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Research 451–480 of 1000+
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- 9. Immunology and Genetics
- Main Plenary Sessions: Summaries of Papers
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- <i>Hoxc13</i> mutant mice lack external hair
- THE PATHOGENESIS OF ALOPECIA AREATA
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Pathways to inflammation: acne pathophysiology
- Treatment of MSCs with Wnt1a-conditioned medium activates DP cells and promotes hair follicle regrowth
- Idiopathic Hirsutism*
- Spinal and bulbar muscular atrophy: pathogenesis and clinical management
- 5-Alpha reductase deficiency
- Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Relationship between betacoronaviruses and the endocrine system: a new key to understand the COVID-19 pandemic—A comprehensive review
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Antiandrogen therapy for androgenetic alopecia
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Hair growth effects of Laminaria japonica extract and growth factor mixture on a C57BL/6 mouse model
- Decay of Skin-Specific Gene Modules in Pangolins
- Dicer- and BSC-dependent miRNAs during murine anagen development
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Integrated multiple machine learning and Mendelian randomization reveal LTF gene as a prognostic biomarker for nonspecific orbital inflammation
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Main Plenary Sessions: Summaries of Papers
- Polymorphism of the Androgen Receptor Gene is Associated with Male Pattern Baldness
- Delineation of Matriptase Protein Expression by Enzymatic Gene Trapping Suggests Diverging Roles in Barrier Function, Hair Formation, and Squamous Cell Carcinogenesis