about
The function of heterodimeric AP-1 comprised of c-Jun and c-Fos in activin mediated Spemann organizer gene expressionHoyeraal-Hreidarsson syndrome with a DKC1 mutation identified by whole-exome sequencingCopy number variation of age-related macular degeneration relevant genes in the Korean populationCombined linkage and association analyses identify a novel locus for obesity near PROX1 in AsiansEstimation of Prognostic Marker Genes by Public Microarray Data in Patients with Ovarian Serous CystadenocarcinomaA genome-wide Asian genetic map and ethnic comparison: the GENDISCAN studyAltered nucleocytoplasmic proteome and transcriptome distributions in an in vitro model of amyotrophic lateral sclerosisHigh prevalence of TP53 mutations is associated with poor survival and an EMT signature in gliosarcoma patients.Transcriptome analyses of chronic traumatic encephalopathy show alterations in protein phosphatase expression associated with tauopathy.Targeted next-generation sequencing at copy-number breakpoints for personalized analysis of rearranged ends in solid tumors.Analysis of Gene Expression in Human Dermal Fibroblasts Treated with Senescence-Modulating COX Inhibitors.Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancerThe first Irish genome and ways of improving sequence accuracyExomic sequencing of immune-related genes reveals novel candidate variants associated with alopecia universalis.Targeted sequencing of cancer-related genes in colorectal cancer using next-generation sequencingGenetic association of APOA5 and APOE with metabolic syndrome and their interaction with health-related behavior in Korean menIsolation of Middle East Respiratory Syndrome Coronavirus from a Patient of the 2015 Korean Outbreak.xCyp26c Induced by Inhibition of BMP Signaling Is Involved in Anterior-Posterior Neural Patterning of Xenopus laevisThe fine-scale and complex architecture of human copy-number variationTargeted resequencing of candidate genes reveals novel variants associated with severe Behçet's uveitisDraft Genome of Toxocara canis, a Pathogen Responsible for Visceral Larva Migrans.RNA editing in RHOQ promotes invasion potential in colorectal cancerRANBP2-ALK fusion combined with monosomy 7 in acute myelomonocytic leukemia.The opsonin MFG-E8 is a ligand for the alphavbeta5 integrin and triggers DOCK180-dependent Rac1 activation for the phagocytosis of apoptotic cells.Findings of a 1303 Korean whole-exome sequencing study.The full-length DNA sequence of Epstein Barr virus from a human gastric carcinoma cell line, SNU-719.Noninvasive prenatal diagnosis of duchenne muscular dystrophy: comprehensive genetic diagnosis in carrier, proband, and fetus.Novel fusion transcripts in human gastric cancer revealed by transcriptome analysis.Genome-wide combination profiling of copy number and methylation offers an approach for deciphering misregulation and development in cancer cells.Genome-wide characterization of the routes to pluripotency.Association between salivary amylase (AMY1) gene copy numbers and insulin resistance in asymptomatic Korean men.Glutaminase 2 expression is associated with regional heterogeneity of 5-aminolevulinic acid fluorescence in glioblastoma.Clinical whole exome sequencing in early onset diabetes patients.Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis.MicroRNA Expression Profiles in Gastric CarcinogenesisI148M variant in PNPLA3 reduces central adiposity and metabolic disease risks while increasing nonalcoholic fatty liver diseaseTargeted next-generation DNA sequencing identifies Notch signaling pathway mutation as a predictor of radiation responseDevelopment of a common platform for the noninvasive prenatal diagnosis of X-linked diseasesUnstable Genome and Transcriptome Dynamics during Tumor Metastasis Contribute to Therapeutic Heterogeneity in Colorectal CancersComparative genomics of Mycoplasma pneumoniae isolated from children with pneumonia: South Korea, 2010-2016
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Jong-Il Kim
@ast
Jong-Il Kim
@en
Jong-Il Kim
@es
Jong-Il Kim
@nl
type
label
Jong-Il Kim
@ast
Jong-Il Kim
@en
Jong-Il Kim
@es
Jong-Il Kim
@nl
prefLabel
Jong-Il Kim
@ast
Jong-Il Kim
@en
Jong-Il Kim
@es
Jong-Il Kim
@nl
P106
P31
P496
0000-0002-7240-3744