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Research 31–60 of 1000+
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Reversing wrinkled skin and hair loss in mice by restoring mitochondrial function
- 666 Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in follicular dystrophy and primary cicatricial alopecia
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Normalization of hair growth in sparse fur-abnormal skin and hair (SPF-ASH) mice by introduction of the rat ornithine transcarbamylase (OTC) gene
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Insertional mutation of the hairless locus on mouse Chromosome 14
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- Skin-specific expression of a truncated E1a oncoprotein binding to p105-Rb leads to abnormal hair follicle maturation without increased epidermal proliferation.
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- β-catenin Activity in the Dermal Papilla Regulates Morphogenesis and Regeneration of Hair
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Laminin-511 is an epithelial message promoting dermal papilla development and function during early hair morphogenesis
- A missense mutation in Lama3 causes androgen alopecia
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype