Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Sridharan, Rajamani"'
Autor:
Hongfei Ge, Gongxin Liu, Tracy M. Yamawaki, Caroline Tao, Shawn T. Alexander, Kimberly Ly, Preston Fordstrom, Artem A. Shkumatov, Chi-Ming Li, Sridharan Rajamani, Mingyue Zhou, Brandon Ason
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Heart failure (HF) and cardiac arrhythmias share overlapping pathological mechanisms that act cooperatively to accelerate disease pathogenesis. Cardiac fibrosis is associated with both pathological conditions. Our previous work identified a
Externí odkaz:
https://doaj.org/article/2f56b69ee6d54d0caa04b1fc1525bcf7
Autor:
Elisa Darkow, Dilmurat Yusuf, Sridharan Rajamani, Rolf Backofen, Peter Kohl, Ursula Ravens, Rémi Peyronnet
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 13, p 10961 (2023)
The cardiac cell mechanical environment changes on a beat-by-beat basis as well as in the course of various cardiac diseases. Cells sense and respond to mechanical cues via specialized mechano-sensors initiating adaptive signaling cascades. With the
Externí odkaz:
https://doaj.org/article/c284abcd34964d36b1db2fc631f21d46
Autor:
Kristjan Norland, Gardar Sveinbjornsson, Rosa B. Thorolfsdottir, Olafur B. Davidsson, Vinicius Tragante, Sridharan Rajamani, Anna Helgadottir, Solveig Gretarsdottir, Jessica van Setten, Folkert W. Asselbergs, Jon Th. Sverrisson, Sigurdur S. Stephensen, Gylfi Oskarsson, Emil L. Sigurdsson, Karl Andersen, Ragnar Danielsen, Gudmundur Thorgeirsson, Unnur Thorsteinsdottir, David O. Arnar, Patrick Sulem, Hilma Holm, Daniel F. Gudbjartsson, Kari Stefansson
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Aberrant morphology of the QRS complex in an electrocardiogram can be associated with cardiac morbidity and mortality. Here, the authors perform genome-wide association studies for ten measures of the QRS complex in 81,192 individuals and find 86 pre
Externí odkaz:
https://doaj.org/article/013cd3a5a1cd47ec9888561074de6288
Autor:
Elisa Darkow, Thong T. Nguyen, Marina Stolina, Fabian A. Kari, Constanze Schmidt, Felix Wiedmann, István Baczkó, Peter Kohl, Sridharan Rajamani, Ursula Ravens, Rémi Peyronnet
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
In search of more efficacious and safe pharmacological treatments for atrial fibrillation (AF), atria-selective antiarrhythmic agents have been promoted that target ion channels principally expressed in the atria. This concept allows one to engage an
Externí odkaz:
https://doaj.org/article/ddf44bced1ca4c75b664065aa511da6e
Autor:
Peyronnet, Elisa Darkow, Dilmurat Yusuf, Sridharan Rajamani, Rolf Backofen, Peter Kohl, Ursula Ravens, Rémi
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 13; Pages: 10961
The cardiac cell mechanical environment changes on a beat-by-beat basis as well as in the course of various cardiac diseases. Cells sense and respond to mechanical cues via specialized mechano-sensors initiating adaptive signaling cascades. With the
Autor:
Caroline Tao, Shawn T. Alexander, Sridharan Rajamani, Preston Fordstrom, Mingyue Zhou, Hongfei Ge, Gongxin Liu, Kimberly Ly, Tracy M. Yamawaki, Chi-Ming Li, Brandon Ason, Artem Shkumatov
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports
Scientific Reports
Heart failure (HF) and cardiac arrhythmias share overlapping pathological mechanisms that act cooperatively to accelerate disease pathogenesis. Cardiac fibrosis is associated with both pathological conditions. Our previous work identified a link betw
