المؤلفون: Le Goff, Caroline

المصدر: Experimental Physiology, 108 (10), 1257 - 1258 (2023-10)

مصطلحات موضوعية: Galectin-3, cardiac fibrosis, endurance, sport, suppression of tumorigenicity 2, Biomarkers, Galectin 3, IL1RL1 protein, human, Interleukin-1 Receptor-Like 1 Protein, LGALS3 protein, human, Humans, Biomarkers/analysis, Fibrosis/genetics, Fibrosis/pathology, Galectin 3/analysis, Galectin 3/genetics, Heart Diseases/genetics, Heart Diseases/metabolism, Heart Diseases/pathology, Interleukin-1 Receptor-Like 1 Protein/analysis, Interleukin-1 Receptor-Like 1 Protein/genetics, Sports, Fibrosis, Heart Diseases, Physiology, Nutrition and Dietetics, Physiology (medical), Human health sciences, Cardiovascular & respiratory systems, Sciences de la santé humaine, Systèmes cardiovasculaire & respiratoire

العلاقة: urn:issn:0958-0670; urn:issn:1469-445X

الوصول الحر: https://orbi.uliege.be/handle/2268/311817Test

المؤلفون: Smeland, Marie F, McClenaghan, Conor, Roessler, Helen I, Savelberg, Sanne, Hansen, Geir Åsmund Myge, Hjellnes, Helene, Arntzen, Kjell Arne, Müller, Kai Ivar, Dybesland, Andreas Rosenberger, Harter, Theresa, Sala-Rabanal, Monica, Emfinger, Chris H, Huang, Yan, Singareddy, Soma S, Gunn, Jamie, Wozniak, David F, Kovacs, Attila, Massink, Maarten, Tessadori, Federico, Kamel, Sarah M, Bakkers, Jeroen, Remedi, Maria S, Van Ghelue, Marijke, Nichols, Colin G, van Haaften, Gijs

المساهمون: Genetica Groep Van Haaften, Genetica Sectie Genoomdiagnostiek, Child Health, Medische Fysiologie, Circulatory Health, CMM Sectie Genomics and Bioinformatics, Cancer

مصطلحات موضوعية: Adenosine Triphosphate/metabolism, Adolescent, Adult, Amino Acid Sequence, Animals, Cardiomegaly/genetics, Cell Line, Channelopathies/metabolism, Child, Disease Models, Animal, Facies, Female, Genetic Diseases, X-Linked/genetics, Genetic Predisposition to Disease/genetics, Heart, Heart Diseases/genetics, Homozygote, Humans, Hypertrichosis/genetics, Intellectual Disability/metabolism, Male, Mediator Complex/metabolism, Membrane Proteins/metabolism, Mice, Muscular Diseases/genetics, Mutation, Neurodevelopmental Disorders/genetics, Osteochondrodysplasias/genetics

