Detalhe da pesquisa
1.
Whole genome transcriptomic reveals heat stroke molecular signatures in humans.
J Physiol
; 601(12): 2407-2423, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36951421
2.
Impact of Genetic Variations on Thromboembolic Risk in Saudis with Sickle Cell Disease.
Genes (Basel)
; 14(10)2023 10 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37895268
3.
Blockade of p38 MAPK overcomes AML stem cell line KG1a resistance to 5-Fluorouridine and the impact on miRNA profiling.
PLoS One
; 17(5): e0267855, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35511922
4.
Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo CDC42 Gene Defect: Expanding the Molecular and Phenotypic Spectrum.
Genes (Basel)
; 12(2)2021 02 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33672558
5.
Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay.
Ann Clin Transl Neurol
; 7(6): 956-964, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32431071
6.
Differential Gene Expression in Peripheral White Blood Cells with Permissive Underfeeding and Standard Feeding in Critically Ill Patients: A Descriptive Sub-study of the PermiT Randomized Controlled Trial.
Sci Rep
; 8(1): 17984, 2018 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30573851