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Research 121–150 of 1000+
- Biology of the Hair Follicle: The Basics
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- Seasonal Gene Expression Profile Responsible For Hair Follicle Development In Angora Goats
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Investigating RNA-Seq-based differential gene expression during hair follicle development in Angora goat skin
- The 5alpha-reductase type 1, but not type 2, gene is expressed in anagen hairs plucked from the vertex area of the scalp of hirsute women and normal individuals
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Disease causing homozygous variants in the human hairless gene
- Zebrafish Model of Hereditary Pigmentary Disorders
- The role of mutations on gene AR, in androgenetic alopecia syndrome
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Directed Expression of a Chimeric Type II Keratin Partially Rescues Keratin 5-null Mice
- Effects of FGF5-mediated LncRNA on the skin fibroblast growth of Liaoning Cashmere goats
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Distinct mechanisms for sebaceous gland self-renewal and regeneration provide durability in response to injury
- Loose anagen hair syndrome in two patients with epidermolysis bullosa simplex, Dowling-Meara type
- The organization of the keratin I and II gene clusters in placental mammals and marsupials show a striking similarity
- Polymorphism of Keratin Gene KRT71 and Its Relationship with Wool Properties in Gansu Alpine Fine-Wool Sheep
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Hair Today
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families