وصف الملف: application/pdf

العلاقة: https://dspace.library.uu.nl/handle/1874/439266Test

الإتاحة: https://dspace.library.uu.nl/handle/1874/439266Test

المؤلفون: Warrington, N.M., Beaumont, R.N., Horikoshi, M., Day, F.R., Helgeland, Ø., Laurin, C., Bacelis, J., Peng, S., Hao, K., Feenstra, B., Wood, A.R., Mahajan, A., Tyrrell, J., Robertson, N.R., Rayner, N.W., Qiao, Z., Moen, G.H., Vaudel, M., Marsit, C.J., Chen, J., Nodzenski, M., Schnurr, T.M., Zafarmand, M.H., Bradfield, J.P., Grarup, N., Kooijman, M.N., Li-Gao, R., Geller, F., Ahluwalia, T.S., Paternoster, L., Rueedi, R., Huikari, V., Hottenga, J.J., Lyytikäinen, L.P., Cavadino, A., Metrustry, S., Cousminer, D.L., Wu, Y., Thiering, E., Wang, C.A., Have, C.T., Vilor-Tejedor, N., Joshi, P.K., Painter, J.N., Ntalla, I., Myhre, R., Pitkänen, N., van Leeuwen, E.M., Joro, R., Lagou, V., Richmond, R.C., Espinosa, A., Barton, S.J., Inskip, H.M., Holloway, J.W., Santa-Marina, L., Estivill, X., Ang, W., Marsh, J.A., Reichetzeder, C., Marullo, L., Hocher, B., Lunetta, K.L., Murabito, J.M., Relton, C.L., Kogevinas, M., Chatzi, L., Allard, C., Bouchard, L., Hivert, M.F., Zhang, G., Muglia, L.J., Heikkinen, J., Morgen, C.S., van Kampen, AHC, van Schaik, BDC, Mentch, F.D., Langenberg, C., Luan, J., Scott, R.A., Zhao, J.H., Hemani, G., Ring, S.M., Bennett, A.J., Gaulton, K.J., Fernandez-Tajes, J., van Zuydam, N.R., Medina-Gomez, C., de Haan, H.G., Rosendaal, F.R., Kutalik, Z., Marques-Vidal, P., Das, S., Willemsen, G., Mbarek, H., Müller-Nurasyid, M., Standl, M., Appel, EVR, Fonvig, C.E., Trier, C., van Beijsterveldt, CEM, Murcia, M., Bustamante, M., Bonas-Guarch, S., Hougaard, D.M., Mercader, J.M., Linneberg, A., Schraut, K.E., Lind, P.A., Medland, S.E., Shields, B.M., Knight, B.A., Chai, J.F., Panoutsopoulou, K., Bartels, M., Sánchez, F., Stokholm, J., Torrents, D., Vinding, R.K., Willems, S.M., Atalay, M., Chawes, B.L., Kovacs, P., Prokopenko, I., Tuke, M.A., Yaghootkar, H., Ruth, K.S., Jones, S.E., Loh, P.R., Murray, A., Weedon, M.N., Tönjes, A., Stumvoll, M., Michaelsen, K.F., Eloranta, A.M., Lakka, T.A., van Duijn, C.M., Kiess, W., Körner, A., Niinikoski, H., Pahkala, K., Raitakari, O.T., Jacobsson, B., Zeggini, E., Dedoussis, G.V., Teo, Y.Y., Saw, S.M., Montgomery, G.W., Campbell, H., Wilson, J.F., Vrijkotte, TGM, Vrijheid, M., de Geus, EJCN, Hayes, M.G., Kadarmideen, H.N., Holm, J.C., Beilin, L.J., Pennell, C.E., Heinrich, J., Adair, L.S., Borja, J.B., Mohlke, K.L., Eriksson, J.G., Widén, E.E., Hattersley, A.T., Spector, T.D., Kähönen, M., Viikari, J.S., Lehtimäki, T., Boomsma, D.I., Sebert, S., Vollenweider, P., Sørensen, TIA, Bisgaard, H., Bønnelykke, K., Murray, J.C., Melbye, M., Nohr, E.A., Mook-Kanamori, D.O., Rivadeneira, F., Hofman, A., Felix, J.F., Jaddoe, VWV, Hansen, T., Pisinger, C., Vaag, A.A., Pedersen, O., Uitterlinden, A.G., Järvelin, M.R., Power, C., Hyppönen, E., Scholtens, D.M., Lowe, W.L., Davey Smith, G., Timpson, N.J., Morris, A.P., Wareham, N.J., Hakonarson, H., Grant, SFA, Frayling, T.M., Lawlor, D.A., Njølstad, P.R., Johansson, S., Ong, K.K., McCarthy, M.I., Perry, JRB, Evans, D.M., Freathy, R.M.

المساهمون: EGG Consortium

المصدر: Nature genetics, vol. 51, no. 5, pp. 804-814

مصطلحات موضوعية: Adult, Birth Weight/genetics, Blood Pressure/genetics, Body Height/genetics, Diabetes Mellitus, Type 2/etiology, Type 2/genetics, Female, Fetal Development/genetics, Genetic Predisposition to Disease, Genome-Wide Association Study, Heart Diseases/etiology, Heart Diseases/genetics, Humans, Infant, Newborn, Male, Maternal Inheritance/genetics, Maternal-Fetal Exchange/genetics, Metabolic Diseases/etiology, Metabolic Diseases/genetics, Models, Genetic, Polymorphism, Single Nucleotide, Pregnancy, Risk Factors

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31043758; info:eu-repo/semantics/altIdentifier/eissn/1546-1718; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_56910884CABD6; https://serval.unil.ch/notice/serval:BIB_56910884CABDTest; urn:issn:1061-4036; https://serval.unil.ch/resource/serval:BIB_56910884CABD.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_56910884CABD6Test

