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Research 181–210 of 1000+
- Interrelation of immunity and tissue repair or regeneration
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Pharmacological Options for Treatment of Hyperandrogenic Disorders
- Cardiac biopsy in myocarditis
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- Persistent hair growth during treatment with the EGFR inhibitor erlotinib
- Biotin and biotinidase deficiency
- Wnt Signaling, Lgr5, and Stem Cells in the Intestine and Skin
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Retinol Esterification by DGAT1 Is Essential for Retinoid Homeostasis in Murine Skin
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- New clinico‐genetic classification of trichothiodystrophy
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- The chemokine SDF-1/CXCL12 regulates the migration of melanocyte progenitors in mouse hair follicles
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- Oral Presentations
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype