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L Kearney

Showing results (181-190 of 214) with videos related to

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Journal of the American College of Cardiology|September 14, 1999
The detection of viral genomes by polymerase chain reaction in the myocardium of pediatric patients with advanced HIV diseaseN E Bowles, D L Kearney, J Ni, et al.
Iscience|March 4, 2021
Signaling Heterogeneity is Defined by Pathway Architecture and Intercellular Variability in Protein ExpressionDougall Norris, Pengyi Yang, Sung-Young Shin, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|July 20, 2023
Atypical infiltrates on endomyocardial biopsy are associated with adverse outcomes in pediatric heart transplantationKyle D Hope, Shaine A Morris, Debra L Kearney, et al.
Blood|August 9, 2001
A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemiaR J Jaju, C Fidler, O A Haas, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|December 12, 2018
Predicted heart mass is the optimal metric for size match in heart transplantationEvan P Kransdorf, Michelle M Kittleson, Lillian R Benck, et al.
Leukemia|November 13, 2014
Clonal origins of ETV6-RUNX1⁺ acute lymphoblastic leukemia: studies in monozygotic twinsD Alpar, D Wren, L Ermini, et al.
Genomics|April 11, 2000
Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemiaN McDonell, J Ramser, F Francis, et al.
Blood|July 9, 1999
A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG)R J Jaju, O A Haas, M Neat, et al.
American Journal of Human Genetics|October 30, 1998
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1D Johnson, S W Horsley, D M Moloney, et al.
Circulation|December 13, 1997
Association of parvovirus B19 genome in children with myocarditis and cardiac allograft rejection: diagnosis using the polymerase chain reactionK O Schowengerdt, J Ni, S W Denfield, et al.
Pageof 22

Showing results (181-190 of 214) with videos related to

Sort By:
Pageof 22
Journal of the American College of Cardiology|September 14, 1999
The detection of viral genomes by polymerase chain reaction in the myocardium of pediatric patients with advanced HIV diseaseN E Bowles, D L Kearney, J Ni, et al.
Iscience|March 4, 2021
Signaling Heterogeneity is Defined by Pathway Architecture and Intercellular Variability in Protein ExpressionDougall Norris, Pengyi Yang, Sung-Young Shin, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|July 20, 2023
Atypical infiltrates on endomyocardial biopsy are associated with adverse outcomes in pediatric heart transplantationKyle D Hope, Shaine A Morris, Debra L Kearney, et al.
Blood|August 9, 2001
A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemiaR J Jaju, C Fidler, O A Haas, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|December 12, 2018
Predicted heart mass is the optimal metric for size match in heart transplantationEvan P Kransdorf, Michelle M Kittleson, Lillian R Benck, et al.
Leukemia|November 13, 2014
Clonal origins of ETV6-RUNX1⁺ acute lymphoblastic leukemia: studies in monozygotic twinsD Alpar, D Wren, L Ermini, et al.
Genomics|April 11, 2000
Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemiaN McDonell, J Ramser, F Francis, et al.
Blood|July 9, 1999
A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG)R J Jaju, O A Haas, M Neat, et al.
American Journal of Human Genetics|October 30, 1998
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1D Johnson, S W Horsley, D M Moloney, et al.
Circulation|December 13, 1997
Association of parvovirus B19 genome in children with myocarditis and cardiac allograft rejection: diagnosis using the polymerase chain reactionK O Schowengerdt, J Ni, S W Denfield, et al.
Pageof 22