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Research 481–510 of 1000+
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Inherited Disorders of the Hair
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- Testosterone target therapy: focus on immune response, controversies and clinical implications in patients with COVID-19 infection
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Hair and nail involvement in lupus erythematosus
- Analyzing the innate immunity of NIH hairless mice and the impact of gut microbial polymorphisms on<i>Listeria monocytogenes</i>infection
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- The evaluation of IL-4 intron 3 VNTR and TNF-α (rs1799964) gene polymorphisms in Egyptian patients with Alopecia Areata: a case-control study
- Natural Killer Group 2 Type D (NKG2D) Gene Polymorphism in Systemic Lupus Erythematosus-Suez Canal Region - Egypt
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- Animal Models and the Developmental Origins of Polycystic Ovary Syndrome: Increasing Evidence for the Role of Androgens in Programming Reproductive and Metabolic Dysfunction
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- Association between genetically predicted rheumatoid arthritis and alopecia areata: a two-sample Mendelian randomization study
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Androgen receptor gene polymorphism and biological age markers in men
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- The Clinical Presentation of Systemic Lupus Erythematosus
- Polycystic ovary syndrome
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness
- Protein Kinase C<i>ε</i>, Which Is Linked to Ultraviolet Radiation-Induced Development of Squamous Cell Carcinomas, Stimulates Rapid Turnover of Adult Hair Follicle Stem Cells
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review