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Institution

Incyte

CompanyWilmington, Delaware, United States
About: Incyte is a company organization based out in Wilmington, Delaware, United States. It is known for research contribution in the topics: Expression vector & Ruxolitinib. The organization has 1262 authors who have published 1875 publications receiving 75015 citations. The organization is also known as: Incyte Corporation & Incyte Inc..


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Journal ArticleDOI
Midori A. Harris, Jennifer I. Clark1, Ireland A1, Jane Lomax1, Michael Ashburner2, Michael Ashburner1, R. Foulger2, R. Foulger1, Karen Eilbeck1, Karen Eilbeck3, Suzanna E. Lewis3, Suzanna E. Lewis1, B. Marshall3, B. Marshall1, Christopher J. Mungall1, Christopher J. Mungall3, J. Richter1, J. Richter3, Gerald M. Rubin1, Gerald M. Rubin3, Judith A. Blake1, Carol J. Bult1, Dolan M1, Drabkin H1, Janan T. Eppig1, Hill Dp1, L. Ni1, Ringwald M1, Rama Balakrishnan4, Rama Balakrishnan1, J. M. Cherry1, J. M. Cherry4, Karen R. Christie4, Karen R. Christie1, Maria C. Costanzo4, Maria C. Costanzo1, Selina S. Dwight4, Selina S. Dwight1, Stacia R. Engel4, Stacia R. Engel1, Dianna G. Fisk1, Dianna G. Fisk4, Jodi E. Hirschman4, Jodi E. Hirschman1, Eurie L. Hong4, Eurie L. Hong1, Robert S. Nash4, Robert S. Nash1, Anand Sethuraman1, Anand Sethuraman4, Chandra L. Theesfeld4, Chandra L. Theesfeld1, David Botstein5, David Botstein1, Kara Dolinski5, Kara Dolinski1, Becket Feierbach5, Becket Feierbach1, Tanya Z. Berardini1, Tanya Z. Berardini6, S. Mundodi1, S. Mundodi6, Seung Y. Rhee6, Seung Y. Rhee1, Rolf Apweiler1, Daniel Barrell1, Camon E1, E. Dimmer1, Lee1, Rex L. Chisholm, Pascale Gaudet7, Pascale Gaudet1, Warren A. Kibbe7, Warren A. Kibbe1, Ranjana Kishore8, Ranjana Kishore1, Erich M. Schwarz1, Erich M. Schwarz8, Paul W. Sternberg1, Paul W. Sternberg8, M. Gwinn1, Hannick L1, Wortman J1, Matthew Berriman1, Matthew Berriman9, Wood9, Wood1, de la Cruz N1, de la Cruz N10, Peter J. Tonellato1, Peter J. Tonellato10, Pankaj Jaiswal1, Pankaj Jaiswal11, Seigfried T12, Seigfried T1, White R1, White R13 
TL;DR: The Gene Ontology (GO) project as discussed by the authors provides structured, controlled vocabularies and classifications that cover several domains of molecular and cellular biology and are freely available for community use in the annotation of genes, gene products and sequences.
Abstract: The Gene Ontology (GO) project (http://www.geneontology.org/) provides structured, controlled vocabularies and classifications that cover several domains of molecular and cellular biology and are freely available for community use in the annotation of genes, gene products and sequences. Many model organism databases and genome annotation groups use the GO and contribute their annotation sets to the GO resource. The GO database integrates the vocabularies and contributed annotations and provides full access to this information in several formats. Members of the GO Consortium continually work collectively, involving outside experts as needed, to expand and update the GO vocabularies. The GO Web resource also provides access to extensive documentation about the GO project and links to applications that use GO data for functional analyses.

3,565 citations

Journal ArticleDOI
TL;DR: Using cDNA microarrays to explore the variation in expression of approximately 8,000 unique genes among the 60 cell lines used in the National Cancer Institute's screen for anti-cancer drugs provided a novel molecular characterization of this important group of human cell lines and their relationships to tumours in vivo.
Abstract: We used cDNA microarrays to explore the variation in expression of approximately 8,000 unique genes among the 60 cell lines used in the National Cancer Institute's screen for anti-cancer drugs. Classification of the cell lines based solely on the observed patterns of gene expression revealed a correspondence to the ostensible origins of the tumours from which the cell lines were derived. The consistent relationship between the gene expression patterns and the tissue of origin allowed us to recognize outliers whose previous classification appeared incorrect. Specific features of the gene expression patterns appeared to be related to physiological properties of the cell lines, such as their doubling time in culture, drug metabolism or the interferon response. Comparison of gene expression patterns in the cell lines to those observed in normal breast tissue or in breast tumour specimens revealed features of the expression patterns in the tumours that had recognizable counterparts in specific cell lines, reflecting the tumour, stromal and inflammatory components of the tumour tissue. These results provided a novel molecular characterization of this important group of human cell lines and their relationships to tumours in vivo.

