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Institution

Rockefeller University

EducationNew York, New York, United States
About: Rockefeller University is a education organization based out in New York, New York, United States. It is known for research contribution in the topics: Population & Gene. The organization has 15867 authors who have published 32938 publications receiving 2940261 citations. The organization is also known as: Rockefeller University & Rockefeller Institute.
Topics: Population, Gene, Virus, RNA, Antigen


Papers
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Journal ArticleDOI
TL;DR: It is demonstrated that TRANCE activates the antiapoptotic serine/threonine kinase Akt/PKB through a signaling complex involving c-Src and TRAF6 and evidence of cross-talk between TRAF proteins and Src family kinases is provided.

598 citations

Journal ArticleDOI
TL;DR: Results indicate that ABI5 acts downstream of ABI3 to reactivate late embryogenesis programmes and to arrest growth of germinating embryos.
Abstract: The development of a germinating embryo into an autotrophic seedling is arrested under conditions of water deficit. This ABA-mediated developmental checkpoint requires the bZIP transcription factor ABI5. Here, we used abi3-1, which is also unable to execute this checkpoint, to investigate the relative role of ABI3 and ABI5 in this process. In wild-type Arabidopsis plants, ABI3 expression and activity parallel those described for ABI5 following stratification. During this process, transcript levels of late embryogenesis genes such as AtEm1 and AtEm6 are also re-induced, which might be responsible for the acquired osmotic tolerance in germinated embryos whose growth is arrested. ABI5 expression is greatly reduced in abi3-1 mutants, which has low AtEm1 or AtEm6 expression. Cross complementation experiments showed that 35S-ABI5 could complement abi3-1, whereas 35S-ABI3 cannot complement abi5-4. These results indicate that ABI5 acts downstream of ABI3 to reactivate late embryogenesis programmes and to arrest growth of germinating embryos. Although ABI5 is consistently located in the nucleus, chromosomal immunoprecipitation (ChIP) experiments revealed that ABA increases ABI5 occupancy on the AtEm6 promoter.

597 citations

Journal ArticleDOI
TL;DR: It is suggested that progerin-induced aging can be used to reveal late-onset age-related disease features in hiPSC-based disease models.

597 citations

Journal ArticleDOI
TL;DR: The identification and purification of a new inflammatory monokine synthesized by the macrophage tumor cell line RAW 264.7 suggest that MIP is an endogenous mediator that may play a role in the host responses that occur during endotoxemia and other inflammatory events.
Abstract: We report the identification and purification of a new inflammatory monokine synthesized by the macrophage tumor cell line RAW 264.7 in response to endotoxin. This monokine, which we term "macrophage inflammatory protein" (MIP), is a doublet with an apparent molecular mass of approximately 8,000 daltons on SDS-PAGE but forms aggregates of greater than 2 x 10(6) daltons as assessed by gel filtration. Partial NH2-terminal amino acid sequence data reveal no significant homology with any previously described protein. Although the monokine is anionic under physiological conditions, it is one of two major macrophage-secreted proteins that bind to heparin at high salt concentrations. At 100 ng/ml or greater, MIP is chemokinetic for human polymorphonuclear cells and triggers hydrogen peroxide production. Subcutaneous injection of 10 ng or greater of MIP into footpads of C3H/HeJ mice elicits an inflammatory response, characterized by neutrophil infiltration. These findings suggest that MIP is an endogenous mediator that may play a role in the host responses that occur during endotoxemia and other inflammatory events.

595 citations

Journal ArticleDOI
TL;DR: Evidence was obtained that the site on the lymphocyte membrane responsible for binding aggregates was distinct from surface Ig, which was irreversible and independent of complement, pH, temperature, protein content of the medium, and divalent cations.
Abstract: Specific binding of aggregated gamma-globulin to a subpopulation of lymphocytes was demonstrated. This subpopulation was identified as the Ig-staining or B lymphocytes. The binding was irreversible and independent of complement, pH, temperature, protein content of the medium, and divalent cations. Aggregates of large size were needed for optimal visualization. Evidence was obtained that the site on the lymphocyte membrane responsible for binding aggregates was distinct from surface Ig.

594 citations


Authors

Showing all 15925 results

NameH-indexPapersCitations
Bruce S. McEwen2151163200638
David Baltimore203876162955
Ronald M. Evans199708166722
Lewis C. Cantley196748169037
Ronald Klein1941305149140
Scott M. Grundy187841231821
Jie Zhang1784857221720
Andrea Bocci1722402176461
Ralph M. Steinman171453121518
Masayuki Yamamoto1711576123028
Zena Werb168473122629
Nahum Sonenberg167647104053
Michel C. Nussenzweig16551687665
Harvey F. Lodish165782101124
Dennis R. Burton16468390959
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202314
202284
2021873
2020792
2019716
2018767