Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 1 |
2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 2 |
Search Results
5 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Insights into organoid-based modeling of COVID-19 pathology.
Virol J. 2023 Feb 25;20(1):37. doi: 10.1186/s12985-023-01996-2.
Virol J. 2023.
PMID: 36841795
Free PMC article.
Review.
Critical Role for Cold Shock Protein YB-1 in Cytokinesis.
Mehta S, Algie M, Al-Jabry T, McKinney C, Kannan S, Verma CS, Ma W, Zhang J, Bartolec TK, Masamsetti VP, Parker K, Henderson L, Gould ML, Bhatia P, Harfoot R, Chircop M, Kleffmann T, Cohen SB, Woolley AG, Cesare AJ, Braithwaite A.
Mehta S, et al. Among authors: al jabry t.
Cancers (Basel). 2020 Sep 1;12(9):2473. doi: 10.3390/cancers12092473.
Cancers (Basel). 2020.
PMID: 32882852
Free PMC article.
Item in Clipboard
Biallelic PTRHD1 Frameshift Variants Associated with Intellectual Disability, Spasticity, and Parkinsonism.
Al-Kasbi G, Al-Saegh A, Al-Qassabi A, Al-Jabry T, Zadjali F, Al-Yahyaee S, Al-Maawali A.
Al-Kasbi G, et al. Among authors: al jabry t.
Mov Disord Clin Pract. 2021 Sep 20;8(8):1253-1257. doi: 10.1002/mdc3.13342. eCollection 2021 Nov.
Mov Disord Clin Pract. 2021.
PMID: 34765690
Free PMC article.
Item in Clipboard
LRP4 site-specific variants in the third β-propeller domain causes congenital myasthenic syndrome type 17.
Al Jabry T, Al-Hashmi N, Abdelhadi B, Al-Maawali A.
Al Jabry T, et al.
Eur J Med Genet. 2024 Feb;67:104903. doi: 10.1016/j.ejmg.2023.104903. Epub 2023 Dec 13.
Eur J Med Genet. 2024.
PMID: 38101565
Free article.
Review.
Item in Clipboard
Revisiting Exome Data Identified Missed Splice Site Variant of the Asparagine Synthetase ( ASNS ) Gene.
Al-Kasbi G, Al-Murshedi F, Al-Futaisi A, Al-Jabry T, Zadjali F, Al-Yahyaee S, Al-Maawali A.
Al-Kasbi G, et al. Among authors: al jabry t.
J Pediatr Genet. 2022 Oct 13;13(1):1-5. doi: 10.1055/s-0042-1757193. eCollection 2024 Mar.
J Pediatr Genet. 2022.
PMID: 38567172
Free PMC article.
Item in Clipboard
Cite
Cite