2,192 citations

Journal ArticleDOI
Robert L. Strausberg, Elise A. Feingold1, Lynette H. Grouse1, Jeffery G. Derge2, Richard D. Klausner1, Francis S. Collins1, Lukas Wagner1, Carolyn M. Shenmen1, Gregory D. Schuler1, Stephen F. Altschul1, Barry R. Zeeberg1, Kenneth H. Buetow1, Carl F. Schaefer1, Narayan K. Bhat1, Ralph F. Hopkins1, Heather Jordan1, Troy Moore3, Steve I Max3, Jun Wang3, Florence Hsieh, Luda Diatchenko, Kate Marusina, Andrew A Farmer, Gerald M. Rubin4, Ling Hong4, Mark Stapleton4, M. Bento Soares5, Maria de Fatima Bonaldo5, Thomas L. Casavant5, Todd E. Scheetz5, Michael J. Brownstein1, Ted B. Usdin1, Shiraki Toshiyuki, Piero Carninci, Christa Prange6, Sam S Raha7, Naomi A Loquellano7, Garrick J Peters7, Rick D Abramson7, Sara J Mullahy7, Stephanie Bosak, Paul J. McEwan, Kevin McKernan, Joel A. Malek, Preethi H. Gunaratne8, Stephen Richards8, Kim C. Worley8, Sarah Hale8, Angela M. Garcia8, Stephen W. Hulyk8, Debbie K Villalon8, Donna M. Muzny8, Erica Sodergren8, Xiuhua Lu8, Richard A. Gibbs8, Jessica Fahey9, Erin Helton9, Mark Ketteman9, Anuradha Madan9, Stephanie Rodrigues9, Amy Sanchez9, Michelle Whiting9, Anup Madan9, Alice C. Young1, Yuriy O. Shevchenko1, Gerard G. Bouffard1, Robert W. Blakesley1, Jeffrey W. Touchman1, Eric D. Green1, Mark Dickson10, Alex Rodriguez10, Jane Grimwood10, Jeremy Schmutz10, Richard M. Myers10, Yaron S.N. Butterfield11, Martin Krzywinski11, Ursula Skalska11, Duane E. Smailus11, Angelique Schnerch11, Jacqueline E. Schein11, Steven J.M. Jones11, Marco A. Marra11 
TL;DR: The National Institutes of Health Mammalian Gene Collection (MGC) Program is a multiinstitutional effort to identify and sequence a cDNA clone containing a complete ORF for each human and mouse gene.
Abstract: The National Institutes of Health Mammalian Gene Collection (MGC) Program is a multiinstitutional effort to identify and sequence a cDNA clone containing a complete ORF for each human and mouse gene. ESTs were generated from libraries enriched for full-length cDNAs and analyzed to identify candidate full-ORF clones, which then were sequenced to high accuracy. The MGC has currently sequenced and verified the full ORF for a nonredundant set of >9,000 human and >6,000 mouse genes. Candidate full-ORF clones for an additional 7,800 human and 3,500 mouse genes also have been identified. All MGC sequences and clones are available without restriction through public databases and clone distribution networks (see http:mgc.nci.nih.gov).

2,184 citations

Journal ArticleDOI
01 Jan 1999-Science
TL;DR: The temporal program of gene expression during a model physiological response of human cells, the response of fibroblasts to serum, was explored with a complementary DNA microarray representing 8600 different human genes.
Abstract: The temporal program of gene expression during a model physiological response of human cells, the response of fibroblasts to serum, was explored with a complementary DNA microarray representing about 8600 different human genes. Genes could be clustered into groups on the basis of their temporal patterns of expression in this program. Many features of the transcriptional program appeared to be related to the physiology of wound repair, suggesting that fibroblasts play a larger and richer role in this complex multicellular response than had previously been appreciated.

2,062 citations

Journal ArticleDOI
01 Apr 2004-Nature
TL;DR: This first comprehensive analysis of the genome sequence of the Brown Norway (BN) rat strain is reported, which is the third complete mammalian genome to be deciphered, and three-way comparisons with the human and mouse genomes resolve details of mammalian evolution.
Abstract: The laboratory rat (Rattus norvegicus) is an indispensable tool in experimental medicine and drug development, having made inestimable contributions to human health. We report here the genome sequence of the Brown Norway (BN) rat strain. The sequence represents a high-quality 'draft' covering over 90% of the genome. The BN rat sequence is the third complete mammalian genome to be deciphered, and three-way comparisons with the human and mouse genomes resolve details of mammalian evolution. This first comprehensive analysis includes genes and proteins and their relation to human disease, repeated sequences, comparative genome-wide studies of mammalian orthologous chromosomal regions and rearrangement breakpoints, reconstruction of ancestral karyotypes and the events leading to existing species, rates of variation, and lineage-specific and lineage-independent evolutionary events such as expansion of gene families, orthology relations and protein evolution.

1,964 citations


Authors

Showing all 1267 results

NameH-indexPapersCitations
Patrick O. Brown183755200985
David Botstein165468212787
Inês Barroso11330176241
Alessandro M. Vannucchi9471535482
Ana M. Valdes8433426627
Mark C. Genovese7936426945
Michael B. Eisen7117089150
Jingyue Ju6116918952
Jeanne F. Loring6017714503
James Z. Wang5722521890
Emmett V. Schmidt501509304
Günther Sperk5012410246
Robert C. Newton441117369
Magnus Pfahl44878064
William V. Williams441687278
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20231
20225
202158
202093
201985
201882