193 related articles for article (PubMed ID: 12754508)
21. Targeted deletion of the murine corneodesmosin gene delineates its essential role in skin and hair physiology.
Matsumoto M; Zhou Y; Matsuo S; Nakanishi H; Hirose K; Oura H; Arase S; Ishida-Yamamoto A; Bando Y; Izumi K; Kiyonari H; Oshima N; Nakayama R; Matsushima A; Hirota F; Mouri Y; Kuroda N; Sano S; Chaplin DD
Proc Natl Acad Sci U S A; 2008 May; 105(18):6720-4. PubMed ID: 18436651
[TBL] [Abstract][Full Text] [Related]
22. Familial hypotrichosis simplex of the scalp associated with a novel heterozygous nonsense variant in CDSN.
Rayinda T; McSweeney SM; Lalagianni N; Liu L; Guy A; Fenton D; Stefanato CM; Dand N; McGrath JA; Tziotzios C
Clin Exp Dermatol; 2023 Apr; 48(5):579-583. PubMed ID: 36864587
[No Abstract] [Full Text] [Related]
23. Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease.
Oji V; Eckl KM; Aufenvenne K; Nätebus M; Tarinski T; Ackermann K; Seller N; Metze D; Nürnberg G; Fölster-Holst R; Schäfer-Korting M; Hausser I; Traupe H; Hennies HC
Am J Hum Genet; 2010 Aug; 87(2):274-81. PubMed ID: 20691404
[TBL] [Abstract][Full Text] [Related]
24. Human hair growth deficiency is linked to a genetic defect in the phospholipase gene LIPH.
Kazantseva A; Goltsov A; Zinchenko R; Grigorenko AP; Abrukova AV; Moliaka YK; Kirillov AG; Guo Z; Lyle S; Ginter EK; Rogaev EI
Science; 2006 Nov; 314(5801):982-5. PubMed ID: 17095700
[TBL] [Abstract][Full Text] [Related]
25. APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex.
Shimomura Y; Agalliu D; Vonica A; Luria V; Wajid M; Baumer A; Belli S; Petukhova L; Schinzel A; Brivanlou AH; Barres BA; Christiano AM
Nature; 2010 Apr; 464(7291):1043-7. PubMed ID: 20393562
[TBL] [Abstract][Full Text] [Related]
26. A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.
Betz RC; Lee YA; Bygum A; Brandrup F; Bernal AI; Toribio J; Alvarez JI; Kukuk GM; Ibsen HH; Rasmussen HB; Wienker TF; Reis A; Propping P; Kruse R; Cichon S; Nöthen MM
Am J Hum Genet; 2000 Jun; 66(6):1979-83. PubMed ID: 10793007
[TBL] [Abstract][Full Text] [Related]
27. Mutations in the lipase-H gene causing autosomal recessive hypotrichosis and woolly hair.
Mehmood S; Jan A; Muhammad D; Ahmad F; Mir H; Younus M; Ali G; Ayub M; Ansar M; Ahmad W
Australas J Dermatol; 2015 Aug; 56(3):e66-70. PubMed ID: 24628704
[TBL] [Abstract][Full Text] [Related]
28. Transforming growth factor-beta receptor II is preferentially expressed in the companion layer of the human anagen hair follicle.
Sowden HM; Karoo RO; Tobin DJ
Br J Dermatol; 2007 Jul; 157(1):161-4. PubMed ID: 17578439
[TBL] [Abstract][Full Text] [Related]
29. [Hypotrichosis congenita hereditaria Maria Unna].
Wirth G; Bindewald I; Küster W; Goerz G
Hautarzt; 1985 Oct; 36(10):577-80. PubMed ID: 4066319
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. A novel mutation in LPAR6 causes autosomal recessive hypotrichosis of the scalp.
Nahum S; Morice-Picard F; Taieb A; Sprecher E
Clin Exp Dermatol; 2011 Mar; 36(2):188-94. PubMed ID: 21070332
[TBL] [Abstract][Full Text] [Related]
32. Mutations in the desmoglein 4 gene underlie localized autosomal recessive hypotrichosis with monilethrix hairs and congenital scalp erosions.
Schaffer JV; Bazzi H; Vitebsky A; Witkiewicz A; Kovich OI; Kamino H; Shapiro LS; Amin SP; Orlow SJ; Christiano AM
J Invest Dermatol; 2006 Jun; 126(6):1286-91. PubMed ID: 16543896
[TBL] [Abstract][Full Text] [Related]
33. Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings.
Indelman M; Leibu R; Jammal A; Bergman R; Sprecher E
Br J Dermatol; 2005 Sep; 153(3):635-8. PubMed ID: 16120155
[TBL] [Abstract][Full Text] [Related]
34. A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2).
Jelani M; Wasif N; Ali G; Chishti M; Ahmad W
Clin Genet; 2008 Aug; 74(2):184-8. PubMed ID: 18445047
[TBL] [Abstract][Full Text] [Related]
35. Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament.
Tanaka S; Miura I; Yoshiki A; Kato Y; Yokoyama H; Shinogi A; Masuya H; Wakana S; Tamura M; Shiroishi T
Genomics; 2007 Dec; 90(6):703-11. PubMed ID: 17920809
[TBL] [Abstract][Full Text] [Related]
36. Inflammatory peeling skin syndrome caused a novel mutation in CDSN.
Telem DF; Israeli S; Sarig O; Sprecher E
Arch Dermatol Res; 2012 Apr; 304(3):251-5. PubMed ID: 22146835
[TBL] [Abstract][Full Text] [Related]
37. Localization of a novel autosomal recessive hypotrichosis locus (LAH3) to chromosome 13q14.11-q21.32.
Wali A; Chishti M; Ayub M; Yasinzai M; Kafaitullah ; Ali G; John P; Ahmad W
Clin Genet; 2007 Jul; 72(1):23-9. PubMed ID: 17594396
[TBL] [Abstract][Full Text] [Related]
38. Expression of vascular endothelial growth factor, apoptosis inhibitors (survivin and p16) and CCL27 in alopecia areata before and after diphencyprone treatment: an immunohistochemical study.
Simonetti O; Lucarini G; Bernardini ML; Simoncini C; Biagini G; Offidani A
Br J Dermatol; 2004 May; 150(5):940-8. PubMed ID: 15149507
[TBL] [Abstract][Full Text] [Related]
39. A
Jacinto JGP; Markey AD; Veiga IMB; Paris JM; Welle M; Beever JE; Drögemüller C
Genes (Basel); 2021 Jul; 12(7):. PubMed ID: 34356054
[TBL] [Abstract][Full Text] [Related]
40. CD10 is expressed in dermal sheath cells of the hair follicles in human scalp.
Lee KJ; Choi YL; Kim WS; Lee JH; Yang JM; Lee ES; Lee DY; Jang KT
Br J Dermatol; 2006 Oct; 155(4):858-60. PubMed ID: 16965452
[No Abstract] [Full Text] [Related]
[Previous] [Next] [New Search]
