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دورية أكاديمية

Computational Methods of Discovering Gene Modules and Constructing Regulatory Networks

المؤلفون: Molong Li

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://cmgm.stanford.edu/biochem218/Projects%202008/LI2008.pdfTest.

وصف الملف: application/pdf

العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.181.80Test; http://cmgm.stanford.edu/biochem218/Projects%202008/LI2008.pdfTest

الإتاحة: http://cmgm.stanford.edu/biochem218/Projects%202008/LI2008.pdfTest

View record in BASE

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Human Disease Modeling Reveals Integrated Transcriptional and Epigenetic Mechanisms of NOTCH1 Haploinsufficiency

المؤلفون: Deepak Srivastava, Mark P. White, Daniel He, Molong Li, Katherine S. Pollard, Christina V. Theodoris, Benoit G. Bruneau, Lei Liu

المصدر: Cell, vol 160, iss 6
Theodoris, CV; Li, M; White, MP; Liu, L; He, D; Pollard, KS; et al.(2015). Human disease modeling reveals integrated transcriptional and epigenetic mechanisms of NOTCH1 haploinsufficiency. Cell, 160(6), 1072-1086. doi: 10.1016/j.cell.2015.02.035. UCSF: Retrieved from: http://www.escholarship.org/uc/item/7t5564z6Test

مصطلحات موضوعية: Male, Transcription, Genetic, Gene regulatory network, Haploinsufficiency, Regenerative Medicine, Medical and Health Sciences, Epigenesis, Genetic, Osteogenesis, 2.1 Biological and endogenous factors, Histone code, Gene Regulatory Networks, Receptor, Notch1, Aetiology, Induced pluripotent stem cell, Derepression, Pediatric, Genetics, Biological Sciences, Pedigree, Cell biology, Histone Code, embryonic structures, cardiovascular system, Female, biological phenomena, cell phenomena, and immunity, Transcription, Receptor, Induced Pluripotent Stem Cells, Biology, Stress, General Biochemistry, Genetics and Molecular Biology, Genetic, Humans, Epigenetics, Enhancer, Transcription factor, Inflammation, Notch1, Stem Cell Research - Induced Pluripotent Stem Cell, Biochemistry, Genetics and Molecular Biology(all), Endothelial Cells, Stem Cell Research, Mechanical, Congenital Structural Anomalies, Stress, Mechanical, sense organs, Epigenesis, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::471acba0d188deefdfe70157798f0c2eTest
https://doi.org/10.1016/j.cell.2015.02.035Test

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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

المؤلفون: Joshua C. Bis, Daniel I. Chasman, Archie Campbell, J. Wouter Jukema, Yoichiro Kamatani, Joylene E. Siland, Siegfried Perz, Jie Huang, Jorge A. Wong, Jared W. Magnani, Stefan Weiss, Caroline Hayward, Christopher D. Anderson, Carolina Roselli, Alexander P. Reiner, Maartje N. Niemeijer, Efthymia Vlachopoulou, David R. Van Wagoner, Elsayed Z. Soliman, Lenore J. Launer, Claudia Schurmann, Jeffrey Haessler, Joshua C. Denny, Qiong Yang, Mika Kähönen, Henry J. Lin, Lu-Chen Weng, Molong Li, Paul L. Huang, Terho Lehtimäki, Bruno H. Stricker, Lewin Eisele, Christopher Newton-Cheh, Marcus E. Kleber, Alexander Teumer, Rainer Malik, Juha Sinisalo, Siew-Kee Low, Xiaoyan Yin, Stéphanie Debette, Jennifer A. Brody, Marco V Perez, Derek Klarin, Farid Radmanesh, Ian Ford, Dan M. Roden, Paul M. Ridker, Jan Heeringa, Jonathan Rosand, Andrew P. Morris, Winfried März, Stefan Gustafsson, Xiuqing Guo, Nathan R. Tucker, Dawood Darbar, Daniel J. Rader, Martin Dichgans, Stefan Kääb, Lars Lind, Patrick T. Ellinor, Nancy L. Pedersen, Stefanie Aeschbacher, Erwin B. Bottinger, Leo-Pekka Lyytikäinen, Peter Lichtner, Marcus Dörr, Svati H. Shah, Lin Y. Chen, Alvaro Alonso, Marja-Liisa Lokki, Albert V. Smith, Guillaume Paré, Ruth J. F. Loos, Christine M. Albert, Markku Eskola, Jonathan D. Smith, Kjell Nikus, Martina Müller-Nurasyid, Yanick Hagemeijer, Lorenz Risch, Nona Sotoodehnia, Jussi Hernesniemi, Albert Y. Sun, Man Li, Jemma C. Hopewell, Olle Melander, Albert Hofman, Annette Peters, Pim van der Harst, Michiel Rienstra, Ilkka Seppälä, Kent D. Taylor, Charles Kooperberg, Moritz F. Sinner, Jerome I. Rotter, Stuart A. Scott, Toshihiro Tanaka, Steven A. Lubitz, Uwe Völker, Marju Orho-Melander, Patrik K. E. Magnusson, Jari Laurikka, M. Benjamin Shoemaker, Niek Verweij, J. Gustav Smith, José Eduardo Krieger, Sébastien Thériault, Andrea R. V. R. Horimoto, Natalia S. Rost, André G. Uitterlinden, Oscar H. Franco, David Conen, Cecilia M. Lindgren, Sekar Kathiresan, Michiaki Kubo, Marina Arendt, Graciela Delgado, Anders Hamsten, Rajat Deo, Lars Lannfelt, Sebastian Clauss, Sandosh Padmanabhan, Emelia J. Benjamin, Roopinder K. Sandhu, Bruce M. Psaty, Peter Weeke, Mark Chaffin, Traci M. Bartz, Erik Ingelsson, Alfredo José Mansur, Nathan A. Bihlmeyer, Christian M. Shaffer, Lynne J. Hocking, Stella Trompet, Melanie Waldenberger, Honghuang Lin, Stephan B. Felix, David J. Porteous, Vilmundur Gudnason, Eric Boerwinkle, Dan E. Arking, Alexandre C. Pereira, Bastiaan Geelhoed, Susan R. Heckbert, Jie Yao, Bradford B. Worrall, Ingrid E. Christophersen, Jennifer Kriebel, Peter Almgren, Blair H. Smith, Jennifer E. Huffman, Seung Hoan Choi, Mina K. Chung, Karl-Heinz Jöckel, Yingchang Lu, Yii-Der Ida Chen, Peter W. Macfarlane, John Barnard, Tamara B. Harris, Kathryn L. Lunetta, Stefanie Heilmann-Heimbach, Ganesh Chauhan

