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Research 961–990 of 1000+
- 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
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Characterization of Hydrogels of Gelatin/O-Carboxymethyl Chitosan in Ovule Form with Curcumin and Retinyl Palmitate as a Treatment for Cervical Cancer
- KCNQ4 K+ channels tune mechanoreceptors for normal touch sensation in mouse and man
- Disorders of Keratinization
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- 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
- New developments in the molecular treatment of ichthyosis: review of the literature
- 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.
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Growth Hormone and the Human Hair Follicle
- AN UPDATE OF HAIR SHAFT DISORDERS
- The Wound Reporting in Animal and Human Preclinical Studies (WRAHPS) Guidelines
- Towards the Development of AgoKirs: New Pharmacological Activators to Study Kir2.x Channel and Target Cardiac Disease
- Essential Role of STAT3 Signaling in Hair Follicle Homeostasis
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Heterozygous Arrhythmogenic Cardiomyopathy-desmoplakin Mutation Carriers Exhibit a Subclinical Cutaneous Phenotype with Cell Membrane Disruption and Lack of Intercellular Adhesion
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Dermatologic manifestations of thyroid disease: a literature review
- Pathogenesis of androgenetic alopecia
- Relationship of a Novel c.429delC Deletion in Hairless Gene HR with Alopecia in Two Families from Southern Punjab, Pakistan
- Insertional mutation of the hairless locus on mouse Chromosome 14