المساهمون: Jiyon Yu, Yoon Jeong Choi, Sung-Hwan Choi, Han-Sung Jung, Ji Hyun Lee, Jung-Yul Cha

مصطلحات موضوعية: Adolescent, Adult, Bicuspid / surgery, Case-Control Studies, Duration of Therapy, Female, Gene Expression, Gene Frequency, Genetic Predisposition to Disease, Genotype, Haplotypes, Humans, Male, Membrane Proteins / genetics, Middle Aged, Orthodontics / methods, Osteopontin / genetics, Polymorphism, Single Nucleotide, RANK Ligand / genetics, Receptors, Purinergic P2X7 / genetics, Retrospective Studies, Transcriptome, Treatment Outcome, Wnt3A Protein / genetics

وصف الملف: application/pdf

العلاقة: SCIENTIFIC REPORTS; J02646; OAK-2021-07493; https://ir.ymlib.yonsei.ac.kr/handle/22282913/186828Test; T202104708; SCIENTIFIC REPORTS, Vol.11(1) : 15942, 2021-08

الإتاحة: https://doi.org/10.1038/s41598-021-94979-8Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/186828Test

المؤلفون: Kilpeläinen, T.O., Bentley, A.R., Noordam, R., Sung, Y.J., Schwander, K., Winkler, T.W., Jakupović, H., Chasman, D.I., Manning, A., Ntalla, I., Aschard, H., Brown, M.R., de Las Fuentes, L., Franceschini, N., Guo, X., Vojinovic, D., Aslibekyan, S., Feitosa, M.F., Kho, M., Musani, S.K., Richard, M., Wang, H., Wang, Z., Bartz, T.M., Bielak, L.F., Campbell, A., Dorajoo, R., Fisher, V., Hartwig, F.P., Horimoto, ARVR, Li, C., Lohman, K.K., Marten, J., Sim, X., Smith, A.V., Tajuddin, S.M., Alver, M., Amini, M., Boissel, M., Chai, J.F., Chen, X., Divers, J., Evangelou, E., Gao, C., Graff, M., Harris, S.E., He, M., Hsu, F.C., Jackson, A.U., Zhao, J.H., Kraja, A.T., Kühnel, B., Laguzzi, F., Lyytikäinen, L.P., Nolte, I.M., Rauramaa, R., Riaz, M., Robino, A., Rueedi, R., Stringham, H.M., Takeuchi, F., van der Most, P.J., Varga, T.V., Verweij, N., Ware, E.B., Wen, W., Li, X., Yanek, L.R., Amin, N., Arnett, D.K., Boerwinkle, E., Brumat, M., Cade, B., Canouil, M., Chen, Y.I., Concas, M.P., Connell, J., de Mutsert, R., de Silva, H.J., de Vries, P.S., Demirkan, A., Ding, J., Eaton, C.B., Faul, J.D., Friedlander, Y., Gabriel, K.P., Ghanbari, M., Giulianini, F., Gu, C.C., Gu, D., Harris, T.B., He, J., Heikkinen, S., Heng, C.K., Hunt, S.C., Ikram, M.A., Jonas, J.B., Koh, W.P., Komulainen, P., Krieger, J.E., Kritchevsky, S.B., Kutalik, Z., Kuusisto, J., Langefeld, C.D., Langenberg, C., Launer, L.J., Leander, K., Lemaitre, R.N., Lewis, C.E., Liang, J., Liu, J., Mägi, R., Manichaikul, A., Meitinger, T., Metspalu, A., Milaneschi, Y., Mohlke, K.L., Mosley, T.H., Murray, A.D., Nalls, M.A., Nang, E.K., Nelson, C.P., Nona, S., Norris, J.M., Nwuba, C.V., O'Connell, J., Palmer, N.D., Papanicolau, G.J., Pazoki, R., Pedersen, N.L., Peters, A., Peyser, P.A., Polasek, O., Porteous, D.J., Poveda, A., Raitakari, O.T., Rich, S.S., Risch, N., Robinson, J.G., Rose, L.M., Rudan, I., Schreiner, P.J., Scott, R.A., Sidney, S.S., Sims, M., Smith, J.A., Snieder, H., Sofer, T., Starr, J.M., Sternfeld, B., Strauch, K., Tang, H., Taylor, K.D., Tsai, M.Y., Tuomilehto, J., Uitterlinden, A.G., van der Ende, M.Y., van Heemst, D., Voortman, T., Waldenberger, M., Wennberg, P., Wilson, G., Xiang, Y.B., Yao, J., Yu, C., Yuan, J.M., Zhao, W., Zonderman, A.B., Becker, D.M., Boehnke, M., Bowden, D.W., de Faire, U., Deary, I.J., Elliott, P., Esko, T., Freedman, B.I., Froguel, P., Gasparini, P., Gieger, C., Kato, N., Laakso, M., Lakka, T.A., Lehtimäki, T., Magnusson, PKE, Oldehinkel, A.J., Penninx, BWJH, Samani, N.J., Shu, X.O., van der Harst, P., Van Vliet-Ostaptchouk, J.V., Vollenweider, P., Wagenknecht, L.E., Wang, Y.X., Wareham, N.J., Weir, D.R., Wu, T., Zheng, W., Zhu, X., Evans, M.K., Franks, P.W., Gudnason, V., Hayward, C., Horta, B.L., Kelly, T.N., Liu, Y., North, K.E., Pereira, A.C., Ridker, P.M., Tai, E.S., van Dam, R.M., Fox, E.R., Kardia, SLR, Liu, C.T., Mook-Kanamori, D.O., Province, M.A., Redline, S., van Duijn, C.M., Rotter, J.I., Kooperberg, C.B., Gauderman, W.J., Psaty, B.M., Rice, K., Munroe, P.B., Fornage, M., Cupples, L.A., Rotimi, C.N., Morrison, A.C., Rao, D.C., Loos, RJF

