Alam Q - Search Results

1

Multitargeted inhibitory effect of Mitoxantrone 2HCl on cervical cancer cell cycle regulatory proteins: a multitargeted docking-based MM\GBSA and MD simulation study.

Alshehri MA, Asiri SA, Alzahrani A, Alazragi RS, Alqahtani LS, Alqosaibi AI, Alnamshan MM, Alam Q, Rafeeq MM. Alshehri MA, et al. Among authors: alam q. Med Oncol. 2023 Oct 20;40(11):337. doi: 10.1007/s12032-023-02203-6. Med Oncol. 2023. PMID: 37864019

2

Unveiling the multitargeted potency of Sodium Danshensu against cervical cancer: a multitargeted docking-based, structural fingerprinting and molecular dynamics simulation study.

Alghamdi S, Baeissa HM, Azhar Kamal M, Rafeeq MM, Al Zahrani A, Maslum AA, Hakeem IJ, Alazragi RS, Alam Q. Alghamdi S, et al. Among authors: alam q. J Biomol Struct Dyn. 2024 Oct;42(16):8268-8280. doi: 10.1080/07391102.2023.2248260. Epub 2023 Aug 20. J Biomol Struct Dyn. 2024. PMID: 37599470

3

Biocomputational Prediction Approach Targeting FimH by Natural SGLT2 Inhibitors: A Possible Way to Overcome the Uropathogenic Effect of SGLT2 Inhibitor Drugs.

Mashraqi MM, Chaturvedi N, Alam Q, Alshamrani S, Bahnass MM, Ahmad K, Alqosaibi AI, Alnamshan MM, Ahmad SS, Beg MMA, Mishra A, Shaikh S, Rizvi SMD. Mashraqi MM, et al. Among authors: alam q. Molecules. 2021 Jan 22;26(3):582. doi: 10.3390/molecules26030582. Molecules. 2021. PMID: 33499241 Free PMC article.

4

A Novel Homozygous Missense Mutation in the Zinc Finger DNA Binding Domain of GLI1 Causes Recessive Post-Axial Polydactyly.

Umair M, Ahmad F, Ahmad S, Alam Q, Rehan M, Alqosaibi AI, Alnamshan MM, Rafeeq MM, Haque S, Sain ZM, Ismail M, Alfadhel M. Umair M, et al. Among authors: alam q. Front Genet. 2021 Oct 15;12:746949. doi: 10.3389/fgene.2021.746949. eCollection 2021. Front Genet. 2021. PMID: 34721536 Free PMC article.

5

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: alam q. Front Genet. 2022 Apr 28;13:878274. doi: 10.3389/fgene.2022.878274. eCollection 2022. Front Genet. 2022. PMID: 35571055 Free PMC article.

6

Case report: A novel de novo loss of function variant in the DNA-binding domain of TBX2 causes severe osteochondrodysplasia.

Rafeeq MM, Murad HAS, Najumuddin, Ullah S, Ahmed Z, Alam Q, Bilal M, Habib AH, Sain ZM, Khan MJ, Umair M. Rafeeq MM, et al. Among authors: alam q. Front Genet. 2023 Jan 17;13:1117500. doi: 10.3389/fgene.2022.1117500. eCollection 2022. Front Genet. 2023. PMID: 36733940 Free PMC article.

7

Targeted exome sequencing identified a novel frameshift variant in the PGAM2 gene causing glycogen storage disease type X.

Nayab A, Alam Q, Alzahrani OR, Khan R, Sarfaraz S, Albaz AA, Rafeeq MM, Sain ZM, Waqas A, Umair M. Nayab A, et al. Among authors: alam q. Eur J Med Genet. 2021 Sep;64(9):104283. doi: 10.1016/j.ejmg.2021.104283. Epub 2021 Jul 5. Eur J Med Genet. 2021. PMID: 34237446

8

Targeting Kaposi's sarcoma associated herpesvirus encoded protease (ORF17) by a lysophosphatidic acid molecule for treating KSHV associated diseases.

Rafeeq MM, Habib AH, Nahhas AF, Binothman N, Aljadani M, Almulhim J, Sain ZM, Alam MZ, Alturki NA, Alam Q, Manish M, Singh RK. Rafeeq MM, et al. Among authors: alam mz, alam q. Front Cell Dev Biol. 2023 Jan 17;11:1060156. doi: 10.3389/fcell.2023.1060156. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 36733461 Free PMC article.

9

Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type A.

Umair M, Palander O, Bilal M, Almuzzaini B, Alam Q, Ahmad F, Younus M, Khan A, Waqas A, Rafeeq MM, Alfadhel M. Umair M, et al. Among authors: alam q. Genomics. 2021 Jul;113(4):2495-2502. doi: 10.1016/j.ygeno.2021.05.015. Epub 2021 May 20. Genomics. 2021. PMID: 34022343 Free article.

10

Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome.

Nawaz H, Mujahid, Khan SA, Bibi F, Waqas A, Bari A, Fardous, Khan N, Muhammad N, Khan A, Paracha SA, Alam Q, Kamal MA, Rafeeq MM, Muhammad N, Haq FU, Khan S, Mahmood A, Khan S, Umair M. Nawaz H, et al. Among authors: alam q. Genes (Basel). 2023 May 19;14(5):1113. doi: 10.3390/genes14051113. Genes (Basel). 2023. PMID: 37239474 Free PMC article.

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