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Research 421–450 of 1000+
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Prediction of the Development of Depression in Patients with Autoimmune Thyroiditis and Hypothyroidism
- Dietary and Genetic Aspects of Polycystic Ovary Syndrome (PCOS) in Polish Women-Part II: Association of
- Correlation and regression analysis of the <i>KRT27</i> and <i>ELOVL4</i> genes in cashmere fineness and other production performances in Liaoning cashmere goats
- Algorithms For Preventive Measures For Disease Prevention And Antioxidant Protection
- A Study on the Clinical Profile and Pharmacogenetics of Methotrexate Treatment in Patients with Rheumatoid Arthritis.
- Becker nevus of the face with asymmetrical growth of beard hair
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- POLY CYSTIC OVARIAN SYNDROME: AN UPDATED REVIEW
- INNOVATIVE APPROACH TO CRC PREVENTION: THE ROLE OF LOW-PENETRATION GENES
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- A review of genetic researches of and rogenic alopecia
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Nucleation and growth of macrofibrils in trichocyte (hard-α) keratins
- Novel TMEM173 Mutation and the Role of Disease Modifying Alleles
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Hepatitis C virus: host, environmental and viral factors promoting spontaneous clearance
- Copper Deficiency a New Reason of Androgenetic Alopecia?
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- 9. Immunology and Genetics
- Androgen receptor CAG repeat length is associated with ovarian reserve but not with ovarian response
- Tissue Retinol‐Binding Protein 4 Expression and Its Genetic Variants (rs3758539) in Patients With Severe and Treatment‐Refractory Alopecia Areata: Association With Response to Baricitinib
- Eziopatogenesi e terapia dell'acne:studio epidemiologico delle caratteristiche cliniche di una popolazione di pazienti affetti da acne e analisi dei polimorfismi del gene codificante per il recettore degli androgeni e del gene codificante per il citocromo P-450 1A1
- 420 Severe thiopurine-induced myelotoxicity and hair loss in Japanese patients with NUDT15 gene variant: A retrospective case-control study
- <i>IGF2BP2</i> and <i>IGFBP3</i> Genotypes, Haplotypes, and Genetic Models Studies in Polycystic Ovary Syndrome
- Study on the mechanism that SNPs related to sex hormone metabolism regulate the imbalance of sex hormones and lead to BPH in rats