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David Baltimore

Researcher at California Institute of Technology

Publications -  882
Citations -  168784

David Baltimore is an academic researcher from California Institute of Technology. The author has contributed to research in topics: RNA & Virus. The author has an hindex of 203, co-authored 876 publications receiving 162955 citations. Previous affiliations of David Baltimore include Thomas Jefferson University & Johns Hopkins University.

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Biología celular y molecular

James Darnell, +2 more
TL;DR: Las colagenasas, metaloproteasas , elastasas y otras enzimas degradativas conforman el amplio mundo de proteasas that se encargan de degradar la matriz extracelular.
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A normal cell protein cross-reactive to the major Abelson murine leukaemia virus gene product

Owen N. Witte, +3 more
- 04 Oct 1979 - 
TL;DR: An anti-A-MuLV syngeneic tumour regressor serum with defined specificities is used to search for cross-reacting normal cellular proteins and a protein of MW 150,000 (NCP150) is identified in metabolically labelled thymus and other lymphoid organs.
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Transcriptomics identified a critical role for Th2 cell-intrinsic miR-155 in mediating allergy and antihelminth immunity

Isobel S. Okoye, +12 more
- 29 Jul 2014 - 
TL;DR: It is reported here that distinct regulatory miRNA networks operate to regulate Th2 cells in house dust mite-allergic or helminth-infected animals and in vitro Th1, Th2, Th9, Th17, and Treg cells, which are distinguishable from other T cells.
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Localization of two cellular forms of the vesicular stomatitis viral glycoprotein.

David M. Knipe, +2 more
- 01 Mar 1977 - 
TL;DR: Two cell-associated forms of the glycoprotein (G) of vesicular stomatitis virus, termed G1 and G2, have been resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, suggesting that partial clycosylation of G occurs concomitantly with or immediately after its synthesis.
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Isopycnic Separation of Subcellular Components from Poliovirus-Infected and Normal HeLa Cells

David Baltimore, +1 more
- 01 Nov 1968 - 
TL;DR: The poliovirus replication complex has been separated from polyribosomes and its density has been found to be unaffected by treatment with ethylene-diaminetetraacetic acid.