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Research 331–360 of 1000+
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- 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
- Morphological Approach to Hair Disorders
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Trichoscopy in Hair Shaft Disorders
- 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
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Afamin serum concentrations are associated with insulin resistance and metabolic syndrome in polycystic ovary syndrome
- 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
- Variation in the caprine keratin-associated protein 15-1 (KAP15-1) gene affects cashmere fibre diameter
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- 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
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- 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
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle