Varaico: Literature-Extracted Genetic Variants

Gene:CAT
Variant:p.D389A
Back to variants list

CAT

NM_001752.4:p.D389A

Associated Papers

Association of maternal angiotensin II type 1 and type 2 receptor combination genotypes with susceptibility to early-onset preeclampsia.

Satra M et al.

Journal of Human Hypertension, 2022

Angiotensin-converting enzyme insertion/deletion (rs106180) and angiotensin type 1 receptor A1166 C (rs106165) genotypes and psoriasis: Correlation with cellular immunity, lipid profile, and oxidative stress markers.

Tanhapour M et al.

Journal of Cellular Biochemistry, 2019

Renin-angiotensin system genetic polymorphisms: lack of association with CRP levels in patients with coronary artery disease.

Bahramali E et al.

Journal of the Renin-angiotensin-aldosterone System : Jraas, 2014

Genetic polymorphisms of the renin-angiotensin system in breast cancer patients.

Fishchuk LE et al.

Experimental Oncology, 2013

Association of angiotensin-converting enzyme polymorphism with coronary artery disease in Iranian patients with unipolar depression.

Firouzabadi N et al.

Clinical Biochemistry, 2012

Genetic polymorphisms in the renin-angiotensin system confer increased risk of stroke independently of blood pressure: a nested case-control study.

Möllsten A et al.

Journal of Hypertension, 2008

Assessment of 115 candidate genes for diabetic nephropathy by transmission/disequilibrium test.

Ewens KG et al.

Diabetes, 2005

Angiotensinogen M235T gene polymorphism and recurrent restenosis after repeated percutaneous transluminal coronary angiography.

Hertwig S et al.

Clinical Science (london, England : 1979), 2002

Variance of ACE and AT1 receptor gene does not influence the risk of neonatal acute renal failure.

Nobilis A et al.

Pediatric Nephrology (berlin, Germany), 2001

Polymorphisms in candidate genes for blood pressure regulation in young men with normal or elevated screening blood pressure.

Fossum E et al.

Blood Pressure, 2001

Angiotensinogen T235 and ACE insertion/deletion polymorphisms associated with albuminuria in Chinese type 2 diabetic patients.

Young RP et al.

Diabetes Care, 1998

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."