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Marian Case

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British Journal of Haematology|September 15, 2005
The V617F mutation in Jak2 is not found in childhood acute lymphoblastic leukaemiaSarina Sulong, Marian Case, Lynne Minto, et al.
Haematologica|December 3, 2009
Flow minimal residual disease monitoring of candidate leukemic stem cells defined by the immunophenotype, CD34+CD38lowCD19+ in B-lineage childhood acute lymphoblastic leukemiaKerrie Wilson, Marian Case, Lynne Minto, et al.
Genes, Chromosomes & Cancer|November 11, 2011
Casitas B lymphoma mutations in childhood acute lymphoblastic leukemiaLindsay Nicholson, Thomas Knight, Elizabeth Matheson, et al.
Cancer Research|August 15, 2008
Mutation of genes affecting the RAS pathway is common in childhood acute lymphoblastic leukemiaMarian Case, Elizabeth Matheson, Lynne Minto, et al.
Haematologica|January 19, 2019
Glucocorticoids and selumetinib are highly synergistic in RAS pathway-mutated childhood acute lymphoblastic leukemia through upregulation of BIMElizabeth C Matheson, Huw Thomas, Marian Case, et al.
Haematologica|November 24, 2022
Hyperactive CREB subpopulations increase during therapy in pediatric B-lineage acute lymphoblastic leukemiaDino Masic, Kayleigh Fee, Hayden Bell, et al.
Haematologica|April 21, 2009
Establishment and validation of a standard protocol for the detection of minimal residual disease in B lineage childhood acute lymphoblastic leukemia by flow cytometry in a multi-center settingJulie Irving, Jenny Jesson, Paul Virgo, et al.
Blood|September 26, 2014
Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibitionJulie Irving, Elizabeth Matheson, Lynne Minto, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|February 25, 2020
Label-Free Leukemia Monitoring by Computer VisionMinh Doan, Marian Case, Dino Masic, et al.
Genes, Chromosomes & Cancer|September 4, 2008
The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1Helen Parker, Qian An, Kerry Barber, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
British Journal of Haematology|September 15, 2005
The V617F mutation in Jak2 is not found in childhood acute lymphoblastic leukaemiaSarina Sulong, Marian Case, Lynne Minto, et al.
Haematologica|December 3, 2009
Flow minimal residual disease monitoring of candidate leukemic stem cells defined by the immunophenotype, CD34+CD38lowCD19+ in B-lineage childhood acute lymphoblastic leukemiaKerrie Wilson, Marian Case, Lynne Minto, et al.
Genes, Chromosomes & Cancer|November 11, 2011
Casitas B lymphoma mutations in childhood acute lymphoblastic leukemiaLindsay Nicholson, Thomas Knight, Elizabeth Matheson, et al.
Cancer Research|August 15, 2008
Mutation of genes affecting the RAS pathway is common in childhood acute lymphoblastic leukemiaMarian Case, Elizabeth Matheson, Lynne Minto, et al.
Haematologica|January 19, 2019
Glucocorticoids and selumetinib are highly synergistic in RAS pathway-mutated childhood acute lymphoblastic leukemia through upregulation of BIMElizabeth C Matheson, Huw Thomas, Marian Case, et al.
Haematologica|November 24, 2022
Hyperactive CREB subpopulations increase during therapy in pediatric B-lineage acute lymphoblastic leukemiaDino Masic, Kayleigh Fee, Hayden Bell, et al.
Haematologica|April 21, 2009
Establishment and validation of a standard protocol for the detection of minimal residual disease in B lineage childhood acute lymphoblastic leukemia by flow cytometry in a multi-center settingJulie Irving, Jenny Jesson, Paul Virgo, et al.
Blood|September 26, 2014
Ras pathway mutations are prevalent in relapsed childhood acute lymphoblastic leukemia and confer sensitivity to MEK inhibitionJulie Irving, Elizabeth Matheson, Lynne Minto, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|February 25, 2020
Label-Free Leukemia Monitoring by Computer VisionMinh Doan, Marian Case, Dino Masic, et al.
Genes, Chromosomes & Cancer|September 4, 2008
The complex genomic profile of ETV6-RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1Helen Parker, Qian An, Kerry Barber, et al.
Pageof 2