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Research 30 of 99
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- 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
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Mutation in human hair keratin hHb6 in monilethrix: clinical variation is not due to genetic variation.
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- [Analysis of human hair basic keratin 6 gene mutation in a Chinese Han family with monilethrix].
- Sequences and differential expression of three novel human type-II hair keratins
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- A cDNA encoding the human type I hair keratin hHa1
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Detection of Type IIHair Keratin Gene in a Family with Monilethrix
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- The hair shaft: normality, abnormality, and genetics
- Monilethrix
- <i>De novo</i> mutations in monilethrix
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Discreet monilethrix: De novo mutation on the example of polish families
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- The Catalog of Human Hair Keratins
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- The human keratins: biology and pathology
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis