Salemi R - Search Results

1

Clinical outcome and pathological features associated with NRAS mutation in cutaneous melanoma.

Devitt B, Liu W, Salemi R, Wolfe R, Kelly J, Tzen CY, Dobrovic A, McArthur G. Devitt B, et al. Among authors: salemi r. Pigment Cell Melanoma Res. 2011 Aug;24(4):666-72. doi: 10.1111/j.1755-148X.2011.00873.x. Epub 2011 Jun 22. Pigment Cell Melanoma Res. 2011. PMID: 21615881

2

Mutations in KIT occur at low frequency in melanomas arising from anatomical sites associated with chronic and intermittent sun exposure.

Handolias D, Salemi R, Murray W, Tan A, Liu W, Viros A, Dobrovic A, Kelly J, McArthur GA. Handolias D, et al. Among authors: salemi r. Pigment Cell Melanoma Res. 2010 Apr;23(2):210-5. doi: 10.1111/j.1755-148X.2010.00671.x. Epub 2010 Jan 20. Pigment Cell Melanoma Res. 2010. PMID: 20088873

3

Clinical responses observed with imatinib or sorafenib in melanoma patients expressing mutations in KIT.

Handolias D, Hamilton AL, Salemi R, Tan A, Moodie K, Kerr L, Dobrovic A, McArthur GA. Handolias D, et al. Among authors: salemi r. Br J Cancer. 2010 Apr 13;102(8):1219-23. doi: 10.1038/sj.bjc.6605635. Epub 2010 Apr 6. Br J Cancer. 2010. PMID: 20372153 Free PMC article.

4

Targeted-capture massively-parallel sequencing enables robust detection of clinically informative mutations from formalin-fixed tumours.

Wong SQ, Li J, Salemi R, Sheppard KE, Do H, Tothill RW, McArthur GA, Dobrovic A. Wong SQ, et al. Among authors: salemi r. Sci Rep. 2013 Dec 13;3:3494. doi: 10.1038/srep03494. Sci Rep. 2013. PMID: 24336498 Free PMC article.

5

Dual targeting of the epidermal growth factor receptor using the combination of cetuximab and erlotinib: preclinical evaluation and results of the phase II DUX study in chemotherapy-refractory, advanced colorectal cancer.

Weickhardt AJ, Price TJ, Chong G, Gebski V, Pavlakis N, Johns TG, Azad A, Skrinos E, Fluck K, Dobrovic A, Salemi R, Scott AM, Mariadason JM, Tebbutt NC. Weickhardt AJ, et al. Among authors: salemi r. J Clin Oncol. 2012 May 1;30(13):1505-12. doi: 10.1200/JCO.2011.38.6599. Epub 2012 Mar 12. J Clin Oncol. 2012. PMID: 22412142 Clinical Trial.

6

Rarity of AKT1 and AKT3 E17K mutations in squamous cell carcinoma of lung.

Do H, Salemi R, Murone C, Mitchell PL, Dobrovic A. Do H, et al. Among authors: salemi r. Cell Cycle. 2010 Nov 1;9(21):4411-2. doi: 10.4161/cc.9.21.13654. Epub 2010 Nov 13. Cell Cycle. 2010. PMID: 20980808 No abstract available.

7

Alpers syndrome with mutations in POLG: clinical and investigative features.

Hunter MF, Peters H, Salemi R, Thorburn D, Mackay MT. Hunter MF, et al. Among authors: salemi r. Pediatr Neurol. 2011 Nov;45(5):311-8. doi: 10.1016/j.pediatrneurol.2011.07.008. Pediatr Neurol. 2011. PMID: 22000311

8

Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial disease.

Sugiana C, Pagliarini DJ, McKenzie M, Kirby DM, Salemi R, Abu-Amero KK, Dahl HH, Hutchison WM, Vascotto KA, Smith SM, Newbold RF, Christodoulou J, Calvo S, Mootha VK, Ryan MT, Thorburn DR. Sugiana C, et al. Among authors: salemi r. Am J Hum Genet. 2008 Oct;83(4):468-78. doi: 10.1016/j.ajhg.2008.09.009. Am J Hum Genet. 2008. PMID: 18940309 Free PMC article.

9

Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the United States explained by single ancient European founders.

Hakonen AH, Davidzon G, Salemi R, Bindoff LA, Van Goethem G, Dimauro S, Thorburn DR, Suomalainen A. Hakonen AH, et al. Among authors: salemi r. Eur J Hum Genet. 2007 Jul;15(7):779-83. doi: 10.1038/sj.ejhg.5201831. Epub 2007 Apr 11. Eur J Hum Genet. 2007. PMID: 17426723

10

NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency.

Kirby DM, Salemi R, Sugiana C, Ohtake A, Parry L, Bell KM, Kirk EP, Boneh A, Taylor RW, Dahl HH, Ryan MT, Thorburn DR. Kirby DM, et al. Among authors: salemi r. J Clin Invest. 2004 Sep;114(6):837-45. doi: 10.1172/JCI20683. J Clin Invest. 2004. PMID: 15372108 Free PMC article.

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