A. Sen

发表

Structure, organization, and expression of the rat cardiac myosin light chain-2 gene. Identification of a 250-base pair fragment which confers cardiac-specific expression.

K. Chien, S. Henderson, M. Spencer, 1989, The Journal of biological chemistry.

Accumulation of Unesterified Arachidonic Acid in Ischemic Canine Myocardium: Relationship to a Phosphatidylcholine Deacylation‐Reacylation Cycle and the Depletion of Membrane Phospholipids

K. Chien, J. Willerson, L. Buja, 1984, Circulation research.

Mechanisms of accumulation of arachidonic acid in cultured myocardial cells during ATP depletion.

K. Chien, J. Willerson, A. Chang, 1985, The American journal of physiology.

Inhibition of the release of arachidonic acid prevents the development of sarcolemmal membrane defects in cultured rat myocardial cells during adenosine triphosphate depletion.

K. Chien, J. Willerson, L. Buja, 1988, The Journal of clinical investigation.

Fatty acylcarnitine accumulation and membrane injury in ischemic canine myocardium.

K. Chien, J. Willerson, L. Buja, 1983, The American journal of cardiology.

Accumulation of arachidonate in triacylglycerols and unesterified fatty acids during ischemia and reflow in the isolated rat heart. Correlation with the loss of contractile function and the development of calcium overload.

K. Chien, J. Willerson, L. Buja, 1986, The American journal of pathology.

Cloning, sequencing, and expression of a cDNA encoding rat liver mitochondrial carnitine palmitoyltransferase II.

C. Slaughter, M. Mcphaul, J. McGarry, 1990, The Journal of biological chemistry.

Phorbol esters induce immediate-early genes and activate cardiac gene transcription in neonatal rat myocardial cells.

K. Chien, S. Henderson, A. Sen, 1990, Journal of molecular and cellular cardiology.

New insights into the mitochondrial carnitine palmitoyltransferase enzyme system.

J. McGarry, K. Woeltje, D. W. Foster, 1991, Biochimie.

Characterization of a potentially reversible increase in beta-adrenergic receptors in isolated, neonatal rat cardiac myocytes with impaired energy metabolism.

K. Chien, J. Willerson, L. Buja, 1985, Circulation research.

Purification and characterization of protein kinase C isozymes from rat heart

J. Torchia, A. Sen, Y. Qu, 1991, Molecular and Cellular Biochemistry.

Expression of precursor and mature carnitine palmitoyltransferase II in Escherichia coli and in vitro: differential behaviour of rat and human isoforms.

J. McGarry, N. Brown, D. W. Foster, 1993, The Biochemical journal.

Membrane phospholipid metabolism during myocardial ischaemia: past, present and future.

K. Chien, J. Willerson, L. Buja, 1987, Basic research in cardiology.

Release of arachidonate from membrane phospholipids in cultured neonatal rat myocardial cells during adenosine triphosphate depletion. Correlation with the progression of cell injury.

K. Chien, J. Willerson, M. Gunn, 1985, The Journal of clinical investigation.

Terminally differentiated neonatal rat myocardial cells proliferate and maintain specific differentiated functions following expression of SV40 large T antigen.

K. Chien, R. Gerard, A Sen, 1988, The Journal of biological chemistry.

Alpha 1-adrenergic stimulation of rat myocardial cells increases protein synthesis.

K. Chien, R. S. Meidell, S. Henderson, 1986, The American journal of physiology.

Protein kinase C mediated activation and phosphorylation of Ca(2+)-pump in cardiac sarcolemma.

J. Torchia, A. Sen, Y. Qu, 1992, Canadian Journal of Physiology and Pharmacology.

Carbachol-stimulated phosphorylation of a 170-kDa endogenous protein in avian salt gland cells.

J. Torchia, A. Sen, D. Pon, 1991, The American journal of physiology.

A PHOSPHORYLATED INTERMEDIATE IN ADENOSINE TRIPHOSPHATE-DEPENDENT SODIUM AND POTASSIUM TRANSPORT ACROSS KIDNEY MEMBRANES.

A. Sen, R. Post, A. Rosenthal, 1965, The Journal of biological chemistry.

Endogenous substrates of rat heart protein kinase C type I, II, and III isozymic forms in cardiac sarcolemma.

J. Torchia, A. Sen, Y. Qu, 1992, Biochemistry and cell biology = Biochimie et biologie cellulaire.