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1.
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
2.
Progress in research on the reproductive function in the sand rat (Psammomys obesus): A review.
Gen Comp Endocrinol;
331: 114161, 2023 01 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-36368440
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.
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
5.
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
6.
Global patterns of apparent copy number variation in birds revealed by cross-species comparative genomic hybridization.
Chromosome Res;
22(1): 59-70, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24570127
7.
Novel tools for characterising inter and intra chromosomal rearrangements in avian microchromosomes.
Chromosome Res;
22(1): 85-97, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-24696127
8.
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
9.
Advances in research on the biology of the desert rodent Gerbillus tarabuli: a review.
Lab Anim;
56(4): 319-330, 2022 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-35216536
10.
Genetic diversity, antifungal evaluation and molecular docking studies of Cu-chitosan nanoparticles as prospective stem rust inhibitor candidates among some Egyptian wheat genotypes.
PLoS One;
16(11): e0257959, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34767570
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.
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.
Cell Biosci;
10: 126, 2020.
Artículo
en Inglés
| MEDLINE | ID: mdl-33133516
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.
Genistein Induces Alterations of Epigenetic Modulatory Signatures in Human Cervical Cancer Cells.
Anticancer Agents Med Chem;
18(3): 412-421, 2018.
Artículo
en Inglés
| MEDLINE | ID: mdl-28925878
16.
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
17.
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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