血管内皮生长因子（VEGF）基因3'-非翻译区多态性（C702T、C936T和G1612A）与发生晚期早产儿视网膜病变（ROP）风险之间无关联。 - Suppr

Suppr

超能文献

Lack of association of VEGF gene 3'- UTR polymorphisms (C702T, C936T and G1612A) and the risk of developing advanced retinopathy of prematurity (ROP).

作者信息

Gismondi Daniela, Ndoja Livja, Qu Xianggui, Shastry Barkur S

出版信息

Graefes Arch Clin Exp Ophthalmol. 2013 Jan;251(1):413-5. doi: 10.1007/s00417-011-1913-4. Epub 2012 Jan 7.

DOI:10.1007/s00417-011-1913-4

PMID:22227643

Abstract

摘要

相似文献

Lack of association of VEGF gene 3'- UTR polymorphisms (C702T, C936T and G1612A) and the risk of developing advanced retinopathy of prematurity (ROP).血管内皮生长因子（VEGF）基因3'-非翻译区多态性（C702T、C936T和G1612A）与发生晚期早产儿视网膜病变（ROP）风险之间无关联。

Graefes Arch Clin Exp Ophthalmol. 2013 Jan;251(1):413-5. doi: 10.1007/s00417-011-1913-4. Epub 2012 Jan 7.

Single nucleotide polymorphisms in the 3' untranslated region of vascular endothelial growth factor gene in Japanese population with or without renal cell carcinoma.日本有或没有肾细胞癌人群中血管内皮生长因子基因3'非翻译区的单核苷酸多态性

Tohoku J Exp Med. 2002 Nov;198(3):181-90. doi: 10.1620/tjem.198.181.

Lack of association of VEGF (-2578 C-->A) and ANG 2 (-35 G-->C) gene polymorphisms with the progression of retinopathy of prematurity.血管内皮生长因子（VEGF，-2578 C→A）和血管生成素2（ANG 2，-35 G→C）基因多态性与早产儿视网膜病变进展之间无关联。

Graefes Arch Clin Exp Ophthalmol. 2009 Jun;247(6):859-60. doi: 10.1007/s00417-008-0988-z. Epub 2008 Nov 19.

Polymorphisms of Vascular Endothelial Growth Factor and Retinopathy of Prematurity.血管内皮生长因子多态性与早产儿视网膜病变

J Pediatr Ophthalmol Strabismus. 2015 Jul-Aug;52(4):245-53. doi: 10.3928/01913913-20150506-02. Epub 2015 May 11.

Norrie disease gene sequence variants in an ethnically diverse population with retinopathy of prematurity.早产儿视网膜病变的不同种族人群中的诺里病基因序列变异

Mol Vis. 2005 Jul 14;11:501-8.

Lack of association of the VEGF gene promoter (-634 G-->C and -460 C-->T) polymorphism and the risk of advanced retinopathy of prematurity.血管内皮生长因子（VEGF）基因启动子（-634 G→C和-460 C→T）多态性与早产儿晚期视网膜病变风险之间无关联。

Graefes Arch Clin Exp Ophthalmol. 2007 May;245(5):741-3. doi: 10.1007/s00417-006-0480-6. Epub 2006 Nov 22.

Associations of VEGF/VEGF-receptor and HGF/c-Met promoter polymorphisms with progression/regression of retinopathy of prematurity.VEGF/VEGF 受体和 HGF/c-Met 启动子多态性与早产儿视网膜病变进展/消退的相关性。

Curr Eye Res. 2013 Jan;38(1):137-42. doi: 10.3109/02713683.2012.731550. Epub 2012 Oct 24.

The clinical role of vascular endothelial growth factor (VEGF) system in the pathogenesis of retinopathy of prematurity.血管内皮生长因子（VEGF）系统在早产儿视网膜病变发病机制中的临床作用。

Graefes Arch Clin Exp Ophthalmol. 2008 Oct;246(10):1467-75. doi: 10.1007/s00417-008-0865-9. Epub 2008 Jun 11.

Genetic polymorphisms of vascular endothelial growth factor and angiopoietin 2 in retinopathy of prematurity.早产儿视网膜病变中血管内皮生长因子和血管生成素2的基因多态性

Curr Eye Res. 2006 Jul-Aug;31(7-8):685-90. doi: 10.1080/02713680600801123.

