Levitas A - Search Results

1

Functional defects in hiPSCs-derived cardiomyocytes from patients with a PLEKHM2-mutation associated with dilated cardiomyopathy and left ventricular non-compaction.

Korover N, Etzion S, Cherniak A, Rabinski T, Levitas A, Etzion Y, Ofir R, Parvari R, Cohen S. Korover N, et al. Among authors: levitas a. Biol Res. 2023 Jun 23;56(1):34. doi: 10.1186/s40659-023-00442-5. Biol Res. 2023. PMID: 37349842 Free PMC article.

2

Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase.

Levitas A, Muhammad E, Harel G, Saada A, Caspi VC, Manor E, Beck JC, Sheffield V, Parvari R. Levitas A, et al. Eur J Hum Genet. 2010 Oct;18(10):1160-5. doi: 10.1038/ejhg.2010.83. Epub 2010 Jun 16. Eur J Hum Genet. 2010. PMID: 20551992 Free PMC article.

3

The mutations associated with dilated cardiomyopathy.

Parvari R, Levitas A. Parvari R, et al. Among authors: levitas a. Biochem Res Int. 2012;2012:639250. doi: 10.1155/2012/639250. Epub 2012 Jul 9. Biochem Res Int. 2012. PMID: 22830024 Free PMC article.

4

D117N in Cypher/ZASP may not be a causative mutation for dilated cardiomyopathy and ventricular arrhythmias.

Levitas A, Konstantino Y, Muhammad E, Afawi Z, Marc Weinstein J, Amit G, Etzion Y, Parvari R. Levitas A, et al. Eur J Hum Genet. 2016 May;24(5):666-71. doi: 10.1038/ejhg.2015.195. Epub 2015 Sep 30. Eur J Hum Genet. 2016. PMID: 26419279 Free PMC article.

5

PLEKHM2 mutation leads to abnormal localization of lysosomes, impaired autophagy flux and associates with recessive dilated cardiomyopathy and left ventricular noncompaction.

Muhammad E, Levitas A, Singh SR, Braiman A, Ofir R, Etzion S, Sheffield VC, Etzion Y, Carrier L, Parvari R. Muhammad E, et al. Among authors: levitas a. Hum Mol Genet. 2015 Dec 20;24(25):7227-40. doi: 10.1093/hmg/ddv423. Epub 2015 Oct 12. Hum Mol Genet. 2015. PMID: 26464484 Free PMC article.

6

CAP2 mutation leads to impaired actin dynamics and associates with supraventricular tachycardia and dilated cardiomyopathy.

Aspit L, Levitas A, Etzion S, Krymko H, Slanovic L, Zarivach R, Etzion Y, Parvari R. Aspit L, et al. Among authors: levitas a. J Med Genet. 2019 Apr;56(4):228-235. doi: 10.1136/jmedgenet-2018-105498. Epub 2018 Dec 5. J Med Genet. 2019. PMID: 30518548

7

A Novel Recessive Mutation in SPEG Causes Early Onset Dilated Cardiomyopathy.

Levitas A, Muhammad E, Zhang Y, Perea Gil I, Serrano R, Diaz N, Arafat M, Gavidia AA, Kapiloff MS, Mercola M, Etzion Y, Parvari R, Karakikes I. Levitas A, et al. PLoS Genet. 2020 Sep 14;16(9):e1009000. doi: 10.1371/journal.pgen.1009000. eCollection 2020 Sep. PLoS Genet. 2020. PMID: 32925938 Free PMC article.

8

Dock10 Regulates Cardiac Function under Neurohormonal Stress.

Segal L, Etzion S, Elyagon S, Shahar M, Klapper-Goldstein H, Levitas A, Kapiloff MS, Parvari R, Etzion Y. Segal L, et al. Among authors: levitas a. Int J Mol Sci. 2022 Aug 25;23(17):9616. doi: 10.3390/ijms23179616. Int J Mol Sci. 2022. PMID: 36077014 Free PMC article.

9

Duchenne Muscular Dystrophy and Early Onset Hypertrophic Cardiomyopathy associated with Mutations in Dystrophin and Hypertrophic Cardiomyopathy-Associated Genes.

Aspit L, Arwas N, Krymko H, Etzion Y, Parvari R, Levitas A. Aspit L, et al. Among authors: levitas a. J Pediatr Genet. 2020 Nov 19;11(4):304-308. doi: 10.1055/s-0040-1718724. eCollection 2022 Dec. J Pediatr Genet. 2020. PMID: 36267863 Free PMC article.

10

A Missense Variation in PHACTR2 Associates with Impaired Actin Dynamics, Dilated Cardiomyopathy, and Left Ventricular Non-Compaction in Humans.

Majdalani P, Levitas A, Krymko H, Slanovic L, Braiman A, Hadad U, Dabsan S, Horev A, Zarivach R, Parvari R. Majdalani P, et al. Among authors: levitas a. Int J Mol Sci. 2023 Jan 10;24(2):1388. doi: 10.3390/ijms24021388. Int J Mol Sci. 2023. PMID: 36674904 Free PMC article.

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