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Research 211–240 of 1000+
- Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization
- The Genetics of Human Skin Disease
- New developments in the molecular treatment of ichthyosis: review of the literature
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Third International Research Workshop on Alopecia Areata
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Dermatologic Manifestations of Mitochondrial Dysfunction: A Review of the Literature
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- The molecular pathogenesis of Trichilemmal carcinoma
- A Hairy Cituation – PADIs in Regeneration and Alopecia
- Neurobiology, Stem Cell Biology, and Immunology: An Emerging Triad for Understanding Tissue Homeostasis and Repair
- The Rho GTPase exchange factor Vav2 promotes extensive age-dependent rewiring of the hair follicle stem cell transcriptome
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Current Progress Regarding Cordyceps militaris, Its Metabolite Function, and Its Production
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- K <sub>ATP</sub> Channels and Cardiovascular Disease