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.
130 related articles for article (PubMed ID: 8281013)
21. The near-naked hairless (Hr(N)) mutation disrupts hair formation but is not due to a mutation in the Hairless coding region. Liu Y; Das S; Olszewski RE; Carpenter DA; Culiat CT; Sundberg JP; Soteropoulos P; Liu X; Doktycz MJ; Michaud EJ; Voy BH J Invest Dermatol; 2007 Jul; 127(7):1605-14. PubMed ID: 17330134 [TBL] [Abstract][Full Text] [Related]
22. Vesicle formation and follicular root sheath separation in mice homozygous for deleterious alleles at the balding (bal) locus. Montagutelli X; Lalouette A; Boulouis HJ; Guénet JL; Sundberg JP J Invest Dermatol; 1997 Sep; 109(3):324-8. PubMed ID: 9284099 [TBL] [Abstract][Full Text] [Related]
23. Spatially restricted hypopigmentation associated with an Ednrbs-modifying locus on mouse chromosome 10. Rhim H; Dunn KJ; Aronzon A; Mac S; Cheng M; Lamoreux ML; Tilghman SM; Pavan WJ Genome Res; 2000 Jan; 10(1):17-29. PubMed ID: 10645946 [TBL] [Abstract][Full Text] [Related]
24. Kyoto rhino rats derived by ENU mutagenesis undergo congenital hair loss and exhibit focal glomerulosclerosis. Kuramoto T; Kuwamura M; Tagami F; Mashimo T; Nose M; Serikawa T Exp Anim; 2011; 60(1):57-63. PubMed ID: 21325752 [TBL] [Abstract][Full Text] [Related]
25. Phenotypic and molecular analysis of a transgenic insertional allele of the mouse Fused locus. Perry WL; Vasicek TJ; Lee JJ; Rossi JM; Zeng L; Zhang T; Tilghman SM; Costantini F Genetics; 1995 Sep; 141(1):321-32. PubMed ID: 8536979 [TBL] [Abstract][Full Text] [Related]
26. Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5. Johnson KR; Lane PW; Cook SA; Harris BS; Ward-Bailey PF; Bronson RT; Lyons BL; Shultz LD; Davisson MT Genomics; 2003 Jan; 81(1):6-14. PubMed ID: 12573256 [TBL] [Abstract][Full Text] [Related]
27. Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene. Ahmad W; Ratterree MS; Panteleyev AA; Aita VM; Sundberg JP; Christiano AM Lab Anim; 2002 Jan; 36(1):61-7. PubMed ID: 11831740 [TBL] [Abstract][Full Text] [Related]
28. Molecular basis for the rhino Yurlovo (hr(rhY)) phenotype: severe skin abnormalities and female reproductive defects associated with an insertion in the hairless gene. Panteleyev AA; Ahmad W; Malashenko AM; Ignatieva EL; Paus R; Sundberg JP; Christiano AM Exp Dermatol; 1998 Oct; 7(5):281-8. PubMed ID: 9832316 [TBL] [Abstract][Full Text] [Related]
29. Balding: a new mutation on mouse chromosome 18 causing hair loss and immunological defects. Davisson MT; Cook SA; Johnson KR; Eicher EM J Hered; 1994; 85(2):134-6. PubMed ID: 8182278 [No Abstract] [Full Text] [Related]
30. Morphological analysis of hair in the hr-2 mutant deer mouse (Peromyscus maniculatus). Knapp LW; Dawson WD J Hered; 1991; 82(5):431-4. PubMed ID: 1940285 [TBL] [Abstract][Full Text] [Related]
31. [Gene angora as a modifier of the mouse hairless gene]. Koniukhov BV; Martynova MIu; Nesterova AP Genetika; 2007 Feb; 43(2):254-60. PubMed ID: 17385325 [TBL] [Abstract][Full Text] [Related]
32. The Charles River "hairless" rat mutation maps to chromosome 1: allelic with fuzzy and a likely orthologue of mouse frizzy. Ahearn K; Akkouris G; Berry PR; Chrissluis RR; Crooks IM; Dull AK; Grable S; Jeruzal J; Lanza J; Lavoie C; Maloney RA; Pitruzzello M; Sharma R; Stoklasek TA; Tweeddale J; King TR J Hered; 2002; 93(3):210-3. PubMed ID: 12195039 [TBL] [Abstract][Full Text] [Related]
33. [The mouse hairless gene: its function in hair root and at the heart of a subtle pleiotropy]. Nonchev S; Brancaz MV; Folco E; Romero Y; Iratni R Med Sci (Paris); 2006 May; 22(5):525-30. PubMed ID: 16687122 [TBL] [Abstract][Full Text] [Related]
34. Fuzzy, a hypotrichotic mutant in linkage group I of the Norway rat. Palm J; Ferguson FG J Hered; 1976; 67(5):284-8. PubMed ID: 1010929 [TBL] [Abstract][Full Text] [Related]
35. Phenotypic characterization of the transgenic mouse insertional mutation, legless. McNeish JD; Thayer J; Walling K; Sulik KK; Potter SS; Scott WJ J Exp Zool; 1990 Feb; 253(2):151-62. PubMed ID: 2313245 [TBL] [Abstract][Full Text] [Related]
36. Identification of a new chemically induced allele (Lp(m1Jus)) at the loop-tail locus: morphology, histology, and genetic mapping. Kibar Z; Underhill DA; Canonne-Hergaux F; Gauthier S; Justice MJ; Gros P Genomics; 2001 Mar; 72(3):331-7. PubMed ID: 11401449 [TBL] [Abstract][Full Text] [Related]
37. Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia. Cichon S; Anker M; Vogt IR; Rohleder H; Pützstück M; Hillmer A; Farooq SA; Al-Dhafri KS; Ahmad M; Haque S; Rietschel M; Propping P; Kruse R; Nöthen MM Hum Mol Genet; 1998 Oct; 7(11):1671-9. PubMed ID: 9736769 [TBL] [Abstract][Full Text] [Related]
38. Alopecia universalis associated with a mutation in the human hairless gene. Ahmad W; Faiyaz ul Haque M; Brancolini V; Tsou HC; ul Haque S; Lam H; Aita VM; Owen J; deBlaquiere M; Frank J; Cserhalmi-Friedman PB; Leask A; McGrath JA; Peacocke M; Ahmad M; Ott J; Christiano AM Science; 1998 Jan; 279(5351):720-4. PubMed ID: 9445480 [TBL] [Abstract][Full Text] [Related]
39. Gaping lids, gp, a mutation on centromeric chromosome 11 that causes defective eyelid development in mice. Juriloff DM; Harris MJ; Banks KG; Mah DG Mamm Genome; 2000 Jun; 11(6):440-7. PubMed ID: 10818208 [TBL] [Abstract][Full Text] [Related]
40. A null mutation at the mouse Phosphoglucomutase-1 locus and a new locus Pgm-3. Johnson FM; Hendren RW; Chasalow F; Barnett LB; Lewis SE Biochem Genet; 1981 Jun; 19(5-6):599-615. PubMed ID: 6457600 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]