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miR-27a-3p regulates expression of intercellular junctions at the brain endothelium and controls the endothelial barrier permeability

PloS one, 2022-01, Vol.17 (1), p.e0262152-e0262152

2022

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Silencing miR-202-3p increases MMP-1 and promotes a brain invasive phenotype in metastatic breast cancer cells

PloS one, 2020-10, Vol.15 (10), p.e0239292-e0239292

2020

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

Human genetics, 2022-04, Vol.141 (3-4), p.595-605

2022

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

Breast cancer research and treatment, 2021-06, Vol.187 (3), p.695-713

2021

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Genetic analysis of 106 sporadic cases with hearing loss in the UAE population

Human genomics, 2024-06, Vol.18 (1), p.59-8

2024

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Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families

Human genomics, 2023-05, Vol.17 (1), p.42-42, Article 42

2023

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The Segregation of p.Arg68Ter- CLDN14 Mutation in a Syrian Deaf Family, Phenotypic Variations, and Comparative Analysis with the GJB2 Gene

Genes, 2024-05, Vol.15 (5), p.588

2024

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Loss of miR-101-3p Promotes Transmigration of Metastatic Breast Cancer Cells through the Brain Endothelium by Inducing COX-2/MMP1 Signaling

Pharmaceuticals (Basel, Switzerland), 2020-07, Vol.13 (7), p.144

2020

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Congenital anomalies of the kidney and urinary tract

Frontiers in medicine, 2024-07, Vol.11, p.1384676

2024

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

PloS one, 2017-09, Vol.12 (9), p.e0185281-e0185281

2017

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Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population

Journal of advanced research, 2021-07, Vol.31, p.13-24

2021

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Functional consequences of Genetics variant in TMC1 and TMC2 within a United Arab Emirates family with Pre-lingual hearing loss

Saudi journal of biological sciences, 2023-02, Vol.30 (2), p.103520-103520, Article 103520

2023

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

Frontiers in genetics, 2019-11, Vol.10

2019

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Genetic Diversity in Casein Gene Cluster in a Dromedary Camel ( C. dromedarius ) Population from the United Arab Emirates

Genes, 2021-09, Vol.12 (9), p.1417

2021

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Whole exome sequencing, in silico and functional studies confirm the association of the GJB2 mutation p.Cys169Tyr with deafness and suggest a role for the TMEM59 gene in the hearing process

Saudi journal of biological sciences, 2021-08, Vol.28 (8), p.4421-4429

2021

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Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region

Frontiers in neurology, 2023-03, Vol.14, p.1092887

2023

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Fast, highly sensitive and label free detection of small genetic sequence difference of DNA using novel Surface-Enhanced Raman Spectroscopy nanostructured sensor

Sensing and Bio-Sensing Research, 2021-06, Vol.32, p.100406, Article 100406

2021

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Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria

Journal of human genetics, 2014-04, Vol.59 (4), p.216-222

2014

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Mutations of LRTOMT , a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

Nature genetics, 2008-11, Vol.40 (11), p.1335-1340

2008

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The Segregation of p.Arg68Ter-ICLDN14/I Mutation in a Syrian Deaf Family, Phenotypic Variations, and Comparative Analysis with the IGJB2/I Gene

Genes, 2024-05, Vol.15 (5)

2024

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Two new mutations, ESPN c.2257T>C and ESRRB c.10583 C>A, cause hearing loss in UAE families

Hamdan Medical Journal, 2020, Vol.13 (2), p.115

2020

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Dual phenomenon of surface plasmon and laser optics induced EM enhancement for rapid DNA detection with semiconductor nanostructures (SiNWs/AgNPs)

Journal of physics. Conference series, 2022-08, Vol.2327 (1), p.12018

2022

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Mitochondrial genes modulate the phenotypic expression of congenital scoliosis syndrome caused by mutations in the TBXT gene

Gene, 2024-07, Vol.914, p.148388-148388, Article 148388

2024

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Evidence of Mutational Heterogeneity of the ALDH7A1 Gene in Tunisian Families： Molecular and Insilico Investigations

Journal of materials science and engineering. B, 2016-08, Vol.6 (4), p.196-200

Abdelaziz Tlili Marwa kharrat Emna Mkaouar-Rebai Nadia Hamida-Hentati Sawssan Ben Romdhan Nourhene Fendri-Kriaa Faiza Fakhfakh

2016

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Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome

The Journal of clinical investigation, 2018-08, Vol.128 (8), p.3382-3401

2018

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miR-27a-3p regulates expression of intercellular junctions at the brain endothelium and controls the endothelial barrier permeability

Silencing miR-202-3p increases MMP-1 and promotes a brain invasive phenotype in metastatic breast cancer cells

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

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

Genetic analysis of 106 sporadic cases with hearing loss in the UAE population

Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families

The Segregation of p.Arg68Ter- CLDN14 Mutation in a Syrian Deaf Family, Phenotypic Variations, and Comparative Analysis with the GJB2 Gene

Loss of miR-101-3p Promotes Transmigration of Metastatic Breast Cancer Cells through the Brain Endothelium by Inducing COX-2/MMP1 Signaling

Congenital anomalies of the kidney and urinary tract

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

Novel pathogenic mutations and further evidence for clinical relevance of genes and variants causing hearing impairment in Tunisian population

Functional consequences of Genetics variant in TMC1 and TMC2 within a United Arab Emirates family with Pre-lingual hearing loss

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

Genetic Diversity in Casein Gene Cluster in a Dromedary Camel ( C. dromedarius ) Population from the United Arab Emirates

Whole exome sequencing, in silico and functional studies confirm the association of the GJB2 mutation p.Cys169Tyr with deafness and suggest a role for the TMEM59 gene in the hearing process

Case report: Functional analysis of the p.Arg507Trp variant of the PIGT gene supporting the moderate epilepsy phenotype of mutations in the C-terminal region

Fast, highly sensitive and label free detection of small genetic sequence difference of DNA using novel Surface-Enhanced Raman Spectroscopy nanostructured sensor

Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria

Mutations of LRTOMT , a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans

The Segregation of p.Arg68Ter-ICLDN14/I Mutation in a Syrian Deaf Family, Phenotypic Variations, and Comparative Analysis with the IGJB2/I Gene

Two new mutations, ESPN c.2257T>C and ESRRB c.10583 C>A, cause hearing loss in UAE families

Dual phenomenon of surface plasmon and laser optics induced EM enhancement for rapid DNA detection with semiconductor nanostructures (SiNWs/AgNPs)

Mitochondrial genes modulate the phenotypic expression of congenital scoliosis syndrome caused by mutations in the TBXT gene

Evidence of Mutational Heterogeneity of the ALDH7A1 Gene in Tunisian Families： Molecular and Insilico Investigations

Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome

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