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Research 481–510 of 492
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Pharmacogenetics of the Androgen Metabolic Pathway
- Male-pattern hair loss: Comprehensive identification of the associated genes as a basis for understanding pathophysiology
- Oxidative Stress and Skin Diseases: The Role of Lipid Peroxidation
- Marine Health-Promoting Compounds: Recent Trends for Their Characterization and Human Applications
- Secondary Metabolites with Antifungal Activities from Mangrove Derived Fungus Monascus purpureus WMD2424
- Side gland of Suncus murinus as a new model of sebaceous gland: 5?-reductase, androgen receptor, and nuclear androgen content in male and female animals
- Isolation, Structural Elucidation and Therapeutic Potentials of Root of Cucurbita pepo
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Buschke-Ollendorff syndrome
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Ehlers-Danlos syndrome: From bedside to bench
- <i>WNT10A</i> , dermatology and dentistry
- Sulphation catalysed by the human cytosolic sulphotransferases - chemical defence or molecular terrorism?
- Familial and Sporadic Porphyria Cutanea Tarda
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Ovarian Hypertension: Polycystic Ovary Syndrome
- Androgen receptor gene CAG repeat polymorphism in women with polycystic ovary syndrome
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Congenital adrenal hyperplasia
- Genomic and transcriptomic landscape to decipher the genetic basis of hyperpigmentation in Lanping black-boned sheep (Ovis aries)
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Cutaneous signals of immune system disease
- 12 Treatment of hirsutism with 5α-reductase inhibitors