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Research 61–90 of 1000+
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Miz1 is required for hair follicle structure and hair morphogenesis
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- A comparison of transcriptomic patterns measured in the skin of Chinese fine and coarse wool sheep breeds
- An LRH-RSL4 feedback regulatory loop controls the determinate growth of root hairs in Arabidopsis
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- A review of genotrichoses and hair pathology associated with inherited skin diseases
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- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- RSPO1, a potent inducer of pancreatic β cell neogenesis
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Function of KLF4 in Stem Cell Biology
- Novel small molecules downregulate CDK1 expression and inhibit Wnt/β-catenin signaling in cutaneous squamous cell carcinoma by targeting its distinct tumor-specific cellular landscape
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Kyoto Rhino Rats Derived by ENU Mutagenesis Undergo Congenital Hair Loss and Exhibit Focal Glomerulosclerosis
- Disease causing homozygous variants in the human hairless gene
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Fatal autoimmunity results from the conditional deletion of Snai2 and Snai3
- Cellular Plasticity in Cutaneous Wound Healing
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Skin manifestations among<i>GATA2</i>-deficient patients
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- A family business: stem cell progeny join the niche to regulate homeostasis
- The Molecular Basis of Androgen Insensitivity