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Diabetic nephropathy: FRMD3 in diabetic nephropathy--guilt by association.

作者信息

Palmer Nicholette D, Freedman Barry I

机构信息

Department of Biochemistry, Wake Forest School of Medicine, Medical Center Boulevard, Winston-Salem, NC 27157, USA.

出版信息

Nat Rev Nephrol. 2013 Jun;9(6):313-4. doi: 10.1038/nrneph.2013.81. Epub 2013 Apr 30.

DOI:10.1038/nrneph.2013.81
PMID:23629636
Abstract
摘要

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Family-based association analysis confirms the role of the chromosome 9q21.32 locus in the susceptibility of diabetic nephropathy.基于家系的关联分析证实了染色体 9q21.32 位点在糖尿病肾病易感性中的作用。
PLoS One. 2013;8(3):e60301. doi: 10.1371/journal.pone.0060301. Epub 2013 Mar 29.
2
From single nucleotide polymorphism to transcriptional mechanism: a model for FRMD3 in diabetic nephropathy.从单核苷酸多态性到转录机制：糖尿病肾病中 FRMD3 的模型。
Diabetes. 2013 Jul;62(7):2605-12. doi: 10.2337/db12-1416. Epub 2013 Feb 22.
3
A family-based association study after genome-wide linkage analysis identified two genetic loci for renal function in a Mongolian population.
中国黑龙江省9号染色体单核苷酸多态性与缺血性脑卒中的关联
Int J Clin Exp Pathol. 2021 Jun 15;14(6):726-733. eCollection 2021.
4
Diabetic kidney disease in type 2 diabetes: a review of pathogenic mechanisms, patient-related factors and therapeutic options.2型糖尿病中的糖尿病肾病：致病机制、患者相关因素及治疗选择综述
PeerJ. 2021 Apr 19;9:e11070. doi: 10.7717/peerj.11070. eCollection 2021.
5
Genetic and Epigenetic Studies in Diabetic Kidney Disease.糖尿病肾病的遗传与表观遗传学研究
Front Genet. 2019 Jun 7;10:507. doi: 10.3389/fgene.2019.00507. eCollection 2019.
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rs1888747 polymorphism in the FRMD3 gene, gene and protein expression: role in diabetic kidney disease.FRMD3基因中的rs1888747多态性、基因与蛋白表达：在糖尿病肾病中的作用
Diabetol Metab Syndr. 2016 Jan 8;8:3. doi: 10.1186/s13098-015-0121-5. eCollection 2016.
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FRMD3 gene: its role in diabetic kidney disease. A narrative review.FRMD3基因：其在糖尿病肾病中的作用。一篇叙述性综述。
Diabetol Metab Syndr. 2015 Dec 30;7:118. doi: 10.1186/s13098-015-0114-4. eCollection 2015.
8
Identifying Common Genetic Risk Factors of Diabetic Neuropathies.识别糖尿病神经病变的常见遗传风险因素。
Front Endocrinol (Lausanne). 2015 May 28;6:88. doi: 10.3389/fendo.2015.00088. eCollection 2015.
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Evaluation of neurotrophic tyrosine receptor kinase 2 (NTRK2) as a positional candidate gene for variation in estimated glomerular filtration rate (eGFR) in Mexican American participants of San Antonio Family Heart study.在圣安东尼奥家族心脏研究的墨西哥裔美国参与者中，评估神经营养性酪氨酸受体激酶2（NTRK2）作为估计肾小球滤过率（eGFR）变异的定位候选基因。
J Biomed Sci. 2015 Mar 25;22(1):23. doi: 10.1186/s12929-015-0123-5.
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全基因组连锁分析后的家系关联研究在蒙古族人群中鉴定出两个与肾功能相关的遗传位点。
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