Department of Laboratory Medicine
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t(5;12)(q13;p13) in acute myeloid leukemia with preceding granulocytic sarcoma.
Cancer genetics and cytogenetics Sep, 2007 | Pubmed ID: 17854675
A der(1;15)(q10;q10) is a rare nonrandom whole-arm translocation in patients with acute lymphoblastic leukemia.
Cancer genetics and cytogenetics Dec, 2007 | Pubmed ID: 18036400
[Evaluation of the Abbott Cell-Dyn Sapphire hematology analyzer].
The Korean journal of laboratory medicine Jun, 2007 | Pubmed ID: 18094570
Investigation of von Willebrand factor gene mutations in Korean von Willebrand disease patients.
The Korean journal of laboratory medicine Jun, 2007 | Pubmed ID: 18094571
8p11 myeloproliferative syndrome preceded by t(8;9)(p11;q33), CEP110/FGFR1 fusion transcript: morphologic, molecular, and cytogenetic characterization of myeloid neoplasms associated with eosinophilia and FGFR1 abnormality.
Cancer genetics and cytogenetics Mar, 2008 | Pubmed ID: 18295660
A novel missense MSH2 gene mutation in a patient of a Korean family with hereditary nonpolyposis colorectal cancer.
Cancer genetics and cytogenetics Apr, 2008 | Pubmed ID: 18406877
Paracentric inversion-associated t(8;21) variant in de novo acute myelogenous leukemia: characteristic patterns of conventional cytogenetics, FISH, and multicolor banding analysis.
Cancer genetics and cytogenetics May, 2008 | Pubmed ID: 18474302
Preceding orbital granulocytic sarcoma in an adult patient with acute myelogenous leukemia with t(8;21): a case study and review of the literature.
Cancer genetics and cytogenetics Aug, 2008 | Pubmed ID: 18656695
Complex t(8;19;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia.
Cancer genetics and cytogenetics Sep, 2008 | Pubmed ID: 18722881
Tetrasomy 8 in a patient with acute monoblastic leukemia.
The Korean journal of laboratory medicine Aug, 2008 | Pubmed ID: 18728374
Acute erythroleukemia with der(1;7)(q10;p10) as a sole acquired abnormality after treatment with azathioprine.
Cancer genetics and cytogenetics Oct, 2008 | Pubmed ID: 18786444
Rare translocations involving chromosome band 8p11 in myeloid neoplasms.
Cancer genetics and cytogenetics Oct, 2008 | Pubmed ID: 18940479
[Evaluation of multiplex PCR assay using dual priming oligonucleotide system for detection mutation in the Duchenne muscular dystrophy gene].
The Korean journal of laboratory medicine Oct, 2008 | Pubmed ID: 18971620
Linear relationship between ADAMTS13 activity and platelet dynamics even before severe thrombocytopenia.
Annals of clinical and laboratory science , 2008 | Pubmed ID: 18988930
MLL rearrangement with t(6;11)(q15;q23) as a sole abnormality in a patient with de novo acute myeloid leukemia: conventional cytogenetics, FISH, and multicolor FISH analyses for detection of rare MLL-related chromosome abnormalities.
Cancer genetics and cytogenetics Nov, 2008 | Pubmed ID: 18992643
Trisomy 8 in an elderly patient with acute lymphoblastic leukemia as a sole abnormality.
Cancer genetics and cytogenetics Nov, 2008 | Pubmed ID: 18992645
Acute promyelocytic leukemia relapsing as secondary acute myelogenous leukemia with translocation t(3;21)(q26;q22) and RUNX1-MDS1-EVI1 fusion transcript.
Cancer genetics and cytogenetics Dec, 2008 | Pubmed ID: 19027486
Acute promyelocytic leukemia in early pregnancy with translocation t(15;17) and variant PML/RARA fusion transcripts.
Cancer genetics and cytogenetics Jan, 2009 | Pubmed ID: 19061780
Three new nonsense mutations of MLH1 and MSH2 genes in Korean families with hereditary nonpolyposis colorectal cancer.
Cancer genetics and cytogenetics Jan, 2009 | Pubmed ID: 19100506
Acute promyelocytic leukemia with insertion of PML exon 7a and partial deletion of exon 3 of RARA: a novel variant transcript related to aggressive course and not detected with real-time polymerase chain reaction analysis.
Cancer genetics and cytogenetics Jan, 2009 | Pubmed ID: 19100514
Biphenotypic acute leukemia with b2a2 fusion transcript and trisomy 21.
Cancer genetics and cytogenetics Jan, 2009 | Pubmed ID: 19100520
Therapy-related myelodysplastic syndrome with der(17)t(12;17)(q13;p13) as a new recurrent cytogenetic abnormality after treatment for chronic lymphocytic leukemia.