المساهمون: Lifelines Cohort Study, Alizadeh, B.Z., Boezen, H.M., Franke, L., Navis, G., Rots, M., Swertz, M., Wolffenbuttel, BHR, Wijmenga, C.

المصدر: Nature communications, vol. 10, no. 1, pp. 376

مصطلحات موضوعية: Adolescent, Adult, African Continental Ancestry Group/genetics, Aged, 80 and over, Asian Continental Ancestry Group/genetics, Brazil, Calcium-Binding Proteins/genetics, Cholesterol/blood, Cholesterol, HDL/blood, HDL/genetics, LDL/blood, LDL/genetics, European Continental Ancestry Group/genetics, Exercise, Female, Genetic Loci/genetics, Genome-Wide Association Study, Genotype, Hispanic Americans/genetics, Humans, LIM-Homeodomain Proteins/genetics, Lipid Metabolism/genetics, Lipids/blood, Lipids/genetics, Male, Membrane Proteins/genetics, Microtubule-Associated Proteins/genetics, Middle Aged

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/30670697; info:eu-repo/semantics/altIdentifier/eissn/2041-1723; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_1B8EF42248BA4; https://serval.unil.ch/notice/serval:BIB_1B8EF42248BATest; urn:issn:2041-1723; https://serval.unil.ch/resource/serval:BIB_1B8EF42248BA.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_1B8EF42248BA4Test

الإتاحة: https://doi.org/10.1038/s41467-018-08008-wTest
https://serval.unil.ch/notice/serval:BIB_1B8EF42248BATest
https://serval.unil.ch/resource/serval:BIB_1B8EF42248BA.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_1B8EF42248BA4Test

المساهمون: College of Medicine, Dept. of Pharmacology, Carolin E. Sadowski, Svjetlana Lovric, Shazia Ashraf, Werner L. Pabst, Heon Yung Gee, Stefan Kohl, Susanne Engelmann, Virginia Vega-Warner, Humphrey Fang, Jan Halbritter, Michael J. Somers, Weizhen Tan, Shirlee Shril, In챔s Fessi, Richard P. Lifton, Detlef Bockenhauer, Sherif El-Desoky, Jameela A. Kari, Martin Zenker, Markus J. Kemper, Dominik Mueller, Hanan M. Fathy, Neveen A. Soliman, Friedhelm Hildebrandt, Gee, Heon Yung

مصطلحات موضوعية: Adolescent, Adult, Age of Onset, Child, Preschool, Cohort Studies, Female, Genes, Wilms Tumor, Genetic Association Studies, Genetic Predisposition to Disease/epidemiology, Genotype, Heterozygote, Humans, Incidence, Infant, Intracellular Signaling Peptides and Proteins/genetics, Male, Membrane Proteins/genetics, Middle Aged, Mutation, Nephrotic Syndrome/congenital, Nephrotic Syndrome/epidemiology, Nephrotic Syndrome/genetics, Nephrotic Syndrome/physiopathology, Pedigree, Phenotype, Real-Time Polymerase Chain Reaction, Retrospective Studies, Risk Assessment

العلاقة: JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY; J01779; OAK-2015-05412; https://ir.ymlib.yonsei.ac.kr/handle/22282913/156712Test; http://jasn.asnjournals.org/content/26/6/1279.abstractTest; T201504426; JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, Vol.26(6) : 1279-1289, 2015

الإتاحة: https://doi.org/10.1681/ASN.2014050489Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/156712Test
http://jasn.asnjournals.org/content/26/6/1279.abstractTest

المساهمون: Eun Su Moon, Hak Sun Kim, Veushj Sharma, Jin Oh Park, Hwan Mo Lee, Sung Hwan Moon, Hyon Su Chong, Kim, Hak Sun, Moon, Seong Hwan, Moon, Eun Su, Park, Jin Oh, Lee, Hwan Mo, Chong, Hyon Su

المصدر: T201300333.pdf

مصطلحات موضوعية: Adolescent, Disease Progression, Female, Genetic Predisposition to Disease, Genotype, Humans, Insulin-Like Growth Factor I/genetics, Korea, Male, Membrane Proteins/genetics, Oncogene Proteins/genetics, Polymorphism, Single Nucleotide, Radiography, Scoliosis/diagnostic imaging, Scoliosis/genetics, Scoliosis/pathology, Adolescent idiopathic scoliosis, gene, single nucleotide polymorphism

