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Research 661–690 of 1000+
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Epidermal stem cell fate: what can we learn from embryonic stem cells?
- TRPV Channels in Osteoarthritis: A Comprehensive Review
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Hair Loss Caused by Gain-of-Function Mutant TRPV3 Is Associated with Premature Differentiation of Follicular Keratinocytes
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Non-classical congenital adrenal hyperplasia: current insights into clinical implications, diagnosis and treatment
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Identification of Beta-Sitosterol and Stigmasterol as Possible Inhibitors of 5 Alpha-Reductase 1: An In-Silico Study
- TRPV3 Ion Channel: From Gene to Pharmacology
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Dermatologic care of patients with differences of sex development
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Understanding Type 3 Innate Lymphoid Cells and Crosstalk with the Microbiota: A Skin Connection
- A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report
- Biomedical engineering approaches for the delivery of JAGGED1 as a potential tissue regenerative therapy
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- In Vitro Assembly and Structure of Trichocyte Keratin Intermediate Filaments
- Does prostaglandin D<sub>2</sub> hold the cure to male pattern baldness?
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath