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Research 841–870 of 1000+
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells
- <i>Hoxc13</i> mutant mice lack external hair
- Signaling Involved in Hair Follicle Morphogenesis and Development
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Functional identification of the phosphorylation sites of Arabidopsis PIN-FORMED3 for its subcellular localization and biological role
- Membrane androgen receptors may mediate androgen reinforcement
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Bendamustine: an Old Drug in the New Era for Patients with Non-Hodgkin Lymphomas and Chronic Lymphocytic Leukemia
- The Critical Roles of Serum/Glucocorticoid-Regulated Kinase 3 (SGK3) in the Hair Follicle Morphogenesis and Homeostasis
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- Clinical Snippets
- Insights learned from L457(3.43)R, an activating mutant of the human lutropin receptor
- Dermatologic Care of the Transplant Patient
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Current Progress Regarding Cordyceps militaris, Its Metabolite Function, and Its Production
- Effectiveness of Botulinum Toxin Type A for Trichodynia Associated with Hair Loss Disorders: A Retrospective Study
- Decoding Hyperpigmentation from Biological Mechanisms to Actives with Clinically Proven Topical Efficacy: A Narrative Review
- The genetic basis of dermatophytosis skin infection susceptibility
- SnapshotDx Quiz: February 2018
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Roles of GasderminA3 in Catagen–Telogen Transition During Hair Cycling
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Two Dogs with Juvenile-Onset Skin Diseases with Involvement of Extremities
- Biotinidase deficiency characterized by skin and hair findings
- Inherited Epidermolysis Bullosa: A Clinical Case
- Editors' Picks
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency