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Research 31–60 of 53
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Genetic Hair Disorders: A Review
- Diseases of Periocular Hair
- Biology and Genetics of Hair
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Westwood Carolina Conference on Clinical Dermatology
- Dermatoscopy of hair shaft disorders
- Signaling Involved in Hair Follicle Morphogenesis and Development
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Trichotillomania in Children
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo
- CXCL12+ dermal fibroblasts promote neutrophil recruitment and host defense by recognition of IL-17
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- The Developmental & Molecular Requirements for Ensuring that Human Pluripotent Stem Cell-Derived Hair Follicle Bulge Stem Cells Have Acquired Competence for Hair Follicle Generation Following Transplantation
- STAT3 Partly Inhibits Cell Proliferation via Direct Negative Regulation of FST Gene Expression
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerating Healing
- Recent Findings with Computerized Methods for Scalp Hair Growth Measurements
- Trichorhinophalangeal Syndrome
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I