Lack of association of genetic polymorphisms of angiotensin-converting enzyme gene I/D and glutathione-S-transferase enzyme T1 and M1 with retinopathy of prematures.

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Genetics and Molecular Research

• Publication date

  2010-10-26

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.4238/vol9-4gmr887PMID 21038299
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Glutathione Transferases

  2010cited by this paper
• Lack of association of VEGF (−2578 C → A) and ANG 2 (−35 G → C) gene polymorphisms with the progression of retinopathy of prematurity

  2009cited by this paper
• Endothelial nitric oxide synthase gene T−786C and 27-bp repeat gene polymorphisms in retinopathy of prematurity

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• Role of GSTM1 and GSTT1 polymorphism: Susceptibility to hypertension in Arabs residing in UAE

  2025cites this paper
• Association of ACE and AGTR1 variants with retinopathy of prematurity: a case–control study and meta-analysis

  2024cites this paper
• No Association of Angiotensin-Converting Enzyme Insertion/Deletion (ACE I/D) Gene Polymorphism in the Susceptibility to Diabetic Retinopathy in Type 2 Diabetes Mellitus Patients: An Updated Meta-Analysis

  2023cites this paper
• The Genetics of Disorders Affecting the Premature Newborn

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• Association of ACE I/D and PAI-1 4G/5G polymorphisms with susceptibility to type 2 diabetes mellitus

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• Retinopathy prematurity: a systematic review and meta-analysis study based on neonatal and maternal risk factors

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• Association of eNOS and ACE Polymorphisms with Retinopathy of Prematurity: A Systematic Review and Meta-Analysis

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• Interaction of renin-angiotensin system gene polymorphisms with hypertension in Chinese patients with type 1 diabetes and retinopathy

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• The relationship between ACE/AGT gene polymorphisms and the risk of diabetic retinopathy in Chinese patients with type 2 diabetes

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• Influence of polymorphisms in VEGF, ACE, TNF and GST genes on the susceptibility to retinopathy of prematurity among Chinese infants.

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• Investigation of TNF-alpha gene (G308A) and GSTP1 gene (Ilel05Val) polymorphisms in Turkish patients with retinopathy of prematurity.

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• Association of the ACE I/D Gene Polymorphisms with JAK2V617F-Positive Polycythemia Vera and Essential Thrombocythemia

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• Investigating GSTT1 and GSTM1 null genotype as the risk factor of diabetes type 2 retinopathy

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• Impact of Genetic Variations of the CYP1A1, GSTT1, and GSTM1 Genes on the Risk of Coronary Artery Disease

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• The Role of Reactive Oxygen Species and Oxidative Signaling in Retinopathy of Prematurity

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• The Association of Angiotensin-Converting Enzyme Gene Insertion/Deletion Polymorphisms with Obstructive Sleep Apnoea: A Meta-analysis

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