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Institution

University of Cologne

EducationCologne, Germany
About: University of Cologne is a education organization based out in Cologne, Germany. It is known for research contribution in the topics: Population & Gene. The organization has 32050 authors who have published 66350 publications receiving 2210092 citations. The organization is also known as: Universität zu Köln & Universitatis Coloniensis.
Topics: Population, Gene, Transplantation, Medicine, Cancer


Papers
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Journal ArticleDOI
01 Jun 1995-Nature
TL;DR: The infected mutant mice developed a significantly stronger Thl type of immune response than the wild-type or heterozygous mice, and showed reduced nonspecific inflammatory response to carrageenin, and were resistant to lipopolysaccharide-induced mortality.
Abstract: NITRIC oxide (NO) is important in many biological functions1–5. It is generated from L-arginine by the enzyme NO synthase (NOS). The cytokine-inducible NOS (iNOS) is activated by several immunological stimuli, leading to the production of large quantities of NO which can be cytotoxic6. To define the biological role of iNOS further, we generated iNOS mutant mice. These are viable, fertile and without evident histopathological abnormalities. However, in contrast to wild-type and heterozygous mice, which are highly resistant to the protozoa parasite Leishmania major infection, mutant mice are uniformly susceptible. The infected mutant mice developed a significantly stronger Thl type of immune response than the wild-type or heterozygous mice. The mutant mice showed reduced nonspecific inflammatory response to carrageenin, and were resistant to lipopolysaccharide-induced mortality.

1,305 citations

Journal ArticleDOI
TL;DR: Ceritinib was highly active in patients with advanced, ALK-rearranged NSCLC, including those who had had disease progression during crizotinib treatment, regardless of the presence of resistance mutations in ALK.
Abstract: BackgroundNon–small-cell lung cancer (NSCLC) harboring the anaplastic lymphoma kinase gene (ALK) rearrangement is sensitive to the ALK inhibitor crizotinib, but resistance invariably develops. Ceritinib (LDK378) is a new ALK inhibitor that has shown greater antitumor potency than crizotinib in preclinical studies. MethodsIn this phase 1 study, we administered oral ceritinib in doses of 50 to 750 mg once daily to patients with advanced cancers harboring genetic alterations in ALK. In an expansion phase of the study, patients received the maximum tolerated dose. Patients were assessed to determine the safety, pharmacokinetic properties, and antitumor activity of ceritinib. Tumor biopsies were performed before ceritinib treatment to identify resistance mutations in ALK in a group of patients with NSCLC who had had disease progression during treatment with crizotinib. ResultsA total of 59 patients were enrolled in the dose-escalation phase. The maximum tolerated dose of ceritinib was 750 mg once daily; dose-l...

