Al Mutery A - Search Results

1

Genistein Induces Alterations of Epigenetic Modulatory Signatures in Human Cervical Cancer Cells.

Sundaram MK, Ansari MZ, Al Mutery A, Ashraf M, Nasab R, Rai S, Rais N, Hussain A. Sundaram MK, et al. Among authors: al mutery a. Anticancer Agents Med Chem. 2018;18(3):412-421. doi: 10.2174/1871520617666170918142114. Anticancer Agents Med Chem. 2018. PMID: 28925878

2

Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.

Tlili A, Al Mutery A, Kamal Eddine Ahmad Mohamed W, Mahfood M, Hadj Kacem H. Tlili A, et al. Among authors: al mutery a. Genet Test Mol Biomarkers. 2017 Nov;21(11):686-691. doi: 10.1089/gtmb.2017.0130. Epub 2017 Oct 10. Genet Test Mol Biomarkers. 2017. PMID: 29016196

3

Novel mutation in the DSG1 gene causes autosomal-dominant striate palmoplantar keratoderma in a large Syrian family.

Abi Zamer B, Mahfood M, Saleh B, Al Mutery AF, Tlili A. Abi Zamer B, et al. Among authors: al mutery af. Ann Hum Genet. 2019 Nov;83(6):472-476. doi: 10.1111/ahg.12335. Epub 2019 Jun 13. Ann Hum Genet. 2019. PMID: 31192455

4

Genetic diversity, antifungal evaluation and molecular docking studies of Cu-chitosan nanoparticles as prospective stem rust inhibitor candidates among some Egyptian wheat genotypes.

Omar HS, Al Mutery A, Osman NH, Reyad NEA, Abou-Zeid MA. Omar HS, et al. Among authors: al mutery a. PLoS One. 2021 Nov 12;16(11):e0257959. doi: 10.1371/journal.pone.0257959. eCollection 2021. PLoS One. 2021. PMID: 34767570 Free PMC article.

5

Clinical Exome Sequencing Identifies a Frameshift Mutation Within the STRC Gene in a United Arab Emirates Family with Profound Nonsyndromic Hearing Loss.

Mahfood M, Kamal Eddine Ahmad Mohamed W, Al Mutery A, Tlili A. Mahfood M, et al. Among authors: al mutery a. Genet Test Mol Biomarkers. 2019 Mar;23(3):204-208. doi: 10.1089/gtmb.2018.0264. Epub 2019 Feb 13. Genet Test Mol Biomarkers. 2019. PMID: 30758234

6

Significant transcriptomic changes are associated with differentiation of bone marrow-derived mesenchymal stem cells into neural progenitor-like cells in the presence of bFGF and EGF.

Khan AA, Huat TJ, Al Mutery A, El-Serafi AT, Kacem HH, Abdallah SH, Reza MF, Abdullah JM, Jaafar H. Khan AA, et al. Among authors: al mutery a. Cell Biosci. 2020 Oct 28;10:126. doi: 10.1186/s13578-020-00487-z. eCollection 2020. Cell Biosci. 2020. PMID: 33133516 Free PMC article.

7

[No title available]

[No authors listed] [No authors listed] PMID: 33292454

8

Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countries.

Al Mutery A, Mahfood M, Chouchen J, Tlili A. Al Mutery A, et al. Hum Genet. 2022 Apr;141(3-4):595-605. doi: 10.1007/s00439-021-02323-x. Epub 2021 Aug 2. Hum Genet. 2022. PMID: 34338889 Review.

9

Mitochondrial mutations in non-syndromic hearing loss at UAE.

Mohamed WKE, Arnoux M, Cardoso THS, Almutery A, Tlili A. Mohamed WKE, et al. Int J Pediatr Otorhinolaryngol. 2020 Nov;138:110286. doi: 10.1016/j.ijporl.2020.110286. Epub 2020 Aug 7. Int J Pediatr Otorhinolaryngol. 2020. PMID: 32871514

10

A Novel Nonsense Mutation (c.414G>A; p.Trp138*) in CLDN14 Causes Hearing Loss in Yemeni Families: A Case Report.

Mohamed WKE, Mahfood M, Al Mutery A, Abdallah SH, Tlili A. Mohamed WKE, et al. Among authors: al mutery a. Front Genet. 2019 Nov 8;10:1087. doi: 10.3389/fgene.2019.01087. eCollection 2019. Front Genet. 2019. PMID: 31781163 Free PMC article.

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