العلاقة: YONSEI MEDICAL JOURNAL; J02813; OAK-2013-00266; https://ir.ymlib.yonsei.ac.kr/handle/22282913/86385Test; T201300333; YONSEI MEDICAL JOURNAL, Vol.54(2) : 500-509, 2013

الإتاحة: https://doi.org/10.3349/ymj.2013.54.2.500Test
https://ir.ymlib.yonsei.ac.kr/handle/22282913/86385Test

المؤلفون: Ko, Jae Sung, Kim, Kyung Mo, Oh, Young Lyun, Seo, Jeong Kee

المساهمون: 고재성, 김경모, 오영련, 서정기

مصطلحات موضوعية: Adolescent, Antigens, Bacterial/*genetics, Bacterial Outer Membrane Proteins/*genetics, Bacterial Proteins/*genetics, Child, Preschool, Endoscopy, Digestive System, Female, Gastritis/diagnosis/*microbiology, Genotype, Helicobacter Infections/*genetics/*microbiology, Helicobacter pylori/classification/*genetics/isolation &, purification, Humans, Korea, Male, Severity of Illness Index, Virulence Factors/genetics

العلاقة: Pediatr Int. 2008; 50(5): 628-631; 1442-200X (Electronic); http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=19261108Test; http://hdl.handle.net/10371/68143Test

الإتاحة: https://doi.org/10.1111/j.1442-200X.2008.02641.xTest
http://hdl.handle.net/10371/68143Test
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=19261108Test

المؤلفون: Basamat Almoallem, Gavin Arno, Anne Destree, Elfride De Baere, Denise Williams, Anthony T. Moore, Thomy de Ravel, Ingele Casteels, Andrew R. Webster, Sarah Hull, Irina Balikova, Bart P. Leroy, Martina Suzani, Julie De Zaeytijd, John R. Ainsworth, Hannah Verdin, Michelle Y. Peng

المساهمون: Medical Genetics

المصدر: Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Scientific reports, vol 10, iss 1
SCIENTIFIC REPORTS

مصطلحات موضوعية: 0301 basic medicine, Male, lcsh:Medicine, Gene mutation, PHENOTYPE, Compound heterozygosity, Microphthalmia, Cohort Studies, Exon, 0302 clinical medicine, Genotype, Medicine and Health Sciences, 2.1 Biological and endogenous factors, Microphthalmos, Aetiology, lcsh:Science, Child, Genetics, Multidisciplinary, Molecular medicine, ASSOCIATION, Middle Aged, Disease gene identification, Microphthalmos/genetics, Child, Preschool, Female, FRIZZLED-RELATED PROTEIN, Adult, Serine Proteases/genetics, Heterozygote, Adolescent, DNA Copy Number Variations, Biology, Article, 03 medical and health sciences, Clinical Research, RETINITIS-PIGMENTOSA, GENE MUTATION, Retinitis pigmentosa, medicine, Humans, Family, Allele, Membrane Proteins/genetics, Preschool, Alleles, Aged, IDENTIFICATION, Whole Genome Sequencing, HIGH HYPEROPIA, lcsh:R, Membrane Proteins, Hereditary eye disease, medicine.disease, Brain Disorders, 030104 developmental biology, Mutation, 030221 ophthalmology & optometry, FOVEOSCHISIS, lcsh:Q, Serine Proteases

وصف الملف: application/pdf; Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c67f6b56f74c44ecf74e0f3c5839b48Test
https://pubmed.ncbi.nlm.nih.gov/31992737Test