الإتاحة: https://doi.org/10.1038/s41588-019-0403-1Test
https://serval.unil.ch/notice/serval:BIB_56910884CABDTest
https://serval.unil.ch/resource/serval:BIB_56910884CABD.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_56910884CABD6Test

المؤلفون: Chen, Huimei, Moreno-Moral, Aida, Pesce, Francesco, Devapragash, Nithya, Mancini, Massimiliano, Heng, Ee Ling, Rotival, Maxime, Srivastava, Prashant, K, Harmston, Nathan, Shkura, Kirill, Rackham, Owen, J L, Yu, Wei-Ping, Sun, Xi-Ming, Gui Zhen Tee, Nicole, Li San Tan, Elisabeth, Barton, Paul, J R, Felkin, Leanne, E, Lara-Pezzi, Enrique, Angelini, Gianni, Beltrami, Cristina, Pravenec, Michal, Schafer, Sebastian, Bottolo, Leonardo, Hubner, Norbert, Emanueli, Costanza, Cook, Stuart, Petretto, Enrico

المساهمون: Cardiovascular and Metabolic Disorders Singapor (cvmd), Duke-NUS Medical School Singapore, Università degli studi di Bari Aldo Moro = University of Bari Aldo Moro (UNIBA), Ospedale San Giovanni di Dio, Firenze, National Heart and Lung Institute London (NHLI), Imperial College London-Royal Brompton and Harefield NHS Foundation Trust, Génétique Evolutive Humaine - Human Evolutionary Genetics, Institut Pasteur Paris (IP)-Centre National de la Recherche Scientifique (CNRS), Faculty of Medicine London, UK, Imperial College London, Agency for science, technology and research Singapore (A*STAR), Institute of Molecular and Cell Biology, National University of Singapore (NUS)-Agency for science, technology and research Singapore (A*STAR), MRC London Institute of Medical Sciences (LMC), National Heart Centre Singapore (NHCS), Royal Brompton and Harefield NHS Foundation Trust, Cardiovascular Research Centre London, Centro Nacional de Investigaciones Cardiovasculares Carlos III Madrid, Spain (CNIC), Instituto de Salud Carlos III Madrid (ISC), University of Bristol Bristol, Institute of Physiology Prague, Czech Academy of Sciences Prague (CAS), University of Cambridge UK (CAM), The Alan Turing Institute, MRC Biostatistics Unit Cambridge, UK, Max Delbrück Center for Molecular Medicine Berlin (MDC), Helmholtz-Gemeinschaft = Helmholtz Association, German Center for Cardiovascular Research (DZHK), Berlin Institute of Health (BIH), Charité - UniversitätsMedizin = Charité - University Hospital Berlin, The research was primarily supported by National Medical Research Council (NMRC) Singapore grant NMRC/CBRG/0106/2016 (to E.P.) and the British Heart Foundation (BHF) Ph.D. Studentship grant FS/11/25/28740 (to E.P). We acknowledge additional funding support from European Union FP7 CardioNeT-ITN-289600 (to E.L.-P., S.A.C., and P.J.R.B.), Heart Research UK (to P.J.R.B.), NIHR CV BRU of Royal Brompton and Harefield, NHS Foundation Trust (to S.A.C. and P.J.R.B.), BHF (to S.A.C.), Leducq Foundation (to S.A.C.), MRC UK (to S.A.C.), BHF Program Grant no. RG/15/5/31446 (to C.E. and E.P.). M.P. was supported by Praemium Academiae award of the Czech Academy of Sciences and grant 14-36804G from the Czech Science Foundation., We wish to thank Dr. Jacques Behmoaras for contributing critical and constructive comments to the manuscript., European Project: 289600,EC:FP7:PEOPLE,FP7-PEOPLE-2011-ITN,CARDIONET(2012)

المصدر: ISSN: 2041-1723.

