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Research 811–840 of 1000+
- <i>WNT10A</i> , dermatology and dentistry
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- 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
- Inducing hair follicle neogenesis with secreted proteins enriched in embryonic skin
- A pilot study evaluating the efficacy of topically applied niacin derivatives for treatment of female pattern alopecia
- Stem cells and aberrant signaling of molecular systems in skin aging
- Defining the identity of mouse embryonic dermal fibroblasts
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- A curated catalog of canine and equine keratin genes
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Deciphering principles of morphogenesis from temporal and spatial patterns on the integument
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Comparison of mitochondrial transplantation by using a stamp-type multineedle injector and platelet-rich plasma therapy for hair aging in naturally aging mice
- Minoxidil Sulfotransferase Enzyme (SULT1A1) genetic variants predicts response to oral minoxidil treatment for female pattern hair loss
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- RNA sequence analysis of dermal papilla cells’ regeneration in 3D culture
- Endocrinology & Metabolism News, August 2005
- The seasonal development dynamics of the yak hair cycle transcriptome
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Hair shaft structures in EDAR induced ectodermal dysplasia
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Urinary 5-ene-steroid excretion in non-classical congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency (NC-3BHSD)
- H2AK119ub dynamics control hair follicle stem cell quiescence
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Nuclear Topology, Epigenetics, and Keratinocyte Differentiation
- Neuroactive Steroids and Ethanol Exposure: Relevance to Ethanol Sensitivity and Alcohol Use Disorders Risk