المؤلفون: Michael R. Brown, Christian Gieger, André G. Uitterlinden, Diana van Heemst, Alison D. Murray, Stephen B. Kritchevsky, Timo A. Lakka, Karen Schwander, Federica Laguzzi, Stephen S. Rich, Rajkumar Dorajoo, Yun Ju Sung, Xiaofeng Zhu, Hugues Aschard, Jing Hua Zhao, Gregory P. Wilson, Kenneth Rice, Barbara Sternfeld, Kent D. Taylor, Paul Elliott, Ei-Ei Khaing Nang, Ilja M. Nolte, Heather M. Stringham, Bruce M. Psaty, Heming Wang, Tangchun Wu, Caroline Hayward, Vilmundur Gudnason, Fernando Pires Hartwig, Paolo Gasparini, Jingjing Liang, Neil Risch, Albertine J. Oldehinkel, Ani Manichaikul, Tibor V. Varga, Michael Y. Tsai, Niek Verweij, Xueling Sim, Norihiro Kato, Evangelos Evangelou, Philippe Froguel, Xiuqing Guo, Traci M. Bartz, Nicholette D. Palmer, Woon-Puay Koh, Rozenn N. Lemaitre, Caizheng Yu, Mike A. Nalls, Mariaelisa Graff, Eric Boerwinkle, Dabeeru C. Rao, Thomas Meitinger, Virginia Fisher, Mario Sims, Charles Kooperberg, Carl D. Langefeld, Jaakko Tuomilehto, Reedik Mägi, Wei Zhao, Wanqing Wen, Donna K. Arnett, Ervin R. Fox, Lynda M. Rose, Maris Alver, Ayse Demirkan, Solomon K. Musani, Dennis O. Mook-Kanamori, Andres Metspalu, Jerome I. Rotter, Barry I. Freedman, Jiang He, Hermina Jakupović, Steven C. Hunt, Marco Brumat, Maria Pina Concas, Rob M. van Dam, Rico Rueedi, Jonathan Marten, Chi Charles Gu, Tõnu Esko, Peter Vollenweider, Zoltán Kutalik, Olli T. Raitakari, Ya X. Wang, Yong-Bing Xiang, Pamela J. Schreiner, Antonietta Robino, Tanika N. Kelly, Igor Rudan, Mathilde Boissel, Claudia Langenberg, Yii-Der Ida Chen, Anne U. Jackson, Lawrence F. Bielak, Brenda W.J.H. Penninx, Brigitte Kühnel, Christopher P. Nelson, Konstantin Strauch, Albert V. Smith, Daniel I. Chasman, Jasmin Divers, Lisa R. Yanek, M. Arfan Ikram, Melissa A. Richard, Nilesh J. Samani, Lisa de las Fuentes, H. Janaka de Silva, Jana V. van Vliet-Ostaptchouk, Yongmei Liu, Peter J. van der Most, Fang-Chi Hsu, Jeffrey R. O'Connell, Alexandre C. Pereira, Raymond Noordam, Changwei Li, Jie Yao, Trudy Voortman, Zhe Wang, Thomas H. Mosley, Diane M. Becker, Charles N. Rotimi, Sami Heikkinen, Archie Campbell, John M. C. Connell, Lenore J. Launer, Hua Tang, Rainer Rauramaa, Ruth J. F. Loos, Pirjo Komulainen, Amy R. Bentley, Patrik Wennberg, Chew-Kiat Heng, Kari E. North, Salman M. Tajuddin, Renée de Mutsert, David J. Porteous, Susan Redline, Sarah E. Harris, Tamara B. Harris, Raha Pazoki, Mickaël Canouil, Robert A. Scott, Jingzhong Ding, Mary F. Feitosa, Jost B. Jonas, José Eduardo Krieger, John M. Starr, Karin Leander, Jennifer A. Smith, Paul W. Franks, Charles B. Eaton, Sharon L.R. Kardia, E. Shyong Tai, Jill M. Norris, Annette Peters, Chiamaka Vivian Nwuba, Jianjun Liu, Stella Aslibekyan, Nora Franceschini, Kurt Lohman, Myriam Fornage, Dina Vojinovic, Erin B. Ware, Xiaoyin Li, Najaf Amin, Johanna Kuusisto, M. Yldau van der Ende, Cora E. Lewis, Lynne E. Wagenknecht, Jennifer G. Robinson, Franco Giulianini, Ulf de Faire, Yechiel Friedlander, Nicholas J. Wareham, Meian He, George J. Papanicolau, Nancy L. Pedersen, Bernardo L. Horta, Karen L. Mohlke, Kelley Pettee Gabriel, Minjung Kho, Michele K. Evans, Ozren Polasek, Markku Laakso, Tuomas O. Kilpeläinen, Ching-Ti Liu, Michael Boehnke, Jin-Fang Chai, Ioanna Ntalla, Cornelia M. van Duijn, L. Adrienne Cupples, Yuri Milaneschi, Stephen Sidney, Alan B. Zonderman, Leo-Pekka Lyytikäinen, Mohsen Ghanbari, Harold Snieder, Donald W. Bowden, Aldi T. Kraja, Alaitz Poveda, Terho Lehtimäki, Paul S. de Vries, Dongfeng Gu, Sotoodehnia Nona, Thomas W. Winkler, Muhammad Riaz, Ian J. Deary, Fumihiko Takeuchi, Pim van der Harst, Alisa K. Manning, Michael A. Province, Andrea R. V. R. Horimoto, David R. Weir, Wei Zheng, Alanna C. Morrison, Marzyeh Amini, Jian-Min Yuan, W. James Gauderman, Paul M. Ridker, Melanie Waldenberger, Chuan Gao, Xiao-Ou Shu, Patricia B. Munroe, Patricia A. Peyser, Jessica D. Faul, Xu Chen, Brian E. Cade, Patrik K. E. Magnusson, Tamar Sofer

