J
Jeffrey M. Leiden
Researcher at Harvard University
Publications - 126
Citations - 20557
Jeffrey M. Leiden is an academic researcher from Harvard University. The author has contributed to research in topics: T cell & Enhancer. The author has an hindex of 69, co-authored 126 publications receiving 19911 citations. Previous affiliations of Jeffrey M. Leiden include Brigham and Women's Hospital & Loyola University Medical Center.
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Journal ArticleDOI
An Integrated Stress Response Regulates Amino Acid Metabolism and Resistance to Oxidative Stress
Heather P. Harding,Yuhong Zhang,Huiquing Zeng,Isabel Novoa,Phoebe D. Lu,Marcella Calfon,Navid Sadri,Chi Yun,Brian Popko,Richard S. Paules,David F. Stojdl,John C. Bell,Thore Hettmann,Jeffrey M. Leiden,David Ron +14 more
TL;DR: A signaling pathway initiated by eIF2alpha phosphorylation protects cells against metabolic consequences of ER oxidation by promoting the linked processes of amino acid sufficiency and resistance to oxidative stress.
Journal ArticleDOI
GATA4 transcription factor is required for ventral morphogenesis and heart tube formation.
Chay T. Kuo,Edward E. Morrisey,Roshani T. Anandappa,Kirsten Sigrist,Min M. Lu,Michael S. Parmacek,Claire Soudais,Jeffrey M. Leiden +7 more
TL;DR: Analysis of cardiac development in the GATA4-/- mice demonstrated that these embryos developed splanchnic mesoderm, which differentiated into primitive cardiac myocytes that expressed contractile proteins that formed aberrant cardiac structures in the anterior and dorsolateral regions of the embryo.
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CD28 activation pathway regulates the production of multiple T-cell-derived lymphokines/cytokines
Craig B. Thompson,Tullia Lindsten,J A Ledbetter,Steven L. Kunkel,Howard A. Young,Stephen G. Emerson,Jeffrey M. Leiden,Carl H. June +7 more
TL;DR: It is shown that CD28 stimulation augments T- cell immune responses by specifically inducing a 5- to 50-fold enhancement in the expression and secretion of interleukin 2, tumor necrosis factor type alpha, lymphotoxin, interferon gamma, and granulocyte-macrophage colony-stimulating factor in normal human T cells stimulated to proliferate by crosslinking of the T-cell receptor/CD3 complex.
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Immune responses to transgene–encoded proteins limit the stability of gene expression after injection of replication–defective adenovirus vectors
TL;DR: It is demonstrated that immune responses directed against foreign transgene–encoded proteins are the major determinants of the stability of gene expression following i.m. injection of RDAd.
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Transcription factor GATA-3 is required for development of the T-cell lineage.
TL;DR: The results show that GATA-3−/− ES cells can contribute to the development of the mature ery-throid, myelomonocytic and B-cell lineages, but fail to give rise to thymocytes or mature peripheral T cells, suggesting that Gata-3 is an essential and specific regulator of early thymocyte development.