Sort by
Items per page

Send to

Choose Destination

Search results

Items: 15


Inter-species comparative antioxidant assay and HPTLC analysis of sakuranetin in the chloroform and ethanol extracts of aerial parts of Rhus retinorrhoea and Rhus tripartita.

Alam P, Parvez MK, Arbab AH, Siddiqui NA, Al-Dosary MS, Al-Rehaily AJ, Ahmed S, Kalam MA, Ahmad MS.

Pharm Biol. 2017 Dec;55(1):1450-1457. doi: 10.1080/13880209.2017.1304428.


The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy.

Dombi E, Diot A, Morten K, Carver J, Lodge T, Fratter C, Ng YS, Liao C, Muir R, Blakely EL, Hargreaves I, Al-Dosary M, Sarkar G, Hickman SJ, Downes SM, Jayawant S, Yu-Wai-Man P, Taylor RW, Poulton J.

Neurology. 2016 May 17;86(20):1921-3. doi: 10.1212/WNL.0000000000002688. Epub 2016 Apr 22. No abstract available.


Design, synthesis and anticancer activity of some novel thioureido-benzenesulfonamides incorporated biologically active moieties.

Ghorab MM, Alsaid MS, Al-Dosary MS, Nissan YM, Attia SM.

Chem Cent J. 2016 Apr 7;10:19. doi: 10.1186/s13065-016-0161-4. eCollection 2016.


In-Vitro Anticancer Evaluation and Docking Study of Novel Benzo[g] Quinazoline-sulfonamide Derivatives.

Ghorab MM, Alsaid MS, Al-Dosary MS, El-Gazzar MG.

Med Chem. 2016;12(5):448-56.


ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder.

Al-Hassnan ZN, Al-Dosary M, Alfadhel M, Faqeih EA, Alsagob M, Kenana R, Almass R, Al-Harazi OS, Al-Hindi H, Malibari OI, Almutari FB, Tulbah S, Alhadeq F, Al-Sheddi T, Alamro R, AlAsmari A, Almuntashri M, Alshaalan H, Al-Mohanna FA, Colak D, Kaya N.

J Med Genet. 2015 Mar;52(3):186-94. doi: 10.1136/jmedgenet-2014-102592. Epub 2014 Dec 24.


Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly.

Faqeih EA, Al-Owain M, Colak D, Kenana R, Al-Yafee Y, Al-Dosary M, Al-Saman A, Albalawi F, Al-Sarar D, Domiaty D, Daghestani M, Kaya N.

Am J Med Genet A. 2014 Jun;164A(6):1565-70. doi: 10.1002/ajmg.a.36482. Epub 2014 Mar 25.


Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay.

Al-Sayed MD, Al-Zaidan H, Albakheet A, Hakami H, Kenana R, Al-Yafee Y, Al-Dosary M, Qari A, Al-Sheddi T, Al-Muheiza M, Al-Qubbaj W, Lakmache Y, Al-Hindi H, Ghaziuddin M, Colak D, Kaya N.

Am J Hum Genet. 2013 Oct 3;93(4):721-6. doi: 10.1016/j.ajhg.2013.08.001. Epub 2013 Sep 26.


Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy.

Tuppen HA, Naess K, Kennaway NG, Al-Dosary M, Lesko N, Yarham JW, Bruhn H, Wibom R, Nennesmo I, Weleber RG, Blakely EL, Taylor RW, McFarland R.

Eur J Hum Genet. 2012 Aug;20(8):897-904. doi: 10.1038/ejhg.2012.44. Epub 2012 Feb 29. Erratum in: Eur J Hum Genet. 2012 Aug;20(8):910.


A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations.

Yarham JW, Al-Dosary M, Blakely EL, Alston CL, Taylor RW, Elson JL, McFarland R.

Hum Mutat. 2011 Nov;32(11):1319-25. doi: 10.1002/humu.21575. Epub 2011 Sep 19.


Effects of Riyadh cement industry pollutions on some physiological and morphological factors of Datura innoxia Mill. plant.

Salama HM, Al-Rumaih MM, Al-Dosary MA.

Saudi J Biol Sci. 2011 Jul;18(3):227-37. doi: 10.1016/j.sjbs.2011.05.001. Epub 2011 May 6.


The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families.

Tuppen HA, Hogan VE, He L, Blakely EL, Worgan L, Al-Dosary M, Saretzki G, Alston CL, Morris AA, Clarke M, Jones S, Devlin AM, Mansour S, Chrzanowska-Lightowlers ZM, Thorburn DR, McFarland R, Taylor RW.

Brain. 2010 Oct;133(10):2952-63. doi: 10.1093/brain/awq232. Epub 2010 Sep 6.


Morphology of the egg shell and the developing embryo of the Red Palm Weevil, Rhynchophorus ferrugineus (Oliver).

Al-Dosary MM, Al-Bekairi AM, Moursy EB.

Saudi J Biol Sci. 2010 Apr;17(2):177-83. doi: 10.1016/j.sjbs.2010.02.012. Epub 2010 Feb 6.


Neuromuscular disease presentation with three genetic defects involving two genomes.

Al-Dosary M, Whittaker RG, Haughton J, McFarland R, Goodship J, Turnbull DM, Taylor RW.

Neuromuscul Disord. 2009 Dec;19(12):841-4. doi: 10.1016/j.nmd.2009.10.001. Epub 2009 Oct 22.


A novel mitochondrial DNA mutation in COX1 leads to strokes, seizures, and lactic acidosis.

Tam EW, Feigenbaum A, Addis JB, Blaser S, Mackay N, Al-Dosary M, Taylor RW, Ackerley C, Cameron JM, Robinson BH.

Neuropediatrics. 2008 Dec;39(6):328-34. doi: 10.1055/s-0029-1202287. Epub 2009 Jun 30.


Supplemental Content

Loading ...
Support Center