المساهمون: Home Office, Medical Research Council (MRC), National Institute for Health Research, Imperial College Healthcare NHS Trust- BRC Funding, UK DRI Ltd, Psychiatry, Amsterdam Neuroscience - Complex Trait Genetics, APH - Mental Health, APH - Digital Health, IT University of Copenhagen, Icahn School of Medicine at Mount Sinai [New York] (MSSM), National Institutes of Health [Bethesda] (NIH), Leiden University Medical Center (LUMC), Washington University School of Medicine in St. Louis, Washington University in Saint Louis (WUSTL), University of Regensburg, Brigham and Women's Hospital [Boston], Harvard Medical School [Boston] (HMS), Massachusetts General Hospital [Boston], Queen Mary University of London (QMUL), Département de Biologie Computationnelle - Department of Computational Biology, Institut Pasteur [Paris]-Centre National de la Recherche Scientifique (CNRS), The University of Texas Health Science Center at Houston (UTHealth), Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP), University of Washington [Seattle], The present work was largely supported by a grant from the US National Heart, Lung,and Blood Institute (NHLBI) of the National Institutes of Health (R01HL118305)., Kilpeläinen, Tuomas O., Bentley, Amy R., Noordam, Raymond, Sung, Yun Ju, Schwander, Karen, Winkler, Thomas W., Jakupović, Hermina, Chasman, Daniel I., Manning, Alisa, Ntalla, Ioanna, Aschard, Hugue, Brown, Michael R., de las Fuentes, Lisa, Franceschini, Nora, Guo, Xiuqing, Vojinovic, Dina, Aslibekyan, Stella, Feitosa, Mary F., Kho, Minjung, Musani, Solomon K., Richard, Melissa, Wang, Heming, Wang, Zhe, Bartz, Traci M., Bielak, Lawrence F., Campbell, Archie, Dorajoo, Rajkumar, Fisher, Virginia, Hartwig, Fernando P., Horimoto, Andrea R. V. R., Li, Changwei, Lohman, Kurt K., Marten, Jonathan, Sim, Xueling, Smith, Albert V., Tajuddin, Salman M., Alver, Mari, Amini, Marzyeh, Boissel, Mathilde, Chai, Jin Fang, Chen, Xu, Divers, Jasmin, Evangelou, Evangelo, Gao, Chuan, Graff, Mariaelisa, Harris, Sarah E., He, Meian, Hsu, Fang-Chi, Jackson, Anne U., Zhao, Jing Hua, Kraja, Aldi T., Kühnel, Brigitte, Laguzzi, Federica, Lyytikäinen, Leo-Pekka, Nolte, Ilja M., Rauramaa, Rainer, Riaz, Muhammad, Robino, Antonietta, Rueedi, Rico, Stringham, Heather M., Takeuchi, Fumihiko, van der Most, Peter J., Varga, Tibor V., Verweij, Niek, Ware, Erin B., Wen, Wanqing, Li, Xiaoyin, Yanek, Lisa R., Amin, Najaf, Arnett, Donna K., Boerwinkle, Eric, Brumat, Marco, Cade, Brian, Canouil, Mickaël, Chen, Yii-Der Ida, Concas, Maria Pina, Connell, John, de Mutsert, Renée, de Silva, H. Janaka, de Vries, Paul S., Demirkan, Ayşe, Ding, Jingzhong, Eaton, Charles B., Faul, Jessica D., Friedlander, Yechiel, Gabriel, Kelley P., Ghanbari, Mohsen, Giulianini, Franco, Gu, Chi Charle, Gu, Dongfeng, Harris, Tamara B., He, Jiang, Heikkinen, Sami, Heng, Chew-Kiat, Hunt, Steven C., Ikram, M. Arfan, Jonas, Jost B., Koh, Woon-Puay, Komulainen, Pirjo, Krieger, Jose E., Kritchevsky, Stephen B., Kutalik, Zoltán, Kuusisto, Johanna, Langefeld, Carl D., Langenberg, Claudia, Launer, Lenore J., Leander, Karin, Lemaitre, Rozenn N., Lewis, Cora E., Liang, Jingjing, Alizadeh, Behrooz Z., Boezen, H. Marike, Franke, Lude, Navis, Gerjan, Rots, Marianne, Swertz, Morri, Wolffenbuttel, Bruce H. R., Wijmenga, Cisca, Liu, Jianjun, Mägi, Reedik, Manichaikul, Ani, Meitinger, Thoma, Metspalu, Andre, Milaneschi, Yuri, Mohlke, Karen L., Mosley, Thomas H., Murray, Alison D., Nalls, Mike A., Nang, Ei-Ei Khaing, Nelson, Christopher P., Nona, Sotoodehnia, Norris, Jill M., Nwuba, Chiamaka Vivian, O’Connell, Jeff, Palmer, Nicholette D., Papanicolau, George J., Pazoki, Raha, Pedersen, Nancy L., Peters, Annette, Peyser, Patricia A., Polasek, Ozren, Porteous, David J., Poveda, Alaitz, Raitakari, Olli T., Rich, Stephen S., Risch, Neil, Robinson, Jennifer G., Rose, Lynda M., Rudan, Igor, Schreiner, Pamela J., Scott, Robert A., Sidney, Stephen S., Sims, Mario, Smith, Jennifer A., Snieder, Harold, Sofer, Tamar, Starr, John M., Sternfeld, Barbara, Strauch, Konstantin, Tang, Hua, Taylor, Kent D., Tsai, Michael Y., Tuomilehto, Jaakko, Uitterlinden, André G., van der Ende, M. Yldau, van Heemst, Diana, Voortman, Trudy, Waldenberger, Melanie, Wennberg, Patrik, Wilson, Gregory, Xiang, Yong-Bing, Yao, Jie, Yu, Caizheng, Yuan, Jian-Min, Zhao, Wei, Zonderman, Alan B., Becker, Diane M., Boehnke, Michael, Bowden, Donald W., de Faire, Ulf, Deary, Ian J., Elliott, Paul, Esko, Tõnu, Freedman, Barry I., Froguel, Philippe, Gasparini, Paolo, Gieger, Christian, Kato, Norihiro, Laakso, Markku, Lakka, Timo A., Lehtimäki, Terho, Magnusson, Patrik K. E., Oldehinkel, Albertine J., Penninx, Brenda W. J. H., Samani, Nilesh J., Shu, Xiao-Ou, van der Harst, Pim, Van Vliet-Ostaptchouk, Jana V., Vollenweider, Peter, Wagenknecht, Lynne E., Wang, Ya X., Wareham, Nicholas J., Weir, David R., Wu, Tangchun, Zheng, Wei, Zhu, Xiaofeng, Evans, Michele K., Franks, Paul W., Gudnason, Vilmundur, Hayward, Caroline, Horta, Bernardo L., Kelly, Tanika N., Liu, Yongmei, North, Kari E., Pereira, Alexandre C., Ridker, Paul M., Tai, E. Shyong, van Dam, Rob M., Fox, Ervin R., Kardia, Sharon L. R., Liu, Ching-Ti, Mook-Kanamori, Dennis O., Province, Michael A., Redline, Susan, van Duijn, Cornelia M., Rotter, Jerome I., Kooperberg, Charles B., Gauderman, W. Jame, Psaty, Bruce M., Rice, Kenneth, Munroe, Patricia B., Fornage, Myriam, Cupples, L. Adrienne, Rotimi, Charles N., Morrison, Alanna C., Rao, Dabeeru C., Loos, Ruth J. F., Bentley, Amy R [0000-0002-0827-9101], Jakupović, Hermina [0000-0001-9667-9406], Manning, Alisa [0000-0003-0247-902X], Aschard, Hugues [0000-0003-0907-2548], de Las Fuentes, Lisa [0000-0002-4689-325X], Richard, Melissa [0000-0003-0129-9860], Liu, Ching-Ti [0000-0002-0703-0742], Rice, Kenneth [0000-0002-3071-7278], Munroe, Patricia B [0000-0002-4176-2947], Loos, Ruth JF [0000-0002-8532-5087], Apollo - University of Cambridge Repository, Epidemiology, Radiology & Nuclear Medicine, Erasmus MC other, Internal Medicine, Læknadeild (HÍ), Faculty of Medicine (UI), Heilbrigðisvísindasvið (HÍ), School of Health Sciences (UI), Háskóli Íslands, University of Iceland, IT University of Copenhagen (ITU), Universiteit Leiden, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Life Course Epidemiology (LCE), Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI), Groningen Research Institute for Asthma and COPD (GRIAC), Lifestyle Medicine (LM), Groningen Kidney Center (GKC), Value, Affordability and Sustainability (VALUE), Damage and Repair in Cancer Development and Cancer Treatment (DARE), Restoring Organ Function by Means of Regenerative Medicine (REGENERATE), Interdisciplinary Centre Psychopathology and Emotion regulation (ICPE), Cardiovascular Centre (CVC), Center for Liver, Digestive and Metabolic Diseases (CLDM), Stem Cell Aging Leukemia and Lymphoma (SALL), Real World Studies in PharmacoEpidemiology, -Genetics, -Economics and -Therapy (PEGET), Lifelines Cohort Study, Alizadeh, B.Z., Boezen, H.M., Franke, L., Navis, G., Rots, M., Swertz, M., Wolffenbuttel, BHR, Wijmenga, C.

