De novo mutations in monilethrix-Reference-Cited by-同舟云学术

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De novo mutations in monilethrix

Published:2003-12 Issue:6 Volume:12 Page:882-885
ISSN:0906-6705
Container-title:Experimental Dermatology
language:en
Short-container-title:Exp Dermatol

Author:

Horev Liran,Djabali Karima,Green Jack,Sinclair Rodney,Martinez-Mir Amalia,Ingber Arieh,Christiano Angela M.,Zlotogorski Abraham

Publisher

Wiley

Subject

Dermatology,Molecular Biology,Biochemistry

Reference18 articles.

1. Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

2. A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix

3. 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

4. Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype

5. A Novel Missense Mutation, A118E, in the Helix Initiation Motif of the Type II Hair Cortex Keratin hHb6, Causing Monilethrix

Cited by 23 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Autosomal dominant monilethrix with incomplete penetrance due to a novel KRT86 mutation in a Chinese family;Anais Brasileiros de Dermatologia;2024-07

2. De novo filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks;FEBS Open Bio;2021-04-03

3. Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential;Experimental Dermatology;2019-05

4. Treatment of monilethrix with oral minoxidil;JAAD Case Reports;2016-05

5. NovelKRT83andKRT86mutations associated with monilethrix;Experimental Dermatology;2015-02-26

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