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Research 211–240 of 1000+
- Skin Development and Disease: A Molecular Perspective
- The Roles of EDA2R in Ageing and Disease
- Obesity in Adults: Position Statement of Polish Association for the Study on Obesity, Polish Association of Endocrinology, Polish Association of Cardiodiabetology, Polish Psychiatric Association, Section of Metabolic and Bariatric Surgery of the Association of Polish Surgeons, and the College of Family Physicians in Poland
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Genetics
- Genome-wide association study in alopecia areata implicates both innate and adaptive immunity
- Polycystic ovary syndrome
- Keratins of the Human Hair Follicle
- Genetic Basis of Male Pattern Baldness
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Characterization of the Human Hair Keratin–Associated Protein 2 (KRTAP2) Gene Family
- Significance of stress keratin expression in normal and diseased epithelia
- Deciphering the Complex Immunopathogenesis of Alopecia Areata
- Malt1 Protease Is Critical in Maintaining Function of Regulatory T Cells and May Be a Therapeutic Target for Antitumor Immunity
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? 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
- Thyroid diseases and skin autoimmunity
- Ptosis in childhood
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Immunological and Metabolic Causes of Infertility in Polycystic Ovary Syndrome
- Acne Syndromes and Mosaicism
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Does Complement Have a Role in the Pathogenesis of Alopecia Areata?