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Research 91–120 of 1000+
- Alopecia areata
- Embryology, Histology, and Physiology of the Hair Follicle
- Alopecia in Epidermolysis Bullosa
- VINCENT BARRANCO, M.D., EDITOR 2121 EAST 21ST STREET, P.O. BOX 52588 TUESA, OK 74152-0588.
- Hair structure anatomy and comparative anatomy1 1Dedicated to the memory of the late Dr. R. E. Rivett whose untimely death prevented his role in co-authorship.
- Skin of the Baikal Seal (Pusa sibirica, Phocidae): Norm and Pathology
- Skin of the Baikal seal (<i>Pusa sibirica</i>, Phocidae): norm and pathology
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Lesions in the skin, intestine, and central nervous system induced by an antimetabolite of niacin.
- Segmental Vitiligo
- Cornification in reptilian epidermis occurs through the deposition of keratin‐associated beta‐proteins (beta‐keratins) onto a scaffold of intermediate filament keratins
- Wool fiber curvature is correlated with abundance of K38 and specific keratin‐associated proteins
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Acquired perforating dermatosis in renal and diabetic patients
- Immunolocalization of Scaffoldin, a Trichohyalin‐Like Protein, in the Epidermis of the Chicken Embryo
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Distribution of keratin and associated proteins in the epidermis of monotreme, marsupial, and placental mammals
- Three-dimensional architecture of macrofibrils in the human scalp hair cortex
- Ageing processes influence keratin and KAP expression in human hair follicles
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Myotonic Dystrophy—A Progeroid Disease?
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Suprabasal Desmoglein 3 Expression in the Epidermis of Transgenic Mice Results in Hyperproliferation and Abnormal Differentiation
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Recently Identified Forms of Epidermolysis Bullosa