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Sun-Hee Kim

Showing results (241-250 of 605) with videos related to

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Blood Research|October 19, 2017
Clinical impact of CD5 expression in Korean patients with diffuse large B-cell lymphomaHyun-Young Kim, Mi-Ae Jang, Hee-Jin Kim, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 18, 2010
Establishment of reference intervals for von Willebrand factor antigen and eight coagulation factors in a Korean population following the Clinical and Laboratory Standards Institute guidelinesJa-Hyun Jang, Ja-Young Seo, Sung-Hwan Bang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 24, 2010
Novel deleterious mutation in the F12 gene in a Korean family with severe coagulation factor XII deficiencyHee-Jung Kim, Hee-Jin Kim, Eui-Hoon Kwon, et al.
Brain Research|October 27, 2006
Influence of age on the response to fibroblast growth factor-2 treatment in a rat model of strokeSeok Joon Won, Lin Xie, Sun Hee Kim, et al.
Journal of Korean Medical Science|August 30, 2008
Screening of subtelomeric rearrangements in 100 Korean Pediatric patients with unexplained mental retardation and anomalies using subtelomeric FISH (fluorescence in situ hybridization)Hyun-Kyung Park, Hee-Jin Kim, Hyun-Jun Kim, et al.
Cancer Genetics and Cytogenetics|July 15, 2009
A novel four-way t(6;16;21;8)(p21.3;p11.2;q22;q22) in acute myeloid leukemia with RUNX1/RUNX1T1 rearrangementKyoung-Jin Park, Hyung-Doo Park, Hee-Jin Kim, et al.
Journal of Clinical Laboratory Analysis|November 12, 2014
Mutant Enrichment with 3'-Modified Oligonucleotides (MEMO)-Quantitative PCR for Detection of NPM1 Mutations in Acute Myeloid LeukemiaSang-Yong Shin, Chang-Seok Ki, Hee-Jin Kim, et al.
Medicine|February 1, 2020
Congenital factor V deficiency from compound heterozygous mutations with a novel variant c.2426del (p.Pro809Hisfs*2) in the F5 gene: A case reportChang-Hun Park, Min-Seung Park, Ki-O Lee, et al.
Annals of Clinical and Laboratory Science|August 16, 2015
A Novel de novo Mutation in the G6PD Gene in a Korean Boy with Glucose-6-phosphate Dehydrogenase Deficiency: Case ReportMi-Ae Jang, Ji-Yoon Kim, Ki-O Lee, et al.
Cancer Genetics and Cytogenetics|August 1, 2006
PML/RARA rearrangement associated with a t(15;19;17) in a case of acute myeloid leukemia with abundant myelocytes with salmon-pink cytoplasmIn-Suk Kim, Hee-Jin Kim, Hee-Suk Choung, et al.
Pageof 61

Showing results (241-250 of 605) with videos related to

Sort By:
Pageof 61
Blood Research|October 19, 2017
Clinical impact of CD5 expression in Korean patients with diffuse large B-cell lymphomaHyun-Young Kim, Mi-Ae Jang, Hee-Jin Kim, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 18, 2010
Establishment of reference intervals for von Willebrand factor antigen and eight coagulation factors in a Korean population following the Clinical and Laboratory Standards Institute guidelinesJa-Hyun Jang, Ja-Young Seo, Sung-Hwan Bang, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|August 24, 2010
Novel deleterious mutation in the F12 gene in a Korean family with severe coagulation factor XII deficiencyHee-Jung Kim, Hee-Jin Kim, Eui-Hoon Kwon, et al.
Brain Research|October 27, 2006
Influence of age on the response to fibroblast growth factor-2 treatment in a rat model of strokeSeok Joon Won, Lin Xie, Sun Hee Kim, et al.
Journal of Korean Medical Science|August 30, 2008
Screening of subtelomeric rearrangements in 100 Korean Pediatric patients with unexplained mental retardation and anomalies using subtelomeric FISH (fluorescence in situ hybridization)Hyun-Kyung Park, Hee-Jin Kim, Hyun-Jun Kim, et al.
Cancer Genetics and Cytogenetics|July 15, 2009
A novel four-way t(6;16;21;8)(p21.3;p11.2;q22;q22) in acute myeloid leukemia with RUNX1/RUNX1T1 rearrangementKyoung-Jin Park, Hyung-Doo Park, Hee-Jin Kim, et al.
Journal of Clinical Laboratory Analysis|November 12, 2014
Mutant Enrichment with 3'-Modified Oligonucleotides (MEMO)-Quantitative PCR for Detection of NPM1 Mutations in Acute Myeloid LeukemiaSang-Yong Shin, Chang-Seok Ki, Hee-Jin Kim, et al.
Medicine|February 1, 2020
Congenital factor V deficiency from compound heterozygous mutations with a novel variant c.2426del (p.Pro809Hisfs*2) in the F5 gene: A case reportChang-Hun Park, Min-Seung Park, Ki-O Lee, et al.
Annals of Clinical and Laboratory Science|August 16, 2015
A Novel de novo Mutation in the G6PD Gene in a Korean Boy with Glucose-6-phosphate Dehydrogenase Deficiency: Case ReportMi-Ae Jang, Ji-Yoon Kim, Ki-O Lee, et al.
Cancer Genetics and Cytogenetics|August 1, 2006
PML/RARA rearrangement associated with a t(15;19;17) in a case of acute myeloid leukemia with abundant myelocytes with salmon-pink cytoplasmIn-Suk Kim, Hee-Jin Kim, Hee-Suk Choung, et al.
Pageof 61