Leukemia research Jul, 2009 | Pubmed ID: 19155067
JAK2 V617F/C618R mutation in a patient with polycythemia vera: a case study and review of the literature.
Cancer genetics and cytogenetics Feb, 2009 | Pubmed ID: 19167611
Non-age related Y chromosome loss in an elderly patient with acute promyelocytic leukemia.
Leukemia research Aug, 2009 | Pubmed ID: 19195699
Detection of a novel CBFB/MYH11 variant fusion transcript (K-type) showing partial insertion of exon 6 of CBFB gene using two commercially available multiplex RT-PCR kits.
Cancer genetics and cytogenetics Mar, 2009 | Pubmed ID: 19215788
A tandem triplication, trp(1)(q21q32), in a patient with follicular lymphoma: a case study and review of the literature.
Cancer genetics and cytogenetics Mar, 2009 | Pubmed ID: 19215795
BCR/ABL rearrangement with b3a3 fusion transcript in a case of childhood acute lymphoblastic leukemia.
Cancer genetics and cytogenetics Mar, 2009 | Pubmed ID: 19215796
Concomitant t(3;3)(q21;q26), trisomy 19, and E255V mutation associated with imatinib mesylate resistance in chronic myelogenous leukemia.
Cancer genetics and cytogenetics Apr, 2009 | Pubmed ID: 19264234
der(1)t(1;19)(p13;p13.1) in two elderly patients with myeloid neoplasms: new case reports and review of the literature.
Leukemia research Aug, 2009 | Pubmed ID: 19345416
Therapy-related acute lymphoblastic leukemia with t(9;22)(q34;q11.2):a case study and review of the literature.
Cancer genetics and cytogenetics May, 2009 | Pubmed ID: 19389510
Three-way Philadelphia variant t(9;22;14)(q34;q11.2;p11) in chronic myeloid leukemia.
Cancer genetics and cytogenetics May, 2009 | Pubmed ID: 19389511
Concomitant isochromosome 17q and trisomy 14 in a patient with myelodysplastic syndrome in leukemic transformation.
Annals of clinical and laboratory science , 2009 | Pubmed ID: 19429805
A novel PHEX mutation in a Korean patient with sporadic hypophosphatemic rickets.
Annals of clinical and laboratory science , 2009 | Pubmed ID: 19429806
Two case reports of 1q triplication in myeloproliferative neoplasms.
Cancer genetics and cytogenetics Jun, 2009 | Pubmed ID: 19446749
Association between acute promyelocytic leukemia and ring chromosome 6.
Cancer genetics and cytogenetics Jul, 2009 | Pubmed ID: 19480938
Chronic myelomonocytic leukemia with der(9)t(1;9)(q11;q34) as a sole abnormality.
Annals of clinical and laboratory science , 2009 | Pubmed ID: 19667417
A novel t(1;12)(q21;q24) in a patient with myelodysplastic syndrome.
Annals of hematology May, 2010 | Pubmed ID: 19697027
Detection of FUS-ERG chimeric transcript in two cases of acute myeloid leukemia with t(16;21)(p11.2;q22) with unusual characteristics.
Cancer genetics and cytogenetics Oct, 2009 | Pubmed ID: 19781443
A novel in-frame deletion in the factor V C1 domain associated with severe coagulation factor V deficiency in a Korean family.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis Mar, 2009 | Pubmed ID: 19786944
CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia.
Cancer genetics and cytogenetics Nov, 2009 | Pubmed ID: 19837277
Therapy-related myelodysplastic syndrome/acute myeloid leukemia after treatment with temozolomide in a patient with glioblastoma multiforme.
Annals of clinical and laboratory science , 2009 | Pubmed ID: 19880768
Three-way translocation involving MLL, MLLT1, and a novel third partner, NRXN1, in a patient with acute lymphoblastic leukemia and t(2;19;11) (p12;p13.3;q23).
Cancer genetics and cytogenetics Feb, 2010 | Pubmed ID: 20113834
Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia.
Cancer genetics and cytogenetics Mar, 2010 | Pubmed ID: 20193844
Automated detection of malaria-associated pseudoeosinophilia and abnormal WBC scattergram by the Sysmex XE-2100 hematology analyzer: a clinical study with 1,801 patients and real-time quantitative PCR analysis in vivax malaria-endemic area.
The American journal of tropical medicine and hygiene Mar, 2010 | Pubmed ID: 20207865
Constitutional pericentric inversion 9 in Korean patients with chronic myelogenous leukemia.
The Korean journal of laboratory medicine Jun, 2010 | Pubmed ID: 20603579
Molecular characterization of alternative SET-NUP214 fusion transcripts in a case of acute undifferentiated leukemia.
