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Items: 12

1.

Whole exome sequencing detects novel variants in Saudi children diagnosed with eczema.

Bogari NM, Amin AA, Rayes HH, Abdelmotelb A, Al-Allaf FA, Dannoun A, Al-Amodi HS, Sedayo AA, Almalk H, Moulana A, Balkhair R, Jambi F, Madani F, Abutalib M, Taher MM, Bouazzaoui A, Aljohani A, Bogari MN, G K UR, Fawzy A, Alharbi KK, Ali Khan I.

J Infect Public Health. 2019 Jun 15. pii: S1876-0341(19)30188-1. doi: 10.1016/j.jiph.2019.05.020. [Epub ahead of print]

2.

Identification of six novel factor viii gene variants using next generation sequencing and molecular dynamics simulation.

Al-Allaf FA, Abduljaleel Z, Bogari NM, Owaidah TMA, Taher MM, Athar M, Elsendiony A, Abalkhail H, Abdellatif A, Elbjeirami W, Bouazzaoui A.

Acta Biochim Pol. 2019 Feb 22;66(1):23-31. doi: 10.18388/abp.2018_2339.

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.

Bogari NM, Aljohani A, Amin AA, Al-Allaf FA, Dannoun A, Taher MM, Elsayed A, Rednah DI, Elkhatee O, Porqueddu M, Alamanni F, Khogeer SAA, Fawzy A.

BMC Cardiovasc Disord. 2019 Jan 3;19(1):2. doi: 10.1186/s12872-018-0965-3.

4.

Pattern of Thyroid Lesions in Western Region of Saudi Arabia: A Retrospective Analysis and Literature Review.

Saeed MI, Hassan AA, Butt ME, Baniyaseen KA, Siddiqui MI, Bogari NM, Al-Allaf FA, Taher MM.

J Clin Med Res. 2018 Feb;10(2):106-116. doi: 10.14740/jocmr3202w. Epub 2017 Dec 30.

5.

Molecular Analysis of Factor VIII and Factor IX Genes in Hemophilia Patients: Identification of Novel Mutations and Molecular Dynamics Studies.

Al-Allaf FA, Taher MM, Abduljaleel Z, Bouazzaoui A, Athar M, Bogari NM, Abalkhail HA, Owaidah TM.

J Clin Med Res. 2017 Apr;9(4):317-331. doi: 10.14740/jocmr2876w. Epub 2017 Feb 21.

6.

Next generation sequencing (NGS) in glucose-6-phosphate dehydrogenase (G6PD) deficiency studies.

Bogari NM.

Bioinformation. 2016 Apr 10;12(2):41-43. doi: 10.6026/97320630012041. eCollection 2016.

7.

A novel SNP in 3' UTR of INS gene: A case report of neonatal diabetes mellitus.

Bogari NM, Rayes HH, Mostafa F, Abdel-Latif AM, Ramadan A, Al-Allaf FA, Taher MM, Fawzy A.

Diabetes Res Clin Pract. 2015 Sep;109(3):e14-7. doi: 10.1016/j.diabres.2015.06.002. Epub 2015 Jul 10.

PMID:
26212367
8.

No association of apolipoprotein B gene polymorphism and blood lipids in obese Egyptian subjects.

Bogari NM, Abdel-Latif AM, Hassan MA, Ramadan A, Fawzy A.

J Negat Results Biomed. 2015 Mar 18;14:7. doi: 10.1186/s12952-015-0026-8.

9.

Transporter TAP1-637G and immunoproteasome PSMB9-60H variants influence the risk of developing vitiligo in the Saudi population.

Elhawary NA, Bogari N, Jiffri EH, Rashad M, Fatani A, Tayeb M.

Dis Markers. 2014;2014:260732. doi: 10.1155/2014/260732. Epub 2014 Dec 7.

10.

The MTHFR 677T allele may influence the severity and biochemical risk factors of Alzheimer's disease in an Egyptian population.

Elhawary NA, Hewedi D, Arab A, Teama S, Shaibah H, Tayeb MT, Bogari N.

Dis Markers. 2013;35(5):439-46. doi: 10.1155/2013/524106. Epub 2013 Oct 1.

11.

Molecular updating of β-thalassemia mutations in the Upper Egyptian population.

Jiffri EH, Bogari N, Zidan KH, Teama S, Elhawary NA.

Hemoglobin. 2010;34(6):538-47. doi: 10.3109/03630269.2010.526440.

PMID:
21077761
12.

Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patients.

Kyriakou T, Pontefract DE, Viturro E, Hodgkinson CP, Laxton RC, Bogari N, Cooper G, Davies M, Giblett J, Day IN, Simpson IA, Albrecht C, Ye S.

Hum Mol Genet. 2007 Jun 15;16(12):1412-22. Epub 2007 Apr 5.

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