المساهمون: Epidemiology, Internal Medicine, Cardiovascular Centre (CVC)

المصدر: Nature Genetics, 49(6), 946-+. Nature Publishing Group
Nature Genetics
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Nature Genetics, 49(6), 946
Nature Genetics, 49(6), 946-952. Nature Publishing Group
Christophersen, I E, Rienstra, M, Roselli, C, Yin, X, Geelhoed, B, Barnard, J, Lin, H, Arking, D E, Smith, A V, Albert, C M, Chaffin, M, Tucker, N R, Li, M, Klarin, D, Bihlmeyer, N A, Low, S-K, Weeke, P E, Müller-nurasyid, M, Smith, J G, Brody, J A, Niemeijer, M N, Dörr, M, Trompet, S, Huffman, J, Gustafsson, S, Schurmann, C, Kleber, M E, Lyytikäinen, L-P, Seppälä, I, Malik, R, Horimoto, A R V R, Perez, M, Sinisalo, J, Aeschbacher, S, Thériault, S, Yao, J, Radmanesh, F, Weiss, S, Teumer, A, Choi, S H, Weng, L-C, Clauss, S, Deo, R, Rader, D J, Shah, S H, Sun, A, Morris, A P, Campbell, A, Porteous, D & Hayward, C 2017, ' Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation ', Nature Genetics, vol. 49, no. 6, pp. 946-952 . https://doi.org/10.1038/ng.3843Test
Nat. Genet. 49, 946-952 (2017)
Nature genetics 49(6), 946-952 (2017). doi:10.1038/ng.3843

مصطلحات موضوعية: 0301 basic medicine, Quantitative Trait Loci, Medizin, genetics [White People], SNP, Genome-wide association study, 030204 cardiovascular system & hematology, Biology, SUSCEPTIBILITY, Bioinformatics, GENOMAS, ANNOTATION, White People, 03 medical and health sciences, 0302 clinical medicine, ddc:570, Genetic variation, Atrial Fibrillation, Genetics, medicine, Journal Article, TOOL, Humans, Genetic Predisposition to Disease, genetics [Atrial Fibrillation], GENOME-WIDE ASSOCIATION, Stroke, METAANALYSIS, Genetic association, RISK, genetics [Black or African American], GENETIC-VARIATION, Atrial fibrillation, medicine.disease, R1, 3. Good health, Black or African American, genetics [European Continental Ancestry Group], 030104 developmental biology, Genetic Loci, Heart failure, Meta-analysis, VISUALIZATION, genetics [African Americans], BURDEN, Genome-Wide Association Study