154 related articles for article (PubMed ID: 25557232)
1. Novel KRT83 and KRT86 mutations associated with monilethrix.
van Steensel M; Vreeburg M; Urbina MT; López P; Morice-Picard F; van Geel M
Exp Dermatol; 2015 Mar; 24(3):222-4. PubMed ID: 25557232
[TBL] [Abstract][Full Text] [Related]
2. A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance.
De Cruz R; Horev L; Green J; Babay S; Sladden M; Zlotogorski A; Sinclair R
Br J Dermatol; 2012 Jun; 166 Suppl 2():20-6. PubMed ID: 22670615
[TBL] [Abstract][Full Text] [Related]
3. A novel KRT86 mutation in a Turkish family with monilethrix, and identification of maternal mosaicism.
Redler S; Pasternack SM; Wolf S; Stienen D; Wenzel J; Nöthen MM; Betz RC
Clin Exp Dermatol; 2015 Oct; 40(7):781-5. PubMed ID: 25809918
[TBL] [Abstract][Full Text] [Related]
4. Recessive progressive symmetric erythrokeratoderma results from a homozygous loss-of-function mutation of
Shah K; Ansar M; Mughal ZU; Khan FS; Ahmad W; Ferrara TM; Spritz RA
J Med Genet; 2017 Mar; 54(3):186-189. PubMed ID: 27965375
[TBL] [Abstract][Full Text] [Related]
5. Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix.
Ye ZZ; Nan X; Zhao HS; Chen XR; Song QH
Chin Med J (Engl); 2013 Aug; 126(16):3103-6. PubMed ID: 23981620
[TBL] [Abstract][Full Text] [Related]
6. Identification of a novel missense KRT86 mutation in a Chinese family with monilethrix.
Deng Y; Xia D; Wang L; Li M; Li W
J Dermatol; 2018 Nov; 45(11):e298-e300. PubMed ID: 29701253
[No Abstract] [Full Text] [Related]
7. Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
Celep F; Uzumcu A; Sonmez FM; Uyguner O; Balci YI; Bahadir S; Karaguzel A
Genet Couns; 2009; 20(1):1-8. PubMed ID: 19400537
[TBL] [Abstract][Full Text] [Related]
8. A new KRT86 mutation in a Chinese family with monilethrix.
Li XY; Wang S; Chen XM
Clin Exp Dermatol; 2022 Feb; 47(2):461-463. PubMed ID: 34610158
[No Abstract] [Full Text] [Related]
9. A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix.
Wu J; Lin Y; Xu W; Li Z; Fan W
J Biomed Res; 2011 Jan; 25(1):49-55. PubMed ID: 23554671
[TBL] [Abstract][Full Text] [Related]
10. Congenital monilethrix and hereditary unilateral external auditory canal atresia are co-inherited in a Chinese pedigree with recurrent KRT86 mutation.
Feng YG; Xiao SX; Xu AL; Feng JY; Wang JM
J Dermatol; 2012 Sep; 39(9):817-9. PubMed ID: 22568869
[No Abstract] [Full Text] [Related]
11. A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene.
Farooq M; Ito M; Naito M; Shimomura Y
Br J Dermatol; 2011 Aug; 165(2):425-31. PubMed ID: 21495994
[TBL] [Abstract][Full Text] [Related]
12. Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene.
Nedoszytko B; Lewicka-Potocka Z; Szczerkowska-Dobosz A; Gleń J; Bykowska B; Świątecka-Czaj J; Nowicki R
J Eur Acad Dermatol Venereol; 2017 Sep; 31(9):e409-e410. PubMed ID: 28299823
[No Abstract] [Full Text] [Related]
13. Autosomal recessive monilethrix: Novel variants of the DSG4 gene in three Chinese families.
Zhou C; Wang P; Yang D; Liao W; Guo Q; Li J; Wen G; Zheng S; Zhang X; Wang R; Zhang J
Mol Genet Genomic Med; 2022 Apr; 10(4):e1889. PubMed ID: 35146972
[TBL] [Abstract][Full Text] [Related]
14. Keratins: the hair shaft's backbone revealed.
Ramot Y; Zlotogorski A
Exp Dermatol; 2015 Jun; 24(6):416-7. PubMed ID: 25653108
[No Abstract] [Full Text] [Related]
15. Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family.
Dai R; Wang T; Wu X
An Bras Dermatol; 2024; 99(4):606-609. PubMed ID: 38594178
[No Abstract] [Full Text] [Related]
16. Annotation of sheep keratin intermediate filament genes and their patterns of expression.
Yu Z; Wildermoth JE; Wallace OA; Gordon SW; Maqbool NJ; Maclean PH; Nixon AJ; Pearson AJ
Exp Dermatol; 2011 Jul; 20(7):582-8. PubMed ID: 21554405
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix.
Winter H; Rogers MA; Langbein L; Stevens HP; Leigh IM; Labrèze C; Roul S; Taieb A; Krieg T; Schweizer J
Nat Genet; 1997 Aug; 16(4):372-4. PubMed ID: 9241275
[TBL] [Abstract][Full Text] [Related]
18. Monilethrix: a novel mutation (Glu402Lys) in the helix termination motif and the first causative mutation (Asn114Asp) in the helix initiation motif of the type II hair keratin hHb6.
Winter H; Clark RD; Tarras-Wahlberg C; Rogers MA; Schweizer J
J Invest Dermatol; 1999 Aug; 113(2):263-6. PubMed ID: 10469314
[TBL] [Abstract][Full Text] [Related]
19. Hair keratin KRT81 is expressed in normal and breast cancer cells and contributes to their invasiveness.
Nanashima N; Horie K; Yamada T; Shimizu T; Tsuchida S
Oncol Rep; 2017 May; 37(5):2964-2970. PubMed ID: 28405679
[TBL] [Abstract][Full Text] [Related]
20. Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity.
Birch-Machin MA; Healy E; Turner R; Haldane F; Belgaid CE; Darlington S; Stephenson AM; Munro C; Messenger AG; Rees JL
Br J Dermatol; 1997 Sep; 137(3):339-43. PubMed ID: 9349326
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]