Autor:
Elisa Darkow, Dilmurat Yusuf, Sridharan Rajamani, Rolf Backofen, Peter Kohl, Ursula Ravens, Rémi Peyronnet
Cardiac cell mechanical environment changes on a beat-by-beat basis and also in the course of various cardiac diseases. Cells sense and adapt to such mechanical cues via specialized mechano-sensors mediating adaptive signaling cascades. Here, we repo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34109258ba43e76adf8c4f7bf360f072
https://doi.org/10.1101/2022.07.21.492231
https://doi.org/10.1101/2022.07.21.492231
Autor:
Gaetano Thiene, Leander Beekman, Sridharan Rajamani, Adrián Ruiz-Villalba, Antonius Baartscheer, Carol Ann Remme, Gerard A Marchal, Ingeborg van der Made, Esther E. Creemers, Mathilde R. Rivaud, Cristina Basso, Connie R. Bezzina, Toon A.B. van Veen, John A. Jansen, Luiz Belardinelli, Rianne Wolswinkel
Publikováno v:
Europace
EP Europace, 22(10), 1579-1589. Oxford University Press
EP Europace, 22(10), 1579-1589. Oxford University Press
Aims SCN5A mutations are associated with arrhythmia syndromes, including Brugada syndrome, long QT syndrome type 3 (LQT3), and cardiac conduction disease. Long QT syndrome type 3 patients display atrio-ventricular (AV) conduction slowing which may co
Autor:
Hongfei Ge, Gongxin Liu, Tracy M. Yamawaki, Caroline Tao, Shawn T. Alexander, Kimberly Ly, Preston Fordstrom, Artem A. Shkumatov, Chi-Ming Li, Sridharan Rajamani, Mingyue Zhou, Brandon Ason
Heart failure (HF) and cardiac arrhythmias share overlapping pathological mechanisms that act cooperatively to accelerate disease pathogenesis. Cardiac fibrosis is associated with both pathological conditions. Our previous work identified a link betw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ce3fe8820e3e500f4067a77295017a9
https://doi.org/10.21203/rs.3.rs-474251/v1
https://doi.org/10.21203/rs.3.rs-474251/v1
Autor:
Jon K. Sigurdsson, Gudmundur Thorgeirsson, Ingileif Jonsdottir, Søren Brunak, Mette Nyegaard, Bjarni Torfason, Henrik Ullum, Hildur M Aegisdottir, Gudmundur L. Norddahl, Stefan Jonsson, Hilma Holm, Lilja Stefansdottir, Christian Torp-Pedersen, Ben Michael Brumpton, Asmundur Oddsson, Daniel F. Gudbjartsson, Vinicius Tragante, Kristoffer Sølvsten Burgdorf, Kari Stefansson, Erna V. Ivarsdottir, Stefania Benonisdottir, Kristjan E. Hjorleifsson, Cristen J. Willer, Kristian Hveem, David O. Arnar, Gardar Sveinbjornsson, Sridharan Rajamani, Rosa B. Thorolfsdottir, Karina Banasik, Ole Birger Pedersen, Solveig Gretarsdottir, Atli S Valgardsson, David Westergaard, Erik Sørensen, Gudmar Thorleifsson, Peter Weeke, Unnur Thorsteinsdottir, Olafur B. Davidsson, Gisli H. Halldorsson, Michael L. Frigge, Anna Helgadottir, Wei Zhou, Patrick Sulem, Henning Bundgaard, Kaspar René Nielsen
Publikováno v:
Thorsteinsdottir, U, Gudbjartsson, D F, Holm, H, Stefansson, K & DBDS Genomic Consortium 2021, ' Genetic insight into sick sinus syndrome ', European Heart Journal, vol. 42, no. 20, pp. 1959-1971 . https://doi.org/10.1093/eurheartj/ehaa1108
