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Research 151–180 of 826
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Enhancing the Growth of Natural Eyelashes: The Mechanism of Bimatoprost-Induced Eyelash Growth
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- ‘Black dots’ seen under trichoscopy are not specific for alopecia areata
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Bovine besnoitiosis in Germany
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Phenotypic variability associated with<i>WNT10A</i>nonsense mutations
- Intragenic deletion in the Desmoglein 4 gene underlies the skin phenotype in the Iffa Credo “hairless” rat
- Pubic Hair Transplantation
- Genetic Hair Disorders: A Review
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- The Genetics of Human Skin Disease
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- Genetics of Structural Hair Disorders
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Disorders of hair in infants and children other than alopecia
- Dermatopathology and molecular genetics
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- A new type of pachyonychia congenita.
- Identification of 736T>A mutation of lipase H in Japanese siblings with autosomal recessive woolly hair
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles
- Manganese Ethylene Bis(Maneb)-Induced Degeneration of Hair Follicle Epithelia in the Dosal Skin of WBN/ILA-Ht Rats.
- Sebaceous adenitis in a cat.
- Desmogleins: Hair perspective
- Cardiomiopatia dilatada em cão com hipotireoidismo e megaesôfago
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen