Cargando…

Whole-genome re-sequencing for the identification of high contribution susceptibility gene variants in patients with type 2 diabetes

There is increasing evidence that several genes are associated with an increased risk of type 2 diabetes (T2D); genome-wide association investigations and whole-genome re-sequencing investigations offer a useful approach for the identification of genes involved in common human diseases. To further i...

Descripción completa

Detalles Bibliográficos
Autores principales:	SUN, XIAOJUAN, SUI, WEIGUO, WANG, XIAOBING, HOU, XIANLIANG, OU, MINGLIN, DAI, YONG, XIANG, YUEYING
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2016
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4838165/ https://www.ncbi.nlm.nih.gov/pubmed/27035118 http://dx.doi.org/10.3892/mmr.2016.5014

Ejemplares similares

Whole-genome resequencing of 100 healthy individuals using DNA pooling
por: Wang, Xiaobin, et al.
Publicado: (2016)

Single-cell sequencing reveals the potential oncogenic expression atlas of human iPSC-derived cardiomyocytes
por: Ou, Minglin, et al.
Publicado: (2021)

High-throughput sequencing reveals Jatrorrhizine inhibits colorectal cancer growth by ferroptosis-related genes
por: Huang, Lingyu, et al.
Publicado: (2023)

Determination of the complexity and diversity of the TCR β-chain CDR3 repertoire in bladder cancer using high-throughput sequencing
por: Ma, Jingsheng, et al.
Publicado: (2019)

Comparison of immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH) assessment for Her-2 status in breast cancer
por: Sui, Weiguo, et al.
Publicado: (2009)

Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing
por: Varzari, Alexander, et al.
Publicado: (2022)

Re-Ranking Sequencing Variants in the Post-GWAS Era for Accurate Causal Variant Identification
por: Faye, Laura L., et al.
Publicado: (2013)

Identification of breast cancer susceptibility genes using whole exome sequencing
por: Thompson, E, et al.
Publicado: (2012)

Whole-Exome Sequencing for the Identification of Susceptibility Genes of Kashin–Beck Disease
por: Yang, Zhenxing, et al.
Publicado: (2014)

A genetic risk factor for thrombophilia in a Han Chinese family
por: Sun, Guoping, et al.
Publicado: (2017)

Identification of genome variations in patients with lung adenocarcinoma using whole genome re-sequencing
por: Li, Guiyuan, et al.
Publicado: (2017)

Genetic characteristics of Jiaji Duck by whole genome re-sequencing
por: Gu, Lihong, et al.
Publicado: (2020)

Integrating Spatial Transcriptomics and Single-Cell RNA-seq Reveals the Gene Expression Profling of the Human Embryonic Liver
por: Hou, Xianliang, et al.
Publicado: (2021)

Discovery of Variants Underlying Host Susceptibility to Virus Infection Using Whole-Exome Sequencing
por: Leiva-Torres, Gabriel A., et al.
Publicado: (2017)

Whole-exome sequencing analysis identifies novel variants associated with Kawasaki disease susceptibility
por: Zhang, Xing, et al.
Publicado: (2023)

A case of anti-myelin oligodendrocyte glycoprotein (MOG)-immunoglobulin G (IgG) associated disorder (MOGAD) with clinical manifestations of acute disseminated encephalomyelitis: Secondary to mycoplasma pneumoniae infection
por: Huang, Xiangui, et al.
Publicado: (2023)

Identification and Characterization of Genes Related to the Prognosis of Hepatocellular Carcinoma Based on Single-Cell Sequencing
por: Chen, Wenbiao, et al.
Publicado: (2022)

Comparative proteomic analysis of membranous nephropathy biopsy tissues using quantitative proteomics
por: SUI, WEIGUO, et al.
Publicado: (2015)

Dynamic Metabolomics Study of the Bile Acid Pathway During Perioperative Primary Hepatic Carcinoma Following Liver Transplantation
por: Sui, Weiguo, et al.
Publicado: (2020)

Identification and Validation of Immune-Related Gene Prognostic Signature for Hepatocellular Carcinoma
por: Chen, Wenbiao, et al.
Publicado: (2020)

Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing
por: Crooks, Lucy, et al.
Publicado: (2020)

Identification of novel variants in retinitis pigmentosa genes by whole-exome sequencing
por: Kocaaga, Ayca, et al.
Publicado: (2023)

Initial whole-genome sequencing and analysis of the host genetic contribution to COVID-19 severity and susceptibility
por: Wang, Fang, et al.
Publicado: (2020)

Contribution of rare whole-genome sequencing variants to plasma protein levels and the missing heritability
por: Kierczak, Marcin, et al.
Publicado: (2022)

Optimal sequencing depth design for whole genome re-sequencing in pigs
por: Jiang, Yifan, et al.
Publicado: (2019)

Favored single nucleotide variants identified using whole genome Re-sequencing of Austrian and Chinese cattle breeds
por: Naji, Maulana M., et al.
Publicado: (2022)

Identification of risk variants related to malignant tumors in children with birth defects by whole genome sequencing
por: Liu, Yichuan, et al.
Publicado: (2022)

Identification of recurrent variants implicated in disease in bicuspid aortic valve patients through whole-exome sequencing
por: Chen, Shasha, et al.
Publicado: (2022)

Integrated microRNA and protein expression analysis reveals novel microRNA regulation of targets in fetal down syndrome
por: Lin, Hua, et al.
Publicado: (2016)

Characteristic analysis of TCR β-chain CDR3 repertoire for pre- and post-liver transplantation
por: Yang, Guiqi, et al.
Publicado: (2018)

Differential expression profile study and gene function analysis of maternal foetal-derived circRNA for screening for Down's syndrome
por: Sui, Weiguo, et al.
Publicado: (2020)

Correction: Characteristic analysis of TCR β-chain CDR3 repertoire for preand post-liver transplantation
por: Yang, Guiqi, et al.
Publicado: (2020)

Evaluation of variant identification methods for whole genome sequencing data in dairy cattle
por: Baes, Christine F, et al.
Publicado: (2014)

Identification of potential genetic causal variants for rheumatoid arthritis by whole-exome sequencing
por: Li, Ying, et al.
Publicado: (2017)

Identification of potential causal variants for premature ovarian failure by whole exome sequencing
por: Jin, Haengun, et al.
Publicado: (2020)

Identification of rare coding variants associated with Kawasaki disease by whole exome sequencing
por: Kim, Jae-Jung, et al.
Publicado: (2021)

Identification of Rare Variants Involved in High Myopia Unraveled by Whole Genome Sequencing
por: Haarman, Annechien E.G., et al.
Publicado: (2023)

Whole-Genome Sequencing-Based Re-Identification of Pseudomonas putida/fluorescens Clinical Isolates Identified by Biochemical Bacterial Identification Systems
por: Tohya, Mari, et al.
Publicado: (2022)

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program
por: Wheeler, Marsha M., et al.
Publicado: (2022)

Validation of Pooled Whole-Genome Re-Sequencing in Arabidopsis lyrata
por: Fracassetti, Marco, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_s75etoefbdcorsvhib3ksp1b0p