Bashayer R Al-Mubarak
Overview
Explore the profile of Bashayer R Al-Mubarak including associated specialties, affiliations and a list of published articles.
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11
Citations
82
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Recent Articles
1.
Mohamed W, Eltantawi M, Mecheri Y, Zewde Y, Kamel W, Al-Mubarak B, et al.
Lancet Neurol
. 2024 Jan;
23(2):140-141.
PMID: 38267182
No abstract available.
2.
Ostrozovicova M, Mecheri Y, Al-Mubarak B, Al-Tassan N, Makarious M, Perinan M, et al.
Brain
. 2023 Jul;
146(12):e120-e124.
PMID: 37467482
No abstract available.
3.
Abomelha F, Aldhalaan H, Ghaziuddin M, Al-Tassan N, Al-Mubarak B
Genes (Basel)
. 2022 Sep;
13(9).
PMID: 36140719
Even in the era of information "prosperity" in the form of databases and registries that compile a wealth of data, information about ASD and ADHD remains scattered and disconnected. These...
4.
Al-Mubarak B, Bell K, Chowdhry S, Meakin P, Baxter P, McKay S, et al.
Redox Biol
. 2021 Oct;
47:102158.
PMID: 34626892
The transcription factor Nrf2 is a stress-responsive master regulator of antioxidant, detoxification and proteostasis genes. In astrocytes, Nrf2-dependent gene expression drives cell-autonomous cytoprotection and also non-cell-autonomous protection of nearby neurons,...
5.
Baxter P, Markus N, Dando O, He X, Al-Mubarak B, Qiu J, et al.
Cell Death Dis
. 2021 Feb;
12(2):218.
PMID: 33637689
Many neurodegenerative diseases are associated with neuronal misfolded protein accumulation, indicating a need for proteostasis-promoting strategies. Here we show that de-repressing the transcription factor Nrf2, epigenetically shut-off in early neuronal...
6.
Al-Mubarak B, Omar A, Baz B, Al-Abdulaziz B, Magrashi A, Al-Yemni E, et al.
Eur J Hum Genet
. 2020 Apr;
28(8):1098-1110.
PMID: 32238911
Several types of genetic alterations occurring at numerous loci have been described in attention deficit hyperactivity disorder (ADHD). However, the role of rare single nucleotide variants (SNVs) remains under investigated....
7.
Alabdullah A, Al-Abdulaziz B, Alsalem H, Magrashi A, Pulicat S, Almzroua A, et al.
BMC Res Notes
. 2019 Apr;
12(1):225.
PMID: 30987672
Objective: Delivery of constructs for silencing or over-expressing genes or their modified versions is a crucial step for studying neuronal cell biology. Therefore, efficient transfection is important for the success...
8.
Mustafa A, Faquih T, Baz B, Kattan R, Al-Issa A, Tahir A, et al.
Genes (Basel)
. 2018 May;
9(5).
PMID: 29789446
Quick and accurate molecular testing is necessary for the better management of many inherited diseases. Recent technological advances in various next generation sequencing (NGS) platforms, such as target panel-based sequencing,...
9.
Bohlega S, Al-Mubarak B, Alyemni E, Abouelhoda M, Monies D, Mustafa A, et al.
BMC Res Notes
. 2016 Jun;
9:295.
PMID: 27268037
Background: Recessive mutations in PLA2G6 have been associated with different neurodegenerative disorders, including infantile neuroaxonal dystrophy, neurodegeneration with brain iron accumulation and more recently, early-onset dystonia parkinsonism. Method: Targeted-next generation...
10.
Al-Mubarak B, Bohlega S, Alkhairallah T, Magrashi A, Alturki M, Khalil D, et al.
PLoS One
. 2015 Aug;
10(8):e0135950.
PMID: 26274610
Parkinson's disease (PD) is one of the major causes of parkinsonism syndrome. Its characteristic motor symptoms are attributable to dopaminergic neurons loss in the midbrain. Genetic advances have highlighted underlying...