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The Journal of Clinical Investigation
|
October 19, 1999
Mutations in Igalpha (CD79a) result in a complete block in B-cell development
Y Minegishi, E Coustan-Smith, L Rapalus, et al.
AJNR. American Journal of Neuroradiology
|
April 14, 2006
Diffuse CNS vasculopathy with chronic Epstein-Barr virus infection in X-linked lymphoproliferative disease
J K Weeks, K J Helton, M E Conley, et al.
Human Molecular Genetics
|
October 1, 1994
Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase
M E Conley, M E Fitch-Hilgenberg, J L Cleveland, et al.
The Journal of Allergy and Clinical Immunology
|
July 1, 1991
Retrospective analysis of the incidence of pulmonary disease in hypogammaglobulinemia
S K Sweinberg, R A Wodell, M P Grodofsky, et al.
The New England Journal of Medicine
|
April 12, 1990
Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysis
J M Puck, C M Krauss, S M Puck, et al.
The American Journal of Physiology
|
July 1, 1997
Activation of glycolysis in human muscle in vivo
K E Conley, M L Blei, T L Richards, et al.
The Journal of Physiology
|
September 30, 2003
Acidosis inhibits oxidative phosphorylation in contracting human skeletal muscle in vivo
Sharon A Jubrias, Gregory J Crowther, Eric G Shankland, et al.
Hospital & Health Services Administration
|
December 7, 1981
Development and use of a method of assessing patient perception of care
P W Taylor, E Nelson-Wernick, H S Currey, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1993
Individual variation in contractile cost and recovery in a human skeletal muscle
M L Blei, K E Conley, I B Odderson, et al.
Blood
|
May 1, 1986
A chromosomal breakage syndrome with profound immunodeficiency
M E Conley, N B Spinner, B S Emanuel, et al.
Page
of 27
Search research articles
Search
Showing results (151-160 of 264) with videos related to
Sort By:
Page
of 27
The Journal of Clinical Investigation
|
October 19, 1999
Mutations in Igalpha (CD79a) result in a complete block in B-cell development
Y Minegishi, E Coustan-Smith, L Rapalus, et al.
AJNR. American Journal of Neuroradiology
|
April 14, 2006
Diffuse CNS vasculopathy with chronic Epstein-Barr virus infection in X-linked lymphoproliferative disease
J K Weeks, K J Helton, M E Conley, et al.
Human Molecular Genetics
|
October 1, 1994
Screening of genomic DNA to identify mutations in the gene for Bruton's tyrosine kinase
M E Conley, M E Fitch-Hilgenberg, J L Cleveland, et al.
The Journal of Allergy and Clinical Immunology
|
July 1, 1991
Retrospective analysis of the incidence of pulmonary disease in hypogammaglobulinemia
S K Sweinberg, R A Wodell, M P Grodofsky, et al.
The New England Journal of Medicine
|
April 12, 1990
Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysis
J M Puck, C M Krauss, S M Puck, et al.
The American Journal of Physiology
|
July 1, 1997
Activation of glycolysis in human muscle in vivo
K E Conley, M L Blei, T L Richards, et al.
The Journal of Physiology
|
September 30, 2003
Acidosis inhibits oxidative phosphorylation in contracting human skeletal muscle in vivo
Sharon A Jubrias, Gregory J Crowther, Eric G Shankland, et al.
Hospital & Health Services Administration
|
December 7, 1981
Development and use of a method of assessing patient perception of care
P W Taylor, E Nelson-Wernick, H S Currey, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1993
Individual variation in contractile cost and recovery in a human skeletal muscle
M L Blei, K E Conley, I B Odderson, et al.
Blood
|
May 1, 1986
A chromosomal breakage syndrome with profound immunodeficiency
M E Conley, N B Spinner, B S Emanuel, et al.
Page
of 27