Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Shiraz Haron-Khun"'
Autor:
Hanna Bueno-Levy, David Weisbrod, Dor Yadin, Shiraz Haron-Khun, Asher Peretz, Edith Hochhauser, Michael Arad, Bernard Attali
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2020)
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited, stressed-provoked ventricular arrhythmia. CPVT is treated by β-adrenergic receptor blockers, Na+ channel inhibitors, sympathetic denervation, or by implanting a defibrilla
Externí odkaz:
https://doaj.org/article/5f912df24fcc4112ae6d5f854b56f575
Autor:
Shiraz Haron‐Khun, David Weisbrod, Hanna Bueno, Dor Yadin, Joachim Behar, Asher Peretz, Ofer Binah, Edith Hochhauser, Michael Eldar, Yael Yaniv, Michael Arad, Bernard Attali
Publikováno v:
EMBO Molecular Medicine, Vol 9, Iss 4, Pp 415-429 (2017)
Abstract Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a stress‐provoked ventricular arrhythmia, which also manifests sinoatrial node (SAN) dysfunction. We recently showed that SK4 calcium‐activated potassium channels are import
Externí odkaz:
https://doaj.org/article/f81d60e628cd448aa9f2afc49e1e9d69
Autor:
Michael Arad, Bernard Attali, David Weisbrod, Edith Hochhauser, Dor Yadin, Hanna Bueno-Levy, Shiraz Haron-Khun, Asher Peretz
Publikováno v:
Frontiers in Pharmacology, Vol 10 (2020)
Frontiers in Pharmacology
Frontiers in Pharmacology
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited, stressed-provoked ventricular arrhythmia. CPVT is treated by β-adrenergic receptor blockers, Na+ channel inhibitors, sympathetic denervation, or by implanting a defibrilla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19b6ad416168dd662ea15e1938f23cb9
https://www.frontiersin.org/article/10.3389/fphar.2019.01566/full
https://www.frontiersin.org/article/10.3389/fphar.2019.01566/full
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
https://doi.org/10.1016/j.hrthm.2017.09.024
Autor:
Asher Peretz, Bernard Attali, Yael Yaniv, Michael Eldar, Edith Hochhauser, Joachim Behar, Ofer Binah, Shiraz Haron-Khun, Michael Arad, Dor Yadin, Hanna Bueno, David Weisbrod
Publikováno v:
EMBO Molecular Medicine
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a stress‐provoked ventricular arrhythmia, which also manifests sinoatrial node (SAN) dysfunction. We recently showed that SK4 calcium‐activated potassium channels are important for a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::765536e5a1345c51e3045a9e3eb69bf1
http://europepmc.org/articles/PMC5376763
http://europepmc.org/articles/PMC5376763
Publikováno v:
Acta pharmacologica Sinica. 37(1)
The proper expression and function of the cardiac pacemaker is a critical feature of heart physiology. The sinoatrial node (SAN) in human right atrium generates an electrical stimulation approximately 70 times per minute, which propagates from a cond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eabe4135e5bd51d16b230663a357e93f
https://pubmed.ncbi.nlm.nih.gov/26725737
https://pubmed.ncbi.nlm.nih.gov/26725737
Autor:
Michael, Arad, Lorenzo, Monserrat, Shiraz, Haron-Khun, Jonathan G, Seidman, Christine E, Seidman, Eloisa, Arbustini, Michael, Glikson, Dov, Freimark
Publikováno v:
The Israel Medical Association journal : IMAJ. 16(11)
Hypertrophic cardiomyopathy (HCM) is a familial disease with autosomal dominant inheritance and age-dependent penetrance, caused primarily by mutations of sarcomere genes. Because the clinical variability of HCM is related to its genetic heterogeneit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::79e6b5aa20284bea0f5cbfcefcdd0981
https://pubmed.ncbi.nlm.nih.gov/25558701
https://pubmed.ncbi.nlm.nih.gov/25558701
Autor:
Asher Peretz, Yael Yaniv, David Weisbrod, Bernard Attali, Hanna Bueno, Michael Arad, Joachim Behar, Dor Yadin, Shiraz Haron-Khun
Publikováno v:
Biophysical Journal. 112:35a
The sinoatrial node (SAN) controls the heart rhythm under physiological conditions. We recently showed that SK4 calcium-activated potassium channels (SK4) are important for automaticity of cardiomyocytes derived from human embryonic stem cells. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c84938aa6f90750e0c311aa5bedbfbf9
https://doi.org/10.1016/j.bpj.2016.11.225
https://doi.org/10.1016/j.bpj.2016.11.225
Autor:
Michael Arad, Shiraz Haron-Khun, Asher Peretz, David Weisbrod, Bernard Attali, Dor Yadin, Michael Eldar
Publikováno v:
Biophysical Journal. 110:29a
Catecholaminergic Polymorphic Ventricular Tachychardia (CPVT) is a stressed-provoked ventricular arrhythmia triggered by diastolic intracellular calcium leak, which can lead to sudden death. While many studies have focused on ventricular tachyarrhyth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37abd25495b57e5a2ed7dd57cae85ad1
https://doi.org/10.1016/j.bpj.2015.11.224
https://doi.org/10.1016/j.bpj.2015.11.224