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.
23. Mutation in Mpzl3, a novel [corrected] gene encoding a predicted [corrected] adhesion protein, in the rough coat (rc) mice with severe skin and hair abnormalities. Cao T; Racz P; Szauter KM; Groma G; Nakamatsu GY; Fogelgren B; Pankotai E; He QP; Csiszar K J Invest Dermatol; 2007 Jun; 127(6):1375-86. PubMed ID: 17273165 [TBL] [Abstract][Full Text] [Related]
24. Rhino-9J (hr(rh9J)): a new allele at the hairless locus. Sundberg JP; Boggess D Vet Pathol; 1998 Jul; 35(4):297-9. PubMed ID: 9684974 [TBL] [Abstract][Full Text] [Related]
25. Uncv (uncovered): a new mutation causing hairloss on mouse chromosome 11. Li SR; Wang DP; Yu XL; Ge BS; Wang CE; Lu YF; Li JQ; Wu N; Li RF; Zhu SE; Zhang ZC; Chen YF Genet Res; 1999 Jun; 73(3):233-8. PubMed ID: 10425919 [TBL] [Abstract][Full Text] [Related]
26. A molecular model for the genetic and phenotypic characteristics of the mouse lethal yellow (Ay) mutation. Michaud EJ; Bultman SJ; Klebig ML; van Vugt MJ; Stubbs LJ; Russell LB; Woychik RP Proc Natl Acad Sci U S A; 1994 Mar; 91(7):2562-6. PubMed ID: 8146154 [TBL] [Abstract][Full Text] [Related]
27. Patchy fur, a mouse coat mutation associated with X-Y nondisjunction, maps to the pseudoautosomal boundary region. Korobova O; Lane PW; Perry J; Palmer S; Ashworth A; Davisson MT; Arnheim N Genomics; 1998 Dec; 54(3):556-9. PubMed ID: 9878259 [TBL] [Abstract][Full Text] [Related]
28. The mouse frizzy (fr) and rat 'hairless' (frCR) mutations are natural variants of protease serine S1 family member 8 (Prss8). Spacek DV; Perez AF; Ferranti KM; Wu LK; Moy DM; Magnan DR; King TR Exp Dermatol; 2010 Jun; 19(6):527-32. PubMed ID: 20201958 [TBL] [Abstract][Full Text] [Related]
29. Progressive hair loss and myocardial degeneration in rough coat mice: reduced lysyl oxidase-like (LOXL) in the skin and heart. Hayashi K; Cao T; Passmore H; Jourdan-Le Saux C; Fogelgren B; Khan S; Hornstra I; Kim Y; Hayashi M; Csiszar K J Invest Dermatol; 2004 Nov; 123(5):864-71. PubMed ID: 15482472 [TBL] [Abstract][Full Text] [Related]
30. Role of the Nh (Non-hair) mutation in the development of dermatitis and hyperproduction of IgE in DS-Nh mice. Watanabe A; Takeuchi M; Nagata M; Nakamura K; Nakao H; Yamashita H; Makino S; Harada M; Hirasawa T Exp Anim; 2003 Oct; 52(5):419-23. PubMed ID: 14625409 [TBL] [Abstract][Full Text] [Related]
31. Mapping the mouse craniofacial mutation first arch (Far) to chromosome 2. Juriloff DM; Harris MJ J Hered; 1991; 82(5):402-5. PubMed ID: 1940283 [TBL] [Abstract][Full Text] [Related]
32. HEM dysplasia and ichthyosis are likely laminopathies and not due to 3beta-hydroxysterol Delta14-reductase deficiency. Wassif CA; Brownson KE; Sterner AL; Forlino A; Zerfas PM; Wilson WK; Starost MF; Porter FD Hum Mol Genet; 2007 May; 16(10):1176-87. PubMed ID: 17403717 [TBL] [Abstract][Full Text] [Related]
33. Epidermis is the site of action of tabby (Ta) in the mouse. Mayer TC; Green MC Genetics; 1978 Sep; 90(1):125-31. PubMed ID: 359407 [TBL] [Abstract][Full Text] [Related]
34. Angora mouse mutation: altered hair cycle, follicular dystrophy, phenotypic maintenance of skin grafts, and changes in keratin expression. Sundberg JP; Rourk MH; Boggess D; Hogan ME; Sundberg BA; Bertolino AP Vet Pathol; 1997 May; 34(3):171-9. PubMed ID: 9163872 [TBL] [Abstract][Full Text] [Related]
35. Retinal degeneration 12 (rd12): a new, spontaneously arising mouse model for human Leber congenital amaurosis (LCA). Pang JJ; Chang B; Hawes NL; Hurd RE; Davisson MT; Li J; Noorwez SM; Malhotra R; McDowell JH; Kaushal S; Hauswirth WW; Nusinowitz S; Thompson DA; Heckenlively JR Mol Vis; 2005 Feb; 11():152-62. PubMed ID: 15765048 [TBL] [Abstract][Full Text] [Related]
36. A lysosomal storage disorder in mice characterized by the accumulation of several sphingolipids. Pentchev PG; Gal AE; Boothe AD; Fouks J; Omodeo-Sale F; Brady RO Birth Defects Orig Artic Ser; 1980; 16(1):225-30. PubMed ID: 7448355 [TBL] [Abstract][Full Text] [Related]
37. The Igh-V locus of MRL mice: restriction fragment length polymorphism in eleven strains of mice as determined with VH and D gene probes. Trepicchio W; Barrett KJ J Immunol; 1985 Apr; 134(4):2734-9. PubMed ID: 2982952 [TBL] [Abstract][Full Text] [Related]
38. Fine mapping of the circling (cir) gene on the distal portion of mouse chromosome 9. Cho KI; Lee JW; Kim KS; Lee EJ; Suh JG; Lee HJ; Kim HT; Hong SH; Chung WH; Chang KT; Hyun BH; Oh YS; Ryoo ZY Comp Med; 2003 Dec; 53(6):642-8. PubMed ID: 14727813 [TBL] [Abstract][Full Text] [Related]
39. Location of plucked (pk) on chromosome 18 of the mouse. Lane PW; Eicher EM J Hered; 1985; 76(6):476-7. PubMed ID: 4086792 [TBL] [Abstract][Full Text] [Related]
40. The mouse frizzy mutation (fr) maps between D7Csu5 and D7Mit165. Paul EL; Badal R; Thompson DS; Magnan DR; Soucy FM; Khan IM; Haughton RA; King TR Exp Dermatol; 2008 Aug; 17(8):640-4. PubMed ID: 18177347 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]