مصطلحات موضوعية: Ubiquitin ligases, Cardiomyopathies, MESH: Adolescent, MESH: Adult, MESH: Fibrosis / genetics, MESH: Fibrosis / metabolism, MESH: Mice, Transgenic, MESH: Gene Regulatory Networks, MESH: Genetic Predisposition to Disease* / genetics, MESH: Heart Diseases / genetics, MESH: Heart Diseases / metabolism, MESH: Humans, MESH: Male, MESH: Ubiquitin-Protein Ligases / metabolism, MESH: Middle Aged, MESH: Aged, MESH: Protein Isoforms, MESH: Smad2 Protein / genetics, MESH: Smad2 Protein / metabolism, MESH: Transforming Growth Factor beta / metabolism, MESH: Ubiquitin-Protein Ligases / genetics, MESH: Young Adult, MESH: Gene Expression Regulation, MESH: Animals, MESH: Cardiomyopathies / genetics, MESH: Cardiomyopathies / metabolism, MESH: Extracellular Matrix Proteins / metabolism, MESH: Female, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/31399586; info:eu-repo/grantAgreement/EC/FP7/289600/EU/Translational Training network on the Cellular and Molecular Bases of Heart Homeostasis and Repair/CARDIONET; pasteur-02868982; https://pasteur.hal.science/pasteur-02868982Test; https://pasteur.hal.science/pasteur-02868982/documentTest; https://pasteur.hal.science/pasteur-02868982/file/Chen_Nature%20Communication_2019.pdfTest; PUBMED: 31399586; PUBMEDCENTRAL: PMC6689010

الإتاحة: https://doi.org/10.1038/s41467-019-11551-9Test
https://pasteur.hal.science/pasteur-02868982Test
https://pasteur.hal.science/pasteur-02868982/documentTest
https://pasteur.hal.science/pasteur-02868982/file/Chen_Nature%20Communication_2019.pdfTest

المؤلفون: Kristoffersson, Ulf

المصدر: Läkartidningen. 102(11):7-826

مصطلحات موضوعية: Biomedical Research, Cardiovascular Diseases: genetics, Heart Diseases: genetics, Humans, Knowledge, Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics

الوصول الحر: https://lup.lub.lu.se/record/136172Test
http://ltarkiv.lakartidningen.se/artNo29939Test

المؤلفون: Balogh, Johanna, Merisckay, M, Li, Z, Paulin, D, Arner, Anders

المصدر: Cardiovascular Research. 53(2):439-450

مصطلحات موضوعية: Myosins/analysis, Perfusion, Support, Non-U.S. Gov't, Inbred C57BL, Mice, Intermediate Filaments/metabolism, In Vitro, Actins/analysis, Calcium/metabolism, Animal, Myocardium/metabolism, Myocardial Contraction/*physiology, Transgenic, Desmin/genetics/metabolism/*physiology, Female, Heart Diseases/genetics/*physiopathology, Medicin och hälsovetenskap, Klinisk medicin, Kardiologi, Medical and Health Sciences, Clinical Medicine, Cardiac and Cardiovascular Systems

الوصول الحر: https://lup.lub.lu.se/record/106186Test
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=11827695&dopt=AbstractTest
http://dx.doi.org/10.1016/S0008-6363Test(01)00500-4

المؤلفون: Lasserre, A.M., Strippoli, M.F., Glaus, J., Gholam-Rezaee, M., Vandeleur, C.L., Castelao, E., Marques-Vidal, P., Waeber, G., Vollenweider, P., Preisig, M.

المصدر: Molecular psychiatry, vol. 22, no. 7, pp. 1026-1034

مصطلحات موضوعية: Adult, Blood Glucose/metabolism, Cholesterol, HDL/blood, Comorbidity, Depression/complications, Depressive Disorder, Major/classification, Major/complications, Major/diagnosis, Major/metabolism, Female, Heart Diseases/genetics, Heart Diseases/metabolism, Humans, Incidence, Life Style, Male, Metabolic Diseases/genetics, Metabolic Diseases/metabolism, Metabolic Syndrome X/epidemiology, Middle Aged, Prospective Studies, Risk Factors, Switzerland, Triglycerides/blood, Waist Circumference

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/27725658; info:eu-repo/semantics/altIdentifier/eissn/1476-5578; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_4C8F5CF44AE36; https://serval.unil.ch/notice/serval:BIB_4C8F5CF44AE3Test; urn:issn:1359-4184; https://serval.unil.ch/resource/serval:BIB_4C8F5CF44AE3.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_4C8F5CF44AE36Test

الإتاحة: https://doi.org/10.1038/mp.2016.178Test
https://serval.unil.ch/notice/serval:BIB_4C8F5CF44AE3Test
https://serval.unil.ch/resource/serval:BIB_4C8F5CF44AE3.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_4C8F5CF44AE36Test

المؤلفون: Bagnall, Richard D, Singer, Emma S, Wacker Bou Puigdefabregas, Julie Caroline, Nowak, Natalie, Ingles, Jodie, King, Ingrid, Macciocca, Ivan, Crowe, Joshua, Ronan, Anne, Weintraub, Robert G, Semsarian, Christopher

المصدر: ISSN: 2574-8300 ; Circulation. Genomic and precision medicine, vol. 15, no. 6 (2022) e003686.

