BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

330 related articles for article (PubMed ID: 15708289)

  • 1. Genetic hair and nail disorders.
    Sprecher E
    Clin Dermatol; 2005; 23(1):47-55. PubMed ID: 15708289
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Unraveling the molecular mechanisms of hair and nail genodermatoses.
    Stratigos AJ; Baden HP
    Arch Dermatol; 2001 Nov; 137(11):1465-71. PubMed ID: 11708949
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Molecular genetics of hereditary hair and nail disease.
    van Steensel MA; van Geel M; Steijlen PM
    Am J Med Genet C Semin Med Genet; 2004 Nov; 131C(1):52-60. PubMed ID: 15468149
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation.
    Rasool M; Nawaz S; Azhar A; Wajid M; Westermark P; Baig SM; Klar J; Dahl N
    Eur J Dermatol; 2010; 20(4):443-6. PubMed ID: 20409997
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Family with "pure" hair-nail ectodermal dysplasia.
    Barbareschi M; Cambiaghi S; Crupi AC; Tadini G
    Am J Med Genet; 1997 Oct; 72(1):91-3. PubMed ID: 9295083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Nail changes in genodermatoses.
    Fistarol SK; Itin PH
    Eur J Dermatol; 2002; 12(2):119-28. PubMed ID: 11872405
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pure hair-nail ectodermal dysplasia maps to chromosome 12p11.1-q21.1 in a consanguineous Pakistani family.
    Naeem M; John P; Ali G; Ahmad W
    Clin Exp Dermatol; 2007 Sep; 32(5):502-5. PubMed ID: 17489990
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type.
    Naeem M; Wajid M; Lee K; Leal SM; Ahmad W
    J Med Genet; 2006 Mar; 43(3):274-9. PubMed ID: 16525032
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutations in the gene HOXC13 underlying pure hair and nail ectodermal dysplasia in consanguineous families.
    Ali RH; Habib R; Ud-Din N; Khan MN; Ansar M; Ahmad W
    Br J Dermatol; 2013 Aug; 169(2):478-80. PubMed ID: 23461661
    [No Abstract]   [Full Text] [Related]  

  • 10. Keratin disorders: from gene to therapy.
    McLean WH; Moore CB
    Hum Mol Genet; 2011 Oct; 20(R2):R189-97. PubMed ID: 21890491
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Familial congenital hypotrichosis with "uncombable hair," retinal pigmentary dystrophy, juvenile cataract and brachymetacarpia: another entity of the ectodermal dysplasia group].
    Bork K; Stender E; Schmidt D; Berzas C; Rochels R
    Hautarzt; 1987 Jun; 38(6):342-7. PubMed ID: 3654205
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in the keratin 85 (KRT85/hHb5) gene underlie pure hair and nail ectodermal dysplasia.
    Shimomura Y; Wajid M; Kurban M; Sato N; Christiano AM
    J Invest Dermatol; 2010 Mar; 130(3):892-5. PubMed ID: 19865094
    [No Abstract]   [Full Text] [Related]  

  • 13. Heritable disorders of hair.
    Birnbaum PS; Baden HP
    Dermatol Clin; 1987 Jan; 5(1):137-53. PubMed ID: 3549074
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
    Tariq M; Chishti MS; Ali G; Ahmad W
    Ann Hum Genet; 2008 Jan; 72(Pt 1):19-25. PubMed ID: 18184143
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Heritable nail diseases.
    Gass SF; Guberman RM; D'Orazi ST; Furci TJ
    Clin Podiatr Med Surg; 1989 Apr; 6(2):339-45. PubMed ID: 2650844
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mosaicism in genetic skin disorders.
    Siegel DH; Sybert VP
    Pediatr Dermatol; 2006; 23(1):87-92. PubMed ID: 16445423
    [No Abstract]   [Full Text] [Related]  

  • 17. [Hair anomalies in syndromic disorders].
    Frank J; Betz RC
    Hautarzt; 2019 Jul; 70(7):514-519. PubMed ID: 31197391
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Connexin disorders of the skin.
    Richard G
    Clin Dermatol; 2005; 23(1):23-32. PubMed ID: 15708286
    [TBL] [Abstract][Full Text] [Related]  

  • 19. GJB6, of which mutations underlie Clouston syndrome, is a potential direct target gene of p63.
    Fujimoto A; Kurban M; Nakamura M; Farooq M; Fujikawa H; Kibbi AG; Ito M; Dahdah M; Matta M; Diab H; Shimomura Y
    J Dermatol Sci; 2013 Feb; 69(2):159-66. PubMed ID: 23219093
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Association of ectodermal dysplasia and syndactylia].
    Boudghene-Stambouli O; Merad-Boudia A
    Ann Dermatol Venereol; 1991; 118(2):107-10. PubMed ID: 1646587
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 17.