Yoonjung Kim

Seoul, Republic of Korea

Last Updated: 09/26/2026

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Found 19 publications

Cost-Effectiveness Analysis of Three Diagnostic Strategies for the Detection of EGFR Mutation in Advanced Non-Small Cell Lung Cancer.

Cost-Effectiveness Analysis of Three Diagnostic Strategies for the Detection of EGFR Mutation in Advanced Non-Small Cell Lung Cancer.

Journal: Annals of laboratory medicine

Published: October 17, 2022

Caspase-10 affects the pathogenesis of primary biliary cholangitis by regulating inflammatory cell death.

Caspase-10 affects the pathogenesis of primary biliary cholangitis by regulating inflammatory cell death.

Journal: Journal of autoimmunity

Published: August 11, 2022

Comparison of Homologous Recombination Repair Gene Next-Generation Sequencing Analysis in Patients With Metastatic Castration-Resistant Prostate Cancer Between Local and Central Laboratories in Korea.

Comparison of Homologous Recombination Repair Gene Next-Generation Sequencing Analysis in Patients With Metastatic Castration-Resistant Prostate Cancer Between Local and Central Laboratories in Korea.

Journal: Annals of laboratory medicine

Published: March 23, 2022

Application of CRISPR/Cas9-based mutant enrichment technique to improve the clinical sensitivity of plasma EGFR testing in patients with non-small cell lung cancer.

Application of CRISPR/Cas9-based mutant enrichment technique to improve the clinical sensitivity of plasma EGFR testing in patients with non-small cell lung cancer.

Journal: Cancer cell international

Published: November 25, 2021

Exosome-based detection of EGFR T790M in plasma and pleural fluid of prospectively enrolled non-small cell lung cancer patients after first-line tyrosine kinase inhibitor therapy.

Exosome-based detection of EGFR T790M in plasma and pleural fluid of prospectively enrolled non-small cell lung cancer patients after first-line tyrosine kinase inhibitor therapy.

Journal: Cancer cell international

Published: September 10, 2020

Selecting short length nucleic acids localized in exosomes improves plasma EGFR mutation detection in NSCLC patients.

Selecting short length nucleic acids localized in exosomes improves plasma EGFR mutation detection in NSCLC patients.

Journal: Cancer cell international

Published: June 02, 2019

A Comparative Study for Detection of EGFR Mutations in Plasma Cell-Free DNA in Korean Clinical Diagnostic Laboratories.

A Comparative Study for Detection of EGFR Mutations in Plasma Cell-Free DNA in Korean Clinical Diagnostic Laboratories.

Journal: BioMed research international

Published: January 04, 2018

Assessment of real-time PCR method for detection of EGFR mutation using both supernatant and cell pellet of malignant pleural effusion samples from non-small-cell lung cancer patients.

Assessment of real-time PCR method for detection of EGFR mutation using both supernatant and cell pellet of malignant pleural effusion samples from non-small-cell lung cancer patients.

Journal: Clinical chemistry and laboratory medicine

Published: September 20, 2016

Concomitant AID Expression and BCL7A Loss Associates With Accelerated Phase Progression and Imatinib Resistance in Chronic Myeloid Leukemia.

Concomitant AID Expression and BCL7A Loss Associates With Accelerated Phase Progression and Imatinib Resistance in Chronic Myeloid Leukemia.

Journal: Annals of laboratory medicine

Published: July 10, 2016

In Vivo Selection of Pan-Drug Resistant Acinetobacter baumannii during Antibiotic Treatment.

In Vivo Selection of Pan-Drug Resistant Acinetobacter baumannii during Antibiotic Treatment.

Journal: Yonsei medical journal

Published: June 13, 2015

Erratum to "Partial Gene Deletions of PMP22 Causing Hereditary Neuropathy with Liability to Pressure Palsies".

Erratum to "Partial Gene Deletions of PMP22 Causing Hereditary Neuropathy with Liability to Pressure Palsies".

Journal: Case reports in genetics

Published: January 26, 2015

Breakpoint mapping by whole genome sequencing identifies PTH2R gene disruption in a patient with midline craniosynostosis and a de novo balanced chromosomal rearrangement.

Breakpoint mapping by whole genome sequencing identifies PTH2R gene disruption in a patient with midline craniosynostosis and a de novo balanced chromosomal rearrangement.

Journal: Journal of medical genetics

Published: January 13, 2015

Showing 1-12 of 19

Last Updated: 09/26/2026