Cargando…

EXOC3L2 rs597668 variant contributes to Alzheimer’s disease susceptibility in Asian population

Recent genome-wide association studies have established the association between EXOC3L2 rs597668 variant and Alzheimer's disease (AD) in European population. However, recent studies reported inconsistent results in Asian population. Here, we performed a systematic review and meta-analysis to ev...

Descripción completa

Detalles Bibliográficos
Autores principales:	Wu, Qing-Jian, Sun, Shu-Yin, Yan, Cheng-Jun, Cheng, Zi-Cui, Yang, Ming-Feng, Li, Zi-Fei, Cheng, Hou-Wen, Fang, Ti-Kun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Impact Journals LLC 2017
Materias:	Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5386745/ https://www.ncbi.nlm.nih.gov/pubmed/28423615 http://dx.doi.org/10.18632/oncotarget.15380

Ejemplares similares

Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer’s disease
por: Miller, Jason E., et al.
Publicado: (2018)

Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival
por: Coulter, Michael E., et al.
Publicado: (2020)

A comprehensive prognostic and immune infiltration analysis of EXOC3L1 in pan-cancer
por: Zhang, Zhan-Fei
Publicado: (2022)

MiR-155 and its functional variant rs767649 contribute to the susceptibility and survival of hepatocellular carcinoma
por: Ji, Jiansong, et al.
Publicado: (2016)

Variants rs2200733 and rs6843082 Show Different Associations in Asian and Non-Asian Populations With Ischemic Stroke
por: Wang, Dongsen, et al.
Publicado: (2022)

BIN1 rs744373 variant shows different association with Alzheimer’s disease in Caucasian and Asian populations
por: Han, Zhifa, et al.
Publicado: (2019)

Mutations in the exocyst component EXOC2 cause severe defects in human brain development
por: Van Bergen, Nicole J., et al.
Publicado: (2020)

EXOC3L1: A Novel Prognostic Biomarker Correlated with Immune Infiltration in Esophageal Squamous Cell Carcinoma
por: Zhang, Zhan-Fei
Publicado: (2023)

EXOC4 Promotes Diffuse-Type Gastric Cancer Metastasis via Activating FAK Signal
por: Li, Haojie, et al.
Publicado: (2022)

Altered methylation pattern in EXOC4 is associated with stroke outcome: an epigenome-wide association study
por: Cullell, Natalia, et al.
Publicado: (2022)

Single Nucleotide Polymorphisms of EXOC1, BCL2, CCAT2, and CARD8 Genes and Susceptibility to Cervical Cancer in the Northern Chinese Han Population
por: Feng, Yanan, et al.
Publicado: (2022)

Case Report: Co-existence of a novel EXOC4‐TRHDE gene fusion with PML-RARA in acute promyelocytic leukemia
por: Liu, Xiaodong, et al.
Publicado: (2023)

Interleukin-1 Beta Gene Polymorphism rs16944 May Associate with Increased Susceptibility to Extremity Chronic Osteomyelitis in Chinese Han Population
por: Yao, Zi-long, et al.
Publicado: (2019)

Genetic Variant rs10757278 on Chromosome 9p21 Contributes to Myocardial Infarction Susceptibility
por: Chen, Guangyuan, et al.
Publicado: (2015)

The contribution of YTHDF2 gene rs3738067 A>G to the Wilms tumor susceptibility
por: Wang, Zhiyuan, et al.
Publicado: (2021)

Tnfaip2/exoc3‐driven lipid metabolism is essential for stem cell differentiation and organ homeostasis
por: Deb, Sarmistha, et al.
Publicado: (2020)

EXOC1 plays an integral role in spermatogonia pseudopod elongation and spermatocyte stable syncytium formation in mice
por: Osawa, Yuki, et al.
Publicado: (2021)

HIF-1α rs11549465 C>T polymorphism contributes to increased cancer susceptibility: Evidence from 49 studies
por: Li, Hu-Nian, et al.
Publicado: (2019)

CDH1 rs9929218 variant at 16q22.1 contributes to colorectal cancer susceptibility
por: Han, Peng, et al.
Publicado: (2016)