Thorolfsdottir, R B, Sveinbjornsson, G, Aegisdottir, H M, Benonisdottir, S, Stefansdottir, L, Ivarsdottir, E V, Halldorsson, G H, Sigurdsson, J K, Torp-Pedersen, C, Weeke, P E, Brunak, S, Westergaard, D, Pedersen, O B, Sorensen, E, Nielsen, K R, Burgdorf, K S, Banasik, K, DBDS Genomic Consortium, Brumpton, B, Zhou, W, Oddsson, A, Tragante, V, Hjorleifsson, K E, Davidsson, O B, Rajamani, S, Jonsson, S, Torfason, B, Valgardsson, A S, Thorgeirsson, G, Frigge, M L, Thorleifsson, G, Norddahl, G L, Helgadottir, A, Gretarsdottir, S, Sulem, P, Jonsdottir, I, Willer, C J, Hveem, K, Bundgaard, H, Ullum, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Holm, H, Stefansson, K & Nyegaard, M 2021, ' Genetic insight into sick sinus syndrome ', European Heart Journal, vol. 42, no. 20, pp. 1959-1971 . https://doi.org/10.1093/eurheartj/ehaa1108
European Heart Journal
Thorolfsdottir, R B, Sveinbjornsson, G, Aegisdottir, H M, Benonisdottir, S, Stefansdottir, L, Ivarsdottir, E V, Halldorsson, G H, Sigurdsson, J K, Torp-Pedersen, C, Weeke, P E, Brunak, S, Westergaard, D, Pedersen, O B, Sorensen, E, Nielsen, K R, Burgdorf, K S, Banasik, K, Brumpton, B, Zhou, W, Oddsson, A, Tragante, V, Hjorleifsson, K E, Davidsson, O B, Rajamani, S, Jonsson, S, Torfason, B, Valgardsson, A S, Thorgeirsson, G, Frigge, M L, Thorleifsson, G, Norddahl, G L, Helgadottir, A, Gretarsdottir, S, Sulem, P, Jonsdottir, I, Willer, C J, Hveem, K, Bundgaard, H, Ullum, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Holm, H, Stefansson, K & DBDS Genomic Consortium (MN part of consortium) 2021, ' Genetic insight into sick sinus syndrome ', European Heart Journal . https://doi.org/10.1093/eurheartj/ehaa1108
Thorolfsdottir, R B, Sveinbjornsson, G, Aegisdottir, H M, Benonisdottir, S, Stefansdottir, L, Ivarsdottir, E V, Halldorsson, G H, Sigurdsson, J K, Torp-Pedersen, C, Weeke, P E, Brunak, S, Westergaard, D, Pedersen, O B, Sorensen, E, Nielsen, K R, Burgdorf, K S, Banasik, K, Brumpton, B, Zhou, W, Oddsson, A, Tragante, V, Hjorleifsson, K E, Davidsson, O B, Rajamani, S, Jonsson, S, Torfason, B, Valgardsson, A S, Thorgeirsson, G, Frigge, M L, Thorleifsson, G, Norddahl, G L, Helgadottir, A, Gretarsdottir, S, Sulem, P, Jonsdottir, I, Willer, C J, Hveem, K, Bundgaard, H, Ullum, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Holm, H, Stefansson, K & DBDS Genomic Consortium 2021, ' Genetic insight into sick sinus syndrome ', European Heart Journal, vol. 42, no. 20, pp. 1959-1971 . https://doi.org/10.1093/eurheartj/ehaa1108
Thorolfsdottir, R B, Sveinbjornsson, G, Aegisdottir, H M, Benonisdottir, S, Stefansdottir, L, Ivarsdottir, E V, Halldorsson, G H, Sigurdsson, J K, Torp-Pedersen, C, Weeke, P E, Brunak, S, Westergaard, D, Pedersen, O B, Sørensen, E, Nielsen, K R, Burgdorf, K S, Banasik, K, Brumpton, B, Zhou, W, Oddsson, A, Tragante, V, Hjorleifsson, K E, Davidsson, O B, Rajamani, S, Jonsson, S, Torfason, B, Valgardsson, A S, Thorgeirsson, G, Frigge, M L, Thorleifsson, G, Norddahl, G L, Helgadottir, A, Gretarsdottir, S, Sulem, P, Jonsdottir, I, Willer, C J, Hveem, K, Bundgaard, H, Ullum, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Holm, H, Stefansson, K & DBDS Genomic Consortium 2021, ' Genetic insight into sick sinus syndrome ', European Heart Journal, vol. 42 . https://doi.org/10.1093/eurheartj/ehaa1108
Thorolfsdottir, R B, Sveinbjornsson, G, Aegisdottir, H M, Benonisdottir, S, Stefansdottir, L, Ivarsdottir, E V, Halldorsson, G H, Sigurdsson, J K, Torp-Pedersen, C, Weeke, P E, Brunak, S, Westergaard, D, Pedersen, O B, Sorensen, E, Nielsen, K R, Burgdorf, K S, Banasik, K, DBDS Genomic Consortium, Brumpton, B, Zhou, W, Oddsson, A, Tragante, V, Hjorleifsson, K E, Davidsson, O B, Rajamani, S, Jonsson, S, Torfason, B, Valgardsson, A S, Thorgeirsson, G, Frigge, M L, Thorleifsson, G, Norddahl, G L, Helgadottir, A, Gretarsdottir, S, Sulem, P, Jonsdottir, I, Willer, C J, Hveem, K, Bundgaard, H, Ullum, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Holm, H, Stefansson, K & Nyegaard, M 2021, ' Genetic insight into sick sinus syndrome ', European Heart Journal, vol. 42, no. 20, pp. 1959-1971 . https://doi.org/10.1093/eurheartj/ehaa1108
European Heart Journal
Thorolfsdottir, R B, Sveinbjornsson, G, Aegisdottir, H M, Benonisdottir, S, Stefansdottir, L, Ivarsdottir, E V, Halldorsson, G H, Sigurdsson, J K, Torp-Pedersen, C, Weeke, P E, Brunak, S, Westergaard, D, Pedersen, O B, Sorensen, E, Nielsen, K R, Burgdorf, K S, Banasik, K, Brumpton, B, Zhou, W, Oddsson, A, Tragante, V, Hjorleifsson, K E, Davidsson, O B, Rajamani, S, Jonsson, S, Torfason, B, Valgardsson, A S, Thorgeirsson, G, Frigge, M L, Thorleifsson, G, Norddahl, G L, Helgadottir, A, Gretarsdottir, S, Sulem, P, Jonsdottir, I, Willer, C J, Hveem, K, Bundgaard, H, Ullum, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Holm, H, Stefansson, K & DBDS Genomic Consortium (MN part of consortium) 2021, ' Genetic insight into sick sinus syndrome ', European Heart Journal . https://doi.org/10.1093/eurheartj/ehaa1108
Thorolfsdottir, R B, Sveinbjornsson, G, Aegisdottir, H M, Benonisdottir, S, Stefansdottir, L, Ivarsdottir, E V, Halldorsson, G H, Sigurdsson, J K, Torp-Pedersen, C, Weeke, P E, Brunak, S, Westergaard, D, Pedersen, O B, Sorensen, E, Nielsen, K R, Burgdorf, K S, Banasik, K, Brumpton, B, Zhou, W, Oddsson, A, Tragante, V, Hjorleifsson, K E, Davidsson, O B, Rajamani, S, Jonsson, S, Torfason, B, Valgardsson, A S, Thorgeirsson, G, Frigge, M L, Thorleifsson, G, Norddahl, G L, Helgadottir, A, Gretarsdottir, S, Sulem, P, Jonsdottir, I, Willer, C J, Hveem, K, Bundgaard, H, Ullum, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Holm, H, Stefansson, K & DBDS Genomic Consortium 2021, ' Genetic insight into sick sinus syndrome ', European Heart Journal, vol. 42, no. 20, pp. 1959-1971 . https://doi.org/10.1093/eurheartj/ehaa1108
Thorolfsdottir, R B, Sveinbjornsson, G, Aegisdottir, H M, Benonisdottir, S, Stefansdottir, L, Ivarsdottir, E V, Halldorsson, G H, Sigurdsson, J K, Torp-Pedersen, C, Weeke, P E, Brunak, S, Westergaard, D, Pedersen, O B, Sørensen, E, Nielsen, K R, Burgdorf, K S, Banasik, K, Brumpton, B, Zhou, W, Oddsson, A, Tragante, V, Hjorleifsson, K E, Davidsson, O B, Rajamani, S, Jonsson, S, Torfason, B, Valgardsson, A S, Thorgeirsson, G, Frigge, M L, Thorleifsson, G, Norddahl, G L, Helgadottir, A, Gretarsdottir, S, Sulem, P, Jonsdottir, I, Willer, C J, Hveem, K, Bundgaard, H, Ullum, H, Arnar, D O, Thorsteinsdottir, U, Gudbjartsson, D F, Holm, H, Stefansson, K & DBDS Genomic Consortium 2021, ' Genetic insight into sick sinus syndrome ', European Heart Journal, vol. 42 . https://doi.org/10.1093/eurheartj/ehaa1108
Aims The aim of this study was to use human genetics to investigate the pathogenesis of sick sinus syndrome (SSS) and the role of risk factors in its development. Methods and results We performed a genome-wide association study of 6469 SSS cases and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd6e6818fe6f5016cfbb473965bbb2c2
https://pure.au.dk/ws/files/277444925/ehaa1108.pdf
https://pure.au.dk/ws/files/277444925/ehaa1108.pdf