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Research 421–450 of 1000+
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- 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
- Tumor Necrosis Factor-Alpha and Polycystic Ovarian Syndrome: A Clinical, Biochemical, and Molecular Genetic Study
- Congenital adrenal hyperplasia
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Nuclear Factor I-C Regulates TGF-β-dependent Hair Follicle Cycling*
- Regulation of melanocyte stem cell behavior by the niche microenvironment
- Friends Turned Foes: Angiogenic Growth Factors beyond Angiogenesis
- The Genetics of Human Skin Disease
- Polyclonal origin and hair induction ability of dermal papillae in neonatal and adult mouse back skin
- Crosstalk between androgen and Wnt/β-catenin leads to changes of wool density in FGF5-knockout sheep
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Alopecia in Epidermolysis Bullosa
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia
- Epimorphic regeneration in mice is p53-independent
- Inhibiting the cytosolic function of CXXC5 accelerates diabetic wound healing by enhancing angiogenesis and skin repair
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Relating neurosteroid modulation of inhibitory neurotransmission to behaviour
- Genetic basis of polycystic ovary syndrome
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Expression patterns of the glial cell line–derived neurotrophic factor, neurturin, their cognate receptors GFRα-1, GFRα-2, and a common signal transduction element c-Ret in the human skin hair follicles
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?