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Research 31–60 of 51
- Genetic Hair Disorders: A Review
- Diseases of Periocular Hair
- Biology and Genetics of Hair
- Westwood Carolina Conference on Clinical Dermatology
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Trichotillomania in Children
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- Signaling Involved in Hair Follicle Morphogenesis and Development
- Human Induced Pluripotent Stem Cell–Derived Ectodermal Precursor Cells Contribute to Hair Follicle Morphogenesis In Vivo
- LHX2 is a direct NF-κB target gene that promotes primary hair follicle placode down-growth
- 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 with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Trichorhinophalangeal Syndrome
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- 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
- <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
- Comprehensive Transcriptome Profiling of Balding and Non-Balding Scalps in Trichorhinophalangeal Syndrome Type I Patient
- Treatment of Hair Loss in the Trichorhinophalangeal Syndrome
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Generalized hypertrichosis after 5% minoxidil solution in trichorhinophalangeal syndrome: A case report and review of the literatures