المصدر: Nature Communications, 10(1):376. Nature Publishing Group
Nature Communications, Vol 10, Iss 1, Pp 1-11 (2019)
Nature Communications
Nature Communications, Nature Publishing Group, 2019, 10 (1), pp.376. ⟨10.1038/s41467-018-08008-w⟩
Kilpeläinen, T O, Bentley, A R & Loos, R J F 2019, ' Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity ', Nature Communications, vol. 10, no. 1, 376 . https://doi.org/10.1038/s41467-018-08008-wTest
Kilpeläinen, T O, Bentley, A R, Noordam, R, Sung, Y J, Schwander, K, Winkler, T W, Jakupović, H, Chasman, D I, Manning, A, Ntalla, I, Aschard, H, Brown, M R, de las Fuentes, L, Franceschini, N, Guo, X, Vojinovic, D, Aslibekyan, S, Feitosa, M F, Kho, M, Musani, S K, Richard, M, Wang, H, Wang, Z, Bartz, T M, Bielak, L F, Campbell, A, Dorajoo, R, Fisher, V, Hartwig, F P, Horimoto, A R V R, Li, C, Lohman, K K, Marten, J, Sim, X, Smith, A V, Tajuddin, S M, Alver, M, Amini, M, Boissel, M, Chai, J F, Chen, X, Divers, J, Evangelou, E, Gao, C, Graff, M, Harris, S E, He, M, Hsu, F C, Zhao, J H, Loos, R J F, LifeLines Cohort Study & V Varga, T 2019, ' Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity ', Nature Communications, vol. 10, 376 . https://doi.org/10.1038/s41467-018-08008-wTest
Kilpeläinen, T O, Bentley, A R, Noordam, R, Sung, Y J, Schwander, K, Winkler, T W, Jakupović, H, Chasman, D I, Manning, A, Ntalla, I, Aschard, H, Brown, M R, de las Fuentes, L, Franceschini, N, Guo, X, Vojinovic, D, Aslibekyan, S, Feitosa, M F, Kho, M, Musani, S K, Richard, M, Wang, H, Wang, Z, Bartz, T M, Bielak, L F, Campbell, A, Dorajoo, R, Fisher, V, Hartwig, F P, Horimoto, A R V R, Li, C, Lohman, K K, Marten, J, Sim, X, Smith, A V, Tajuddin, S M, Alver, M, Amini, M, Boissel, M, Chai, J F, Chen, X, Divers, J, Evangelou, E, Gao, C, Graff, M, Harris, S E, He, M, Milaneschi, Y, Yuan, J-M, Penninx, B W J H, Lifelines Cohort Study, Weir, D R, Franks, P W, Rotter, J I, Kooperberg, C B, Gauderman, W J, Psaty, B M, Rice, K M, Munroe, P B, Fornage, M, Cupples, L A, Rotimi, C N, Morrison, A C, Rao, D C & Loos, R J F 2019, ' Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity ', Nature Communications, vol. 10, no. 1, 376 . https://doi.org/10.1038/s41467-018-08008-wTest
Nature Communications, 10
Nature Communications, 10:376. Nature Publishing Group
Nature Communications, 2019, 10 (1), pp.376. ⟨10.1038/s41467-018-08008-w⟩
Nat. Commun. 10:376 (2019)
Nature communications, vol. 10, no. 1, pp. 376

