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Journal of Clinical Laboratory Analysis|November 7, 2019
Next-generation sequencing reveals unique combination of mutations in cis of CSF3R in atypical chronic myeloid leukemiaJae Won Yun, Jung Yoon, Chul Won Jung, et al.Journal of Agricultural and Food Chemistry|September 13, 2012
Brazilin induces apoptosis and G2/M arrest via inactivation of histone deacetylase in multiple myeloma U266 cellsBonglee Kim, Sun-Hee Kim, Soo-Jin Jeong, et al.American Journal of Hematology|November 29, 2011
Monosomal karyotype in acute myeloid leukemia predicts adverse treatment outcome and associates with high functional multidrug resistance activityHee Kyung Ahn, Jun Ho Jang, Kihyun Kim, et al.Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|February 8, 2011
Molecular characterization of female hemophilia A by multiplex ligation-dependent probe amplification analysis and X-chromosome inactivation studyMin-Jung Song, Hee-Jin Kim, Ki-Young Yoo, et al.Journal of the American Chemical Society|February 26, 2004
An EPR, ESEEM, structural NMR, and DFT study of a synthetic model for the covalently ring-linked tyrosine-histidine structure in the heme-copper oxidasesSun Hee Kim, Constantino Aznar, Marcin Brynda, et al.Biotechnology Letters|May 28, 2014
Coexpression of multiple genes reconstitutes two pathways of very long-chain polyunsaturated fatty acid biosynthesis in Pichia pastorisSun Hee Kim, Kyung Hee Roh, Kwang-Soo Kim, et al.Pediatric Blood & Cancer|December 3, 2009
A novel initiation codon mutation in the ribosomal protein S17 gene (RPS17) in a patient with Diamond-Blackfan anemiaMin-Jung Song, Eun-Hyung Yoo, Ki-O Lee, et al.Structure (London, England : 1993)|November 4, 2015
Mutation-Guided Unbiased Modeling of the Fat Sensor GPR119 for High-Yield Agonist ScreeningChristoffer Norn, Maria Hauge, Maja S Engelstoft, et al.Annals of Laboratory Medicine|February 27, 2016
Usefulness of Flow Cytometric Analysis for Detecting Leptomeningeal Diseases in Non-Hodgkin LymphomaSang Yong Shin, Seung Tae Lee, Hee Jin Kim, et al.International Journal of Hematology|June 22, 2006
A novel mutation W252X in the WAS gene in a Korean patient with Wiskott-Aldrich syndromeHee-Jin Kim, Eun-Hyung Yoo, Chang-Seok Ki, et al.Pageof 56