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Research 301–330 of 1000+
- Maternal PPARγ protects nursing neonates by suppressing the production of inflammatory milk
- Tcf3 and Lef1 regulate lineage differentiation of multipotent stem cells in skin
- A Ca <sup>2+</sup> /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
- Folliculin encoded by the <i>BHD</i> gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling
- Biology of the Hair Follicle: The Basics
- Conditional Gene Expression in the Epidermis of Transgenic Mice Using the Tetracycline-Regulated Transactivators tTA and rTA Linked to the Keratin 5 Promoter
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- An Update of Congenital Adrenal Hyperplasia
- 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
- TGF-β family signaling in stem cells
- Convergent Genesis of an Adult Neural Crest-Like Dermal Stem Cell from Distinct Developmental Origins
- 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
- Hox genes in development and beyond
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Beyond Expectations
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Nonclassic adrenal hyperplasia
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Hoxc-Dependent Mesenchymal Niche Heterogeneity Drives Regional Hair Follicle Regeneration
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- Congenital hair loss disorders: Rare, but not too rare
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment