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Research 271–300 of 1000+
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Congenital Adrenal Hyperplasia
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Genetic Hair Disorders: A Review
- Converging physiological roles of the anthrax toxin receptors
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Whole Genome Scan and Selection Signatures for Climate Adaption in Yanbian Cattle
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Ligand‐independent Regulation of the hairless Promoter by Vitamin D Receptor<sup>†</sup>
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- 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
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Trichoscopy in Hair Shaft Disorders