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Institution

Memorial Sloan Kettering Cancer Center

HealthcareNew York, New York, United States
About: Memorial Sloan Kettering Cancer Center is a healthcare organization based out in New York, New York, United States. It is known for research contribution in the topics: Cancer & Population. The organization has 30293 authors who have published 65381 publications receiving 4462534 citations. The organization is also known as: MSKCC & New York Cancer Hospital.


Papers
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Journal ArticleDOI
TL;DR: Clinical studies investigating single-agent anti-PD-1/PD-L1 therapy and trials of combination approaches with other standard anticancer therapies, in multiple tumor types are reviewed and the key adverse events reported in these studies are summarized.

1,110 citations

Journal ArticleDOI
16 Sep 2011-Science
TL;DR: Anti-HIV broadly neutralizing antibodies with similar specificities and modes of binding were found in multiple HIV-infected individuals, and cloned 576 new HIV antibodies from four unrelated individuals to determine whether they are part of a larger group of related molecules.
Abstract: Passive transfer of broadly neutralizing HIV antibodies can prevent infection, which suggests that vaccines that elicit such antibodies would be protective. Thus far, however, few broadly neutralizing HIV antibodies that occur naturally have been characterized. To determine whether these antibodies are part of a larger group of related molecules, we cloned 576 new HIV antibodies from four unrelated individuals. All four individuals produced expanded clones of potent broadly neutralizing CD4-binding-site antibodies that mimic binding to CD4. Despite extensive hypermutation, the new antibodies shared a consensus sequence of 68 immunoglobulin H (IgH) chain amino acids and arise independently from two related IgH genes. Comparison of the crystal structure of one of the antibodies to the broadly neutralizing antibody VRC01 revealed conservation of the contacts to the HIV spike.

1,110 citations

Journal ArticleDOI
TL;DR: How immune- mediated colonization resistance against antibiotic-resistant intestinal pathogens is influenced by the composition of the commensal microbiota is discussed and recent advances characterizing the ability of different Commensal bacterial families, genera and species to restore colonization resistance to intestinal pathogens in antibiotic-treated hosts are reviewed.
Abstract: Colonization resistance — protection from exogenous pathogens by commensal bacteria — can be mediated by direct antagonism and by indirect effects on the host immune response. This Review outlines our current knowledge of immune-mediated colonization resistance against clinically relevant, antibiotic-resistant intestinal pathogens and how insights into commensal bacterial species and their mechanisms might be therapeutically used to restore resistance.

1,110 citations

Journal ArticleDOI
TL;DR: Among patients with newly diagnosed advanced ovarian cancer who had a response to platinum-based chemotherapy, those who received niraparib had significantly longer progression-free survival thanThose who received placebo, regardless of the presence or absence of homologous-recombination deficiency.
Abstract: Background Niraparib, an inhibitor of poly(adenosine diphosphate [ADP]–ribose) polymerase (PARP), has been associated with significantly increased progression-free survival among patients ...

1,106 citations

Journal ArticleDOI
Sushmita Roy1, Jason Ernst1, Peter V. Kharchenko2, Pouya Kheradpour1, Nicolas Nègre3, Matthew L. Eaton4, Jane M. Landolin5, Christopher A. Bristow1, Lijia Ma3, Michael F. Lin1, Stefan Washietl6, Bradley I. Arshinoff7, Ferhat Ay8, Patrick E. Meyer9, Nicolas Robine10, Nicole L. Washington5, Luisa Di Stefano2, Eugene Berezikov11, Christopher D. Brown3, Rogerio Candeias6, Joseph W. Carlson5, Adrian Carr12, Irwin Jungreis1, Daniel Marbach1, Rachel Sealfon1, Michael Y. Tolstorukov2, Sebastian Will6, Artyom A. Alekseyenko2, Carlo G. Artieri13, Benjamin W. Booth5, Angela N. Brooks14, Qi Dai10, Carrie A. Davis15, Michael O. Duff16, X. Feng, Andrey A. Gorchakov2, Tingting Gu17, Jorja G. Henikoff10, Philipp Kapranov18, Renhua Li13, Heather K. MacAlpine4, John H. Malone13, Aki Minoda5, Jared T. Nordman6, Katsutomo Okamura10, Marc D. Perry7, Sara K. Powell4, Nicole C. Riddle17, Akiko Sakai2, Anastasia Samsonova2, Jeremy E. Sandler5, Yuri B. Schwartz2, Noa Sher6, Rebecca Spokony3, David Sturgill13, Marijke J. van Baren17, Kenneth H. Wan5, Li Yang16, Charles Yu5, Elise A. Feingold13, Peter J. Good13, Mark S. Guyer13, Rebecca F. Lowdon13, Kami Ahmad2, Justen Andrews19, Bonnie Berger1, Steven E. Brenner14, Michael R. Brent17, Lucy Cherbas19, Sarah C. R. Elgin17, Thomas R. Gingeras18, Robert L. Grossman3, Roger A. Hoskins5, Thomas C. Kaufman19, W. J. Kent20, Mitzi I. Kuroda2, Terry L. Orr-Weaver6, Norbert Perrimon2, Vincenzo Pirrotta21, James W. Posakony22, Bing Ren22, Steven Russell12, Peter Cherbas19, Brenton R. Graveley16, Suzanna E. Lewis5, Gos Micklem12, Brian Oliver13, Peter J. Park2, Susan E. Celniker5, Steven Henikoff23, Gary H. Karpen14, Eric C. Lai10, David M. MacAlpine4, Lincoln Stein7, Kevin P. White3, Manolis Kellis1 
24 Dec 2010-Science
TL;DR: The Drosophila Encyclopedia of DNA Elements (modENCODE) project as mentioned in this paper has been used to map transcripts, histone modifications, chromosomal proteins, transcription factors, replication proteins and intermediates, and nucleosome properties across a developmental time course and in multiple cell lines.
Abstract: To gain insight into how genomic information is translated into cellular and developmental programs, the Drosophila model organism Encyclopedia of DNA Elements (modENCODE) project is comprehensively mapping transcripts, histone modifications, chromosomal proteins, transcription factors, replication proteins and intermediates, and nucleosome properties across a developmental time course and in multiple cell lines. We have generated more than 700 data sets and discovered protein-coding, noncoding, RNA regulatory, replication, and chromatin elements, more than tripling the annotated portion of the Drosophila genome. Correlated activity patterns of these elements reveal a functional regulatory network, which predicts putative new functions for genes, reveals stage- and tissue-specific regulators, and enables gene-expression prediction. Our results provide a foundation for directed experimental and computational studies in Drosophila and related species and also a model for systematic data integration toward comprehensive genomic and functional annotation.

1,102 citations


Authors

Showing all 30708 results

NameH-indexPapersCitations
Gordon H. Guyatt2311620228631
Edward Giovannucci2061671179875
Irving L. Weissman2011141172504
Craig B. Thompson195557173172
Joan Massagué189408149951
Gad Getz189520247560
Chris Sander178713233287
Richard B. Lipton1762110140776
Richard K. Wilson173463260000
George P. Chrousos1691612120752
Stephen J. Elledge162406112878
Murray F. Brennan16192597087
Lewis L. Lanier15955486677
David W. Bates1591239116698
Dan R. Littman157426107164
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023163
2022413
20214,330
20204,389
20194,156
20183,686