Detalhe da pesquisa
1.
Association of KIR gene polymorphisms with COVID-19 disease.
Clin Immunol
; 234: 108911, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34929414
2.
Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality.
Genomics
; 113(4): 1733-1741, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33838280
3.
Role of sphingolipid metabolism in neurodegeneration.
J Neurochem
; 158(1): 25-35, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32402091
4.
PDCD6IP, encoding a regulator of the ESCRT complex, is mutated in microcephaly.
Clin Genet
; 98(1): 80-85, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32286682
5.
ADAMTS19-associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype.
Clin Genet
; 98(1): 56-63, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32323311
6.
A missense mutation in the CRBN gene that segregates with intellectual disability and self-mutilating behaviour in a consanguineous Saudi family.
J Med Genet
; 54(4): 236-240, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28143899
7.
Case report: A founder UGDH variant associated with developmental epileptic encephalopathy in Saudi Arabia.
Front Genet
; 14: 1294214, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38292436
8.
Tween 80-Based Self-Assembled Mixed Micelles Boost Valsartan Transdermal Delivery.
Pharmaceuticals (Basel)
; 17(1)2023 Dec 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-38256853
9.
TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy.
J Cardiovasc Dev Dis
; 10(11)2023 Nov 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37998513
10.
Consanguinity and Congenital Heart Disease Susceptibility: Insights into Rare Genetic Variations in Saudi Arabia.
Genes (Basel)
; 13(2)2022 02 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35205398
11.
Correlation between ABO Blood Group Phenotype and the Risk of COVID-19 Infection and Severity of Disease in a Saudi Arabian Cohort.
J Epidemiol Glob Health
; 12(1): 85-91, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-34978705
12.
The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome.
Genes (Basel)
; 13(2)2022 01 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35205281
13.
Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes.
Front Genet
; 13: 886038, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36035137
14.
Fast-Dissolving Nifedipine and Atorvastatin Calcium Electrospun Nanofibers as a Potential Buccal Delivery System.
Pharmaceutics
; 14(2)2022 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35214093
15.
Reply to Zandi, M.; Soltani, S. Comment on "Alfassam et al. Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles. Pharmaceutics 2021, 13, 502".
Pharmaceutics
; 14(9)2022 Sep 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36145626
16.
Development of Epirubicin-Loaded Biocompatible Polymer PLA-PEG-PLA Nanoparticles: Synthesis, Characterization, Stability, and In Vitro Anticancerous Assessment.
Polymers (Basel)
; 13(8)2021 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-33918625
17.
Novel Autosomal Recessive Splice-Altering Variant in PRKD1 Is Associated with Congenital Heart Disease.
Genes (Basel)
; 12(5)2021 04 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-33919081
18.
Development of a Colorimetric Tool for SARS-CoV-2 and Other Respiratory Viruses Detection Using Sialic Acid Fabricated Gold Nanoparticles.
Pharmaceutics
; 13(4)2021 Apr 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33917625
19.
A cell-based drug delivery platform for treating central nervous system inflammation.
J Mol Med (Berl)
; 99(5): 663-671, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33398468
20.
Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.
J Clin Invest
; 131(14)2021 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34043590