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Research 331–360 of 1000+
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Trichoscopy in Hair Shaft Disorders
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Loss of Keratin K2 Expression Causes Aberrant Aggregation of K10, Hyperkeratosis, and Inflammation
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Management of CAH during pregnancy
- Genetic Fate Mapping Using Site-Specific Recombinases
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Friends Turned Foes: Angiogenic Growth Factors beyond Angiogenesis
- The Genetics of Human Skin Disease
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Molecular pathology of skin adnexal tumours
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Hirsutism in the Adolescent Female
- Dermatopathology and molecular genetics
- Polymorphisms in androgen and estrogen receptor genes: effects on male aging
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome