Zobrazeno 1 - 10 of 11 pro vyhledávání: '"Yuval Shemer"'
1
Akademický článek
Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathy.
Autor: Revital Schick, Lucy N Mekies, Yuval Shemer, Binyamin Eisen, Tova Hallas, Ronen Ben Jehuda, Meital Ben-Ari, Agnes Szantai, Lubna Willi, Rita Shulman, Michael Gramlich, Luna Simona Pane, Ilaria My, Dov Freimark, Marta Murgia, Gianluca Santamaria, Mihaela Gherghiceanu, Michael Arad, Alessandra Moretti, Ofer Binah
Publikováno v: PLoS ONE, Vol 13, Iss 10, p e0205719 (2018)
AIMS:Dilated cardiomyopathy (DCM), a myocardial disorder that can result in progressive heart failure and arrhythmias, is defined by ventricular chamber enlargement and dilatation, and systolic dysfunction. Despite extensive research, the pathologica
Externí odkaz: https://doaj.org/article/e1a99e6238e543028fefdc138f726611
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2
Akademický článek
A Method Sustaining the Bioelectric, Biophysical, and Bioenergetic Function of Cultured Rabbit Atrial Cells
Autor: Noa Kirschner Peretz, Sofia Segal, Limor Arbel-Ganon, Ronen Ben Jehuda, Yuval Shemer, Binyamin Eisen, Moran Davoodi, Ofer Binah, Yael Yaniv
Publikováno v: Frontiers in Physiology, Vol 8 (2017)
Culturing atrial cells leads to a loss in their ability to be externally paced at physiological rates and to maintain their shape. We aim to develop a culture method that sustains the shape of atrial cells along with their biophysical and bioenergeti
Externí odkaz: https://doaj.org/article/93024dba45ac4a43bcaca99feb15da0e
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3
Investigating LMNA-Related Dilated Cardiomyopathy Using Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes
Autor: Polina Baskin, Eloisa Arbustini, Ofer Binah, Mihaela Gherghiceanu, Binyamin Eisen, Michael Arad, Yuval Shemer, Lucy N. Mekies, Rita Shulman, Brenda Gerull, Danielle Regev, Eyal Gottlieb, Ronen Ben Jehuda
Publikováno v: International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 7874, p 7874 (2021)
Volume 22
Issue 15
LMNA-related dilated cardiomyopathy is an inherited heart disease caused by mutations in the LMNA gene encoding for lamin A/C. The disease is characterized by left ventricular enlargement and impaired systolic function associated with conduction defe
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39b868c884aec2fe964ff5ee7fdd55f1
http://europepmc.org/articles/PMC8346174
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4
CRISPR correction of the PRKAG2 gene mutation in the patient's induced pluripotent stem cell-derived cardiomyocytes eliminates electrophysiological and structural abnormalities
Autor: Irina Reiter, Ofer Binah, Mihaela Gherghiceanu, Michael Arad, Yuval Shemer, Shiraz Haron-Khun, Kaomei Guan, Silke Sperling, Binyamin Eisen, Huanhuan Cui, Ronen Ben Jehuda, Agnes Szantai, Dov Freimark, Lucy N. Mekies
Publikováno v: Heart Rhythm. 15:267-276
Background Mutations in the PRKAG2 gene encoding the γ-subunit of adenosine monophosphate kinase (AMPK) cause hypertrophic cardiomyopathy (HCM) and familial Wolff-Parkinson-White (WPW) syndrome. Patients carrying the R302Q mutation in PRKAG2 present
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b83e258b747a6401aed630d5b9f7fbc
https://doi.org/10.1016/j.hrthm.2017.09.024
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5
Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients
Autor: Lorenzo Monserrat, Ashley J. Cuttitta, Lubna Willi, Denise Hilfiker-Kleiner, Lucy N. Mekies, Daniel E. Michele, Ofer Binah, Mihaela Gherghiceanu, Michael Arad, Binyamin Eisen, Ronen Ben Jehuda, Michaela Scherr, Polina Baskin, Dov Freimark, Yuval Shemer, Irina Reiter
Publikováno v: Journal of Cellular and Molecular Medicine
Duchenne muscular dystrophy (DMD) is an X‐linked progressive muscle degenerative disease, caused by mutations in the dystrophin gene and resulting in death because of respiratory or cardiac failure. To investigate the cardiac cellular manifestation
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::241de8bce11d966c544cf4883479c23c
https://pubmed.ncbi.nlm.nih.gov/30618214
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6
Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathy
Autor: Yuval Shemer, Lubna Willi, Michael Arad, Michael Gramlich, Ofer Binah, Mihaela Gherghiceanu, Alessandra Moretti, Dov Freimark, Ronen Ben Jehuda, Rita Shulman, Meital Ben-Ari, Luna Simona Pane, Binyamin Eisen, Tova Hallas, Gianluca Santamaria, Revital Schick, Agnes Szantai, Lucy N. Mekies, Ilaria My, Marta Murgia
Publikováno v: PLoS One
PLOS ONE
PLoS ONE
PLOS ONE 13(10), e0205719 (2018). doi:10.1371/journal.pone.0205719
PLoS ONE, Vol 13, Iss 10, p e0205719 (2018)
Aims Dilated cardiomyopathy (DCM), a myocardial disorder that can result in progressive heart failure and arrhythmias, is defined by ventricular chamber enlargement and dilatation, and systolic dysfunction. Despite extensive research, the pathologica
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3123d25edbfb721332acd04884d6e3c7
https://hdl.handle.net/21.11116/0000-0002-F13F-821.11116/0000-0002-F140-521.11116/0000-0002-F13D-A
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8
A Method Sustaining the Bioelectric, Biophysical, and Bioenergetic Function of Cultured Rabbit Atrial Cells
Autor: Sofia Segal, Ofer Binah, Yuval Shemer, Noa Kirschner Peretz, Moran Davoodi, Limor Arbel-Ganon, Binyamin Eisen, Ronen Ben Jehuda, Yael Yaniv
Publikováno v: Frontiers in Physiology, Vol 8 (2017)
Frontiers in Physiology
Culturing atrial cells leads to a loss in their ability to be externally paced at physiological rates and to maintain their shape. We aim to develop a culture method that sustains the shape of atrial cells along with their biophysical and bioenergeti
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f2f3ee5abca0d40e30c0ab92493e887
http://journal.frontiersin.org/article/10.3389/fphys.2017.00584/full
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9
Investigating the cardiac pathology of SCO2-mediated hypertrophic cardiomyopathy using patients induced pluripotent stem cell-derived cardiomyocytes
Autor: Binyamin Eisen, Yeshayahu Katz, Tova Hallas, Revital Schick, Avraham Lorber, Eugene Vlodavsky, Irina Reiter, Katrin Õunap, Yuval Shemer, Richard J. Rodenburg, Lucy N. Mekies, Shulamit Naor, Hanna Mandel, Ofer Binah, Mihaela Gherghiceanu, Sivan Eliyahu, Ronen Ben Jehuda
Publikováno v: Journal of Cellular and Molecular Medicine
Journal of Cellular and Molecular Medicine, 22, 913-925
Journal of Cellular and Molecular Medicine, 22, 2, pp. 913-925
Mutations in SCO2 are among the most common causes of COX deficiency, resulting in reduced mitochondrial oxidative ATP production capacity, often leading to hypertrophic cardiomyopathy (HCM). To date, none of the recent pertaining reports provide dee
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb6eb37b1aedaec124d315ad81e6917d
https://pubmed.ncbi.nlm.nih.gov/29193756
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