scholarly article | Q13442814 |
P2093 | author name string | Iman Salahshourifar | |
Farbod Yaghoubi Hariri | |||
Shohreh Zare Karizi | |||
P2860 | cites work | Evaluation of association between common genetic variants on chromosome 9p21 and coronary artery disease in Turkish population | Q37680668 |
9p21 DNA variants associated with coronary artery disease impair interferon-γ signalling response | Q39048288 | ||
An efficient procedure for genotyping single nucleotide polymorphisms. | Q39098483 | ||
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Enduring mystery of the chromosome 9p21.3 locus | Q44809994 | ||
Risk Factors for Coronary Artery Disease: Historical Perspectives | Q46098769 | ||
The association of polymorphic variants, rs2267788, rs1333049 and rs2383207 with coronary artery disease, its severity and presentation in North Indian population. | Q50137756 | ||
ANRIL rs1333049 C/G polymorphism and coronary artery disease in a North Indian population - Gender and age specific associations | Q90459402 | ||
The 9p21.3 risk locus for coronary artery disease: A 10-year search for its mechanism | Q92759498 | ||
Epigenetic regulation of the INK4b-ARF-INK4a locus: in sickness and in health | Q24604190 | ||
Genetic variants at chromosome 9p21 and risk of first versus subsequent coronary heart disease events: a systematic review and meta-analysis | Q33673402 | ||
Significance of a positive family history for coronary heart disease in patients with a zero coronary artery calcium score (from the Multi-Ethnic Study of Atherosclerosis). | Q34257566 | ||
Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF. | Q34619960 | ||
A common variant in the CDKN2B gene on chromosome 9p21 protects against coronary artery disease in Americans of African ancestry. | Q34816288 | ||
Association Study between Coronary Artery Disease and rs1333049 and rs10757274 Polymorphisms at 9p21 Locus in South-West Iran | Q35369571 | ||
Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease. | Q35824036 | ||
The rs10757278 polymorphism of the 9p21.3 locus is associated with premature coronary artery disease in Polish patients | Q36225325 | ||
Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study | Q36787671 | ||
P433 | issue | 1 | |
P921 | main subject | coronary artery disease | Q844935 |
P304 | page(s) | 58-63 | |
P577 | publication date | 2020-04-01 | |
P1433 | published in | Reports of biochemistry & molecular biology | Q27726936 |
P1476 | title | Association between Coronary Artery Disease and rs10757278 and rs1333049 Polymorphisms in 9p21 Locus in Iran | |
P478 | volume | 9 |
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