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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 5 (of 5 Records)

Query Trace: Disease and MIAT[original query]
Genetic variants in long non-coding RNA MIAT contribute to risk of paranoid schizophrenia in a Chinese Han population.
Schizophrenia research 2015 Aug 166 (1-3): 125-30.
Rao Shu-Quan, Hu Hui-Ling, Ye Ning, Shen Yan, Xu
Promoter polymorphisms in the lncRNA-MIAT gene associated with acute myocardial infarction in Chinese Han population: a case-control study.
Bioscience reports 2020 Feb 40 (2): .
Ma Ruchao, He Xiaohui, Zhu Xiaoyun, Pang Shuchao, Yan
Long Non-Coding RNAs Gene Variants as Molecular Markers for Diabetic Retinopathy Risk and Response to Anti-VEGF Therapy.
Pharmacogenomics and personalized medicine 2021 14 997-1014.
Mohammad Hala M F, Abdelghany Ahmed A, Al Ageeli Essam, Kattan Shahad W, Hassan Ranya, Toraih Eman A, Fawzy Manal S, Mokhtar Nagl
The rs3931283/PVT1 and rs7158663/MEG3 polymorphisms are associated with diabetic kidney disease and markers of renal function in patients with type 2 diabetes mellitus.
Molecular biology reports 2022 12 .
Dieter Cristine, Lemos Natália Emerim, Girardi Eliandra, Ramos Denise Taurino, Pellenz Felipe Mateus, Canani Luís Henrique, Assmann Taís Silveira, Crispim Dai
Association of Angio-LncRNAs MIAT rs1061540/MALAT1 rs3200401 Molecular Variants with Gensini Score in Coronary Artery Disease Patients Undergoing Angiography.
Biomolecules 2022 01 12 (1): .
Elwazir Mohamed Y, Hussein Mohammad H, Toraih Eman A, Al Ageeli Essam, Esmaeel Safya E, Fawzy Manal S, Faisal Sal
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