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Research 691–720 of 1000+
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Morphological Approach to Hair Disorders
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Diagnostic approach to low‐renin hypertension
- Suppression of Wnt/β-catenin signaling by EGF receptor is required for hair follicle development
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Increased Susceptibility to Skin Carcinogenesis Associated with a Spontaneous Mouse Mutation in the Palmitoyl Transferase Zdhhc13 Gene
- A cDNA encoding the human type I hair keratin hHa1
- Characterization of minoxidil/hydroxypropyl-β-cyclodextrin inclusion complex in aqueous alginate gel useful for alopecia management: Efficacy evaluation in male rat
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- CD133-positive dermal papilla-derived Wnt ligands regulate postnatal hair growth
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Dermatopathology and molecular genetics
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Clinical Manifestations of Hyperandrogenism and Ovulatory Dysfunction Are Not Associated with His1058 C/T SNP (rs1799817) Polymorphism of Insulin Receptor Gene Tyrosine Kinase Domain in Kashmiri Women with PCOS
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Hair shaft structures in EDAR induced ectodermal dysplasia
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Le gène<i>hairless</i>de la souris
- Construction of regulatory network for alopecia areata progression and identification of immune monitoring genes based on multiple machine-learning algorithms
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Effect of inhibiting prolactin secretion on secondary hair follicle development in cashmere goats