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1.
Genetic analysis of 106 sporadic cases with hearing loss in the UAE population.
Hum Genomics;
18(1): 59, 2024 Jun 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-38844983
2.
Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families.
Hum Genomics;
17(1): 42, 2023 05 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-37189200
3.
Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countries.
Hum Genet;
141(3-4): 595-605, 2022 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-34338889
4.
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 Res Treat;
187(3): 695-713, 2021 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-34041621
5.
Novel mutation in the DSG1 gene causes autosomal-dominant striate palmoplantar keratoderma in a large Syrian family.
Ann Hum Genet;
83(6): 472-476, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31192455
6.
Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism.
J Assist Reprod Genet;
36(6): 1273-1280, 2019 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-31073722
7.
Functional consequences of Genetics variant in TMC1 and TMC2 within a United Arab Emirates family with Pre-lingual hearing loss.
Saudi J Biol Sci;
30(2): 103520, 2023 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-36568409
8.
miR-27a-3p regulates expression of intercellular junctions at the brain endothelium and controls the endothelial barrier permeability.
PLoS One;
17(1): e0262152, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35025943
9.
miR-623 Targets Metalloproteinase-1 and Attenuates Extravasation of Brain Metastatic Triple-Negative Breast Cancer Cells.
Breast Cancer (Dove Med Press);
14: 187-198, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35936987
10.
Clinical heterogeneity of the SLC26A4 gene in UAE patients with hearing loss and bioinformatics investigation of DFNB4/Pendred syndrome missense mutations.
Int J Pediatr Otorhinolaryngol;
140: 110467, 2021 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-33199029
11.
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 J Biol Sci;
28(8): 4421-4429, 2021 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-34354426
12.
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation.
Front Endocrinol (Lausanne);
12: 684018, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34393998
13.
A Novel Nonsense Mutation (c.414G>A; p.Trp138*) in CLDN14 Causes Hearing Loss in Yemeni Families: A Case Report.
Front Genet;
10: 1087, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31781163
14.
Clinical Exome Sequencing Identifies a Frameshift Mutation Within the STRC Gene in a United Arab Emirates Family with Profound Nonsyndromic Hearing Loss.
Genet Test Mol Biomarkers;
23(3): 204-208, 2019 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-30758234
15.
Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation.
PLoS One;
12(9): e0185281, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28945813
16.
Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
Genet Test Mol Biomarkers;
21(11): 686-691, 2017 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-29016196
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