Maayan C - Search Results

1

Familial Dysautonomia (FD) Human Embryonic Stem Cell Derived PNS Neurons Reveal that Synaptic Vesicular and Neuronal Transport Genes Are Directly or Indirectly Affected by IKBKAP Downregulation.

Lefler S, Cohen MA, Kantor G, Cheishvili D, Even A, Birger A, Turetsky T, Gil Y, Even-Ram S, Aizenman E, Bashir N, Maayan C, Razin A, Reubinoff BE, Weil M. Lefler S, et al. Among authors: maayan c. PLoS One. 2015 Oct 5;10(10):e0138807. doi: 10.1371/journal.pone.0138807. eCollection 2015. PLoS One. 2015. PMID: 26437462 Free PMC article.

2

IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelination.

Cheishvili D, Maayan C, Smith Y, Ast G, Razin A. Cheishvili D, et al. Among authors: maayan c. Hum Mol Genet. 2007 Sep 1;16(17):2097-104. doi: 10.1093/hmg/ddm157. Epub 2007 Jun 25. Hum Mol Genet. 2007. PMID: 17591626

3

IKAP/Elp1 involvement in cytoskeleton regulation and implication for familial dysautonomia.

Cheishvili D, Maayan C, Cohen-Kupiec R, Lefler S, Weil M, Ast G, Razin A. Cheishvili D, et al. Among authors: maayan c. Hum Mol Genet. 2011 Apr 15;20(8):1585-94. doi: 10.1093/hmg/ddr036. Epub 2011 Jan 27. Hum Mol Genet. 2011. PMID: 21273291

4

Dynamic changes in IKBKAP mRNA levels during crisis of familial dysautonomia patients.

Cheishvili D, Laiba E, Rekhtman D, Claman A, Razin A, Maayan C. Cheishvili D, et al. Among authors: maayan c. Auton Neurosci. 2014 Feb;180:59-65. doi: 10.1016/j.autneu.2013.10.009. Epub 2013 Nov 1. Auton Neurosci. 2014. PMID: 24268683

5

IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation.

Cheishvili D, Dietrich P, Maayan C, Even A, Weil M, Dragatsis I, Razin A. Cheishvili D, et al. Among authors: maayan c. PLoS One. 2014 Apr 23;9(4):e94612. doi: 10.1371/journal.pone.0094612. eCollection 2014. PLoS One. 2014. PMID: 24760006 Free PMC article.

6

Tocotrienol Treatment in Familial Dysautonomia: Open-Label Pilot Study.

Cheishvili D, Maayan C, Holzer N, Tsenter J, Lax E, Petropoulos S, Razin A. Cheishvili D, et al. Among authors: maayan c. J Mol Neurosci. 2016 Jul;59(3):382-91. doi: 10.1007/s12031-016-0760-5. Epub 2016 Apr 30. J Mol Neurosci. 2016. PMID: 27129499 Clinical Trial.

7

Uncommon side effects of common drugs in patients with familial dysautonomia.

Perl L, Hakimian D, Maayan C, Rekhtman D, Fried E, Salmon-Divon M, Sapozhnikov DM, Cheishvili D. Perl L, et al. Among authors: maayan c. Pharmacoepidemiol Drug Saf. 2022 Feb;31(2):128-140. doi: 10.1002/pds.5326. Epub 2021 Jul 16. Pharmacoepidemiol Drug Saf. 2022. PMID: 34245206

8

Genetic Polymorphisms in the ESR1 and VDR Genes Do Not Correlate With Osteoporosis in Patients With Familial Dysautonomia.

Cheishvili D, Maayan C, Sapozhnikov DM, Lax E, Dresner-Pollak R. Cheishvili D, et al. Among authors: maayan c. J Clin Densitom. 2018 Apr-Jun;21(2):205-212. doi: 10.1016/j.jocd.2017.01.002. Epub 2017 Feb 1. J Clin Densitom. 2018. PMID: 28161223

9

Phosphatidylserine increases IKBKAP levels in familial dysautonomia cells.

Keren H, Donyo M, Zeevi D, Maayan C, Pupko T, Ast G. Keren H, et al. Among authors: maayan c. PLoS One. 2010 Dec 29;5(12):e15884. doi: 10.1371/journal.pone.0015884. PLoS One. 2010. PMID: 21209961 Free PMC article.

10

[Diagnosis and misdiagnosis in familial dysautonomia].

Maayan C, Kaplan E, Harrari M, Peleg O, Goldberg A. Maayan C, et al. Harefuah. 1994 May 15;126(10):565-7, 628. Harefuah. 1994. PMID: 8034241 Hebrew.

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