These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 21840860)

  • 21. Genetic mapping and analysis of somatostatin expression in Snell dwarf mice.
    O'Hara BF; Bendotti C; Reeves RH; Oster-Granite ML; Coyle JT; Gearhart JD
    Brain Res; 1988 Dec; 464(4):283-92. PubMed ID: 2906811
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Deafness and permanently reduced potassium channel gene expression and function in hypothyroid Pit1dw mutants.
    Mustapha M; Fang Q; Gong TW; Dolan DF; Raphael Y; Camper SA; Duncan RK
    J Neurosci; 2009 Jan; 29(4):1212-23. PubMed ID: 19176829
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hearing loss associated with the modifier of deaf waddler (mdfw) locus corresponds with age-related hearing loss in 12 inbred strains of mice.
    Zheng QY; Johnson KR
    Hear Res; 2001 Apr; 154(1-2):45-53. PubMed ID: 11423214
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Quantitative trait locus mapping identifies the Gpnmb gene as a modifier of mouse macrophage lysosome function.
    Robinet P; Ritchey B; Lorkowski SW; Alzayed AM; DeGeorgia S; Schodowski E; Traughber CA; Smith JD
    Sci Rep; 2021 May; 11(1):10249. PubMed ID: 33986446
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Ahl2, a second locus affecting age-related hearing loss in mice.
    Johnson KR; Zheng QY
    Genomics; 2002 Nov; 80(5):461-4. PubMed ID: 12408962
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation.
    Camper SA; Saunders TL; Katz RW; Reeves RH
    Genomics; 1990 Nov; 8(3):586-90. PubMed ID: 1981057
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Congenic strains of mice for verification and genetic decomposition of quantitative trait loci for femoral bone mineral density.
    Shultz KL; Donahue LR; Bouxsein ML; Baylink DJ; Rosen CJ; Beamer WG
    J Bone Miner Res; 2003 Feb; 18(2):175-85. PubMed ID: 12568393
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genome-wide search for genes that modulate inflammatory arthritis caused by Ali18 mutation in mice.
    Abe K; Klaften M; Narita A; Kimura T; Imai K; Kimura M; Rubio-Aliaga I; Wagner S; Jakob T; Hrabé de Angelis M
    Mamm Genome; 2009 Mar; 20(3):152-61. PubMed ID: 19238339
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genetic dissection of a major mouse obesity QTL (Carfhg2): integration of gene expression and causality modeling.
    Farber CR; Aten JE; Farber EA; de Vera V; Gularte R; Islas-Trejo A; Wen P; Horvath S; Lucero M; Lusis AJ; Medrano JF
    Physiol Genomics; 2009 May; 37(3):294-302. PubMed ID: 19336533
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Identifying quantitative trait loci affecting resistance to congenital hypothyroidism in 129/SvJcl strain mice.
    Hosoda Y; Sasaki N; Kameda Y; Torigoe D; Agui T
    PLoS One; 2012; 7(1):e31035. PubMed ID: 22299049
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Quantitative trait loci for BMD in an SM/J by NZB/BlNJ intercross population and identification of Trps1 as a probable candidate gene.
    Ishimori N; Stylianou IM; Korstanje R; Marion MA; Li R; Donahue LR; Rosen CJ; Beamer WG; Paigen B; Churchill GA
    J Bone Miner Res; 2008 Sep; 23(9):1529-37. PubMed ID: 18442308
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Identification of Soat1 as a quantitative trait locus gene on mouse chromosome 1 contributing to hyperlipidemia.
    Lu Z; Yuan Z; Miyoshi T; Wang Q; Su Z; Chang CC; Shi W
    PLoS One; 2011; 6(10):e25344. PubMed ID: 22022387
    [TBL] [Abstract][Full Text] [Related]  

  • 33. QTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations.
    Dang R; Torigoe D; Sasaki N; Agui T
    PLoS One; 2011; 6(11):e27902. PubMed ID: 22132166
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Quantitative lymphatic vessel trait analysis suggests Vcam1 as candidate modifier gene of inflammatory bowel disease.
    Jurisic G; Sundberg JP; Bleich A; Leiter EH; Broman KW; Buechler G; Alley L; Vestweber D; Detmar M
    Genes Immun; 2010 Apr; 11(3):219-31. PubMed ID: 20220769
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Locating a modifier gene of Ovum mutant through crosses between DDK and C57BL/6J inbred strains in mice.
    Tan J; Song GD; Song JS; Ren SH; Li CL; Zheng ZY; Zhao WD
    J Genet; 2016 Jun; 95(2):297-302. PubMed ID: 27350672
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Association of a lithogenic Abcg5/Abcg8 allele on Chromosome 17 (Lith9) with cholesterol gallstone formation in PERA/EiJ mice.
    Wittenburg H; Lyons MA; Li R; Kurtz U; Mössner J; Churchill GA; Carey MC; Paigen B
    Mamm Genome; 2005 Jul; 16(7):495-504. PubMed ID: 16151694
    [TBL] [Abstract][Full Text] [Related]  

  • 37. ENU induced single mutation locus on chr 16 leads to high-frequency hearing loss in mice.
    Jiao Y; Cai C; Kermany MH; Yan J; Cai Q; Miller D; Goldowitz D; Li X; Yoo TJ; Gu W
    Genes Genet Syst; 2009 Jun; 84(3):219-24. PubMed ID: 19745570
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Quantitative trait loci on chromosome 5 for susceptibility to frequency-specific effects on hearing in DBA/2J mice.
    Suzuki S; Ishikawa M; Ueda T; Ohshiba Y; Miyasaka Y; Okumura K; Yokohama M; Taya C; Matsuoka K; Kikkawa Y
    Exp Anim; 2015; 64(3):241-51. PubMed ID: 25765874
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of Mom7, a novel modifier of Apc(Min/+) on mouse chromosome 18.
    Kwong LN; Shedlovsky A; Biehl BS; Clipson L; Pasch CA; Dove WF
    Genetics; 2007 Jun; 176(2):1237-44. PubMed ID: 17435219
    [TBL] [Abstract][Full Text] [Related]  

  • 40. New mouse dw allele: genetic location and effects on lifespan and growth hormone levels.
    Eicher EM; Beamer WG
    J Hered; 1980; 71(3):187-90. PubMed ID: 7391543
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.