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Research 451–480 of 866
- Nonclassic congenital adrenal hyperplasia
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Genetic ablation of myelin protein zero-like 3 in mice increases energy expenditure, improves glycemic control, and reduces hepatic lipid synthesis
- No improvement in male-pattern hair loss using laser hair-comb therapy: a 6-month, half-head, assessor-blinded investigation in two men
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- AB0163 ANTI-KU ANTIBODIES: MUCH MORE THAN SCLEROMYOSITIS
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Trichoscopy in Hair Shaft Disorders
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Management of CAH during pregnancy
- The diagnosis of nonclassic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, based on serum basal or post-ACTH stimulation 17-hydroxyprogesterone, can lead to false-positive diagnosis
- Monilethrix Treated with Minoxidil
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Molecular pathology of skin adnexal tumours
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Vitamin D receptor-mediated control of Soggy, Wise, and Hairless gene expression in keratinocytes
- t-Flavanone Improves the Male Pattern of Hair Loss by Enhancing Hair-Anchoring Strength: A Randomized, Double-Blind, Placebo-Controlled Study
- The genetic basis of dermatophytosis skin infection susceptibility
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion