Detalhe da pesquisa
1.
Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21-year single-center experience.
Am J Med Genet A
; 179(8): 1516-1524, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31207162
2.
Chromosomal Abnormalities in Patients with Intellectual Disability: A 21-Year Retrospective Study.
Hum Hered
; 83(5): 274-282, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-31064002
3.
Chromosomal abnormalities in couples with recurrent spontaneous miscarriage: a 21-year retrospective study, a report of a novel insertion, and a literature review.
J Assist Reprod Genet
; 36(3): 499-507, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30470960
4.
Exploring the impact of CYP11A1's missense SNPs on the interaction between CYP11A1 and cholesterol: A comprehensive structural analysis and MD simulation study.
Comput Biol Chem
; 106: 107937, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37552904
5.
Association study of leptin receptor polymorphisms in women with obesity and their impact on protein domains: a case-control study and in silico analyses.
J Biomol Struct Dyn
; 41(14): 6546-6558, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-35968638
6.
Potential inhibitors of SARS-cov-2 RNA dependent RNA polymerase protein: molecular docking, molecular dynamics simulations and MM-PBSA analyses.
J Biomol Struct Dyn
; 40(1): 361-374, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-32873176
7.
Computational screening of potential drugs against COVID-19 disease: the Neuropilin-1 receptor as molecular target.
Virusdisease
; 33(1): 23-31, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-35079600
8.
Attenuation and genetic characteristics of a Moroccan strain of Camel pox virus.
Vaccine
; 40(45): 6471-6480, 2022 10 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-36192275
9.
Identification of p.Met215Ile mutation of the MC4R gene in a Moroccan woman with obesity.
Clin Case Rep
; 9(11): e05059, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34815872
10.
Dominant ACO2 mutations are a frequent cause of isolated optic atrophy.
Brain Commun
; 3(2): fcab063, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34056600
11.
Prediction of the Impact of Deleterious Nonsynonymous Single Nucleotide Polymorphisms on the Human RRM2B Gene: A Molecular Modeling Study.
Biomed Res Int
; 2020: 7614634, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32775440
12.
Identification of deleterious missense variants of human Piwi like RNA-mediated gene silencing 1 gene and their impact on PAZ domain structure, stability, flexibility and dimension: in silico analysis.
J Biomol Struct Dyn
; 38(15): 4600-4606, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-31595844
13.
Computational Analysis of nsSNPs of ADA Gene in Severe Combined Immunodeficiency Using Molecular Modeling and Dynamics Simulation.
J Immunol Res
; 2019: 5902391, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31781678
14.
In Silico Analysis of Coding/Noncoding SNPs of Human RETN Gene and Characterization of Their Impact on Resistin Stability and Structure.
J Diabetes Res
; 2019: 4951627, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31236417