1,297 citations

Journal ArticleDOI
Ludwig Eichinger1, Justin A. Pachebat2, Justin A. Pachebat1, Gernot Glöckner, Marie-Adèle Rajandream3, Richard Sucgang4, Matthew Berriman3, J. Song4, Rolf Olsen5, Karol Szafranski, Qikai Xu4, Budi Tunggal1, Sarah K. Kummerfeld2, Martin Madera2, Bernard Anri Konfortov2, Francisco Rivero1, Alan T. Bankier2, Rüdiger Lehmann, N. Hamlin3, Robert L. Davies3, Pascale Gaudet6, Petra Fey6, Karen E Pilcher6, Guokai Chen4, David L. Saunders3, Erica Sodergren4, P. Davis3, Arnaud Kerhornou3, X. Nie4, Neil Hall3, Christophe Anjard5, Lisa Hemphill4, Nathalie Bason3, Patrick Farbrother1, Brian A. Desany4, Eric M. Just6, Takahiro Morio7, René Rost8, Carol Churcher3, J. Cooper3, Stephen F. Haydock9, N. van Driessche4, Ann Cronin3, Ian Goodhead3, Donna M. Muzny4, T. Mourier3, Arnab Pain3, Mingyang Lu4, D. Harper3, R. Lindsay4, Heidi Hauser3, Kylie R. James3, M. Quiles4, M. Madan Babu2, Tsuneyuki Saito10, Carmen Buchrieser11, A. Wardroper12, A. Wardroper2, Marius Felder, M. Thangavelu, D. Johnson3, Andrew J Knights3, H. Loulseged4, Karen Mungall3, Karen Oliver3, Claire Price3, Michael A. Quail3, Hideko Urushihara7, Judith Hernandez4, Ester Rabbinowitsch3, David Steffen4, Mandy Sanders3, Jun Ma4, Yuji Kohara13, Sarah Sharp3, Mark Simmonds3, S. Spiegler3, Adrian Tivey3, Sumio Sugano14, Brian White3, Danielle Walker3, John Woodward3, Thomas Winckler, Yoshiaki Tanaka7, Gad Shaulsky4, Michael Schleicher8, George M. Weinstock4, André Rosenthal, Edward C. Cox15, Rex L. Chisholm6, Richard A. Gibbs4, William F. Loomis5, Matthias Platzer, Robert R. Kay2, Jeffrey G. Williams16, Paul H. Dear2, Angelika A. Noegel1, Bart Barrell3, Adam Kuspa4 
05 May 2005-Nature
TL;DR: A proteome-based phylogeny shows that the amoebozoa diverged from the animal–fungal lineage after the plant–animal split, but Dictyostelium seems to have retained more of the diversity of the ancestral genome than have plants, animals or fungi.
Abstract: The social amoebae are exceptional in their ability to alternate between unicellular and multicellular forms. Here we describe the genome of the best-studied member of this group, Dictyostelium discoideum. The gene-dense chromosomes of this organism encode approximately 12,500 predicted proteins, a high proportion of which have long, repetitive amino acid tracts. There are many genes for polyketide synthases and ABC transporters, suggesting an extensive secondary metabolism for producing and exporting small molecules. The genome is rich in complex repeats, one class of which is clustered and may serve as centromeres. Partial copies of the extrachromosomal ribosomal DNA (rDNA) element are found at the ends of each chromosome, suggesting a novel telomere structure and the use of a common mechanism to maintain both the rDNA and chromosomal termini. A proteome-based phylogeny shows that the amoebozoa diverged from the animal-fungal lineage after the plant-animal split, but Dictyostelium seems to have retained more of the diversity of the ancestral genome than have plants, animals or fungi.

1,289 citations

Journal ArticleDOI
TL;DR: In this article, the authors introduce a new "pinball" framework of new media's impact on relationships with customers and identify key new media phenomena which companies should take into account when managing their relationships with customer in the new media universe.
Abstract: Recent years have witnessed the rise of new media channels such as Facebook, YouTube, Google, and Twitter, which enable customers to take a more active role as market players and reach (and be reached by) almost everyone anywhere and anytime. These new media threaten long established business models and corporate strategies, but also provide ample opportunities for growth through new adaptive strategies. This paper introduces a new ‘‘pinball’’ framework of new media’s impact on relationships with customers and identifies key new media phenomena which companies should take into account when managing their relationships with customers in the new media universe. For each phenomenon, we identify challenges for researchers and managers which relate to (a) the understanding of consumer behavior, (b) the use of new media to successfully manage customer interactions, and (c) the effective measurement of customers’ activities and outcomes.

1,285 citations


Authors

Showing all 32558 results

NameH-indexPapersCitations
Julie E. Buring186950132967
Stuart H. Orkin186715112182
Cornelia M. van Duijn1831030146009
Dorret I. Boomsma1761507136353
Frederick W. Alt17157795573
Donald E. Ingber164610100682
Klaus Müllen1642125140748
Klaus Rajewsky15450488793
Frederik Barkhof1541449104982
Stefanie Dimmeler14757481658
Detlef Weigel14251684670
Hidde L. Ploegh13567467437
Luca Valenziano13043794728
Peter Walter12684171580
Peter G. Martin12555397257
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023324
2022634
20214,225
20204,052
20193,526
20183,078