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Research 271–300 of 802
- The senescence-like activity of BMS-470539 is associated with anti-fibrotic actions in models of dermal fibrosis
- The human keratins: biology and pathology
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Neurosteroidogenesis Today: Novel Targets for Neuroactive Steroid Synthesis and Action and Their Relevance for Translational Research
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered
- Biology and Genetics of Hair
- Beyond Expectations
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Nonclassic adrenal hyperplasia
- How to diagnose a lipodystrophy syndrome
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Primary cicatricial alopecia: Recent advances in understanding and management
- Trichoscopy in Hair Shaft Disorders
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Hairless is a nuclear receptor corepressor essential for skin function
- Diagnostic approach to low‐renin hypertension
- Testosterone levels in relation to oral contraceptive use and the androgen receptor CAG and GGC length polymorphisms in healthy young women
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Dermatopathology and molecular genetics
- Dermatologic manifestations of endocrine disorders
- Congenital atrichia and hypotrichosis
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population