Chromosomal polymorphisms are independently associated with multinucleated embryo formation
نویسندگان
چکیده
منابع مشابه
Fetal Calcifications Are Associated with Chromosomal Abnormalities
OBJECTIVE The biological importance of calcifications occasionally noted in fetal tissues (mainly liver) at autopsy or ultrasound is largely unexplored. Previous reports hint at an association to infection, circulatory compromise, malformations or chromosomal abnormalities. To identify factors associated with calcifications, we have performed a case-control study on the largest cohort of fetuse...
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results among the patients enrolled, 61 had microalbuminuria (uacr, 30-299) and 133 normoalbuminuria (uacr, < 30). patients with normoalbuminuria showed significantly higher levels of gal-3 than those without (19.9 ± 8.8 vs. 14.6 ± 5.5 ng/ml). the stepwise regression analysis indicated that gal-3 was the first determinant of microalbuminuria (odds ratio [or]: 1.08; 95% confidence interval [ci]:...
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Calcineurin, which functions in calcium signaling, is expressed in skeletal and cardiac muscle and has been linked to sensitivity to muscle strength training. It is also proposed to contribute to individual aerobic endurance. To investigate the relationship between calcineurin-encoding genes and aerobic endurance traits, 126 young-adult Han Chinese males were enrolled in an aerobic exercise tra...
متن کاملAre polymorphisms in MTRR A66G and MTHFR C677T genes associated with congenital heart diseases in Iranian population?
Background: The 5, 10-methyleneterahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) are two essential enzymes involved in folate metabolism. The relationship between genetic polymorphisms and congenital heart defects (CHDs) is inconsistent. Our aim was to investigate the association between two well-known polymorphisms of MTHFR and MTRR genes, C677T and A66G, respectively,...
متن کاملP-206: Mov10l1 Gene Polymorphisms Are Probably Associated to Male Infertility in Azoospermic Men with Complete Maturation Arrest
Background: Thousands of genes are involved in spermatogenesis. Alterations in any of these genes could lead to male infertility. Moloney leukemia virus 10-Like 1 (Mov10l1) gene is one of the genes that are expressed specifically in germ cells. Genetic disruption of this gene in mouse stops spermatogenesis during Meiosis I and causes azoospermia. Materials and Methods: In this study, the geneti...
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ژورنال
عنوان ژورنال: Journal of Assisted Reproduction and Genetics
سال: 2017
ISSN: 1058-0468,1573-7330
DOI: 10.1007/s10815-017-1037-9