Cancer genetics and cytogenetics Sep, 2010 | Pubmed ID: 20682390
Constitutional pericentric inversion 9 and hematological disorders: a Korean tertiary institution's experience over eight years.
Annals of clinical and laboratory science , 2010 | Pubmed ID: 20689141
An SRY-deleted XXY female resulting from a paternally inherited t(Y;22).
Annals of clinical and laboratory science , 2010 | Pubmed ID: 20689145
Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21).
Cancer genetics and cytogenetics Oct, 2010 | Pubmed ID: 20875878
[Parvovirus B19-induced pure red cell aplasia in a liver transplant recipient].
The Korean journal of laboratory medicine Dec, 2010 | Pubmed ID: 21157144
Diagnosis of non-overt disseminated intravascular coagulation made according to the International Society on Thrombosis and Hemostasis criteria with some modifications.
The Korean journal of hematology Dec, 2010 | Pubmed ID: 21253428
Elevated levels of activated and inactivated thrombin-activatable fibrinolysis inhibitor in patients with sepsis.
The Korean journal of hematology Dec, 2010 | Pubmed ID: 21253429
A heparin binding site Arg79Cys missense mutation in the SERPINC1 gene in a Korean patient with hereditary antithrombin deficiency.
Annals of clinical and laboratory science , 2011 | Pubmed ID: 21325262
Acute promyelocytic leukemia with trisomy 8 and del(9)(q22) after treatment of cervical cancer with concurrent chemoradiotherapy: a case report.
Onkologie , 2011 | Pubmed ID: 21734427
Delta neutrophil index: a promising diagnostic and prognostic marker for sepsis.
Shock (Augusta, Ga.) Mar, 2012 | Pubmed ID: 22258230
CD5-negative blastoid variant mantle cell lymphoma with complex CCND1/IGH and MYC aberrations.
Annals of laboratory medicine Jan, 2012 | Pubmed ID: 22259787
A Gly1609Arg missense mutation in the vWF gene in a Korean patient with von Willebrand disease type 2A.
Annals of clinical and laboratory science , 2012 | Pubmed ID: 22371917
Fibrinogen residue γAla341 is necessary for calcium binding and 'A-a' interactions.
Thrombosis and haemostasis May, 2012 | Pubmed ID: 22437918
Comparison study of the rates of manual peripheral blood smear review from 3 automated hematology analyzers, Unicel DxH 800, ADVIA 2120i, and XE 2100, using international consensus group guidelines.
Archives of pathology & laboratory medicine Nov, 2012 | Pubmed ID: 23106587
An engineered fibrinogen variant AαQ328,366P does not polymerise normally, but retains the ability to form α cross-links.
Thrombosis and haemostasis Feb, 2013 | Pubmed ID: 23224113
Immature platelet fraction in diabetes mellitus and metabolic syndrome.
Thrombosis research , 2013 | Pubmed ID: 24140451
Comparison of prothrombin time derived from CoaguChek XS and laboratory test according to fibrinogen level.
Journal of clinical laboratory analysis Jan, 2015 | Pubmed ID: 24687901
The instability of commercial control materials in quality control of mean corpuscular volume.
Clinica chimica acta; international journal of clinical chemistry Jul, 2014 | Pubmed ID: 24769249
Analytical and clinical performance of a new point of care LABGEOIB D-dimer test for diagnosis of venous thromboembolism.
Annals of clinical and laboratory science , 2014 | Pubmed ID: 25117092
Selective serotonin reuptake inhibitors facilitate ANO6 (TMEM16F) current activation and phosphatidylserine exposure.
Pflügers Archiv : European journal of physiology Nov, 2015 | Pubmed ID: 25630304
Capillary-scale direct measurement of hemoglobin concentration of erythrocytes using photothermal angular light scattering.
Biosensors & bioelectronics Dec, 2015 | Pubmed ID: 26176206
Quantitative Influence of ABO Blood Groups on Factor VIII and Its Ratio to von Willebrand Factor, Novel Observations from an ARIC Study of 11,673 Subjects.
PloS one , 2015 | Pubmed ID: 26244499
Clinical Utility of Bone Marrow Study in Gaucher Disease: A Case Report of Gaucher Disease Type 3 With Intractable Myoclonic Seizures.
Annals of laboratory medicine Mar, 2016 | Pubmed ID: 26709268
Automated CH50 liposome-based immunoassay: consideration in dilution and validation of reference interval.
Clinical chemistry and laboratory medicine Oct, 2016 | Pubmed ID: 27016150
Magnetic bead-based nucleic acid purification kit: Clinical application and performance evaluation in stool specimens.
Journal of microbiological methods May, 2016 | Pubmed ID: 27030641
Association of Single Nucleotide Polymorphisms in the ST3GAL4 Gene with VWF Antigen and Factor VIII Activity.
PloS one , 2016 | Pubmed ID: 27584569
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