مصطلحات موضوعية: Genetics and Molecular Biology (all), Male, Genome-wide association study, 02 engineering and technology, Biochemistry, MESH: Genotype, MESH: Nerve Tissue Proteins, lcsh:Science, MESH: Lipid Metabolism, Aged, 80 and over, [STAT.AP]Statistics [stat]/Applications [stat.AP], MESH: Middle Aged, MESH: Asian Continental Ancestry Group, Kólesteról, Hispanic or Latino, MESH: Transcription Factors, MESH: European Continental Ancestry Group, Lipids, ddc, 3. Good health, REVEAL, Cholesterol, MESH: Young Adult, Science & Technology - Other Topics, MESH: Membrane Proteins, MESH: Cholesterol, HDL, Hispanic Americans, 0210 nano-technology, Erfðarannsóknir, MESH: Cholesterol, LDL, MESH: Triglycerides, Genotype, Genetic Loci, Lipid Metabolism, Science, European Continental Ancestry Group, LIM-Homeodomain Proteins, Locus (genetics), EXERCISE, Adolescent, Adult, African Continental Ancestry Group/genetics, Aged, Asian Continental Ancestry Group/genetics, Brazil, Calcium-Binding Proteins/genetics, Cholesterol/blood, Cholesterol, HDL/blood, Cholesterol, HDL/genetics, Cholesterol, LDL/blood, Cholesterol, LDL/genetics, European Continental Ancestry Group/genetics, Exercise, Female, Genetic Loci/genetics, Genome-Wide Association Study, Hispanic Americans/genetics, Humans, LIM-Homeodomain Proteins/genetics, Lipid Metabolism/genetics, Lipids/blood, Lipids/genetics, Membrane Proteins/genetics, Microtubule-Associated Proteins/genetics, Middle Aged, Muscle Proteins/genetics, Nerve Tissue Proteins/genetics, Transcription Factors/genetics, Triglycerides/blood, Triglycerides/genetics, Young Adult, General Biochemistry, Genetics and Molecular Biology, Article, White People, CARBOXYLASE, 03 medical and health sciences, Physics and Astronomy (all), MESH: Muscle Proteins, Asian People, Lifelines Cohort Study, SNP, METAANALYSIS, Ancestry, MESH: Adolescent, Biochemistry, Genetics and Molecular Biology (all), MESH: Humans, Science & Technology, Calcium-Binding Proteins, MESH: Adult, MESH: Microtubule-Associated Proteins, 030104 developmental biology, chemistry, MESH: Genome-Wide Association Study, lcsh:Q, MESH: African Continental Ancestry Group, Chemistry (all), [INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM], MESH: Brazil, MESH: Female, Transcription Factors, 0301 basic medicine, General Physics and Astronomy, Blood lipids, Muscle Proteins, MESH: Calcium-Binding Proteins, chemistry.chemical_compound, MESH: Aged, 80 and over, MESH: Cholesterol, WIDE ASSOCIATION, African Continental Ancestry Group, Genetics, MESH: Aged, Multidisciplinary, Public Health, Global Health, Social Medicine and Epidemiology, 021001 nanoscience & nanotechnology, Multidisciplinary Sciences, lipids (amino acids, peptides, and proteins), Medical Genetics, [STAT.ME]Statistics [stat]/Methodology [stat.ME], Microtubule-Associated Proteins, Asian Continental Ancestry Group, Black People, Nerve Tissue Proteins, Biology, MESH: Genetic Loci, MD Multidisciplinary, Triglycerides, Medicinsk genetik, MESH: LIM-Homeodomain Proteins, Triglyceride, MESH: Hispanic Americans, Cholesterol, HDL, Genome-wide analyses, Membrane Proteins, Lipid metabolism, General Chemistry, Cholesterol, LDL, Arfgengi, MESH: Lipids, MESH: Male, Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi, INDIVIDUALS, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, MESH: Exercise, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie

وصف الملف: application/pdf; ELETTRONICO

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0762057e28a365b8dbed4f0bf77d1b25Test
http://hdl.handle.net/10044/1/66702Test

