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Institution

Medical Research Council

GovernmentLondon, United Kingdom
About: Medical Research Council is a government organization based out in London, United Kingdom. It is known for research contribution in the topics: Population & Malaria. The organization has 16430 authors who have published 19150 publications receiving 1475494 citations.
Topics: Population, Malaria, Poison control, Gene, Antigen


Papers
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Journal ArticleDOI
TL;DR: This trial shows that control of local tumour can lead to an improvement in long term survival and demonstrates the importance of cellular repopulation as a cause of failure in the radiotherapy of NSCLC.

472 citations

Journal ArticleDOI
Padhraig Gormley, Verneri Anttila1, Verneri Anttila2, Bendik S. Winsvold3, Bendik S. Winsvold4, Priit Palta5, Tõnu Esko6, Tõnu Esko7, Tõnu Esko2, Tune H. Pers, Kai-How Farh2, Kai-How Farh1, Kai-How Farh8, Ester Cuenca-León, Mikko Muona, Nicholas A. Furlotte, Tobias Kurth9, Tobias Kurth10, Andres Ingason11, George McMahon12, Lannie Ligthart13, Gisela M. Terwindt14, Mikko Kallela15, Tobias Freilinger16, Tobias Freilinger17, Caroline Ran18, Scott G. Gordon19, Anine H. Stam14, Stacy Steinberg11, Guntram Borck20, Markku Koiranen21, Lydia Quaye22, Hieab H.H. Adams23, Terho Lehtimäki24, Antti-Pekka Sarin5, Juho Wedenoja5, David A. Hinds, Julie E. Buring9, Julie E. Buring1, Markus Schürks25, Paul M. Ridker9, Paul M. Ridker1, Maria Gudlaug Hrafnsdottir, Hreinn Stefansson11, Susan M. Ring12, Jouke-Jan Hottenga13, Brenda W.J.H. Penninx13, Markus Färkkilä15, Ville Artto15, Mari A. Kaunisto5, Salli Vepsäläinen15, Rainer Malik16, Andrew C. Heath26, Pamela A. F. Madden26, Nicholas G. Martin19, Grant W. Montgomery19, Mitja I. Kurki, Mart Kals7, Reedik Mägi7, Kalle Pärn7, Eija Hamalainen5, Hailiang Huang2, Hailiang Huang1, Andrea Byrnes1, Andrea Byrnes2, Lude Franke27, Jie Huang28, Evie Stergiakouli12, Phil Lee2, Phil Lee1, Cynthia Sandor29, Caleb Webber29, Zameel M. Cader29, Zameel M. Cader30, Bertram Müller-Myhsok31, Stefan Schreiber32, Thomas Meitinger33, Johan G. Eriksson34, Johan G. Eriksson5, Veikko Salomaa34, Kauko Heikkilä5, Elizabeth Loehrer1, Elizabeth Loehrer23, André G. Uitterlinden23, Albert Hofman23, Cornelia M. van Duijn23, Lynn Cherkas22, Linda M. Pedersen4, Audun Stubhaug3, Audun Stubhaug4, Christopher Sivert Nielsen35, Christopher Sivert Nielsen4, Minna Männikkö21, Evelin Mihailov7, Lili Milani7, Hartmut Göbel, Ann-Louise Esserlind36, Anne Francke Christensen36, Thomas Hansen36, Thomas Werge37, Thomas Werge38, Thomas Werge36, Jaakko Kaprio5, Jaakko Kaprio34, Arpo Aromaa34, Olli T. Raitakari39, Olli T. Raitakari40, M. Arfan Ikram23, Tim D. Spector22, Marjo-Riitta Järvelin, Andres Metspalu7, Christian Kubisch41, David P. Strachan42, Michel D. Ferrari14, Andrea Carmine Belin18, Martin Dichgans16, Maija Wessman5, Arn M. J. M. van den Maagdenberg14, John-Anker Zwart4, John-Anker Zwart3, Dorret I. Boomsma13, George Davey Smith12, Kari Stefansson43, Kari Stefansson11, Nicholas Eriksson, Mark J. Daly2, Mark J. Daly1, Benjamin M. Neale1, Benjamin M. Neale2, Jes Olesen36, Daniel I. Chasman1, Daniel I. Chasman9, Dale R. Nyholt44, Aarno Palotie 
TL;DR: For example, the authors identified 44 independent single-nucleotide polymorphisms (SNPs) significantly associated with migraine risk (P < 5 × 10−8) that mapped to 38 distinct genomic loci, including 28 loci not previously reported and a locus that to date is the first to be identified on chromosome X.
Abstract: Migraine is a debilitating neurological disorder affecting around one in seven people worldwide, but its molecular mechanisms remain poorly understood. There is some debate about whether migraine is a disease of vascular dysfunction or a result of neuronal dysfunction with secondary vascular changes. Genome-wide association (GWA) studies have thus far identified 13 independent loci associated with migraine. To identify new susceptibility loci, we carried out a genetic study of migraine on 59,674 affected subjects and 316,078 controls from 22 GWA studies. We identified 44 independent single-nucleotide polymorphisms (SNPs) significantly associated with migraine risk (P < 5 × 10−8) that mapped to 38 distinct genomic loci, including 28 loci not previously reported and a locus that to our knowledge is the first to be identified on chromosome X. In subsequent computational analyses, the identified loci showed enrichment for genes expressed in vascular and smooth muscle tissues, consistent with a predominant theory of migraine that highlights vascular etiologies.

