首页> 外文OA文献 >MP855GENETIC TESTING OF WT1, NPHS2 AND NPHS1 GENES IN CZECH PEDIATRIC PATIENTS WITH STEROID-RESISTANT NEPHROTIC SYNDROME IDENTIFIED THE GENETIC BACKGROUND IN 25 CASES

【2h】

MP855GENETIC TESTING OF WT1, NPHS2 AND NPHS1 GENES IN CZECH PEDIATRIC PATIENTS WITH STEROID-RESISTANT NEPHROTIC SYNDROME IDENTIFIED THE GENETIC BACKGROUND IN 25 CASES

机译：捷克儿科患者的WT1，NPHS2和NPHS1基因的MP855生物试验耐药性肾病综合征在25％案件中发现了遗传背景

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者
Sarka Stolbova; Jakub Zieg; Nadezda Simankova; Jitka Lachova; Tomas Rosik; Jiri Dusek; Karel Vondrak; Martin Bezdicka; Ondrej Cinek; Stepanka Pruhova; Tomas Seeman;
展开▼
作者单位

展开▼
年度 2017
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2) [J] . Bernward G. Hinkes, Bettina Mucha, Christopher N. Vlangos, Pediatrics: Official Publication of the American Academy of Pediatrics . 2007,第4期

机译：生命第一年的肾病综合征：三分之二的病例是由4个基因（NPHS1，NPHS2，WT1和LAMB2）的突变引起的
2. A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan [J] . AbidA., KhaliqS., ShahidS., Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function . 2012,第2期

机译：巴基斯坦小儿肾病综合征患者的新NPHS1和NPHS2基因突变谱
3. Genotypic and Phenotypic Features of Both NPHS1 and NPHS2 Genes in Infantile Nephrotic Syndrome and Prognostic Effect of E117K Polymorphism in NPHS1 Gene [J] . Yilmaz Ebru, DINCEL NIDA, Bulut Ipek Kaplan, Iranian journal of pediatrics . 2019,第2期

机译：NPHS1和NPHS2基因的基因型和表型特征在NPHS1基因中E117K多态性的婴儿肾病综合征和预后作用
4. Whole Exome Sequencing Approach to Identify Genetic Variants Causing Sudden Unexplained Death Syndrome [C] . Seok-Hwee Koo, Paul Chui, Chee Seng Ku, Molecular Medicine TRI-CON. . 2014

机译：识别遗传变异突然未解释的死亡综合征的整体exome测序方法
5. Functional studies and population genetic studies of a 25kb haplotype upstream of the AKT1 gene associated with metabolic syndrome. [D] . Devaney, Stephanie. 2009

机译：与代谢综合征相关的AKT1基因上游25kb单倍型的功能研究和群体遗传研究。
6. Screening of the LAMB2 WT1 NPHS1 and NPHS2 Genes in Pediatric Nephrotic Syndrome [O] . Aiysha Abid, Saba Shahid, Madiha Shakoor, 2018

机译：小儿肾病综合征中LAMB2WT1NPHS1和NPHS2基因的筛选
7. Analysis of NPHS1, NPHS2, ACTN4, and WT1 in Japanese patients with congenital nephrotic syndrome [O] . Sako Mayumi, Nakanishi Koichi, Obana Mina, 2005

机译：日本先天性肾病综合征患者NPHS1，NPHS2，ACTN4和WT1的分析

MP855GENETIC TESTING OF WT1, NPHS2 AND NPHS1 GENES IN CZECH PEDIATRIC PATIENTS WITH STEROID-RESISTANT NEPHROTIC SYNDROME IDENTIFIED THE GENETIC BACKGROUND IN 25 CASES

著录项

引文网络

相似文献

相关主题

期刊订阅