Cargando…

Expression quantitative trait loci for PI3K/AKT pathway

A genome-wide association study (GWAS) was conducted to identify expression quantitative trait loci (eQTLs) for the genes involved in phosphatidylinositol-3-kinase/v-akt murine thymoma viral oncogene homolog (PI3K/AKT) pathway. Data on mRNA expression of 341 genes in lymphoblastoid cell lines of 373...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ryu, Dongchan, Lee, Chaeyoung
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2017
Materias:	3500
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5228698/ https://www.ncbi.nlm.nih.gov/pubmed/28072738 http://dx.doi.org/10.1097/MD.0000000000005817

Ejemplares similares

Genome-wide identification of expression quantitative trait loci for human telomerase
por: Kim, Hanseol, et al.
Publicado: (2016)

Strong cis-acting expression quantitative trait loci for the genes encoding SNHG5 and PEX6
por: Lee, Jihyeon, et al.
Publicado: (2016)

Association of IL12A Expression Quantitative Trait Loci (eQTL) With Primary Biliary Cirrhosis in a Chinese Han Population
por: Li, Ping, et al.
Publicado: (2016)

Profile of Differential Promoter Activity by Nucleotide Substitution at GWAS Signals For Multiple Sclerosis
por: Ryu, Jihye, et al.
Publicado: (2014)

Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function
por: Suh, Yujin, et al.
Publicado: (2017)

Genome-wide linkage analysis and regional fine mapping identified variants in the RYR3 gene as a novel quantitative trait locus for circulating adiponectin in Chinese population
por: Chang, Yi-Cheng, et al.
Publicado: (2016)

Potential contribution of the neurodegenerative disorders risk loci to cognitive performance in an elderly male gout population
por: Han, Lin, et al.
Publicado: (2017)

Association of several loci of SMAD7 with colorectal cancer: A meta-analysis based on case–control studies
por: Xiao, Qiang, et al.
Publicado: (2023)

Aberrantly methylated-differentially expressed genes and related pathways in cholangiocarcinoma
por: Lin, Guan, et al.
Publicado: (2022)

Study on the differentially expressed genes and signaling pathways in dermatomyositis using integrated bioinformatics method
por: Liu, Wei, et al.
Publicado: (2020)

Genome-Wide Expression Quantitative Trait Loci Analysis Using Mixed Models
por: Lee, Chaeyoung
Publicado: (2018)

Common Expression Quantitative Trait Loci Shared by Histone Genes
por: Kim, Hanseol, et al.
Publicado: (2017)

Network and pathway-based analyses of genes associated with osteoporosis
por: Gu, Huijie, et al.
Publicado: (2020)

Identification of key genes and pathways in IgA nephropathy using bioinformatics analysis
por: Hu, Shou-Liang, et al.
Publicado: (2020)

Correlation of TGF-β signaling pathway gene polymorphisms with unexplained recurrent spontaneous abortion
por: Xue, Huiqin, et al.
Publicado: (2023)

Identification of hub genes, key pathways, and therapeutic agents in Hutchinson–Gilford Progeria syndrome using bioinformatics analysis
por: Wang, Dengchuan, et al.
Publicado: (2020)

The cGAS-STING pathway-related gene signature can predict patient prognosis and immunotherapy responses in prostate adenocarcinoma
por: Zhuo, Xingxing, et al.
Publicado: (2022)

High expression of MMP28 indicates unfavorable prognosis in pancreatic cancer
por: Chen, Zhitao, et al.
Publicado: (2021)

Expression of LINE-1 retrotransposon in early human spontaneous abortion tissues
por: Lou, Chao, et al.
Publicado: (2022)

Bayesian Inference for Mixed Model-Based Genome-Wide Analysis of Expression Quantitative Trait Loci by Gibbs Sampling
por: Lee, Chaeyoung
Publicado: (2019)

Human epidermal growth factor receptor 2-positive metastatic breast cancer with novel epidermal growth factor receptor -ZNF880 fusion and epidermal growth factor receptor E114K mutations effectively treated with pyrotinib: A case report
por: Yue, Li, et al.
Publicado: (2020)

Expression patterns and prognostic value of m(6)A RNA methylation regulators in adrenocortical carcinoma
por: Fu, Yang, et al.
Publicado: (2021)

NOTCH3 Gene Polymorphism is Associated With the Prognosis of Gliomas in Chinese Patients
por: Shen, Zhipeng, et al.
Publicado: (2015)

Hereditary pancreatitis of 3 Chinese children: Case report and literature review
por: Dai, Li-Na, et al.
Publicado: (2016)

Loss-of-function mutation of PCSK9 as a protective factor in the clinical expression of familial hypercholesterolemia: A case report
por: Bayona, Ane, et al.
Publicado: (2020)

Bioinformatic analysis of differentially expressed profiles of lncRNAs and miRNAs with their related ceRNA network in endometrial cancer
por: Li, Fengfan, et al.
Publicado: (2023)

Effect of TIMP2/TIMP3 genes on the risk of osteosarcoma in Zhejiang population
por: Wu, Zhongwei, et al.
Publicado: (2021)

Constructing gene network for type 1 narcolepsy based on genome-wide association study and differential gene expression analysis (STROBE)
por: Ouyang, Hui, et al.
Publicado: (2020)

Prognostic significance of long intergenic non-protein-coding RNA 511expression in malignant tumors: A systematic review and meta-analysis
por: Chen, Ming, et al.
Publicado: (2020)

Clinicopathological and prognostic significance of NM23 expression in patients with non-small cell lung cancer: A systematic review and meta-analysis
por: Min, Shi-hui, et al.
Publicado: (2021)

Aberrant gene expression pattern in the glycolysis-cholesterol synthesis axis is linked with immune infiltration and prognosis in prostate cancer: A bioinformatics analysis
por: Yuan, Yiwen, et al.
Publicado: (2022)

The effects of NLRP3 and MAVS gene polymorphisms on the risk of asthma: A case–control study
por: Xulong, Cai, et al.
Publicado: (2022)

Genetic polymorphisms of CYP3A4 among Chinese patients with steroid-induced osteonecrosis of the femoral head
por: Wang, Yuan, et al.
Publicado: (2016)

Association of S100B 3’UTR polymorphism with risk of chronic heart failure in a Chinese Han population
por: Chen, Yuewu, et al.
Publicado: (2020)

Whole exome sequencing unveils a frameshift mutation in CNGB3 for cone dystrophy: A case report of an Indian family
por: Gupta, Shashank, et al.
Publicado: (2017)

A novel PMP22 insertion mutation causing Charcot–Marie–Tooth disease type 3: A case report
por: Han, Liang, et al.
Publicado: (2021)

Prenatal detection of terminal 9p24.3 microduplication encompassing DOCK8 gene: A variant of likely benign
por: Yue, Fagui, et al.
Publicado: (2021)

Identification of HIV-1-specific cascaded microRNA-mRNA regulatory relationships by parallel mRNA and microRNA expression profiling with AIDS patients after antiviral treatment
por: Shen, Fangyuan, et al.
Publicado: (2021)

Prenatal detection of a 3q29 microdeletion in a fetus with ventricular septum defect: A case report and literature review
por: Yue, Fagui, et al.
Publicado: (2021)

A novel NOTCH3 mutation and its clinical, neuroimaging and pathological presentation in a Chinese patient with CADASIL: A case report
por: Dang, Jing, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_tfb7j8faf6u1gge7t3u3hf3jj8