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Research 151–180 of 1000+
- Molecular Genetics of Alopecias
- Woolly Antics between the Sheaths
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Hox genes in development and beyond
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- 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>)
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Arabidopsis retromer subunit AtVPS29 is involved in SLY1-mediated gibberellin signaling
- Surface modification and endothelialization of biomaterials as potential scaffolds for vascular tissue engineering applications
- 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
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- 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
- Integrated analysis of coding genes and non-coding RNAs during hair follicle cycle of cashmere goat (Capra hircus)
- Tissue Engineering and Regenerative Medicine: Achievements, Future, and Sustainability in Asia
- HAIR REGROWTH
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- 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
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Beyond Expectations
- Preparation of hair beads and hair follicle germs for regenerative medicine
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- Chrousos syndrome: from molecular pathogenesis to therapeutic management