Alzahrani AS - Search Results

1

A high rate of novel CYP11B1 mutations in Saudi Arabia.

Alzahrani AS, Alswailem MM, Murugan AK, Alhomaidah DS, Capper CP, Auchus RJ, Qasem E, Alzahrani OS, Al-Sagheir A, Bin-Abbas B. Alzahrani AS, et al. Among authors: alzahrani os. J Steroid Biochem Mol Biol. 2017 Nov;174:217-224. doi: 10.1016/j.jsbmb.2017.09.018. Epub 2017 Sep 28. J Steroid Biochem Mol Biol. 2017. PMID: 28962970

2

Epidemiology, clinical and complications profile of diabetes in Saudi Arabia: a review.

Elhadd TA, Al-Amoudi AA, Alzahrani AS. Elhadd TA, et al. Among authors: alzahrani as. Ann Saudi Med. 2007 Jul-Aug;27(4):241-50. doi: 10.5144/0256-4947.2007.241. Ann Saudi Med. 2007. PMID: 17684435 Free PMC article. Review.

3

Paget disease of the bone: does it exist in Saudi Arabia?

Alshaikh OM, Almanea H, Alzahrani AS. Alshaikh OM, et al. Among authors: alzahrani as. Ann Saudi Med. 2011 May-Jun;31(3):305-10. doi: 10.4103/0256-4947.75588. Ann Saudi Med. 2011. PMID: 21242639 Free PMC article.

4

Molecular characterization of a novel p.R118C mutation in the insulin receptor gene from patients with severe insulin resistance.

Alzahrani AS, Zou M, Baitei EY, Parhar RS, Al-Kahtani N, Raef H, Almahfouz A, Amartey JK, Al-Rijjal R, Hammami R, Meyer BF, Al-Mohanna FA, Shi Y. Alzahrani AS, et al. Clin Endocrinol (Oxf). 2012 Apr;76(4):540-7. doi: 10.1111/j.1365-2265.2011.04258.x. Clin Endocrinol (Oxf). 2012. PMID: 22017372

5

Mutations in critical domains confer the human mTOR gene strong tumorigenicity.

Murugan AK, Alzahrani A, Xing M. Murugan AK, et al. J Biol Chem. 2013 Mar 1;288(9):6511-21. doi: 10.1074/jbc.M112.399485. Epub 2013 Jan 15. J Biol Chem. 2013. PMID: 23322780 Free PMC article.

6

Apparent Mineralocorticoid Excess Caused by a Novel Mutation in 11-β Hydroxysteroid Dehydrogenase Type 2 Enzyme: Its Genetics and Response to Therapy.

Alzahrani AS, Aljuhani N, Qasem E, Almohanna M, Hamoudh E, AlOmair A, Alharbi N. Alzahrani AS, et al. Endocr Pract. 2014 Sep;20(9):e151-6. doi: 10.4158/EP14094.CR. Endocr Pract. 2014. PMID: 24936560

7

Divergent gender identity in three siblings with 46XX karyotype and severely virilizing congenital adrenal hyperplasia caused by a novel CYP11B1 mutation.

Bin-Abbas B, Al-Humaida D, Al-Sagheir A, Qasem E, Almohanna M, Alzahrani AS. Bin-Abbas B, et al. Among authors: alzahrani as. Endocr Pract. 2014 Oct;20(10):e191-7. doi: 10.4158/EP14179.CR. Endocr Pract. 2014. PMID: 25100385

8

TERT promoter mutations in thyroid cancer: a report from a Middle Eastern population.

Qasem E, Murugan AK, Al-Hindi H, Xing M, Almohanna M, Alswailem M, Alzahrani AS. Qasem E, et al. Among authors: alzahrani as. Endocr Relat Cancer. 2015 Dec;22(6):901-8. doi: 10.1530/ERC-15-0396. Epub 2015 Sep 9. Endocr Relat Cancer. 2015. PMID: 26354077

9

Absence of somatic mutations of the mTOR gene in differentiated thyroid cancer.

Murugan AK, Humudh EA, Qasem E, Al-Hindi H, Almohanna M, Hassan ZK, Alzahrani AS. Murugan AK, et al. Among authors: alzahrani as. Meta Gene. 2015 Sep 27;6:69-71. doi: 10.1016/j.mgene.2015.08.005. eCollection 2015 Dec. Meta Gene. 2015. PMID: 26504747 Free PMC article.

10

MicroRNAs: Modulators of the Ras Oncogenes in Oral Cancer.

Murugan AK, Munirajan AK, Alzahrani AS. Murugan AK, et al. Among authors: alzahrani as. J Cell Physiol. 2016 Jul;231(7):1424-31. doi: 10.1002/jcp.25269. Epub 2015 Dec 28. J Cell Physiol. 2016. PMID: 26620726 Review.

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