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Karen M Lower

Showing results (1-10 of 23) with videos related to

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Cancer Genetics|October 14, 2017
Trisomy 12 assessment by conventional fluorescence in-situ hybridization (FISH), FISH in suspension (FISH-IS) and laser scanning cytometry (LSC) in chronic lymphocytic leukemiaCuc H Do, Karen M Lower, Cindy Macardle, et al.
Experimental Hematology|April 30, 2018
Aberrant determination of phenotypic markers in chronic lymphocytic leukemia (CLL) lymphocytes after cryopreservationLauren A Thurgood, Karen M Lower, Cindy Macardle, et al.
Journal of Proteomics|January 11, 2017
From genome to proteome: Looking beyond DNA and RNA in chronic lymphocytic leukemiaLauren A Thurgood, Tim K Chataway, Karen M Lower, et al.
British Journal of Haematology|December 5, 2020
A biclonal case of chronic lymphocytic leukaemia with discordant mutational status of the immunoglobulin heavy chain variable region and bimodal CD49d expressionAnya K Hotinski, Oliver G Best, Lauren A Thurgood, et al.
British Journal of Haematology|January 19, 2019
Altered expression of metabolic pathways in CLL detected by unlabelled quantitative mass spectrometry analysisLauren A Thurgood, Eveline S Dwyer, Karen M Lower, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|October 13, 2017
Development of locus specific sub-clone separation by fluorescence in situ hybridization in suspension in chronic lymphocytic leukemiaCuc H Do, Sheree Bailey, Cindy Macardle, et al.
Journal of Diabetes Research|September 9, 2015
Differential Telomere Shortening in Blood versus Arteries in an Animal Model of Type 2 DiabetesSamira Tajbakhsh, Kamelya Aliakbari, Damian J Hussey, et al.
Experimental Hematology|December 13, 2021
Lipid uptake in chronic lymphocytic leukemiaLauren A Thurgood, Oliver G Best, Ashley Rowland, et al.
BMC Medical Genetics|May 10, 2017
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)Shari Javadiyan, Jamie E Craig, Shiwani Sharma, et al.
BMC Research Notes|February 13, 2016
Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataractShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Cancer Genetics|October 14, 2017
Trisomy 12 assessment by conventional fluorescence in-situ hybridization (FISH), FISH in suspension (FISH-IS) and laser scanning cytometry (LSC) in chronic lymphocytic leukemiaCuc H Do, Karen M Lower, Cindy Macardle, et al.
Experimental Hematology|April 30, 2018
Aberrant determination of phenotypic markers in chronic lymphocytic leukemia (CLL) lymphocytes after cryopreservationLauren A Thurgood, Karen M Lower, Cindy Macardle, et al.
Journal of Proteomics|January 11, 2017
From genome to proteome: Looking beyond DNA and RNA in chronic lymphocytic leukemiaLauren A Thurgood, Tim K Chataway, Karen M Lower, et al.
British Journal of Haematology|December 5, 2020
A biclonal case of chronic lymphocytic leukaemia with discordant mutational status of the immunoglobulin heavy chain variable region and bimodal CD49d expressionAnya K Hotinski, Oliver G Best, Lauren A Thurgood, et al.
British Journal of Haematology|January 19, 2019
Altered expression of metabolic pathways in CLL detected by unlabelled quantitative mass spectrometry analysisLauren A Thurgood, Eveline S Dwyer, Karen M Lower, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|October 13, 2017
Development of locus specific sub-clone separation by fluorescence in situ hybridization in suspension in chronic lymphocytic leukemiaCuc H Do, Sheree Bailey, Cindy Macardle, et al.
Journal of Diabetes Research|September 9, 2015
Differential Telomere Shortening in Blood versus Arteries in an Animal Model of Type 2 DiabetesSamira Tajbakhsh, Kamelya Aliakbari, Damian J Hussey, et al.
Experimental Hematology|December 13, 2021
Lipid uptake in chronic lymphocytic leukemiaLauren A Thurgood, Oliver G Best, Ashley Rowland, et al.
BMC Medical Genetics|May 10, 2017
Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)Shari Javadiyan, Jamie E Craig, Shiwani Sharma, et al.
BMC Research Notes|February 13, 2016
Recurrent mutation in the crystallin alpha A gene associated with inherited paediatric cataractShari Javadiyan, Jamie E Craig, Emmanuelle Souzeau, et al.
Pageof 3