Found: 11
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Genetic analysis of 106 sporadic cases with hearing loss in the UAE population.
- Published in:
- Human Genomics, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s40246-024-00630-8
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- Article
Combinatorial targeting of microRNA-26b and microRNA-101 exerts a synergistic inhibition on cyclooxygenase-2 in brain metastatic triple-negative breast cancer cells.
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- Breast Cancer Research & Treatment, 2021, v. 187, n. 3, p. 695, doi. 10.1007/s10549-021-06255-y
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- Article
Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countries.
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- Human Genetics, 2022, v. 141, n. 3/4, p. 595, doi. 10.1007/s00439-021-02323-x
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- Article
A Novel Nonsense Mutation (c.414G>A; p.Trp138*) in CLDN14 Causes Hearing Loss in Yemeni Families: A Case Report.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01087
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- Article
Tunisian Maturity-Onset Diabetes of the Young: A Short Review and a New Molecular and Clinical Investigation.
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- Frontiers in Endocrinology, 2021, v. 12, p. 1, doi. 10.3389/fendo.2021.684018
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- Article
miR-623 Targets Metalloproteinase-1 and Attenuates Extravasation of Brain Metastatic Triple-Negative Breast Cancer Cells.
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- Breast Cancer: Targets & Therapy, 2022, v. 14, p. 187, doi. 10.2147/BCTT.S372083
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- Article
Novel mutation in the DSG1 gene causes autosomal‐dominant striate palmoplantar keratoderma in a large Syrian family.
- Published in:
- Annals of Human Genetics, 2019, v. 83, n. 6, p. 472, doi. 10.1111/ahg.12335
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- Article
Loss-of-function mutations in MYO15A and OTOF cause non-syndromic hearing loss in two Yemeni families.
- Published in:
- Human Genomics, 2023, v. 17, n. 1, p. 1, doi. 10.1186/s40246-023-00489-1
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- Article
Nonstop mutation in the Kisspeptin 1 receptor (KISS1R) gene causes normosmic congenital hypogonadotropic hypogonadism.
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- Journal of Assisted Reproduction & Genetics, 2019, v. 36, n. 6, p. 1273, doi. 10.1007/s10815-019-01468-z
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- Article
miR-27a-3p regulates expression of intercellular junctions at the brain endothelium and controls the endothelial barrier permeability.
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- PLoS ONE, 2022, v. 17, n. 1, p. 1, doi. 10.1371/journal.pone.0262152
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- Article
Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation.
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- PLoS ONE, 2017, v. 12, n. 9, p. 1, doi. 10.1371/journal.pone.0185281
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- Article