مصطلحات موضوعية: Cardiomyopathy, Child, Family, Genetics, Sarcomere, Adult, Humans, Dilated / genetics, Cardiomyopathies / genetics, Genetic Testing, Hypertrophic / genetics, Heart Diseases / genetics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36252119; https://archive-ouverte.unige.ch/unige:174517Test; unige:174517

الإتاحة: https://doi.org/10.1161/CIRCGEN.121.003686Test
https://archive-ouverte.unige.ch/unige:174517Test

المؤلفون: Lu, Y., Day, F.R., Gustafsson, S., Buchkovich, M.L., Na, J., Bataille, V., Cousminer, D.L., Dastani, Z., Drong, A.W., Esko, T., Evans, D.M., Falchi, M., Feitosa, M.F., Ferreira, T., Hedman, Å.K., Haring, R., Hysi, P.G., Iles, M.M., Justice, A.E., Kanoni, S., Lagou, V., Li, R., Li, X., Locke, A., Lu, C., Mägi, R., Perry, J.R., Pers, T.H., Qi, Q., Sanna, M., Schmidt, E.M., Scott, W.R., Shungin, D., Teumer, A., Vinkhuyzen, A.A., Walker, R.W., Westra, H.J., Zhang, M., Zhang, W., Zhao, J.H., Zhu, Z., Afzal, U., Ahluwalia, T.S., Bakker, S.J., Bellis, C., Bonnefond, A., Borodulin, K., Buchman, A.S., Cederholm, T., Choh, A.C., Choi, H.J., Curran, J.E., de Groot, L.C., De Jager, P.L., Dhonukshe-Rutten, R.A., Enneman, A.W., Eury, E., Evans, D.S., Forsen, T., Friedrich, N., Fumeron, F., Garcia, M.E., Gärtner, S., Han, B.G., Havulinna, A.S., Hayward, C., Hernandez, D., Hillege, H., Ittermann, T., Kent, J.W., Kolcic, I., Laatikainen, T., Lahti, J., Mateo Leach, I., Lee, C.G., Lee, J.Y., Liu, T., Liu, Y., Lobbens, S., Loh, M., Lyytikäinen, L.P., Medina-Gomez, C., Michaëlsson, K., Nalls, M.A., Nielson, C.M., Oozageer, L., Pascoe, L., Paternoster, L., Polašek, O., Ripatti, S., Sarzynski, M.A., Shin, C.S., Narančić, N.S., Spira, D., Srikanth, P., Steinhagen-Thiessen, E., Sung, Y.J., Swart, K.M., Taittonen, L., Tanaka, T., Tikkanen, E., van der Velde, N., van Schoor, N.M., Verweij, N., Wright, A.F., Yu, L., Zmuda, J.M., Eklund, N., Forrester, T., Grarup, N., Jackson, A.U., Kristiansson, K., Kuulasmaa, T., Kuusisto, J., Lichtner, P., Luan, J., Mahajan, A., Männistö, S., Palmer, C.D., Ried, J.S., Scott, R.A., Stancáková, A., Wagner, P.J., Demirkan, A., Döring, A., Gudnason, V., Kiel, D.P., Kühnel, B., Mangino, M., Mcknight, B., Menni, C., O'Connell, J.R., Oostra, B.A., Shuldiner, A.R., Song, K., Vandenput, L., van Duijn, C.M., Vollenweider, P., White, C.C., Boehnke, M., Boettcher, Y., Cooper, R.S., Forouhi, N.G., Gieger, C., Grallert, H., Hingorani, A., Jørgensen, T., Jousilahti, P., Kivimaki, M., Kumari, M., Laakso, M., Langenberg, C., Linneberg, A., Luke, A., Mckenzie, C.A., Palotie, A., Pedersen, O., Peters, A., Strauch, K., Tayo, B.O., Wareham, N.J., Bennett, D.A., Bertram, L., Blangero, J., Blüher, M., Bouchard, C., Campbell, H., Cho, N.H., Cummings, S.R., Czerwinski, S.A., Demuth, I., Eckardt, R., Eriksson, J.G., Ferrucci, L., Franco, O.H., Froguel, P., Gansevoort, R.T., Hansen, T., Harris, T.B., Hastie, N., Heliövaara, M., Hofman, A., Jordan, J.M., Jula, A., Kähönen, M., Kajantie, E., Knekt, P.B., Koskinen, S., Kovacs, P., Lehtimäki, T., Lind, L., Orwoll, E.S., Osmond, C., Perola, M., Pérusse, L., Raitakari, O.T., Rankinen, T., Rao, D.C., Rice, T.K., Rivadeneira, F., Rudan, I., Salomaa, V., Sørensen, T.I., Stumvoll, M., Tönjes, A., Towne, B., Tranah, G.J., Tremblay, A., Uitterlinden, A.G., van der Harst, P., Vartiainen, E., Viikari, J.S., Vitart, V., Vohl, M.C., Völzke, H., Walker, M., Wallaschofski, H., Wild, S., Wilson, J.F., Yengo, L., Bishop, D.T., Borecki, I.B., Chambers, J.C., Cupples, L.A., Dehghan, A., Deloukas, P., Fatemifar, G., Fox, C., Furey, T.S., Franke, L., Han, J., Hunter, D.J., Karjalainen, J., Karpe, F., Kaplan, R.C., Kooner, J.S., McCarthy, M.I., Murabito, J.M., Morris, A.P., Bishop, J.A., North, K.E., Ohlsson, C., Ong, K.K., Prokopenko, I., Richards, J.B., Schadt, E.E., Spector, T.D., Widén, E., Willer, C.J., Yang, J., Ingelsson, E., Mohlke, K.L., Hirschhorn, J.N., Pospisilik, J.A., Zillikens, M.C., Lindgren, C., Kilpeläinen, T.O., Loos, R.J.

