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Research 811–840 of 1000+
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- miR-22 promotes stem cell traits via activating Wnt/β-catenin signaling in cutaneous squamous cell carcinoma
- Increased expression of the gene for the Y<sub>1</sub> receptor of neuropeptide Y in the amygdala and paraventricular nucleus of <i>Y</i><sub><i>1</i></sub><i>R/LacZ</i> transgenic mice in response to restraint stress
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Expression of the guinea-pig alpha-lactalbumin gene in transgenic mice
- Strawberry water-extract increases cellular dehydrogenase activity in human follicle dermal papilla cells
- Inflammatory Cytokine TNFα Promotes the Long-Term Expansion of Primary Hepatocytes in 3D Culture
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
- Mitochondrial Reactive Oxygen Species Promote Epidermal Differentiation and Hair Follicle Development
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Melanocytes: The new Black
- Biology and Genetics of Hair
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Learning from nudity: lessons from the nude phenotype
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Neuronal plasticity of the “brain–skin connection”: stress-triggered up-regulation of neuropeptides in dorsal root ganglia and skin via nerve growth factor-dependent pathways
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Overexpression of Bcl-2 Protects from Ultraviolet B-Induced Apoptosis but Promotes Hair Follicle Regression and Chemotherapy-Induced Alopecia
- Strontium ranelate promotes chondrogenesis through inhibition of the Wnt/β-catenin pathway
- Cyclosporin A Promotes Hair Epithelial Cell Proliferation and Modulates Protein Kinase C Expression and Translocation in Hair Epithelial Cells
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Liposomal honokiol promotes hair growth via activating Wnt3a/β-catenin signaling pathway and down regulating TGF-β1 in C57BL/6N mice
- Sinapic Acid Promotes Browning of 3T3‐L1 Adipocytes via p38 MAPK/CREB Pathway