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 *

141 related articles for article (PubMed ID: 9832313)

  • 1. Molecular and functional aspects of the hairless (hr) gene in laboratory rodents and humans.
    Panteleyev AA; Paus R; Ahmad W; Sundberg JP; Christiano AM
    Exp Dermatol; 1998 Oct; 7(5):249-67. PubMed ID: 9832313
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular basis of a novel rhino (hr(rhChr)) phenotype: a nonsense mutation in the mouse hairless gene.
    Ahmad W; Panteleyev AA; Henson-Apollonio V; Sundberg JP; Christiano AM
    Exp Dermatol; 1998 Oct; 7(5):298-301. PubMed ID: 9832318
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. [Mutation of the human hairless gene in atrichia universalis].
    Trüeb RM
    Hautarzt; 1998 Sep; 49(9):687-9. PubMed ID: 9794156
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Molecular basis for hair loss in mice carrying a novel nonsense mutation (Hrrh-R ) in the hairless gene (Hr).
    Liu Y; Sundberg JP; Das S; Carpenter D; Cain KT; Michaud EJ; Voy BH
    Vet Pathol; 2010 Jan; 47(1):167-76. PubMed ID: 20080498
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Of hairless mice and men: the genetic basis of congenital alopecia universalis/congenital atrichia.
    Bale SJ
    J Cutan Med Surg; 1999 Oct; 3(6):309-11. PubMed ID: 10575161
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genomic organization of the human hairless gene (HR) and identification of a mutation underlying congenital atrichia in an Arab Palestinian family.
    Ahmad W; Zlotogorski A; Panteleyev AA; Lam H; Ahmad M; Faiyaz ul Haque M; Abdallah HM; Dragan L; Christiano AM
    Genomics; 1999 Mar; 56(2):141-8. PubMed ID: 10051399
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The hairless mouse in skin research.
    Benavides F; Oberyszyn TM; VanBuskirk AM; Reeve VE; Kusewitt DF
    J Dermatol Sci; 2009 Jan; 53(1):10-8. PubMed ID: 18938063
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Atrichia caused by mutations in the vitamin D receptor gene is a phenocopy of generalized atrichia caused by mutations in the hairless gene.
    Miller J; Djabali K; Chen T; Liu Y; Ioffreda M; Lyle S; Christiano AM; Holick M; Cotsarelis G
    J Invest Dermatol; 2001 Sep; 117(3):612-7. PubMed ID: 11564167
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. Towards defining the pathogenesis of the hairless phenotype.
    Panteleyev AA; van der Veen C; Rosenbach T; Müller-Röver S; Sokolov VE; Paus R
    J Invest Dermatol; 1998 Jun; 110(6):902-7. PubMed ID: 9620297
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [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]  

  • 16. 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]  

  • 17. Congenital atrichia in five Arab Palestinian families resulting from a deletion mutation in the human hairless gene.
    Zlotogorski A; Ahmad W; Christiano AM
    Hum Genet; 1998 Oct; 103(4):400-4. PubMed ID: 9856480
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Patterns of hairless (hr) gene expression in mouse hair follicle morphogenesis and cycling.
    Panteleyev AA; Paus R; Christiano AM
    Am J Pathol; 2000 Oct; 157(4):1071-9. PubMed ID: 11021810
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.