المصدر: Nature Communications, vol. 7, pp. 10495

مصطلحات موضوعية: Adiposity/genetics, Animals, Drosophila melanogaster/genetics, Drosophila melanogaster/metabolism, Gene Expression Regulation/physiology, Gene Knockdown Techniques, Genetic Predisposition to Disease, Genome-Wide Association Study, Heart Diseases/genetics, Humans, Quantitative Trait Loci/genetics

وصف الملف: application/pdf

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/26833246; info:eu-repo/semantics/altIdentifier/eissn/2041-1723; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_3AD8785589CA5; https://serval.unil.ch/notice/serval:BIB_3AD8785589CATest; urn:issn:2041-1723; https://serval.unil.ch/resource/serval:BIB_3AD8785589CA.P001/REF.pdfTest; http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_3AD8785589CA5Test

الإتاحة: https://doi.org/10.1038/ncomms10495Test
https://serval.unil.ch/notice/serval:BIB_3AD8785589CATest
https://serval.unil.ch/resource/serval:BIB_3AD8785589CA.P001/REF.pdfTest
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_3AD8785589CA5Test

المؤلفون: Hertz, Christin Loeth, Christiansen, Sofie Lindgren, Larsen, Maiken Kudahl, Dahl, Morten, Ferrero-Miliani, Laura, Weeke, Peter Ejvin, Pedersen, Oluf, Hansen, Torben, Grarup, Niels, Ottesen, Gyda Lolk, Frank-Hansen, Rune, Banner, Jytte, Morling, Niels

المصدر: Hertz , C L , Christiansen , S L , Larsen , M K , Dahl , M , Ferrero-Miliani , L , Weeke , P E , Pedersen , O , Hansen , T , Grarup , N , Ottesen , G L , Frank-Hansen , R , Banner , J & Morling , N 2016 , ' Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases ' , European Journal of Human Genetics , vol. 24 , no. 6 , pp. 817-822 . https://doi.org/10.1038/ejhg.2015.198Test

مصطلحات موضوعية: Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Heart Diseases/genetics, High-Throughput Nucleotide Sequencing, Humans, Infant, Newborn, Male, Open Reading Frames, Polymorphism, Genetic, Sequence Analysis, DNA, Sudden Infant Death/genetics

العلاقة: https://portal.findresearcher.sdu.dk/da/publications/252bdc5b-b362-4c6c-a7f5-0e343f9989e5Test

الإتاحة: https://doi.org/10.1038/ejhg.2015.198Test
https://portal.findresearcher.sdu.dk/da/publications/252bdc5b-b362-4c6c-a7f5-0e343f9989e5Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867441/pdf/ejhg2015198a.pdfTest