Salleh N. Ehaideb

发表

Mutation of orthologous prickle genes causes a similar epilepsy syndrome in flies and humans

J. Robert Manak, Alexander G. Bassuk, T. Kitamoto, 2016, Annals of clinical and translational neurology.

PRICKLE1 Interaction with SYNAPSIN I Reveals a Role in Autism Spectrum Disorders

Vinit B. Mahajan, J. Robert Manak, Heather C. Mefford, 2013, PloS one.

Seizures Are Regulated by Ubiquitin-specific Peptidase 9 X-linked (USP9X), a De-Ubiquitinase

G. Carvill, I. Scheffer, H. Mefford, 2015, PLoS genetics.

Mutations in prickle orthologs cause seizures in flies, mice, and humans.

J. Rosenfeld, L. Shaffer, M. Scott, 2011, American journal of human genetics.

Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality

S. Yezli, M. Rashid, Salleh N. Ehaideb, 2021, Genomics.

A systematic review uncovers a wide-gap between COVID-19 in humans and animal models

Salleh N. Ehaideb, A. Bouchama, B. Abuyassin, 2020, medRxiv.

Evidence of a wide gap between COVID-19 in humans and animal models: a systematic review

Salleh N. Ehaideb, A. Bouchama, S. Ehaideb, 2020, Critical Care.

Abnormal larval neuromuscular junction morphology and physiology in Drosophila prickle isoform mutants with known axonal transport defects and adult seizure behavior

J. Manak, Chun-Fang Wu, Salleh N. Ehaideb, 2022, Journal of neurogenetics.

prickle modulates microtubule polarity and axonal transport to ameliorate seizures in flies

J. Axelrod, D. Gubb, A. Bassuk, 2014, Proceedings of the National Academy of Sciences.

Elucidating the mechanism of prickle associated epilepsy in flies

Salleh N. Ehaideb, S. Ehaideb, 2015 .

KCNT1‐related epilepsy: An international multicenter cohort of 27 pediatric cases

H. Otsubo, L. Lingappa, T. Hershkovitz, 2020, Epilepsia.

Novel Compensatory Mechanisms Enable the Mutant KCNT1 Channels to Induce Seizures

Salleh N. Ehaideb, D. Davis, Bing Zhang, 2017, bioRxiv.

Abnormal larval neuromuscular junction morphology and physiology in Drosophila Prickle isoform mutants with defective axonal transport and adult seizure behavior

J. Manak, Chun-Fang Wu, Salleh N. Ehaideb, 2022, bioRxiv.

Insights into pathophysiology and therapeutic strategies for heat stroke: Lessons from a baboon model

Salleh N. Ehaideb, Mashan L. Abdullah, George Roberts, 2023, Experimental physiology.

Novel Homozygous Mutation in the WWOX Gene Causes Seizures and Global Developmental Delay: Report and Review

M. Alfadhel, Salleh N. Ehaideb, S. Ehaideb, 2018, Translational neuroscience.