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]