, Eicher EM. The Original Pink-Eyed Dilution Mutation-(P) Arose in Asiatic Mice - Implications for the H4 Minor Histocompatibility Antigen, Myod1 Regulation and the Origin of Inbred Strains. Genetics. 1994 Sep;138(1):203-11.
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 locus

locus gene mice sequence localization germline mutations receptor oculocutaneous albinism mouse risk drosophila families linkage disequilibrium cdna region chromosome association lambda-genes genetic modifiers rflps reductase dioxin yeast NQO2 pairs tyrosine transport transcription B cell receptor mutations linkage gene-expression dt-diaphorase genes mouse chromosome-7 jordan human genome oca2 complex traits p-gene monolayer purification homocysteine chondrodysplasia melanosome transcripts mitf growth-factor-alpha TGFB3 albinism pink-eyed dilution signal integration subunit transgenic mice disorder probabilistic model brown locus coat color Philippines gene targeting acid susceptibility mutation retinoic acid forms isotypic exclusion allelic exclusion angelman syndrome benzodiazepine MSX1 pathway albino locus estrogen-receptor prader-willi syndrome segregation analysis positional cloning laboratory mouse melanocytes Africa OCA2 egf repeats polymorphism precursors variants growth-factors self-tolerance anesthesia confer susceptibility oxidoreductase 2q35 suppressor L STOP steel factor nucleosome NQO1 human collagen-x intragenic deletion Angelman syndrome complex metaanalysis autosomal-dominant inheritance y-chromosome deficiency pseudorheumatoid dysplasia TGFA deacetylase cleft lip genetics hairless biosynthesis acid receptor gene rearrangement tyrosinase gene trp-2 melanin rat-brain MAO light chain messenger-rnas n-cor patient a receptor transcriptional repression maps sox10 homozygosity mapping quinones allele silver locus population expression unstable mutation carcinoma collagen type X immunoglobulin tolerance neural crest melanocyte protein RFLP linkage analysis nad(p)h gaba(a) receptor slaty locus antibody tyrosinase-related protein-1 segments p- kappa-lambda ratio traits finland pooling
Last updated on Thursday, April 02, 2020