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Research 511–540 of 1000+
- Determination of TG5 gene polymorphism and its influence on productivity traits of beef cattle reared in Lithuania
- Histopathological Analysis on keratin2-6 g Expression in Hair Mutant Mouse Hague
- Sickle Cell Disease Complications and BMI Percentiles of Pediatric Patients
- Identification of drug-specific public TCR driving severe cutaneous adverse reactions
- Human genetic basis of coronavirus disease 2019
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- HSD3B1 gene polymorphism and female pattern hair loss in women with polycystic ovary syndrome
- Site of beige (<i>bg</i>) and leaden (<i>ln</i>) pigment gene expression determined by recombinant embryonic skin grafts and aggregation mouse chimaeras employing sash (<i>W</i><sup><i>sh</i></sup>) homozygotes
- A novel 22-bp InDel within <i>FGF7</i> gene is significantly associated with growth traits in goat
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Genetic diversity of Armillaria spp. symbiotic with Polyporus umbellatus in China
- Impact of mutations in PRLR for hair weight, circulating prolactin concentrations, feed intake, and growth of beef cattle in a hot and humid climate
- Pharmacogenomic variation and chemotherapy-related toxicity profiles in pediatric patients with cancer in Tanzania: a cross-sectional study
- Prevalence of rs1998076 and Its Association with Androgenetic Alopecia in Indonesian Population: A Pilot Study
- Exploring the role of CYP19A1 single nucleotide polymorphisms in the pathogenesis of female pattern hair loss
- Genetic and Environmental Factors Affecting Hair Density in East Asian Populations
- Factors Related to Premature Canities; A Cross-sectional Study in Lagos State, Nigeria
- Genetic Association Between Polycystic Ovary Syndrome and the <i>APOA5</i> rs662799 and <i>PLIN1</i> rs894160 Metabolic Variants in the Western Saudi Population: A Case-Control Study
- The Glucocorticoid Resistance Syndrome. Two Cases of a Novel Pathogenic Variant in the Glucocorticoid Receptor Gene
- Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
- A Study on the Clinical Profile and Pharmacogenetics of Methotrexate Treatment in Patients with Rheumatoid Arthritis.
- Molecular genetics of androgen insensitivity
- MLO‐mediated Ca<sup>2+</sup> influx regulates root hair tip growth in Arabidopsis
- The association of Wnt – Factor TCF7L2 (TCF4) gene polymorphism and treated Alopecia Areata (Platelet rich plasma Vs conventional)
- Androgenic alopecia associated with the HSD3B1 (1245a>c) in overweight women with polycystic ovarian syndrome
- Increased lactate dehydrogenase activity is dispensable in squamous carcinoma cells of origin
- A Rare Case Report of Congenital Adrenal Hyperplasia: 46XX at Tertiary Care Centre, Visnagar, North Gujarat.
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- A study of the role of root morphological traits in growth of barley in zinc-deficient soil