BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

95 related articles for article (PubMed ID: 10777357)

  • 1. Marie Unna hereditary hypotrichosis gene maps to human chromosome 8p21 near hairless.
    Sreekumar GP; Roberts JL; Wong CQ; Stenn KS; Parimoo S
    J Invest Dermatol; 2000 Mar; 114(3):595-7. PubMed ID: 10777357
    [No Abstract]   [Full Text] [Related]  

  • 2. Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysis.
    Lefevre P; Rochat A; Bodemer C; Vabres P; Barrandon Y; de Prost Y; Garner C; Hovnanian A
    Eur J Hum Genet; 2000 Apr; 8(4):273-9. PubMed ID: 10854110
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family.
    Cichon S; Kruse R; Hillmer AM; Kukuk G; Anker M; Altland K; Knapp M; Propping P; Nöthen MM
    Br J Dermatol; 2000 Oct; 143(4):811-4. PubMed ID: 11069461
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Refinement of a locus for Marie Unna hereditary hypotrichosis to a 1.1-cM interval at 8p21.3.
    He PP; Zhang XJ; Yang Q; Li M; Liang YH; Yang S; Yan KL; Cui Y; Shen YY; Wang HY; Sun LD; Du WH; Shen YJ; Xu SJ; Huang W
    Br J Dermatol; 2004 May; 150(5):837-42. PubMed ID: 15149494
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Progressive patterned scalp hypotrichosis, with wiry hair, onycholysis, and intermittently associated cleft lip and palate: clinical and genetic distinction from Marie Unna.
    Green J; Fitzpatrick E; de Berker D; Forrest SM; Sinclair RD
    J Investig Dermatol Symp Proc; 2003 Jun; 8(1):121-5. PubMed ID: 12895008
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Marie Unna hereditary hypotrichosis: identification of a U2HR mutation in the family from the original 1925 report.
    Redler S; Kruse R; Eigelshoven S; Hanneken S; Refke M; Wen Y; Zhang X; Cichon S; Betz RC; Nöthen MM
    J Am Acad Dermatol; 2011 Apr; 64(4):e45-50. PubMed ID: 20659777
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript.
    Ramot Y; Horev L; Smolovich I; Molho-Pessach V; Zlotogorski A
    Exp Dermatol; 2010 Aug; 19(8):e320-2. PubMed ID: 20163456
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of a U2HR gene mutation in Turkish families with Marie Unna hereditary hypotrichosis.
    Düzenli S; Redler S; Müller M; Polat M; Dogruer D; Pasternack SM; Betz RC
    Clin Exp Dermatol; 2009 Dec; 34(8):e953-6. PubMed ID: 20055871
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Erythrocyte dematin is a candidate gene for Marie Unna hereditary hypotrichosis and related hairloss disorders.
    Mohseni M; Chishti AH
    Am J Hematol; 2008 May; 83(5):430-2. PubMed ID: 18273904
    [No Abstract]   [Full Text] [Related]  

  • 10. Marie Unna hereditary hypotrichosis.
    Argenziano G; Sammarco E; Rossi A; Delfino M; Calvieri S
    Eur J Dermatol; 1999 Jun; 9(4):278-80. PubMed ID: 10356404
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Marie Unna hereditary hypotrichosis: report of a Chinese family and evidence for genetic heterogeneity.
    Yan KL; He PP; Yang S; Li M; Yang Q; Ren YQ; Cui Y; Gao M; Xiao FL; Huang W; Zhang XJ
    Clin Exp Dermatol; 2004 Sep; 29(5):460-3. PubMed ID: 15347323
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
    Spiegl B; Hundeiker M
    Fortschr Med; 1979 Nov; 97(44):2018-22. PubMed ID: 511082
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.
    van Steensel M; Smith FJ; Steijlen PM; Kluijt I; Stevens HP; Messenger A; Kremer H; Dunnill MG; Kennedy C; Munro CS; Doherty VR; McGrath JA; Covello SP; Coleman CM; Uitto J; McLean WH
    Am J Hum Genet; 1999 Aug; 65(2):413-9. PubMed ID: 10417283
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a novel locus for Marie Unna hereditary hypotrichosis to a 17.5 cM interval at 1p21.1-1q21.3.
    Yang S; Gao M; Cui Y; Yan KL; Ren YQ; Zhang GL; Wang PG; Xiao FL; Du WH; Liang YH; Sun LD; Xu SJ; Huang W; Zhang XJ
    J Invest Dermatol; 2005 Oct; 125(4):711-4. PubMed ID: 16185270
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Marie Unna hereditary hypotrichosis: a Turkish family with loss of eyebrows and a U2HR mutation.
    Mansur AT; Elcioglu NH; Redler S; Serdar ZA; Cetinel S; Betz RC; Akarsu NA
    Am J Med Genet A; 2010 Oct; 152A(10):2628-33. PubMed ID: 20814945
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a novel U2HR mutation in a Korean woman with Marie Unna hereditary hypotrichosis.
    Yun SK; Cho YG; Song KH; Hwang SR; Kim Yoon SJ; Choi KW; Kim HU; Park J
    Int J Dermatol; 2014 Nov; 53(11):1358-61. PubMed ID: 24961381
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Marie Unna hypotrichosis in a Chinese family.
    Wong SN; Giam YC; Lee YS
    Pediatr Dermatol; 2002; 19(3):250-5. PubMed ID: 12047647
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary hypotrichosis (Marie-Unna type) and juvenile macular degeneration (Stargardt's maculopathy).
    Marren P; Wilson C; Dawber RP; Walshe MM
    Clin Exp Dermatol; 1992 May; 17(3):189-91. PubMed ID: 1451298
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Hereditary congenital hypotrichosis, Marie Unna type].
    Chlebarov S
    Z Hautkr; 1985 Apr; 60(7):583-96. PubMed ID: 4002769
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hereditary hypotrichosis (Marie-Unna type) (two cases).
    Hutchinson PE; Wells RS
    Proc R Soc Med; 1975 Aug; 68(8):534-5. PubMed ID: 1202498
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.