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Characteristics of Tumor Infiltrating Lymphocyte and Circulating Lymphocyte Repertoires in Pancreatic Cancer by the Sequencing of T Cell Receptors.Whole Exome Sequencing Identifies Frequent Somatic Mutations in Cell-Cell Adhesion Genes in Chinese Patients with Lung Squamous Cell CarcinomaNovel loci and pathways significantly associated with longevity.Multiple gene mutations identified in patients infected with influenza A (H7N9) virusDetection of clinically relevant genetic variants in autism spectrum disorder by whole-genome sequencingGenome-wide characteristics of de novo mutations in autismDiversity of Gut Microbiota Metabolic Pathways in 10 Pairs of Chinese Infant Twins.High-throughput sequencing of autism spectrum disorders comes of age.Composition and variation analysis of the TCR β-chain CDR3 repertoire in neonatal sepsis.Analysis of the Repertoire Features of TCR Beta Chain CDR3 in Human by High-Throughput Sequencing.Association of MTTP gene variants with pediatric NAFLD: A candidate-gene-based analysis of single nucleotide variations in obese childrenComprehensive investigating of cytokine and receptor related genes variants in patients with chronic hepatitis B virus infection.Comprehensive investigation of cytokine- and immune-related gene variants in HBV-associated hepatocellular carcinoma patients.Increased stool immunoglobulin A level in children with autism spectrum disorders.Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures.High prevalence of serum folate receptor autoantibodies in children with autism spectrum disorders.Mass spectrometry identification of potential biomarker proteins in the 150-kD electrophoretic band in patients with schizophreniaAlterations in Gut Glutamate Metabolism Associated with Changes in Gut Microbiota Composition in Children with Autism Spectrum DisorderAlteration of gut microbiota-associated epitopes in children with autism spectrum disordersWhole-Exome Sequencing Revealing De Novo Heterozygous Variant OF KCNT1 in a Twin Discordant for Benign Epilepsy with Centrotemporal SpikesFrequent mutation of hypoxia-related genes in persistent pulmonary hypertension of the newbornShotgun metagenomics reveals an enrichment of potentially cross-reactive bacterial epitopes in ankylosing spondylitis patients, as well as the effects of TNFi therapy upon microbiome compositionDesign of a Targeted Sequencing Assay to Detect Rare Mutations in Circulating Tumor DNA
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Mingbang Wang
@ast
Mingbang Wang
@en
Mingbang Wang
@es
Mingbang Wang
@nl
type
label
Mingbang Wang
@ast
Mingbang Wang
@en
Mingbang Wang
@es
Mingbang Wang
@nl
prefLabel
Mingbang Wang
@ast
Mingbang Wang
@en
Mingbang Wang
@es
Mingbang Wang
@nl
P106
P1153
57196036249
P21
P31
P496
0000-0002-5989-5377