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Research 211–240 of 1000+
- Defining the identity of mouse embryonic dermal fibroblasts
- Intramembrane Proteolysis of Astrotactins
- Disease causing homozygous variants in the human hairless gene
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- URB expression in human dermal papilla cells
- Melatonin promotes Cashmere goat (<i>Capra hircus</i>) secondary hair follicle growth: a view from integrated analysis of long non-coding and coding RNAs
- Comparative Transcriptome Analysis Reveals that a Ubiquitin-Mediated Proteolysis Pathway Is Important for Primary and Secondary Hair Follicle Development in Cashmere Goats
- Antisense oligonucleotide targeting fibroblast growth factor receptor (FGFR)-1 stimulates cellular activity of hair follicles in an<i>in vitro</i>organ culture system
- Recent advances in the genetics of alopecia areata
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Genetic Fate Mapping Using Site-Specific Recombinases
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Characterization of <i>BMP</i>2 gene expression in embryonic and adult Inner Mongolia Cashmere goat (<i>Capra hircus</i>) hair follicles
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- The promoter of an androgen dependent gene in the hamster flank organ
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- The Rotterdam Study: 2016 objectives and design update
- Cell Types Promoting Goosebumps Form a Niche to Regulate Hair Follicle Stem Cells
- Genome-wide Target Enrichment-aided Chip Design: a 66 K SNP Chip for Cashmere Goat
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives
- Whole-transcriptome analysis reveals the profiles and roles of coding and non-coding RNAs during hair follicle cycling in Rex rabbits
- Implication of Human Bacterial Gut Microbiota on Immune-Mediated and Autoimmune Dermatological Diseases and Their Comorbidities: A Narrative Review
- A comprehensive genome-wide analysis for signatures of selection in goat (genus Capra) revealed new candidate genes for environmental adaptation and productive traits
- Wool Keratin-Associated Protein Genes in Sheep—A Review