Lista de obras - Myungshin Kim - Dominio Público Uruguay

Acute Myeloid Leukemia with a <i>RUNX1-RUNX1T1</i> t(1;21;8)(q21;q22;q22) Novel Variant: A Case Report and Review of the Literature ⬇️

artículo científico publicado el 12 de febrero de 2011

Analytical and Potential Clinical Performance of Oncomine Myeloid Research Assay for Myeloid Neoplasms

artículo científico publicado en 2020

Bone marrow plasma cell assessment before peripheral blood stem cell mobilization in patients with multiple myeloma undergoing autologous stem cell transplantation.

artículo científico publicado en 2014

Budding Yeast Cells in Peripheral Blood Smear: Clue to Candidemia

artículo científico publicado en 2016

CDKN2B downregulation and other genetic characteristics in T-acute lymphoblastic leukemia

artículo científico publicado en 2019

Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea

artículo científico publicado en 2019

Clinical Validity of Next-Generation Sequencing Multi-Gene Panel Testing for Detecting Pathogenic Variants in Patients With Hereditary Breast-Ovarian Cancer Syndrome

scientific article published on 01 March 2020

Clonal Cell Proliferation in Paroxysmal Nocturnal Hemoglobinuria: Evaluation of PIGA Mutations and T-cell Receptor Clonality

scientific article published on 01 September 2019

De Novo Pure Trisomy 20p: Report of a Novel Case of a Marker Chromosome and Literature Review

artículo científico publicado en 2020

Development of immunocompatible pluripotent stem cells via CRISPR-based human leukocyte antigen engineering

article

Diagnosis and Prognosis of Sepsis Based on Use of Cytokines, Chemokines, and Growth Factors

scientific article published on 08 September 2019

Effects of Copy Number Variations on Developmental Aspects of Children With Delayed Development

article

Enumeration of CD34-positive Stem Cells Using the ADAMII Image-based Fluorescence Cell Counter

artículo científico publicado en 2019

Evaluation of Two EGFR Mutation Tests on Tumor and Plasma from Patients with Non-Small Cell Lung Cancer

artículo científico publicado en 2020

Hereditary dehydrated stomatocytosis with splicing site mutation of PIEZO1 mimicking myelodysplastic syndrome diagnosed by targeted next-generation sequencing.

artículo científico publicado en 2018

Hereditary spherocytosis caused by copy number variation in SPTB gene identified through targeted next-generation sequencing

scientific article published on 21 March 2019

High incidence of RAS pathway mutations among sentinel genetic lesions of Korean pediatric BCR-ABL1-like acute lymphoblastic leukemia

scientific article published on 07 May 2020

Passage-dependent accumulation of somatic mutations in mesenchymal stromal cells during in vitro culture revealed by whole genome sequencing.

artículo científico publicado en 2017

Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3.

artículo científico publicado en 2017

Peripheral blood <i>BRCA1</i> methylation profiling to predict familial ovarian cancer

artículo científico publicado en 2021

Practical informativeness of short tandem repeat loci for chimerism analysis in hematopoietic stem cell transplantation.

artículo científico publicado en 2017

Reclassification of Acute Myeloid Leukemia According to the 2016 WHO Classification

scientific article published on 01 May 2019

Seroprevalence of Neutralizing Antibodies against Japanese Encephalitis Virus among Adolescents and Adults in Korea: A Prospective Multicenter Study

artículo científico publicado en 2020

Sex Chromosomes Are Severely Disrupted in Gastric Cancer Cell Lines ⬇️

artículo científico publicado en 2020

Simultaneous Monitoring of Mutation and Chimerism Using Next-Generation Sequencing in Myelodysplastic Syndrome

artículo científico publicado en 2019

Targeted Next-Generation Sequencing of Plasma Cell-Free DNA in Korean Patients with Hepatocellular Carcinoma

artículo científico publicado en 2021

Ubiquitin C decrement plays a pivotal role in replicative senescence of bone marrow mesenchymal stromal cells.

artículo científico publicado en 2018

Lista de obras de Myungshin Kim

Acute Myeloid Leukemia with a &lt;i&gt;RUNX1-RUNX1T1&lt;/i&gt; t(1;21;8)(q21;q22;q22) Novel Variant: A Case Report and Review of the Literature ⬇️

Analytical and Potential Clinical Performance of Oncomine Myeloid Research Assay for Myeloid Neoplasms

Bone marrow plasma cell assessment before peripheral blood stem cell mobilization in patients with multiple myeloma undergoing autologous stem cell transplantation.

Budding Yeast Cells in Peripheral Blood Smear: Clue to Candidemia

CDKN2B downregulation and other genetic characteristics in T-acute lymphoblastic leukemia

Chromosomal Microarray Analysis as a First-Tier Clinical Diagnostic Test in Patients With Developmental Delay/Intellectual Disability, Autism Spectrum Disorders, and Multiple Congenital Anomalies: A Prospective Multicenter Study in Korea

Clinical Validity of Next-Generation Sequencing Multi-Gene Panel Testing for Detecting Pathogenic Variants in Patients With Hereditary Breast-Ovarian Cancer Syndrome

Clonal Cell Proliferation in Paroxysmal Nocturnal Hemoglobinuria: Evaluation of PIGA Mutations and T-cell Receptor Clonality

De Novo Pure Trisomy 20p: Report of a Novel Case of a Marker Chromosome and Literature Review

Development of immunocompatible pluripotent stem cells via CRISPR-based human leukocyte antigen engineering

Diagnosis and Prognosis of Sepsis Based on Use of Cytokines, Chemokines, and Growth Factors

Effects of Copy Number Variations on Developmental Aspects of Children With Delayed Development

Enumeration of CD34-positive Stem Cells Using the ADAMII Image-based Fluorescence Cell Counter

Evaluation of Two EGFR Mutation Tests on Tumor and Plasma from Patients with Non-Small Cell Lung Cancer

Hereditary dehydrated stomatocytosis with splicing site mutation of PIEZO1 mimicking myelodysplastic syndrome diagnosed by targeted next-generation sequencing.

Hereditary spherocytosis caused by copy number variation in SPTB gene identified through targeted next-generation sequencing

High incidence of RAS pathway mutations among sentinel genetic lesions of Korean pediatric BCR-ABL1-like acute lymphoblastic leukemia

Passage-dependent accumulation of somatic mutations in mesenchymal stromal cells during in vitro culture revealed by whole genome sequencing.

Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3.

Peripheral blood <i>BRCA1</i> methylation profiling to predict familial ovarian cancer

Practical informativeness of short tandem repeat loci for chimerism analysis in hematopoietic stem cell transplantation.

Reclassification of Acute Myeloid Leukemia According to the 2016 WHO Classification

Seroprevalence of Neutralizing Antibodies against Japanese Encephalitis Virus among Adolescents and Adults in Korea: A Prospective Multicenter Study

Sex Chromosomes Are Severely Disrupted in Gastric Cancer Cell Lines ⬇️

Simultaneous Monitoring of Mutation and Chimerism Using Next-Generation Sequencing in Myelodysplastic Syndrome

Targeted Next-Generation Sequencing of Plasma Cell-Free DNA in Korean Patients with Hepatocellular Carcinoma

Ubiquitin C decrement plays a pivotal role in replicative senescence of bone marrow mesenchymal stromal cells.

Acute Myeloid Leukemia with a <i>RUNX1-RUNX1T1</i> t(1;21;8)(q21;q22;q22) Novel Variant: A Case Report and Review of the Literature ⬇️