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Research 781–810 of 1000+
- Ductal breast cancer in a male patient
- Nonclassic Congenital Adrenal Hyperplasia: An Overview
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- 666 Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in follicular dystrophy and primary cicatricial alopecia
- Gene that causes woolly hair revealed
- The Agouti Gene in Obesity: Central and Peripheral Mechanisms, and Therapeutic Implications
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Keratins and skin disease
- Activated Kras Alters Epidermal Homeostasis of Mouse Skin, Resulting in Redundant Skin and Defective Hair Cycling
- Current Genetics in Hair Diseases
- Genetics of thyroid lesions updated
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- FGF5 is a crucial regulator of hair length in humans
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Towards Defining the Pathogenesis of the Hairless Phenotype
- N-terminal functional domain of Gasdermin A3 regulates mitochondrial homeostasis via mitochondrial targeting
- FOXN1 Is Critical for Onycholemmal Terminal Differentiation in Nude (Foxn1nu) Mice
- Functional identification of the phosphorylation sites of Arabidopsis PIN-FORMED3 for its subcellular localization and biological role
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Defective control of growth rate and cell diameter in tip-growing root hairs of the<i>rhd4</i>mutant of<i>Arabidopsis thaliana</i>
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice