Abdullah F. Al Mutery

Sharjah, SH, United Arab Emirates

Last Updated: 09/26/2026

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Found 15 publications

Whole-exome sequencing identifies TRIM72 as a candidate gene for autosomal recessive limb-girdle muscular dystrophy.

Whole-exome sequencing identifies TRIM72 as a candidate gene for autosomal recessive limb-girdle muscular dystrophy.

Journal: Human genomics
Published: July 02, 2025

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

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

Journal: Human genomics
Published: February 03, 2024

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

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

Journal: Human genomics
Published: November 27, 2022

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

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

Journal: Saudi journal of biological sciences
Published: July 07, 2022

Advances in research on the biology of the desert rodent Gerbillus tarabuli: a review.

Advances in research on the biology of the desert rodent Gerbillus tarabuli: a review.

Journal: Laboratory animals
Published: February 26, 2022

Progress in research on the reproductive function in the sand rat (Psammomys obesus): A review.

Progress in research on the reproductive function in the sand rat (Psammomys obesus): A review.

Journal: General and comparative endocrinology
Published: January 01, 2022

WITHDRAWN: Distribution of the Novel RFRP-3/receptors system in the epididymis of the seasonal desert rodent, Gerbillus tarabuli, during sexual activity.

WITHDRAWN: Distribution of the Novel RFRP-3/receptors system in the epididymis of the seasonal desert rodent, Gerbillus tarabuli, during sexual activity.

Journal: Morphologie : bulletin de l'Association des anatomistes
Published: August 13, 2021

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

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

Journal: Human genetics
Published: May 23, 2021

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

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

Journal: PloS one
Published: April 20, 2021

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.

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.

Journal: Saudi journal of biological sciences
Published: December 06, 2020

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.

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.

Journal: Cell & bioscience
Published: July 01, 2020

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

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

Journal: Frontiers in genetics
Published: July 26, 2019
Showing 1-12 of 15

Last Updated: 09/26/2026