Follow
Solmaz Etemad
Title
Cited by
Cited by
Year
Differential neuronal targeting of a new and two known calcium channel β4 subunit splice variants correlates with their regulation of gene expression
S Etemad, GJ Obermair, D Bindreither, A Benedetti, R Stanika, V Di Biase, ...
Journal of Neuroscience 34 (4), 1446-1461, 2014
482014
Depletion of oxaloacetate decarboxylase FAHD1 inhibits mitochondrial electron transport and induces cellular senescence in human endothelial cells
M Petit, R Koziel, S Etemad, H Pircher, P Jansen-Dürr
Experimental Gerontology 92, 7-12, 2017
282017
Investigation on Mitochondrial tRNALeu/Lys, NDI and ATPase 6/8 in Iranian Multiple Sclerosis Patients
SE Ahari, M Houshmand, MSS Panahi, S Kasraie, M Moin, MA Bahar
Cellular and Molecular Neurobiology 27, 695-700, 2007
202007
Oxaloacetate decarboxylase FAHD1–a new regulator of mitochondrial function and senescence
S Etemad, M Petit, AKH Weiss, A Schrattenholz, G Baraldo, ...
Mechanisms of Ageing and Development 177, 22-29, 2019
192019
The juvenile myoclonic epilepsy mutant of the calcium channel β4 subunit displays normal nuclear targeting in nerve and muscle cells
S Etemad, M Campiglio, GJ Obermair, BE Flucher
Channels 8 (4), 334-343, 2014
142014
Investigation of tRNALys/Leu and ATPase 6/8 gene mutations in Iranian ataxia telangiectasia patients
M Houshmand, S Kasraie, SE Ahari, M Moin, M Bahar, A Zamani
Archives of Medical Science 7 (3), 523-527, 2011
142011
Investigation of tRNALeu/Lys and ATPase 6 Genes Mutations in Huntington’s Disease
S Kasraie, M Houshmand, MM Banoei, SE Ahari, MSS Panahi, P Shariati, ...
Cellular and molecular neurobiology 28, 933-938, 2008
142008
Structural basis for the bi-functionality of human oxaloacetate decarboxylase FAHD1
AKH Weiss, A Naschberger, JR Loeffler, H Gstach, MW Bowler, ...
Biochemical Journal 475 (22), 3561-3576, 2018
132018
Modulation of serotonin signaling by the putative oxaloacetate decarboxylase FAHD-1 in Caenorhabditis elegans
G Baraldo, S Etemad, AKH Weiss, P Jansen-Dürr, HID Mack
Plos one 14 (8), e0220434, 2019
52019
Point mutations on mitochondrial DNA in Iranian patients with friedreich’s ataxia
S Etemad Ahari, M Houshmand, S Kasraie, M Moin, MA Bahar, ...
Iranian Journal of Child Neurology 2 (1), 41-45, 2008
52008
High glycolytic activity enhances stem cell reprogramming of fahd1-ko mouse embryonic fibroblasts
A Salti, S Etemad, MS Cubero, E Albertini, B Kovacs-Szalka, ...
Cells 10 (8), 2040, 2021
42021
Three Splice Variants of the Calcium Channel Beta4 Subunit Display Differential Targeting and Gene Regulation in Neurons
S Etemad, GJ Obermair, V Burtscher, D Bindreither, BE Flucher
Biophysical Journal 106 (2), 331a, 2014
2014
Monday, February 17, 2014 331a
S Etemad, GJ Obermair, V Burtscher, D Bindreither, BE Flucher
The system can't perform the operation now. Try again later.
Articles 1–13