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Research 601–630 of 1000+
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Table of Contents
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- The Causes of Hair Loss in Women 20-30 Years Old
- Hair & Cutaneous Development
- New aspects of vitamin D metabolism and action — addressing the skin as source and target
- Polycystic ovary syndrome
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Biotin and biotinidase deficiency
- Genetic Disorders and Defects in Vitamin D Action
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Small extracellular vesicles from menstrual blood-derived mesenchymal stem cells (MenSCs) as a novel therapeutic impetus in regenerative medicine
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Advances in the human skin microbiota and its roles in cutaneous diseases
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- The Proteins of Hair and Other Hard α-Keratins
- Ornithine decarboxylase is a target for chemoprevention of basal and squamous cell carcinomas in Ptch1+/– mice
- Ornithine decarboxylase is a target for chemoprevention of basal and squamous cell carcinomas in Ptch1+/– mice
- TREM2 macrophages induced by human lipids drive inflammation in acne lesions
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Endogenous Retinoids in the Pathogenesis of Alopecia Areata
- The Impact of Angiotensin-Converting Enzyme 2 (ACE2) Expression Levels in Patients with Comorbidities on COVID-19 Severity: A Comprehensive Review
- The developmental basis of fingerprint pattern formation and variation
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- Resistance to the Insulin and Elevated Level of Androgen: A Major Cause of Polycystic Ovary Syndrome
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Concise Review: Translating Regenerative Biology into Clinically Relevant Therapies: Are We on the Right Path?
- The role of WNT10B in physiology and disease: A 10-year update
- Calcium regulation of stem cells
- Poster Presentations