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Research 271–300 of 1000+
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Hair for brain trade-off, a metabolic bypass for encephalization
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Gene Variant in Amish a Clue to Better Aging
- News in brief
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- <i>Hoxc13</i> mutant mice lack external hair
- Functional identification of the phosphorylation sites of Arabidopsis PIN-FORMED3 for its subcellular localization and biological role
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Roles of GasderminA3 in Catagen–Telogen Transition During Hair Cycling
- BJD Editor's Choice
- <i>AXR3</i>and<i>SHY2</i>interact to regulate root hair development
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Hair Follicle Disruption Facilitates Pathogenesis to UVB-Induced Cutaneous Inflammation and Basal Cell Carcinoma Development in Ptch+/− Mice
- Generalised Glucocorticoid Resistance
- 892 Behavior of the two circulating androgens testosterone and DHEA and their main intracellular metabolites in an androgen-sensitive sebocyte cell line
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Inherited Epidermolysis Bullosa: A Clinical Case
- 1379 Cell of origin contributes to the melanoma diversity
- Beyond Expectations
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Alopecia areata: a review on diagnosis, immunological etiopathogenesis and treatment options
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Keratins and skin disease