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Salleh N. Ehaideb
Salleh N. Ehaideb
University of Iowa,
E-mail confirmado em kaimrc.edu.sa
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Mutations in prickle orthologs cause seizures in flies, mice, and humans
H Tao, JR Manak, L Sowers, X Mei, H Kiyonari, T Abe, NS Dahdaleh, ...
The American Journal of Human Genetics 88 (2), 138-149, 2011
1602011
Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase
L Paemka, VB Mahajan, SN Ehaideb, JM Skeie, MC Tan, S Wu, AJ Cox, ...
PLoS genetics 11 (3), e1005022, 2015
822015
KCNT1‐related epilepsy: An international multicenter cohort of 27 pediatric cases
F Borlot, A Abushama, N Morrison‐Levy, P Jain, K Puthenveettil Vinayan, ...
Epilepsia 61 (4), 679-692, 2020
562020
Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality
J Alghamdi, M Alaamery, T Barhoumi, M Rashid, H Alajmi, N Aljasser, ...
Genomics 113 (4), 1733-1741, 2021
522021
Evidence of a wide gap between COVID-19 in humans and animal models: a systematic review
SN Ehaideb, ML Abdullah, B Abuyassin, A Bouchama
Critical Care 24, 1-23, 2020
522020
prickle modulates microtubule polarity and axonal transport to ameliorate seizures in flies
SN Ehaideb, A Iyengar, A Ueda, GJ Iacobucci, C Cranston, AG Bassuk, ...
Proceedings of the National Academy of Sciences 111 (30), 11187-11192, 2014
492014
PRICKLE1 interaction with SYNAPSIN I reveals a role in autism spectrum disorders
L Paemka, VB Mahajan, JM Skeie, LP Sowers, SN Ehaideb, ...
PloS one 8 (12), e80737, 2013
492013
Novel homozygous mutation in the WWOX gene causes seizures and global developmental delay: Report and review
SN Ehaideb, MJ Al-Bu Ali, JJ Al-Obaid, KM Aljassim, M Alfadhel
Translational neuroscience 9 (1), 203-208, 2018
322018
Mutation of orthologous prickle genes causes a similar epilepsy syndrome in flies and humans
SN Ehaideb, EA Wignall, J Kasuya, WH Evans, A Iyengar, HL Koerselman, ...
Annals of clinical and translational neurology 3 (9), 695-707, 2016
172016
A systematic review uncovers a wide-gap between COVID-19 in humans and animal models
SN Ehaideb, ML Abdullah, B Abuyassin, A Bouchama
MedRxiv, 2020.07. 15.20147041, 2020
42020
Novel compensatory mechanisms enable the mutant KCNT1 channels to induce seizures
SN Ehaideb, GT Decker, P Smith, D Davis, B Zhang
bioRxiv, 191171, 2017
22017
Insights into pathophysiology and therapeutic strategies for heat stroke: Lessons from a baboon model
M Abdullah, S Ehaideb, G Roberts, A Bouchama
Experimental Physiology 109 (4), 484-501, 2024
2024
Escalating climate-related health risks for Hajj pilgrims to Mecca
S Yezli, S Ehaideb, Y Yassin, B Alotaibi, A Bouchama
Journal of Travel Medicine, taae042, 2024
2024
Abnormal larval neuromuscular junction morphology and physiology in Drosophila prickle isoform mutants with known axonal transport defects and adult seizure …
A Ueda, TCDG O’Harrow, X Xing, S Ehaideb, JR Manak, CF Wu
Journal of neurogenetics 36 (2-3), 65-73, 2022
2022
Abnormal larval neuromuscular junction morphology and physiology in Drosophila Prickle isoform mutants with defective axonal transport and adult seizure behavior
T O’Harrow, A Ueda, X Xing, S Ehaideb, JR Manak, CF Wu
bioRxiv, 2021.12. 31.474668, 2022
2022
A systematic review uncovers a wide-gap between COVID-19 in humans and animal models (preprint)
SN Ehaideb, ML Abdullah, B Abuyassin, A Bouchama
2020
Evidence of a wide gap between COVID-19 in humans and animal models: a systematic
SN Ehaideb, ML Abdullah, B Abuyassin, A Bouchama
2020
Allostatic Compensatory Mechanisms Enable the Mutant KCNT1 Channels to Induce Seizures and Hyperexcitability
SN Ehaideb, GT Decker, P Smith, N Messimore, D Davis, B Zhang
Available at SSRN 3188397, 2018
2018
Elucidating the mechanism of prickle associated epilepsy in flies
SN Ehaideb
The University of Iowa, 2015
2015
The pksple seizure‐associated isoform of prickle is co‐expressed in the same cells as the pkpk isoform in Drosophila larval brains
N Anderson, G Yuan, D Wadkins, S Ehaideb, C Cranston, JR Manak
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