Genetic variant coding for iron regulatory protein HFE contributes to hypertension, the TAMRISK study - Wikidata - awgldk - TriplyDB

Genetic variant coding for iron regulatory protein HFE contributes to hypertension, the TAMRISK study

Genetic variant coding for iron regulatory protein HFE contributes to hypertension, the TAMRISK study

http://www.wikidata.org/entity/Q36153272

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Haplotype analysis of the HFE gene among populations of Northern Eurasia, in patients with metabolic disorders or stomach cancer, and in long-lived people.NLR family pyrin domain containing 3 (NLRP3) inflammasome gene polymorphism rs7512998 (C>T) predicts aging-related increase of blood pressure, the TAMRISK study.Functional Inducible Nitric Oxide Synthase Gene Variants Associate With Hypertension: A Case-Control Study in a Finnish Population-The TAMRISK Study Genetic Polymorphisms of Transcription Factor NRF2 and of its Host Gene Sulfiredoxin (SRXN1) are Associated with Cerebrovascular Disease in a Finnish Cohort, the TAMRISK Study Minor variant of rs 16827043 in the iron regulator hemojuvelin gene (HJV) contributes to hypertension: The TAMRISK study Gene polymorphisms of fibronectin rs2289202 and fibrillin 2 rs331069 associate with vascular disease, the TAMRISK study.Genetic variation in bone morphogenetic proteins family members (BMPs 2 and 4) and hypertension risk in middle-aged men: The TAMRISK study.Transferrin Level Before Treatment and Genetic Polymorphism in HFE Gene as Predictive Markers for Response to Adalimumab in Crohn's Disease Patients.

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Genetic variant coding for iron regulatory protein HFE contributes to hypertension, the TAMRISK study

http://www.wikidata.org/entity/Q36153272

description

2015 nî lūn-bûn

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Genetic variant coding for iro ...... ypertension, the TAMRISK study

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Genetic variant coding for iro ...... ypertension, the TAMRISK study

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Genetic variant coding for iro ...... ypertension, the TAMRISK study

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Genetic variant coding for iro ...... ypertension, the TAMRISK study

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Kirsi M Määttä

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Seppo T Nikkari

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Tarja A Kunnas

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P2860

The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand binding

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

Hepcidin and iron regulation, 10 years later.

Age-specific relevance of usual blood pressure to vascular mortality: a meta-analysis of individual data for one million adults in 61 prospective studies

Global prevalence of putative haemochromatosis mutations

Global burden of hypertension: analysis of worldwide data

Identification of a genetic variant at 2q12.1 associated with blood pressure in East Asians by genome-wide scan including gene-environment interactions

HFE gene and hereditary hemochromatosis: a HuGE review. Human Genome Epidemiology.

Hereditary hemochromatosis--a new look at an old disease.

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