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Research 391–420 of 806
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Clinical biochemistry of dihydrotestosterone
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Keratin Expression Provides Novel Insight into the Morphogenesis and Function of the Companion Layer in Hair Follicles
- Genetic Hair Disorders: A Review
- Skin Development and Disease: A Molecular Perspective
- Converging physiological roles of the anthrax toxin receptors
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- Desmogleins: Hair perspective
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Acne Syndromes and Mosaicism
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Case report: Exploring autosomal recessive woolly hair: genetic and scanning electron microscopic perspectives on a Japanese patient
- Clouston’s syndrome: a rare case report
- Acne-Associated Syndromes
- Genetics of Diabetes in Childhood
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Hirsutism Beyond PCOS: Genome-wide Evidence for Genetic Factors
- Symptomatic zinc deficiency in a full-term breast-fed infant
- Phenotypic heterogeneity in human genetic diseases: ultrasensitivity-mediated threshold effects as a unifying molecular mechanism