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Research 391–420 of 1000+
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Biology of hair pigmentation and its role in premature canities
- 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
- Demographic Characteristics and Association of Serum Vitamin B12, Ferritin and Thyroid Function with Premature Canities in Indian Patients from an Urban Skin Clinic of North India: A Retrospective Analysis of 71 Cases.
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Pathogenesis of androgenetic alopecia
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- 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
- iRhom2 Mutation Leads to Aberrant Hair Follicle Differentiation in Mice
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Acne Syndromes and Mosaicism
- Dermatologic manifestations of thyroid disease: a literature review
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Genome-Wide Association Study and Transcriptome Differential Expression Analysis of the Feather Rate in Shouguang Chickens
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- THE RELATION BETWEEN VITILIGO AND OTHER AUTOIMMUNE DISORDERS
- Hidradenitis suppurativa: pathogenesis and management
- Signaling Involved in Hair Follicle Morphogenesis and Development
- The Pathogenesis of Primary Cicatricial Alopecias
- Unraveling the ECM-Immune Cell Crosstalk in Skin Diseases
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Inflammatory perspectives of polycystic ovary syndrome: role of specific mediators and markers