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Research 91–120 of 99
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Trichoscopy in genetic hair shaft abnormalities
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Dermoscopy: A rapid bedside tool to assess monilethrix
- 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