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Institution

Novartis

CompanyBasel, Switzerland
About: Novartis is a company organization based out in Basel, Switzerland. It is known for research contribution in the topics: Alkyl & Population. The organization has 41930 authors who have published 50566 publications receiving 1978996 citations. The organization is also known as: Novartis International AG.
Topics: Alkyl, Population, Alkoxy group, Receptor, Cancer


Papers
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Journal ArticleDOI
16 Nov 2007-Blood
TL;DR: DKK1 is confirmed as an important therapeutic target in myeloma and the rationale for clinical evaluation of BHQ880 to improve bone disease and to inhibit MM growth is provided.

383 citations

Journal ArticleDOI
TL;DR: This Perspective summarizes recent technological advances in QSAR modeling but it also highlights the applicability of algorithms, modeling methods, and validation practices developed inQSAR to a wide range of research areas outside of traditional QSar boundaries including synthesis planning, nanotechnology, materials science, biomaterials, and clinical informatics.
Abstract: Prediction of chemical bioactivity and physical properties has been one of the most important applications of statistical and more recently, machine learning and artificial intelligence methods in chemical sciences. This field of research, broadly known as quantitative structure–activity relationships (QSAR) modeling, has developed many important algorithms and has found a broad range of applications in physical organic and medicinal chemistry in the past 55+ years. This Perspective summarizes recent technological advances in QSAR modeling but it also highlights the applicability of algorithms, modeling methods, and validation practices developed in QSAR to a wide range of research areas outside of traditional QSAR boundaries including synthesis planning, nanotechnology, materials science, biomaterials, and clinical informatics. As modern research methods generate rapidly increasing amounts of data, the knowledge of robust data-driven modelling methods professed within the QSAR field can become essential for scientists working both within and outside of chemical research. We hope that this contribution highlighting the generalizable components of QSAR modeling will serve to address this challenge.

383 citations

Journal ArticleDOI
Vanessa K. Wong1, Vanessa K. Wong2, Stephen Baker3, Stephen Baker4, Stephen Baker5, Derek Pickard1, Julian Parkhill1, Andrew J. Page1, Nicholas A. Feasey6, Robert A. Kingsley7, Robert A. Kingsley1, Nicholas R. Thomson3, Nicholas R. Thomson1, Jacqueline A. Keane1, François-Xavier Weill8, David J. Edwards9, Jane Hawkey9, Simon R. Harris1, Alison E. Mather1, Amy K. Cain1, James Hadfield1, Peter J. Hart10, Nga Tran Vu Thieu5, Elizabeth J. Klemm1, Dafni A. Glinos1, Robert F. Breiman11, Robert F. Breiman12, Robert F. Breiman13, Conall H. Watson3, Samuel Kariuki13, Samuel Kariuki1, Melita A. Gordon14, Robert S. Heyderman15, Chinyere K. Okoro1, Jan Jacobs16, Jan Jacobs17, Octavie Lunguya, W. John Edmunds3, Chisomo L. Msefula15, José A. Chabalgoity18, Mike Kama, Kylie Jenkins, Shanta Dutta, Florian Marks19, Josefina Campos, Corinne N. Thompson5, Corinne N. Thompson4, Stephen K. Obaro, Calman A. MacLennan20, Calman A. MacLennan10, Calman A. MacLennan1, Christiane Dolecek5, Karen H. Keddy21, Anthony M. Smith21, Christopher M. Parry22, Christopher M. Parry3, Abhilasha Karkey23, E. Kim Mulholland3, James Campbell5, James Campbell4, Sabina Dongol23, Buddha Basnyat23, Muriel Dufour, Don Bandaranayake, Take Toleafoa Naseri, Shalini Singh24, Mochammad Hatta25, Paul N. Newton5, Paul N. Newton26, Robert S. Onsare13, Lupeoletalalei Isaia, David A. B. Dance5, David A. B. Dance26, Viengmon Davong26, Guy E. Thwaites5, Guy E. Thwaites4, Lalith Wijedoru27, John A. Crump28, Elizabeth de Pinna29, Satheesh Nair29, Eric J. Nilles24, Duy Pham Thanh5, Paul Turner5, Paul Turner27, Paul Turner30, Sona Soeng30, Mary Valcanis9, Joan Powling9, Karolina Dimovski9, Geoff Hogg9, Jeremy Farrar4, Jeremy Farrar5, Kathryn E. Holt9, Gordon Dougan1 
TL;DR: This whole-genome sequence analysis of Salmonella enterica serovar Typhi identifies a single dominant MDR lineage, H58, that has emerged and spread throughout Asia and Africa over the last 30 years, and identifies numerous transmissions of H58.
Abstract: The emergence of multidrug-resistant (MDR) typhoid is a major global health threat affecting many countries where the disease is endemic. Here whole-genome sequence analysis of 1,832 Salmonella enterica serovar Typhi (S. Typhi) identifies a single dominant MDR lineage, H58, that has emerged and spread throughout Asia and Africa over the last 30 years. Our analysis identifies numerous transmissions of H58, including multiple transfers from Asia to Africa and an ongoing, unrecognized MDR epidemic within Africa itself. Notably, our analysis indicates that H58 lineages are displacing antibiotic-sensitive isolates, transforming the global population structure of this pathogen. H58 isolates can harbor a complex MDR element residing either on transmissible IncHI1 plasmids or within multiple chromosomal integration sites. We also identify new mutations that define the H58 lineage. This phylogeographical analysis provides a framework to facilitate global management of MDR typhoid and is applicable to similar MDR lineages emerging in other bacterial species.

383 citations

Journal ArticleDOI
TL;DR: The design and implementation of a high-throughput structural genomics pipeline and its application to the proteome of the thermophilic bacterium Thermotoga maritima is described and successfully cloned and attempted expression of 1,376 of the predicted 1,877 genes.
Abstract: Structural genomics is emerging as a principal approach to define protein structure–function relationships. To apply this approach on a genomic scale, novel methods and technologies must be developed to determine large numbers of structures. We describe the design and implementation of a high-throughput structural genomics pipeline and its application to the proteome of the thermophilic bacterium Thermotoga maritima. By using this pipeline, we successfully cloned and attempted expression of 1,376 of the predicted 1,877 genes (73%) and have identified crystallization conditions for 432 proteins, comprising 23% of the T. maritima proteome. Representative structures from TM0423 glycerol dehydrogenase and TM0449 thymidylate synthase-complementing protein are presented as examples of final outputs from the pipeline.

383 citations

Journal ArticleDOI
TL;DR: Visual acuity in SUSTAIN patients with individualized re-treatment based on VA/optical coherence tomography assessment reached on average a maximum after the first 3 monthly injections, decreased slightly under PRN during the next 2 to 3 months, and was then sustained throughout the treatment period.

382 citations


Authors

Showing all 41972 results

NameH-indexPapersCitations
Irving L. Weissman2011141172504
Peter J. Barnes1941530166618
Paul G. Richardson1831533155912
Kenneth C. Anderson1781138126072
Jie Zhang1784857221720
Lei Jiang1702244135205
Marc A. Pfeffer166765133043
Jorge E. Cortes1632784124154
Ian A. Wilson15897198221
Peter G. Schultz15689389716
Bruce D. Walker15577986020
Timothy P. Hughes14583191357
Kurt Wüthrich143739103253
Leonard Guarente14335280169
Christopher D.M. Fletcher13867482484
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
202318
202285
20211,321
20201,377
20191,376
20181,456