471 citations

Journal ArticleDOI
Lavinia Paternoster1, Marie Standl, Johannes Waage2, H. Baurecht3  +151 moreInstitutions (55)
TL;DR: This paper performed a meta-analysis of >15 million genetic variants in 21,399 cases and 95,464 controls from populations of European, African, Japanese and Latino ancestry, followed by replication in 32,059 cases and 228,628 controls from 18 studies.
Abstract: Genetic association studies have identified 21 loci associated with atopic dermatitis risk predominantly in populations of European ancestry. To identify further susceptibility loci for this common, complex skin disease, we performed a meta-analysis of >15 million genetic variants in 21,399 cases and 95,464 controls from populations of European, African, Japanese and Latino ancestry, followed by replication in 32,059 cases and 228,628 controls from 18 studies. We identified ten new risk loci, bringing the total number of known atopic dermatitis risk loci to 31 (with new secondary signals at four of these loci). Notably, the new loci include candidate genes with roles in the regulation of innate host defenses and T cell function, underscoring the important contribution of (auto)immune mechanisms to atopic dermatitis pathogenesis.

471 citations

Journal ArticleDOI
TL;DR: The central stalk in ATP synthase is made of γ, δ and ɛ subunits in the mitochondrial enzyme, and with crystals of F1-ATPase inhibited with dicyclohexylcarbodiimide, the complete structure was revealed.
Abstract: The central stalk in ATP synthase, made of γ, δ and ɛ subunits in the mitochondrial enzyme, is the key rotary element in the enzyme's catalytic mechanism. The γ subunit penetrates the catalytic (αβ)3 domain and protrudes beneath it, interacting with a ring of c subunits in the membrane that drives rotation of the stalk during ATP synthesis. In other crystals of F1-ATPase, the protrusion was disordered, but with crystals of F1-ATPase inhibited with dicyclohexylcarbodiimide, the complete structure was revealed. The δ and ɛ subunits interact with a Rossmann fold in the γ subunit, forming a foot. In ATP synthase, this foot interacts with the c-ring and couples the transmembrane proton motive force to catalysis in the (αβ)3 domain.

471 citations

Journal ArticleDOI
TL;DR: Key issues in interpreting (13)C metabolite labeling patterns are reviewed, with the goal of drawing accurate conclusions from steady state and dynamic stable isotopic tracer experiments.

471 citations


Authors

Showing all 16441 results

NameH-indexPapersCitations
Shizuo Akira2611308320561
Trevor W. Robbins2311137164437
Richard A. Flavell2311328205119
George Davey Smith2242540248373
Nicholas J. Wareham2121657204896
Cyrus Cooper2041869206782
Martin White1962038232387
Frank E. Speizer193636135891
Michael Rutter188676151592
Richard Peto183683231434
Terrie E. Moffitt182594150609
Kay-Tee Khaw1741389138782
Chris D. Frith173524130472
Phillip A. Sharp172614117126
Avshalom Caspi170524113583
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
20236
20229
2021262
2020243
2019231
2018309