The CYP19A1 rs3751592 variant confers susceptibility to Alzheimer disease in the Chinese Han population
por: Zheng, Jiaqiang, et al.
Publicado: (2016)

The Association of an SNP in the EXOC4 Gene and Reproductive Traits Suggests Its Use as a Breeding Marker in Pigs
por: He, Yingting, et al.
Publicado: (2021)

TLR4 promoter rs1927914 variant contributes to the susceptibility of esophageal squamous cell carcinoma in the Chinese population
por: Li, Jiaying, et al.
Publicado: (2021)

Genetic association of RIT2 rs12456492 polymorphism and Parkinson’s disease susceptibility in Asian populations: a meta-analysis
por: Lu, Yanjun, et al.
Publicado: (2015)

Polymorphic variants INSIG2 rs6726538, HLA ‐ DRB1 rs9272143, and GCNT1P5 rs7780883 contribute to the susceptibility of cervical cancer in the Bangladeshi women
por: Hasan, Md. Emtiaz, et al.
Publicado: (2021)

Alzheimer’s Disease Risk Variant rs3865444 in the CD33 Gene: A Possible Role in Susceptibility to Multiple Sclerosis
por: Javor, Juraj, et al.
Publicado: (2022)

EXOC6 (Exocyst Complex Component 6) Is Associated with the Risk of Type 2 Diabetes and Pancreatic β-Cell Dysfunction
por: Sulaiman, Nabil, et al.
Publicado: (2022)

PARP1 rs1136410 Val762Ala contributes to an increased risk of overall cancer in the East Asian population: a meta-analysis
por: Xin, Yijuan, et al.
Publicado: (2021)

Genetic variants of ALDH2-rs671 and CYP2E1-rs2031920 contributed to risk of hepatocellular carcinoma susceptibility in a Chinese population
por: Ye, Xinping, et al.
Publicado: (2018)

IRGM rs13361189 polymorphism may contribute to susceptibility to Crohn’s disease: A meta-analysis
por: LU, YAO, et al.
Publicado: (2014)

CTLA-4 Genetic Variants (rs11571317 and rs3087243): Role in Susceptibility and Progression of Breast Cancer
por: Goske, Maruthi, et al.
Publicado: (2017)

A Functional Variant rs3093023 in CCR6 Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population
por: Zhang, Yue-miao, et al.
Publicado: (2021)

Association of interleukin 10 rs1800896 polymorphism with susceptibility to breast cancer: a meta-analysis
por: Zhu, ZiYin, et al.
Publicado: (2020)

NME8 rs2718058 polymorphism with Alzheimer's disease risk: a replication and meta-analysis
por: Liu, Shu-Lei, et al.
Publicado: (2016)

Modeling the structural implications of an alternatively spliced Exoc3l2, a paralog of the tunneling nanotube-forming M-Sec
por: O’Callaghan, Paul, et al.
Publicado: (2018)

A Functional Variant rs2072915 is Associated with the Susceptibility and Mortality of Cervical Squamous Cell Carcinoma
por: Li, Ren-Liang, et al.
Publicado: (2021)

Common Variant rs9939609 in Gene FTO Confers Risk to Polycystic Ovary Syndrome
por: Li, Tao, et al.
Publicado: (2013)

Genetic variant of miR-146a rs2910164 C>G and gastric cancer susceptibility
por: Xia, Zu-Guang, et al.
Publicado: (2016)

The Common Variant rs11646213 Is Associated with Preeclampsia in Han Chinese Women
por: Wan, Ji-peng, et al.
Publicado: (2013)

Interaction of Alcohol Consumption and ABCG2 rs2231142 Variant Contributes to Hyperuricemia in a Taiwanese Population
por: Chen, I-Chieh, et al.
Publicado: (2021)

A highly significant association between Cathepsin S gene polymorphisms rs12068264 and chronic obstructive pulmonary disease susceptibility in Han Chinese population
por: Gao, Sheng-lan, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_7gikorokrbkqu8bi1cke8eqhsb