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J Colley

Showing results (111-120 of 122) with videos related to

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Glycobiology|June 25, 1998
Two soluble glycosyltransferases glycosylate less efficiently in vivo than their membrane bound counterpartsG Zhu, M L Allende, E Jaskiewicz, et al.
The Journal of Cell Biology|May 11, 2005
Regulation of phototransduction responsiveness and retinal degeneration by a phospholipase D-generated signaling lipidMary M LaLonde, Hilde Janssens, Erica Rosenbaum, et al.
The Journal of Cardiovascular Nursing|October 5, 2021
Increased Quality of Life Among Newly Diagnosed Patients With Heart Failure With Reduced Ejection Fraction in the Months After Initiation of Guideline-Directed Medical Therapy and Wearable Cardioverter Defibrillator PrescriptionAshley E Burch, Byron J Colley, Michael Döring, et al.
Nature|July 7, 1994
An eye-specific G beta subunit essential for termination of the phototransduction cascadeP J Dolph, H Man-Son-Hing, S Yarfitz, et al.
Neuromuscular Disorders : NMD|October 28, 2008
Expression of cardiac alpha-actin spares extraocular muscles in skeletal muscle alpha-actin diseases--quantification of striated alpha-actins by MRM-mass spectrometryGianina Ravenscroft, Stephen M J Colley, Kendall R Walker, et al.
Journal of Medical Genetics|April 14, 2006
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patientsH L Archer, J Evans, S Edwards, et al.
European Heart Journal|June 12, 2024
Therapy duration and improvement of ventricular function in de novo heart failure: the Heart Failure Optimization studyChristian Veltmann, David Duncker, Michael Doering, et al.
Biochemical and Biophysical Research Communications|June 14, 2005
Pleiotrophin induces formation of functional neovasculature in vivoKaren L Christman, Qizhi Fang, Anne J Kim, et al.
The Journal of Biological Chemistry|April 20, 2010
Calnexin deficiency leads to dysmyelinationAllison Kraus, Jody Groenendyk, Karen Bedard, et al.
Gut|June 3, 2008
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3A R Dallosso, S Dolwani, N Jones, et al.
Pageof 13

Showing results (111-120 of 122) with videos related to

Sort By:
Pageof 13
Glycobiology|June 25, 1998
Two soluble glycosyltransferases glycosylate less efficiently in vivo than their membrane bound counterpartsG Zhu, M L Allende, E Jaskiewicz, et al.
The Journal of Cell Biology|May 11, 2005
Regulation of phototransduction responsiveness and retinal degeneration by a phospholipase D-generated signaling lipidMary M LaLonde, Hilde Janssens, Erica Rosenbaum, et al.
The Journal of Cardiovascular Nursing|October 5, 2021
Increased Quality of Life Among Newly Diagnosed Patients With Heart Failure With Reduced Ejection Fraction in the Months After Initiation of Guideline-Directed Medical Therapy and Wearable Cardioverter Defibrillator PrescriptionAshley E Burch, Byron J Colley, Michael Döring, et al.
Nature|July 7, 1994
An eye-specific G beta subunit essential for termination of the phototransduction cascadeP J Dolph, H Man-Son-Hing, S Yarfitz, et al.
Neuromuscular Disorders : NMD|October 28, 2008
Expression of cardiac alpha-actin spares extraocular muscles in skeletal muscle alpha-actin diseases--quantification of striated alpha-actins by MRM-mass spectrometryGianina Ravenscroft, Stephen M J Colley, Kendall R Walker, et al.
Journal of Medical Genetics|April 14, 2006
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patientsH L Archer, J Evans, S Edwards, et al.
European Heart Journal|June 12, 2024
Therapy duration and improvement of ventricular function in de novo heart failure: the Heart Failure Optimization studyChristian Veltmann, David Duncker, Michael Doering, et al.
Biochemical and Biophysical Research Communications|June 14, 2005
Pleiotrophin induces formation of functional neovasculature in vivoKaren L Christman, Qizhi Fang, Anne J Kim, et al.
The Journal of Biological Chemistry|April 20, 2010
Calnexin deficiency leads to dysmyelinationAllison Kraus, Jody Groenendyk, Karen Bedard, et al.
Gut|June 3, 2008
Inherited predisposition to colorectal adenomas caused by multiple rare alleles of MUTYH but not OGG1, NUDT1, NTH1 or NEIL 1, 2 or 3A R Dallosso, S Dolwani, N Jones, et al.
Pageof 13