Tlili A - Search Results

1

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. Among authors: tlili a. 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.

2

Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation.

Tlili A, Fahd Al Mutery A, Mahfood M, Kamal Eddine Ahmad Mohamed W, Bajou K. Tlili A, et al. PLoS One. 2017 Sep 25;12(9):e0185281. doi: 10.1371/journal.pone.0185281. eCollection 2017. PLoS One. 2017. PMID: 28945813 Free PMC article.

3

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. 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

4

CDC14A phosphatase is essential for hearing and male fertility in mouse and human.

Imtiaz A, Belyantseva IA, Beirl AJ, Fenollar-Ferrer C, Bashir R, Bukhari I, Bouzid A, Shaukat U, Azaiez H, Booth KT, Kahrizi K, Najmabadi H, Maqsood A, Wilson EA, Fitzgerald TS, Tlili A, Olszewski R, Lund M, Chaudhry T, Rehman AU, Starost MF, Waryah AM, Hoa M, Dong L, Morell RJ, Smith RJH, Riazuddin S, Masmoudi S, Kindt KS, Naz S, Friedman TB. Imtiaz A, et al. Among authors: tlili a. Hum Mol Genet. 2018 Mar 1;27(5):780-798. doi: 10.1093/hmg/ddx440. Hum Mol Genet. 2018. PMID: 29293958 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: tlili 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

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: tlili a. Ann Hum Genet. 2019 Nov;83(6):472-476. doi: 10.1111/ahg.12335. Epub 2019 Jun 13. Ann Hum Genet. 2019. PMID: 31192455

7

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: tlili a. Front Genet. 2019 Nov 8;10:1087. doi: 10.3389/fgene.2019.01087. eCollection 2019. Front Genet. 2019. PMID: 31781163 Free PMC article.

8

Mitochondrial mutations in non-syndromic hearing loss at UAE.

Mohamed WKE, Arnoux M, Cardoso THS, Almutery A, Tlili A. Mohamed WKE, et al. Among authors: tlili a. 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

9

Clinical heterogeneity of the SLC26A4 gene in UAE patients with hearing loss and bioinformatics investigation of DFNB4/Pendred syndrome missense mutations.

Chouchen J, Mahfood M, Alobathani M, Eldin Mohamed WK, Tlili A. Chouchen J, et al. Among authors: tlili a. Int J Pediatr Otorhinolaryngol. 2021 Jan;140:110467. doi: 10.1016/j.ijporl.2020.110467. Epub 2020 Nov 9. Int J Pediatr Otorhinolaryngol. 2021. PMID: 33199029

10

Combinatorial targeting of microRNA-26b and microRNA-101 exerts a synergistic inhibition on cyclooxygenase-2 in brain metastatic triple-negative breast cancer cells.

Harati R, Mabondzo A, Tlili A, Khoder G, Mahfood M, Hamoudi R. Harati R, et al. Among authors: tlili a. Breast Cancer Res Treat. 2021 Jun;187(3):695-713. doi: 10.1007/s10549-021-06255-y. Epub 2021 May 26. Breast Cancer Res Treat. 2021. PMID: 34041621

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