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Research 31–60 of 40
- Single-cell transcriptomics reveals lineage trajectory of human scalp hair follicle and informs mechanisms of hair graying
- A simple technique to distinguish fibrosing alopecia in a pattern distribution from androgenetic alopecia and concomitant seborrheic dermatitis
- The PCOS Phenotypes in Unselected Populations (P-PUP) study: participant clinical features and data harmonization on analysis of individual participant data
- MicroRNA-181a Targets GNAI2 and Affects the Proliferation and Induction Ability of Dermal Papilla Cells: The Potential Involvement of the Wnt/β-Catenin Signaling Pathway
- Multimodal Non-Invasive Skin Imaging in Dermatology: Current Modalities, Clinical Applications, and Future Integration
- Single-cell transcriptomics reveals hair growth retardation mediated by aberrant connective tissue sheath contraction in male androgenetic alopecia
- Restoration of follicular β-catenin signaling by mesenchymal stem cells promotes hair growth in mice with androgenetic alopecia
- Tissue Expanders for Hair Restoration in the Scalp: Overexpansion Does Matter
- Deciphering the molecular mechanisms of stem cell dynamics in hair follicle regeneration
- Comparative Analysis of mRNA and miRNA Expression between Dermal Papilla Cells and Hair Matrix Cells of Hair Follicles in Yak
- 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
- Molecular pathology of skin adnexal tumours
- 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