![]() ![]() phaseolina in common bean is controlled by two pairs of epistatic genes with complementary effects, and that resistance to charcoal rot could be quantitatively controlled by major effects of two genes. phaseolina was evaluated under greenhouse conditions. Reaction of F 3 lines to a highly virulent isolate of M. Parents, F 1 and F 2 generations and F 1 -parent backcrosses were included in the studies. Experiments were conducted under field conditions at Cotaxtla, Veracruz and in greenhouse at Montecillo, Estado de México. on resistant (BAT 477 and TLP 19) and susceptible (Pinto UI-114 and Rio Tibagi) common bean cultivars were carried out. However, there were no statistically significant associations between any of the 24 DNA variants and TTPP in a population from northeast Mexico.Studies to determine genetic resistance inheritance to M. Based on the analysis, two DNA variants were found to potentially confer an increased risk for TTPP: S1PR1 rs3737576 and AIM rs2330442 (OR, 4.50 95% CI, 1.21‑16.69), and one variant was suggested to be possibly associated with TTPP, namely MUC1 rs4072037 (OR, 3.08 95% CI, 0.841‑1.38). ![]() Only two cases (18%) had a previous diagnosis of hyperthyroidism the rest were diagnosed subsequently with Graves' disease. A total of 11 patients were recruited, comprising nine males and two females (age range, 19‑52 years) and 64 control subjects. A total of 16 gene variants in the genes MUC1, CACNA1S, KCNE3 and SCN4A, and nine ancestry informative markers (AIMs), were analysed by Multiplex TaqMan™ Open Array assay, and a genetic association study was performed. ![]() Gonzalez’ in Monterrey, Nuevo León, Mexico, and were diagnosed with TTPP was performed. A prospective and a retrospective search of the medical records of patients who attended the emergency department at the Hospital Universitario ‘Dr. and epidemiological characteristics of patients with TTPP are described, together with their association with genetic variants reported previously in other populations. Hyperthyroidism has been associated with thyrotoxic periodic paralysis (TTPP) (OMIM TTPP1 and TTPP2), and genetic susceptibility has been implicated. Hypokalemic periodic paralysis type 1 (OMIM HOKPP1) and type 2 (OMIM HOKPP2) are diseases of the muscle characterized by episodes of painless muscle weakness, and is associated with low potassium blood levels. ![]()
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