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Research 661–690 of 1000+
- Androgen receptor gene polymorphism and polycystic ovary syndrome
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Realising the therapeutic potential of neuroactive steroid modulators of the GABAA receptor
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Non polycystic ovary syndrome–related endocrine disorders associated with hirsutism
- Platelet-derived growth factor signaling modulates adult hair follicle dermal stem cell maintenance and self-renewal
- Vitamin D receptor polymorphisms and the polycystic ovary syndrome: A systematic review
- Epigenetic control of skin and hair regeneration after wounding
- Planar cell polarity-dependent and independent functions in the emergence of tissue-scale hair follicle patterns
- Afamin serum concentrations are associated with insulin resistance and metabolic syndrome in polycystic ovary syndrome
- Oncogenic senescence: a multi-functional perspective
- Fate of Prominin-1 Expressing Dermal Papilla Cells during Homeostasis, Wound Healing and Wnt Activation
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- An Ovol2‐Zeb1 transcriptional circuit regulates epithelial directional migration and proliferation
- Removing all obstacles: A critical role for p53 in promoting tissue renewal
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Enzyme Replacement Therapy Ameliorates Multiple Symptoms of Murine Homocystinuria
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- 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
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- Psoriasis patients demonstrate HLA-Cw*06:02 allele dosage-dependent T cell proliferation when treated with hair follicle-derived keratin 17 protein
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- A role for the Tgf-β/Bmp co-receptor Endoglin in the molecular oscillator that regulates the hair follicle cycle
- 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