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2021 6
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2024 0

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New insights on CRISPR/Cas9-based therapy for breast Cancer.
Sabit H, Abdel-Ghany S, Tombuloglu H, Cevik E, Alqosaibi A, Almulhim F, Al-Muhanaa A. Sabit H, et al. Among authors: alqosaibi a. Genes Environ. 2021 Apr 29;43(1):15. doi: 10.1186/s41021-021-00188-0. Genes Environ. 2021. PMID: 33926574 Free PMC article. Review.
Multiple Recurrent Copy Number Variations (CNVs) in Chromosome 22 Including 22q11.2 Associated with Autism Spectrum Disorder.
Alhazmi S, Alzahrani M, Farsi R, Alharbi M, Algothmi K, Alburae N, Ganash M, Azhari S, Basingab F, Almuhammadi A, Alqosaibi A, Alkhatabi H, Elaimi A, Jan M, Aldhalaan HM, Alrafiah A, Alrofaidi A. Alhazmi S, et al. Among authors: alqosaibi a. Pharmgenomics Pers Med. 2022 Jul 20;15:705-720. doi: 10.2147/PGPM.S366826. eCollection 2022. Pharmgenomics Pers Med. 2022. PMID: 35898556 Free PMC article.
Targeting Cytotoxin-Associated Antigen A, a Virulent Factor of Helicobacter pylori-Associated Gastric Cancer: Structure-Based In Silico Screening of Natural Compounds.
He S, Almalki AA, Rafeeq MM, Sain ZM, Alqosaibi AI, Alnamshan MM, Al-Dhuayan IS, Rahaman A, Zhang Y, Banjer HJ, Anjum F, Alzghaibi HAM, Alharbi AH, Jamal QMS. He S, et al. Among authors: alqosaibi ai. Molecules. 2022 Jan 23;27(3):732. doi: 10.3390/molecules27030732. Molecules. 2022. PMID: 35164000 Free PMC article.
Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability.
Waqas A, Nayab A, Shaheen S, Abbas S, Latif M, Rafeeq MM, Al-Dhuayan IS, Alqosaibi AI, Alnamshan MM, Sain ZM, Habib AH, Alam Q, Umair M, Saqib MAN. Waqas A, et al. Among authors: alqosaibi ai. Front Genet. 2022 Apr 28;13:878274. doi: 10.3389/fgene.2022.878274. eCollection 2022. Front Genet. 2022. PMID: 35571055 Free PMC article.
17 results