المؤلفون: Kroes, Hester Y, Monroe, Glen R, van der Zwaag, Bert, Duran, Karen J, de Kovel, Carolien G, van Roosmalen, Mark J, Harakalova, Magdalena, Nijman, Ies J, Kloosterman, Wigard P, Giles, Rachel H, Knoers, Nine V A M, van Haaften, Gijs

المصدر: Kroes , H Y , Monroe , G R , van der Zwaag , B , Duran , K J , de Kovel , C G , van Roosmalen , M J , Harakalova , M , Nijman , I J , Kloosterman , W P , Giles , R H , Knoers , N V A M & van Haaften , G 2016 , ' Joubert syndrome : genotyping a Northern European patient cohort ' , EJHG , vol. 24 , no. 2 , pp. 214-220 . https://doi.org/10.1038/ejhg.2015.84Test ; ISSN:1018-4813

مصطلحات موضوعية: Abnormalities, Multiple/diagnosis, Adaptor Proteins, Signal Transducing/genetics, Adolescent, Cerebellum/abnormalities, Child, Preschool, Eye Abnormalities/diagnosis, Female, Genetic Counseling, Genotype, High-Throughput Nucleotide Sequencing, Humans, Infant, Kidney Diseases, Cystic/diagnosis, Male, Membrane Proteins/genetics, Pathology, Molecular, Proteins/genetics, Retina/abnormalities, Young Adult

الإتاحة: https://doi.org/10.1038/ejhg.2015.84Test
http://hdl.handle.net/11370/01daa816-81eb-4be5-a3b7-183021192272Test
https://research.rug.nl/en/publications/joubert-syndromeTest(01daa816-81eb-4be5-a3b7-183021192272).html

المؤلفون: Ies J Nijman, Wigard P. Kloosterman, Mark van Roosmalen, Magdalena Harakalova, Rachel H. Giles, Carolien G.F. de Kovel, Gijs van Haaften, Karen Duran, Nine V A M Knoers, Hester Y. Kroes, Bert van der Zwaag, Glen R. Monroe

المصدر: EJHG, 24(2), 214-220. Nature Publishing Group
European Journal of Human Genetics

مصطلحات موضوعية: 0301 basic medicine, Male, Signal Transducing/genetics, TMEM67, Adaptor Proteins, Signal Transducing/genetics, Bioinformatics, Cerebellum, Pathology, Eye Abnormalities, Pathology, Molecular, Child, Genetics (clinical), Genetics, Sanger sequencing, education.field_of_study, Cystic/diagnosis, Adaptor Proteins, High-Throughput Nucleotide Sequencing, Eye Abnormalities/diagnosis, Kidney Diseases, Cystic, Child, Preschool, Proteins/genetics, symbols, Kidney Diseases, Cerebellum/abnormalities, Female, Abnormalities, medicine.medical_specialty, Abnormalities, Multiple/diagnosis, Adolescent, Genotype, Population, Genetic Counseling, Consanguinity, Biology, CC2D2A, Retina, Article, Joubert syndrome, 03 medical and health sciences, symbols.namesake, Young Adult, Molecular genetics, medicine, Humans, Abnormalities, Multiple, Membrane Proteins/genetics, Preschool, education, Kidney Diseases, Cystic/diagnosis, Adaptor Proteins, Signal Transducing, Multiple/diagnosis, Genetic heterogeneity, Retina/abnormalities, Molecular, Membrane Proteins, Proteins, Infant, medicine.disease, Adaptor Proteins, Vesicular Transport, Cytoskeletal Proteins, 030104 developmental biology

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efd11d8828c702d788ff0fb87ebf3437Test
https://research.rug.nl/en/publications/01daa816-81eb-4be5-a3b7-183021192272Test

المؤلفون: Smeesters, Pierre, Vergison, Anne, Junior, Dioclécio Campos, Van Melderen, Laurence

المصدر: International journal of antimicrobial agents, 34 (1

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Adolescent, Anti-Bacterial Agents -- pharmacology, Antigens, Bacterial -- genetics, Bacterial Outer Membrane Proteins -- genetics, Bacterial Proteins -- genetics, Bacterial Typing Techniques, Belgium, Brazil, Carrier Proteins -- genetics, Child, Preschool, DNA Gyrase -- genetics, DNA Mutational Analysis, DNA Topoisomerase IV -- genetics, Drug Resistance, Bacterial, Fluoroquinolones -- pharmacology, Genotype, Humans, Infant, Newborn, Molecular Epidemiology, Molecular Sequence Data, Mutation, Missense, Phylogeny, Streptococcal Infections -- microbiology, Streptococcus pyogenes -- drug effects

وصف الملف: 1 full-text file(s): application/pdf

العلاقة: uri/info:doi/10.1016/j.ijantimicag.2009.01.012; uri/info:pii/S0924-8579(09)00058-2; uri/info:pmid/19269141; uri/info:scp/67349252433; https://dipot.ulb.ac.be/dspace/bitstream/2013/51685/1/Elsevier_26803.pdfTest; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51685Test

الإتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51685Test
https://dipot.ulb.ac.be/dspace/bitstream/2013/51685/1/Elsevier_26803.pdfTest