GLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome
نویسندگان
چکیده
منابع مشابه
Examine of Thyroid Function in Pediatric Nephrotic Syndrome; Tehran-Iran
Introduction In children with nephrotic syndrome, it is probable to determine a hypothyroid state because of thyroxine (T4), tri-iodothyronine (T3) and thyroid-binding globulin loss in presence of proteinuria. Objectives: To examine thyroid function in pediatric cases of nephrotic syndrome. Methods: In a cross-sectional study, from march 2010 to march 2012, thyroid function tests were performed...
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Uncovering DNA sequence variations that correlate with phenotypic changes, e.g., diseases, is the aim of sequence variation studies. Common types sequence variations are Single nucleotide polymorphism (SNP, pronounced snip).SNPs are the third-generation molecular marker. SNP represents a DNA sequence variant of a single base pair with the minor allele occurring in more than 1% of a given popula...
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1 Stony Brook Children’s Hospital, Stony Brook, NY, United States, 2 Department of Nephrology, Children’s Hospital of Pittsburgh, Pittsburgh, PA, United States, 3 Department of Cell Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, United States, 4 Division of Pediatric Nephrology, Children’s Hospital at Montefiore, Albert Einstein College of Medicine, New York, NY, United S...
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Single-nucleotide polymorphisms (SNPs) provide an abundant source of DNA polymorphisms in a number of eukaryotic species. Information on the frequency, nature, and distribution of SNPs in plant genomes is limited. Thus, our objectives were (1) to determine SNP frequency in coding and noncoding soybean (Glycine max L. Merr.) DNA sequence amplified from genomic DNA using PCR primers designed to c...
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ژورنال
عنوان ژورنال: Pediatric Nephrology
سال: 2012
ISSN: 0931-041X,1432-198X
DOI: 10.1007/s00467-012-2197-6