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Research 421–450 of 1000+
- Transfection of rat dermal papilla cells with a gene encoding a temperature-sensitive polyomavirus large T antigen generates cell lines retaining a differentiated phenotype
- Relationship of Pantothenic Acid and Inositol to Alopecia in Mice
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Dynamic expression of ornithine decarboxylase in hair growth
- Effects of cepharanthine and minoxidil on proliferation, differentiation and keratinization of cultured cells from the murine hair apparatus
- Selective complete Clq deficiency associated with systemic lupus erythematosus.
- μ-Crystallin, Thyroid Hormone-binding Protein, is Expressed Abundantly in the Murine Inner Root Sheath Cells
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Distinguishing diffuse alopecia areata (AA) from pattern hair loss (PHL) using CD3+ T cells
- Trichoscopy findings in loose anagen hair syndrome: rectangular granular structures and solitary yellow dots
- Characterization of <i>BMP</i>2 gene expression in embryonic and adult Inner Mongolia Cashmere goat (<i>Capra hircus</i>) hair follicles
- Pilomatricoma can differentiate not only towards hair matrix and hair cortex, but also follicular infundibulum, outer root sheath and hair bulge
- Connexin 30, a new marker of hyperproliferative epidermis
- A Study of the Expression of Small Conductance Calcium-Activated Potassium Channels (SK1-3) in Sensory Endings of Muscle Spindles and Lanceolate Endings of Hair Follicles in the Rat
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Ontogeny of enhancing factor in mouse intestines and skin
- Netherton's syndrome and ichthyosis linearis circumflexa.
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- A woman with iatrogenic androgenetic alopecia responding to finasteride
- Bikunin, a Serine Protease Inhibitor, is Present on the Cell Boundary of Epidermis
- Hair changes due to zinc deficiency in a case of sucrose malabsorption
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Comparison of the Pathology of Fascia in Eosinophilic Myalgia Syndrome Patients and Idiopathic Eosinophilic Fasciitis
- Polymorphic Enzyme Systems in Human Hair Sheath Cells
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Histological study of white rhinoceros integument
- Origin and Early Development of Canine Circumanal Glands
- Ultrastructural localization of hair keratins, high sulfur keratin-associated proteins and sulfhydryl oxidase in the human hair
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle