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Research 30 of 48
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Discreet monilethrix: De novo mutation on the example of polish families
- A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- <i>De novo</i> mutations in monilethrix
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- 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
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Nonclassic congenital adrenal hyperplasia
- Molecular pathology of skin adnexal tumours
- Regulation of melanocyte stem cells in the pigmentation of skin and its appendages: Biological patterning and therapeutic potentials
- Defining the transcriptional signature of esophageal-to-skin lineage conversion
- Hétérogénéité tumorale du cancer de la prostate et infection par le SARS-CoV2 : une relation complexe impliquant les vésicules extracellulaires et le récepteur des androgènes
- Guía clínica chilena para el estudio y tratamiento de hidradenitis supurativa. Resumen ejecutivo
- Monilethrix – Case report of a rare disease
- Genetic Basis of Alopecia Areata
- Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature
- Self-Amplifying RNA Approach for Protein Replacement Therapy
- DataSheet1_Single-Cell Transcriptomics Reveals the Molecular Anatomy of Sheep Hair Follicle Heterogeneity and Wool Curvature.zip
- Tissue engineering strategies for human hair follicle regeneration: How far from a hairy goal?
- Reduced serum brain-derived neurotrophic factor in patients with first onset vitiligo
- Clinicopathological characteristics and treatment outcomes of fibrosing alopecia in a pattern distribution: A retrospective cohort study