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Research 31–60 of 52
- Fibroblast Lineage Switching as the Developmental Origin of Scarring and Target for Regenerating Healing
- Diseases of Periocular Hair
- Dermatoscopy of hair shaft disorders
- CXCL12+ dermal fibroblasts promote neutrophil recruitment and host defense by recognition of IL-17
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Biology and Genetics of Hair
- 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
- A systematic simulation-based meta-analytical framework for prediction of physiological biomarkers in alopecia
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- STAT3 Partly Inhibits Cell Proliferation via Direct Negative Regulation of FST Gene Expression
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Developmentally regulated expression of integrin alpha-6 distinguishes neural crest derivatives in the skin
- Recent Findings with Computerized Methods for Scalp Hair Growth Measurements
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo
- Trichorhinophalangeal Syndrome
- Clinical and Trichoscopy Features in Trichorhinophalangeal Syndrome: A Multicenter Retrospective Study
- Trps1 activates a network of secreted Wnt inhibitors and transcription factors crucial to vibrissa follicle morphogenesis
- Genetics of Structural Hair Disorders
- Westwood Carolina Conference on Clinical Dermatology
- Trichotillomania in Children
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient