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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 disease
N 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 Expression
Dougall 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 transplantation
Kyle 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 leukemia
R 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 transplantation
Evan 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 twins
D 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 preleukemia
N 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 7p21.1
D 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 reaction
K O Schowengerdt, J Ni, S W Denfield, et al.
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of 22
Search research articles
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Showing results (181-190 of 214) with videos related to
Sort By:
Page
of 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 disease
N 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 Expression
Dougall 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 transplantation
Kyle 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 leukemia
R 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 transplantation
Evan 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 twins
D 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 preleukemia
N 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 7p21.1
D 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 reaction
K O Schowengerdt, J Ni, S W Denfield, et al.
Page
of 22