首页> 外文OA文献 >Mutational Analysis of the FOXP3 Gene and Evidence for Genetic Heterogeneity in the Immunodysregulation, Polyendocrinopathy, Enteropathy Syndrome

【2h】

Mutational Analysis of the FOXP3 Gene and Evidence for Genetic Heterogeneity in the Immunodysregulation, Polyendocrinopathy, Enteropathy Syndrome

机译：免疫分泌，聚丙烯病变，肠病综合征的抗氟X3基因的突变分析和遗传异质性的证据

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
Catherine J. Owen; Claire E. Jennings; Helen Imrie; Alain Lachaux; Nicola A. Bridges; Tim D. Cheetham; Simon H. S. Pearce;
展开▼
作者单位

展开▼
年度 2003
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. FOXP3 FOXP3 mutations causing early‐onset insulin‐requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked syndrome [J] . Hwang Jessica L, Park Soo‐Young, Ye Honggang, Pediatric diabetes. . 2018,第3期

机译：Foxp3 Foxp3突变导致早起的胰岛素需要糖尿病，但没有其他特征的免疫失调，聚丙烯病，肠病，X键综合征
2. Clinical heterogeneity of immunodysregulation, polyendocrinopathy, enteropathy, X-linked: pulmonary involvement as a non-classical disease manifestation. [J] . Safa Baris, Ilka Schulze, Ahmet Ozen, Journal of Clinical Immunology . 2014,第6期

机译：免疫调节异常，多内分泌病，肠病，X连锁的临床异质性：肺部受累为非经典疾病表现。
3. Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome Associated With a Novel Mutation of FOXP3 Gene [J] . Charalampos Agakidis, Eleni Agakidou, Kosmas Sarafidis, Frontiers in Pediatrics . 2019,第a期

机译：免疫失调，聚丙烯病，肠病，X链接综合征与Foxp3基因的新突变相关
4. Application of the stochastic Moran Model of population genetics to understanding the timing of a driver mutation in Myelodysplastic Syndrome (MDS) [C] . Tomasz Wojdyla, Taly Glaubach, Seth Corey, IFAC World Congress . 2014

机译：人口遗传学随机莫兰模型在骨髓增生综合征（MDS）中驾驶突变的时间
5. A canine model of Imerslund-Grasbeck syndrome: Genetic mapping, mutation identification and functional analysis. [D] . He, Qianchuan. 2005

机译：艾默斯隆-格拉斯贝克综合征的犬科动物模型：遗传作图，突变鉴定和功能分析。
6. Early-onset refractory diarrhea due to immune dysregulation polyendocrinopathy enteropathy X-linked syndrome associated with a novel mutation in the FOXP3 gene: A case report [O] . Na Su, Cheng Chen, Xia Zhou, 2020

机译：免疫功能失调多内分泌病肠病X连锁综合征与FOXP3基因新突变相关的早发型难治性腹泻：病例报告
7. Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation–polyendocrinopathy–enteropathy–X-linked–like syndrome [O] . Gulbu Uzel, Elizabeth P. Sampaio, Monica G. Lawrence, 2013

机译：富申33个野生型免疫功能调整 - 聚泌碱病肠病 - X-连接的综合征偏离函数的常量增益突变
8. JSC Exit Presentation: Effects of Genetics and Mutations on Acquired Long QT Syndrome. [R] . McFadden, R. 2014

机译：JsC退出演示：遗传和突变对获得性长QT综合征的影响。

Mutational Analysis of the FOXP3 Gene and Evidence for Genetic Heterogeneity in the Immunodysregulation, Polyendocrinopathy, Enteropathy Syndrome

著录项

引文网络

相似文献

相关主题

期刊订阅