Proteinuria in AMPD2-deficient mice
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2443.2011.01568.x/fullpdf
Reference39 articles.
1. Molecular analysis of NPHS2 and ACTN4 genes in a series of 33 Italian patients affected by adult-onset nonfamilial focal segmental glomerulosclerosis;Aucella;Nephron. Clin. Pract.,2005
2. Adenosine A2A receptor activation attenuates inflammation and injury in diabetic nephropathy;Awad;Am. J. Physiol. Renal. Physiol.,2006
3. Molecular cloning of AMP deaminase isoform L. Sequence and bacterial expression of human AMPD2 cDNA;Bausch-Jurken;J. Biol. Chem.,1992
4. The purine nucleotide cycle in the regulation of ammoniagenesis during induction and cessation of chronic acidosis in the rat kidney;Bogusky;Biochem. J.,1981
5. Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria;Caridi;Kidney Int.,2004
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. IMPDH2 filaments protect from neurodegeneration in AMPD2 deficiency;EMBO Reports;2024-07-29
2. Frameshift Variant in AMPD2 in Cirneco dell’Etna Dogs with Retinopathy and Tremors;Genes;2024-02-13
3. IMPDH2 filaments protect from neurodegeneration in AMPD2 deficiency;2024-01-22
4. AMPD2 plays important roles in regulating hepatic glucose and lipid metabolism;Molecular and Cellular Endocrinology;2023-11
5. Clinical and genetic spectrum of AMPD2-related pontocerebellar hypoplasia type 9;European Journal of Human Genetics;2018-02-20
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3