Varaico: Literature-Extracted Genetic Variants

Gene:HMOX1
Variant:p.D7H
Back to variants list

HMOX1

NM_002133.3:p.D7H

Associated Papers

Single-Nucleotide Polymorphisms Associated with Mercury Levels and Neurological Symptoms: An Overview.

Perini JA et al.

Toxics, 2024

38535959 (PubMed )
Supplement: toxics-12-00226-s001.zip › toxics-2905208-supplementary.pdf

Heme oxygenase-1 gene rs2071746 polymorphism in retinal vein occlusion.

Posch-Pertl L et al.

Ophthalmic Genetics, 2022

Genetic alterations in necrotizing enterocolitis.

Cuna A et al.

Seminars in Perinatology, 2017

Necrotizing Enterocolitis Is Not Associated With Sequence Variants in Antioxidant Response Genes in Premature Infants.

Sampath V et al.

Journal of Pediatric Gastroenterology and Nutrition, 2016

An association between polymorphism of the heme oxygenase-1 and -2 genes and age-related macular degeneration.

Synowiec E et al.

Molecular Biology Reports, 2012

Association of a matrix metallopeptidase 1 gene polymorphism with long-term outcome of thoracic aortic aneurysm.

Kato K et al.

International Journal of Molecular Medicine, 2012

Genetic analyses of heme oxygenase 1 (HMOX1) in different forms of pancreatitis.

Weis S et al.

Plos One, 2012

Novel strategy to identify genetic risk factors for COPD severity: a genetic isolate.

van Diemen CC et al.

The European Respiratory Journal, 2010

Genetic analysis of heme oxygenase-1 (HO-1) in German Parkinson's disease patients.

Funke C et al.

Journal of Neural Transmission (vienna, Austria : 1996), 2009

Association of genetic variants with chronic kidney disease in Japanese individuals.

Yoshida T et al.

Clinical Journal of the American Society of Nephrology : Cjasn, 2009

Genetic factors for obesity.

Yamada Y et al.

International Journal of Molecular Medicine, 2006

Assessment of genetic factors for type 2 diabetes mellitus.

Yamada Y et al.

International Journal of Molecular Medicine, 2006

The nuclear factor E2-related factor 2 and age-related macular degeneration.

Torres RJA et al.

Arquivos Brasileiros De Oftalmologia, 0

Latest Development on Genetics of Common Retinal Diseases.

Chen LJ et al.

Asia-pacific Journal of Ophthalmology (philadelphia, Pa.), 0

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."