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Research 421–450 of 866
- 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
- 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
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Hair growth promoting effects of adipose tissue-derived stem cells
- 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
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Glucocorticoid Receptor Mutants Demonstrate Increased Motility Inside the Nucleus of Living Cells: Time of Fluorescence Recovery After Photobleaching (FRAP) Is an Integrated Measure of Receptor Function
- Nonclassic Congenital Adrenal Hyperplasia
- Treatment of monilethrix with oral minoxidil
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes