نتایج جستجو برای: phenotype and genetic trends
تعداد نتایج: 16928332 فیلتر نتایج به سال:
background: saccharomyces boulardii (s. boulardii) is the best known probiotic yeast. the genetic engineering of this probiotic strain requires the availability of appropriate mutants to accept various gene constructs carrying different selection markers. as the auxotrophy selection markers are under focus, we have generated a ura3 auxotroph mutant of s. boulardii for use in further genetic man...
In most genomic prediction studies only additive effects will be used in models for estimating genomic breeding values (GEBV). However, dominance genetic effects are an important source of variation for complex traits, considering them into account may improve the accuracy of GEBV. In the present study, performed applying simulated data, the effect of different heritability values (0.1...
Celiac disease is a chronic, systemic and autoimmune disorder of gastrointestinal track that involves approximately 1% of individuals of all ages throughout the world. The collaboration of environmental factor such as gluten proteins and genetic factors, notably HLA-DQ2 and/or HLA-DQ8 trigger the disease. Gluten-free diet is the simply and merely safe and proficient existing treatment. This art...
Background: Autosomal recessive polycystic kidney disorder (ARPCKD) is one of the most prevalent hereditary disorders in neonates and children. Its frequency is between 1/6000 to 1/55000 births. In the most severe cases, it can be diagnosed prenatally by the presence of enlarged, echogenic kidneys and oligohydramnios. However, in the milder forms, clinical manifestations are usually detected in...
Abstract Background and Objectives Thalassemia is a group of inherited hemoglobin disorders with defect in the synthesis of hemoglobin chains. Case The young couple resident in Bandar Abbas, a 23 year old woman with MCV:63fl; MCH:19; HbA2:3.9 and a 25 year old man with MCV:94fl; MCH:32; HbA2:2.1; HbF:36, were referred to the Bandar Abbas Medical Genetic & PND Center for genetic counsell...
ABSTRACT Background: Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder with genetic heterogeneity. Up to three loci are involved in this disease, PKDI on chromosome 16p13.3, PKD2 on 4q21, and a third locus of unknown location. Methods: Here we report the first molecular genetic study of ADPKD and the existence oflocus heterogeneity for ADPKD in the Iranian populatio...
data related to yazd native fowls (obtained during 2000-2008) yazd native fowls were made use of in the present study. the investigated traits consisted of body weight at 8 (bw8) and 12 weeks (bw12), age at sexual maturity (asm), egg number during the first three months of production period (en) and the mean egg weight at 28, 30 and 32 weeks of age (ew). the genetic and phenotypic parameters we...
Background: The prevalence of non-communicable disorders such as metabolic syndrome (MetS) is high in developing countries. Metabolic syndrome is a disorder of energy utilization and storage, diagnosed by a co-occurrence of three out of five of the following medical conditions: abdominal (central) obesity, elevated blood pressure, elevated fasting plasma glucose, high serum triglycerides, and l...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید