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Research 601–630 of 1000+
- A polygenic mouse model of psoriasiform skin disease in CD18-deficient mice.
- Hirsutism, Normal Androgens and Diagnosis of PCOS
- The association between Interleukin (IL)-4 gene intron 3 VNTR polymorphism and alopecia areata (AA) in Turkish population
- Role of testosterone in SARS-CoV-2 infection: A key pathogenic factor and a biomarker for severe pneumonia
- Distinguishing Mouse Strains by Proteomic Analysis of Pelage Hair
- Lithium alters mitotic progression in stamen hair cells of Tradescantia in a time-dependent and reversible fashion.
- Diversity of Trichocyte Keratins and Keratin Associated Proteins
- Prevalence and Risk Factors Associated with the Occurrence of Autoimmune Diseases in Patients with Alopecia Areata
- Characterization of the Human Hair Shaft Cuticle–Specific Keratin-Associated Protein 10 Family
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Genetic prediction of male pattern baldness based on large independent datasets
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- Characterisation of Ovine KRTAP19-3 and Its Impact on Wool Traits in Chinese Tan Sheep
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- Exploring murE protein inhibitors of Tropheryma whipplei through pharmacoinformatic approaches incorporating solubility-enhancing formulation insights
- The Impact of Gender Affirming Hormone Therapy on Physical Performance
- Network-based identification genetic effect of SARS-CoV-2 infections to Idiopathic pulmonary fibrosis (IPF) patients
- Improving the treatment of bacterial infections caused by multidrug-resistant bacteria through drug repositioning
- Runx Family Genes in Tissue Stem Cell Dynamics
- Index of Suspicion
- Human Hair Keratin‐Associated Proteins (KAPs)
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene
- Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome
- Genetics of Diabetes in Childhood
- Biotin and biotinidase deficiency
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- Epidermal Differentiation Complex: A Review on Its Epigenetic Regulation and Potential Drug Targets.