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Research 841–870 of 1000+
- Cardiovascular risk in patients with scarring and nonscarring alopecias: Assessing the current state of evidence
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- TONGUE, RED
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- A randomized double blind study of the effect of finasteride on hair growth in male patients of androgenetic alopecia
- The Genetic Architecture of Alopecia Areata
- Interventions for androgenic alopecia in women
- Metabolic pathways of eicosanoids—derivatives of arachidonic acid and their significance in skin
- A rare case of woolly hair with unusual associations
- Fibroblast bioelectric signaling drives hair growth
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- SkIndia Quiz 24: Itchy papules over face
- Viewpoint 2
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Characterization of Hydrogels of Gelatin/O-Carboxymethyl Chitosan in Ovule Form with Curcumin and Retinyl Palmitate as a Treatment for Cervical Cancer
- Evaluation of Olive Oil-Based Formulations Loaded with Baricitinib for Topical Treatment of Alopecia Areata
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Scoping Review on the Use of Drugs Targeting JAK/STAT Pathway in Atopic Dermatitis, Vitiligo, and Alopecia Areata
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Proof-of-Principle Study of Inflammasome Signaling Proteins as Diagnostic Biomarkers of the Inflammatory Response in Parkinson’s Disease
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases