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 *

193 related articles for article (PubMed ID: 11564167)

  • 1. 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]  

  • 2. Clinical and pathologic correlations in genetically distinct forms of atrichia.
    Zlotogorski A; Hochberg Z; Mirmirani P; Metzker A; Ben-Amitai D; Martinez-Mir A; Panteleyev AA; Christiano AM
    Arch Dermatol; 2003 Dec; 139(12):1591-6. PubMed ID: 14676077
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Interactions of the vitamin D receptor with the corepressor hairless: analysis of hairless mutants in atrichia with papular lesions.
    Wang J; Malloy PJ; Feldman D
    J Biol Chem; 2007 Aug; 282(35):25231-9. PubMed ID: 17609203
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Atrichia with papular lesions in two Pakistani consanguineous families resulting from mutations in the human hairless gene.
    John P; Aslam M; Rafiq MA; Amin-ud-din M; Haque S; Ahmad W
    Arch Dermatol Res; 2005 Nov; 297(5):226-30. PubMed ID: 16211417
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Development and progression of alopecia in the vitamin D receptor null mouse.
    Bikle DD; Elalieh H; Chang S; Xie Z; Sundberg JP
    J Cell Physiol; 2006 May; 207(2):340-53. PubMed ID: 16419036
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The alopecias associated with vitamin D-dependent rickets type IIA and with hairless gene mutations: a comparative clinical, histologic, and immunohistochemical study.
    Bergman R; Schein-Goldshmid R; Hochberg Z; Ben-Izhak O; Sprecher E
    Arch Dermatol; 2005 Mar; 141(3):343-51. PubMed ID: 15781675
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia.
    Malloy PJ; Wang J; Peng L; Nayak S; Sisk JM; Thompson CC; Feldman D
    Arch Biochem Biophys; 2007 Apr; 460(2):285-92. PubMed ID: 17078924
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Atrichia with papular lesions: a report of three novel human hairless gene mutations and a revision of diagnostic criteria.
    Yip L; Horev L; Sinclair R; Zlotogorski A
    Acta Derm Venereol; 2008; 88(4):346-9. PubMed ID: 18709303
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Evidence for pseudodominant inheritance of atrichia with papular lesions.
    Zlotogorski A; Martinez-Mir A; Green J; Lamdagger H; Panteleyevdagger AA; Sinclair R; Christiano AM
    J Invest Dermatol; 2002 May; 118(5):881-6. PubMed ID: 11982769
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Atrichia with papular lesions resulting from a nonsense mutation within the human hairless gene.
    Sprecher E; Lestringant GG; Szargel R; Bergman R; Labay V; Frossard PM; Friedman-Birnbaum R; Cohen N
    J Invest Dermatol; 1999 Oct; 113(4):687-90. PubMed ID: 10504459
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene.
    Wali A; Ansar M; Khan MN; Ahmad W
    Clin Exp Dermatol; 2006 Sep; 31(5):695-8. PubMed ID: 16901311
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nonsense mutations in the hairless gene underlie APL in five families of Pakistani origin.
    Kim H; Wajid M; Kraemer L; Shimomura Y; Christiano AM
    J Dermatol Sci; 2007 Dec; 48(3):207-11. PubMed ID: 17869066
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Compound heterozygous mutations in the vitamin D receptor in a patient with hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia.
    Zhou Y; Wang J; Malloy PJ; Dolezel Z; Feldman D
    J Bone Miner Res; 2009 Apr; 24(4):643-51. PubMed ID: 19049339
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A missense mutation in the zinc-finger domain of the human hairless gene underlies congenital atrichia in a family of Irish travellers.
    Ahmad W; Irvine AD; Lam H; Buckley C; Bingham EA; Panteleyev AA; Ahmad M; McGrath JA; Christiano AM
    Am J Hum Genet; 1998 Oct; 63(4):984-91. PubMed ID: 9758627
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ligand-independent actions of the vitamin D receptor maintain hair follicle homeostasis.
    Skorija K; Cox M; Sisk JM; Dowd DR; MacDonald PN; Thompson CC; Demay MB
    Mol Endocrinol; 2005 Apr; 19(4):855-62. PubMed ID: 15591533
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The molecular basis of congenital atrichia in humans and mice: mutations in the hairless gene.
    Ahmad W; Panteleyev AA; Christiano AM
    J Investig Dermatol Symp Proc; 1999 Dec; 4(3):240-3. PubMed ID: 10674375
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel Hairless mutations in two kindreds with autosomal recessive papular atrichia.
    Kruse R; Cichon S; Anker M; Hillmer AM; Barros-Núñez P; Cantú JM; Leal E; Weinlich G; Schmuth M; Fritsch P; Ruzicka T; Propping P; Nöthen MM
    J Invest Dermatol; 1999 Dec; 113(6):954-9. PubMed ID: 10594736
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ligand-independent regulation of the hairless promoter by vitamin D receptor.
    Engelhard A; Bauer RC; Casta A; Djabali K; Christiano AM
    Photochem Photobiol; 2008; 84(2):515-21. PubMed ID: 18266815
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 10.