Genetic polymorphisms of vascular endothelial growth factor and risk for retinopathy of prematurity in South of Iran.伊朗南部血管内皮生长因子基因多态性与早产儿视网膜病变风险的关系。

Mol Biol Rep. 2013 Jul;40(7):4613-8. doi: 10.1007/s11033-013-2554-y. Epub 2013 May 4.

引用本文的文献

The genetics of retinopathy of prematurity: a model for neovascular retinal disease.早产儿视网膜病变的遗传学：一种新生血管性视网膜疾病模型

Ophthalmol Retina. 2018 Sep;2(9):949-962. doi: 10.1016/j.oret.2018.01.016. Epub 2018 Mar 8.

Retinopathy of prematurity: a review of risk factors and their clinical significance.早产儿视网膜病变：危险因素及其临床意义综述。

Surv Ophthalmol. 2018 Sep-Oct;63(5):618-637. doi: 10.1016/j.survophthal.2018.04.002. Epub 2018 Apr 19.

Association between VEGF polymorphisms (-460 T/C and +936 C/T) and retinopathy of prematurity risk: A meta-analysis.血管内皮生长因子基因多态性（-460 T/C和+936 C/T）与早产儿视网膜病变风险的关联：一项荟萃分析。

Saudi J Ophthalmol. 2016 Jul-Sep;30(3):157-162. doi: 10.1016/j.sjopt.2016.06.003. Epub 2016 Jun 28.

Association of VEGF gene polymorphisms with advanced retinopathy of prematurity: a meta-analysis.血管内皮生长因子基因多态性与早产儿视网膜病变的相关性：一项荟萃分析。

Mol Biol Rep. 2012 Dec;39(12):10731-7. doi: 10.1007/s11033-012-1964-6. Epub 2012 Oct 13.

本文引用的文献

Genetic susceptibility to advanced retinopathy of prematurity (ROP).遗传易感性与早产儿视网膜病变（ROP）的进展。

J Biomed Sci. 2010 Aug 25;17(1):69. doi: 10.1186/1423-0127-17-69.

Genetic variation of vascular endothelial growth factor pathway does not correlate with the severity of retinopathy of prematurity.血管内皮生长因子通路的遗传变异与早产儿视网膜病变的严重程度无关。

J Perinatol. 2011 Apr;31(4):246-50. doi: 10.1038/jp.2010.111. Epub 2010 Aug 12.

Published genetic variants in retinopathy of prematurity: random forest analysis suggests a negligible contribution to risk and severity.早产儿视网膜病变中已发表的基因变异：随机森林分析表明其对风险和严重程度的影响可忽略不计。

Curr Eye Res. 2008 May;33(5):501-5. doi: 10.1080/02713680802018427.

Association of genetic polymorphisms of vascular endothelial growth factor and risk for proliferative retinopathy of prematurity.血管内皮生长因子基因多态性与早产儿增殖性视网膜病变风险的关联。

Pediatr Res. 2005 Mar;57(3):396-8. doi: 10.1203/01.PDR.0000153867.80238.E0. Epub 2005 Jan 5.

Genetic polymorphisms and retinopathy of prematurity.基因多态性与早产儿视网膜病变

Invest Ophthalmol Vis Sci. 2004 Jun;45(6):1712-5. doi: 10.1167/iovs.03-1303.

Tohoku J Exp Med. 2002 Nov;198(3):181-90. doi: 10.1620/tjem.198.181.

A common 936 C/T mutation in the gene for vascular endothelial growth factor is associated with vascular endothelial growth factor plasma levels.血管内皮生长因子基因中常见的936 C/T突变与血管内皮生长因子血浆水平相关。

J Vasc Res. 2000 Nov-Dec;37(6):443-8. doi: 10.1159/000054076.

Regulation of vascular endothelial growth factor by oxygen in a model of retinopathy of prematurity.早产儿视网膜病变模型中氧对血管内皮生长因子的调控

Arch Ophthalmol. 1996 Oct;114(10):1219-28. doi: 10.1001/archopht.1996.01100140419009.

Vascular endothelial growth factor acts as a survival factor for newly formed retinal vessels and has implications for retinopathy of prematurity.血管内皮生长因子作为新生视网膜血管的存活因子，与早产儿视网膜病变有关。

Nat Med. 1995 Oct;1(10):1024-8. doi: 10.1038/nm1095-1024.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验