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1.
Assessment of genetic polymorphism associated with ATP-binding cassette transporter A1 (ABCA1) gene and fluctuations in serum lipid profile levels in patients with coronary artery disease.
Saudi Pharm J
; 29(12): 1458-1465, 2021 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-35002384
2.
Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community.
Hum Genomics
; 12(1): 18, 2018 04 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-29631625
3.
A genetic variant c.553G > T (rs2075291) in the apolipoprotein A5 gene is associated with altered triglycerides levels in coronary artery disease (CAD) patients with lipid lowering drug.
BMC Cardiovasc Disord
; 19(1): 2, 2019 01 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-30606120
4.
Novel LDLR Variant in Familial Hypercholesterolemia: NGS-Based Identification, In Silico Characterization, and Pharmacogenetic Insights.
Life (Basel)
; 13(7)2023 Jul 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-37511917
5.
Anti-E. coli Immunoglobulin Yolk (IgY): Reduction of pathogen receptors and inflammation factors could be caused by decrease in E. coli load.
Heliyon
; 9(3): e13876, 2023 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-36873547
6.
Corrigendum to "Anti- E. coli immunoglobulin yolk (IgY): Reduction of pathogen receptors and inflammation factors could be caused by decrease in E. coli load" [Heliyon 9(3) (February 21, 2023) e13876]>.
Heliyon
; 9(6): e16582, 2023 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-37484345
7.
SARS-CoV-2 vaccine breakthrough infections (VBI) by Omicron variant (B.1.1.529) and consequences in structural and functional impact.
Cell Signal
; 109: 110798, 2023 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-37423342
8.
Genetic Association of rs10757278 on Chromosome 9p21 and Coronary Artery Disease in a Saudi Population.
Int J Gen Med
; 14: 1699-1707, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33981157
9.
Human papillomavirus, gene mutation and estrogen and progesterone receptors in breast cancer: a cross-sectional study.
Pan Afr Med J
; 38: 43, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-33854672
10.
Identification of PKHD1 mutations in Brain, Breast and Rectal tumors by Next Generation DNA Sequencing.
Gulf J Oncolog
; 1(35): 42-53, 2021 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-33716212
11.
Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism.
Clin Chim Acta
; 519: 247-254, 2021 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-34015304
12.
Association between HindIII (rs320) variant in the lipoprotein lipase gene and the presence of coronary artery disease and stroke among the Saudi population.
Saudi J Biol Sci
; 27(8): 2018-2024, 2020 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-32714026
13.
Whole exome sequencing detects novel variants in Saudi children diagnosed with eczema.
J Infect Public Health
; 13(1): 27-33, 2020 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-31213409
14.
Combined Genetic Biomarkers Confer Susceptibility to Risk of Urothelial Bladder Carcinoma in a Saudi Population.
Dis Markers
; 2017: 1474560, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28348449
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