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Research 31–60 of 464
- Congenital hair loss disorders: Rare, but not too rare
- Hairless is a nuclear receptor corepressor essential for skin function
- Low-Level Laser Therapy: A Comprehensive Review of Anti- Inflammatory Applications and Therapeutic Potential
- Comparative biology of tissue repair, regeneration and aging
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- Woolly Antics between the Sheaths
- Learning from nudity: lessons from the nude phenotype
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Immune cell regulation of the hair cycle
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- The Role of Histone Demethylases in Disease
- Inherited Disorders of the Hair
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Transcriptomic analysis reveals critical genes for the hair follicle of Inner Mongolia cashmere goat from catagen to telogen
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Association of long-term 5α-reductase inhibitor use with survival in men with renal cell carcinoma: a nationwide population-based cohort study
- Deletion of adipocyte Sine Oculis Homeobox Homolog 1 prevents lipolysis and attenuates skin fibrosis
- Australasian Society for Dermatology Research Meeting, May 2007
- Biology and Genetics of Hair
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Morpho-Regulation of Ectodermal Organs
- Keratin K15 as a Biomarker of Epidermal Stem Cells
- What causes hidradenitis suppurativa ?—15 years after
- Diagnostic approach to low‐renin hypertension
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)