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- Publications
- Influence
Genome Editing in Induced Pluripotent Stem Cells using CRISPR/Cas9
- Ronen Ben Jehuda, Y. Shemer, O. Binah
- Biology, Medicine
- Stem Cell Reviews and Reports
- 6 April 2018
The development of the reprogramming technology led to generation of induced Pluripotent Stem Cells (iPSC) from a variety of somatic cells. Ever since, fast growing knowledge of different efficient… Expand
Electrophysiological abnormalities in induced pluripotent stem cell‐derived cardiomyocytes generated from Duchenne muscular dystrophy patients
- B. Eisen, Ronen Ben Jehuda, +13 authors O. Binah
- Biology, Medicine
- Journal of cellular and molecular medicine
- 8 January 2019
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.… Expand
CRISPR correction of the PRKAG2 gene mutation in the patient's induced pluripotent stem cell-derived cardiomyocytes eliminates electrophysiological and structural abnormalities.
- Ronen Ben Jehuda, B. Eisen, +11 authors O. Binah
- Biology, Medicine
- Heart rhythm
- 1 September 2017
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.… Expand
Functional abnormalities in induced Pluripotent Stem Cell-derived cardiomyocytes generated from titin-mutated patients with dilated cardiomyopathy
- R. Schick, Lucy N. Mekies, +17 authors O. Binah
- Medicine
- PloS one
- 17 October 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… Expand
Investigating the cardiac pathology of SCO2‐mediated hypertrophic cardiomyopathy using patients induced pluripotent stem cell–derived cardiomyocytes
- T. Hallas, B. Eisen, +14 authors O. Binah
- Medicine
- Journal of cellular and molecular medicine
- 28 November 2017
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… Expand
794Correcting PRKAG2 mutation in induced pluripotent stem cells using CRISPR/Cas9 eliminates arrhythmic firing patterns in the derived cardiomyocytes
- R. B. Jehuda, B. Eisen, Y. Shemer, M. Gherghiceanu, M. Arad, O. Binah
- Medicine
- 1 June 2017
A Method Sustaining the Bioelectric, Biophysical, and Bioenergetic Function of Cultured Rabbit Atrial Cells
- Noa Kirschner Peretz, Sofia Segal, +6 authors Y. Yaniv
- Biology, Medicine
- Front. Physiol.
- 15 August 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… Expand
P3248Investigating dilated cardiomyopathy caused by dystrophin mutations using duchenne muscular dystrophy-patients induced pluripotent stem cell-derived cardiomyocytes
- B. Eisen, R. B. Jehuda, +8 authors O. Binah
- Medicine
- 1 August 2017
CRISPR correction of the PRKAG2 gene mutation in the patient's iPSC-derived cardiomyocytes eliminates the electrophysiological and structural abnormalities
- R. B. Jehuda, B. Eisen, +11 authors O. Binah
- Medicine
- 1 February 2018
BACKGROUND: Mutations in the PRKAG2 gene encoding the {gamma}-subunit of adenosine monophosphate-kinase (AMPK) cause hypertrophic cardiomyopathy (HCM) and familial-Wolff-Parkinson-White syndrome… Expand