154 related articles for article (PubMed ID: 15606503)
1. Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo "hairless" rat.
Bazzi H; Kljuic A; Christiano AM; Christiano AM; Panteleyev AA
Differentiation; 2004 Oct; 72(8):450-64. PubMed ID: 15606503
[TBL] [Abstract][Full Text] [Related]
2. The Charles River "hairless" rat mutation is distinct from the hairless mouse alleles.
Panteleyev AA; Christiano AM
Comp Med; 2001 Feb; 51(1):49-55. PubMed ID: 11926302
[TBL] [Abstract][Full Text] [Related]
3. A spontaneous mutation in the desmoglein 4 gene underlies hypotrichosis in a new lanceolate hair rat model.
Meyer B; Bazzi H; Zidek V; Musilova A; Pravenec M; Kurtz TW; Nurnberg P; Christiano AM
Differentiation; 2004 Dec; 72(9-10):541-7. PubMed ID: 15617564
[TBL] [Abstract][Full Text] [Related]
4. Desmoglein 4 mutations underlie localized autosomal recessive hypotrichosis in humans, mice, and rats.
Bazzi H; Martinez-Mir A; Kljuic A; Christiano AM
J Investig Dermatol Symp Proc; 2005 Dec; 10(3):222-4. PubMed ID: 16382669
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene.
Jahoda CA; Kljuic A; O'Shaughnessy R; Crossley N; Whitehouse CJ; Robinson M; Reynolds AJ; Demarchez M; Porter RM; Shapiro L; Christiano AM
Genomics; 2004 May; 83(5):747-56. PubMed ID: 15081105
[TBL] [Abstract][Full Text] [Related]
7. Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins.
John P; Tariq M; Arshad Rafiq M; Amin-Ud-Din M; Muhammad D; Waheed I; Ansar M; Ahmad W
Arch Dermatol Res; 2006 Aug; 298(3):135-7. PubMed ID: 16770573
[TBL] [Abstract][Full Text] [Related]
8. A new allele of the mouse hairless gene interferes with Hox/LacZ transgene regulation in hair follicle primordia.
Brancaz MV; Iratni R; Morrison A; Mancini SJ; Marche P; Sundberg J; Nonchev S
Exp Mol Pathol; 2004 Apr; 76(2):173-81. PubMed ID: 15010296
[TBL] [Abstract][Full Text] [Related]
9. Desmoglein genes are up-regulated in the pk mutant mouse.
Luo J; Zhang L; Stenn K; Prouty S; Parimoo S
Biochem Biophys Res Commun; 2005 Feb; 327(1):64-9. PubMed ID: 15629430
[TBL] [Abstract][Full Text] [Related]
10. Desmoglein 4 is expressed in highly differentiated keratinocytes and trichocytes in human epidermis and hair follicle.
Bazzi H; Getz A; Mahoney MG; Ishida-Yamamoto A; Langbein L; Wahl JK; Christiano AM
Differentiation; 2006 Mar; 74(2-3):129-40. PubMed ID: 16533311
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular basis for the rhino (hrrh-8J) phenotype: a nonsense mutation in the mouse hairless gene.
Ahmad W; Panteleyev AA; Sundberg JP; Christiano AM
Genomics; 1998 Nov; 53(3):383-6. PubMed ID: 9799606
[TBL] [Abstract][Full Text] [Related]
13. Mutations in lipase H cause autosomal recessive hypotrichosis simplex with woolly hair.
Horev L; Tosti A; Rosen I; Hershko K; Vincenzi C; Nanova K; Mali A; Potikha T; Zlotogorski A
J Am Acad Dermatol; 2009 Nov; 61(5):813-8. PubMed ID: 19766349
[TBL] [Abstract][Full Text] [Related]
14. [Analysis of the effects of mutant hairless genes in chimeric mice].
Martynova MIu; Isaev DA; Koniukhov BV
Genetika; 2003 Sep; 39(9):1252-7. PubMed ID: 14582395
[TBL] [Abstract][Full Text] [Related]
15. Genomic organization and analysis of the hairless gene in four hypotrichotic rat strains.
Kim H; Panteleyev AA; Jahoda CA; Ishii Y; Christiano AM
Mamm Genome; 2004 Dec; 15(12):975-81. PubMed ID: 15599556
[TBL] [Abstract][Full Text] [Related]
16. Mutations in the desmoglein 4 gene are associated with monilethrix-like congenital hypotrichosis.
Shimomura Y; Sakamoto F; Kariya N; Matsunaga K; Ito M
J Invest Dermatol; 2006 Jun; 126(6):1281-5. PubMed ID: 16439973
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions.
Schaffer JV; Bazzi H; Vitebsky A; Witkiewicz A; Kovich OI; Kamino H; Shapiro LS; Amin SP; Orlow SJ; Christiano AM
J Invest Dermatol; 2006 Jun; 126(6):1286-91. PubMed ID: 16543896
[TBL] [Abstract][Full Text] [Related]
18. Beauty is skin deep: the fascinating biology of the epidermis and its appendages.
Fuchs E
Harvey Lect; 1998-1999; 94():47-77. PubMed ID: 11070952
[TBL] [Abstract][Full Text] [Related]
19. The hairless gene of the mouse: relationship of phenotypic effects with expression profile and genotype.
Cachón-González MB; San-José I; Cano A; Vega JA; García N; Freeman T; Schimmang T; Stoye JP
Dev Dyn; 1999 Oct; 216(2):113-26. PubMed ID: 10536052
[TBL] [Abstract][Full Text] [Related]
20. Three variations of hairlessness associated with albinism in the laboratory rat.
Ferguson FG; Irving GW; Stedham MA
Lab Anim Sci; 1979 Aug; 29(4):459-64. PubMed ID: 513614
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]