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Research 391–420 of 1000+
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Molecular Dissection of Mesenchymal–Epithelial Interactions in the Hair Follicle
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Influence of TRPV3 mutation on hair growth cycle in mice
- Dihydrotestosterone inhibits hair growth in mice by inhibiting insulin-like growth factor-I production in dermal papillae
- Differential proteomics of lesional vs. non-lesional biopsies revealed non-immune mechanisms of alopecia areata
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- LncRNA-000133 from secondary hair follicle of Cashmere goat: identification, regulatory network and its effects on inductive property of dermal papilla cells
- Development of Autoimmune Hair Loss Disease Alopecia Areata Is Associated with Cardiac Dysfunction in C3H/HeJ Mice
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- Factors associated with early-onset androgenetic alopecia: A scoping review
- AP-2α/AP-2β transcription factors are key regulators of epidermal homeostasis
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Androgen receptors and their biology
- Nonclassic adrenal hyperplasia
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Androgen receptor gene polymorphism and polycystic ovary syndrome
- Fibroproliferative genes are preferentially expressed in central centrifugal cicatricial alopecia
- 5α-Reductase Inhibitors (5ARIs) and Male Reproduction
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Clinico-investigative profile of patients of hirsutism in a tertiary level institution
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Small Intestinal Organoid-Derived SP Cells Contribute to Repair of Irradiation-Induced Skin Injury
- Protein Kinase C<i>ε</i>, Which Is Linked to Ultraviolet Radiation-Induced Development of Squamous Cell Carcinomas, Stimulates Rapid Turnover of Adult Hair Follicle Stem Cells
- Determination of Secondary Follicle Characteristics, Density, Activity, and Hoxc13 Expression Pattern of Hexi Cashmere Goats Breed
- Hyperandrogenism in Women: Polycystic Ovary Syndrome
- Skin transcriptome reveals the Periodic changes in genes underlying hair follicle cycling in Cashmere goats
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene