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, Andrew J, PRICE, Tim J, SALEMI, Renato, SCOTT, Andrew M, MARIADASON, John M, TEBBUTT, Niall C, CHONG, Geoff, GEBSKI, Val, PAVLAKIS, Nick, JOHNS, Terrance G, AZAD, Arun, SKRINOS, Effie, FLUCK, Kate, DOBROVIC, Alexander
Published in Journal of clinical oncology (01.05.2012)
Published in Journal of clinical oncology (01.05.2012)
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Respiratory chain complex I deficiency caused by mitochondrial DNA mutations
SWALWELL, Helen, KIRBY, Denise M, TURNBULL, Douglass M, MCFARLAND, Robert, TAYLOR, Robert W, THORBURN, David R, BLAKELY, Emma L, MITCHELL, Anna, SALEMI, Renato, SUGIANA, Canny, COMPTON, Alison G, TUCKER, Elena J, KE, Bi-Xia, LAMONT, Phillipa J
Published in European journal of human genetics : EJHG (01.07.2011)
Published in European journal of human genetics : EJHG (01.07.2011)
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Journal Article
Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease
Sugiana, Canny, Pagliarini, David J., McKenzie, Matthew, Kirby, Denise M., Salemi, Renato, Abu-Amero, Khaled K., Dahl, Hans-Henrik M., Hutchison, Wendy M., Vascotto, Katherine A., Smith, Stacey M., Newbold, Robert F., Christodoulou, John, Calvo, Sarah, Mootha, Vamsi K., Ryan, Michael T., Thorburn, David R.
Published in American journal of human genetics (01.10.2008)
Published in American journal of human genetics (01.10.2008)
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Journal Article
NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency
Kirby, Denise M, Salemi, Renato, Sugiana, Canny, Ohtake, Akira, Parry, Lee, Bell, Katrina M, Kirk, Edwin P, Boneh, Avihu, Taylor, Robert W, Dahl, Hans-Henrik M, Ryan, Michael T, Thorburn, David R
Published in The Journal of clinical investigation (01.09.2004)
Published in The Journal of clinical investigation (01.09.2004)
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Journal Article
Rarity of AKT1 and AKT3 E17K mutations in squamous cell carcinoma of lung
Do, Hongdo, Salemi, Renato, Murone, Carmel, Mitchell, Paul L., Dobrovic, Alexander
Published in Cell cycle (Georgetown, Tex.) (01.11.2010)
Published in Cell cycle (Georgetown, Tex.) (01.11.2010)
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Journal Article
Abundance of the POLG disease mutations in Europe, Australia, New Zealand, and the United States explained by single ancient European founders
HAKONEN, Anna H, DAVIDZON, Guido, SALEMI, Renato, BINDOFF, Laurence A, VAN GOETHEM, Gert, DIMAURO, Salvatore, THORBURN, David R, SUOMALAINEN, Anu
Published in European journal of human genetics : EJHG (01.07.2007)
Published in European journal of human genetics : EJHG (01.07.2007)
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Journal Article
Clinical outcome and pathological features associated with NRAS mutation in cutaneous melanoma
Devitt, Bianca, Liu, Wendy, Salemi, Renato, Wolfe, Rory, Kelly, John, Tzen, Chin-Yuan, Dobrovic, Alexander, McArthur, Grant
Published in Pigment cell and melanoma research (01.08.2011)
Published in Pigment cell and melanoma research (01.08.2011)
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Journal Article
Mutations in KIT occur at low frequency in melanomas arising from anatomical sites associated with chronic and intermittent sun exposure
Handolias, Despina, Salemi, Renato, Murray, William, Tan, Angela, Liu, Wendy, Viros, Amaya, Dobrovic, Alexander, Kelly, John, McArthur, Grant A.
Published in Pigment cell and melanoma research (01.04.2010)
Published in Pigment cell and melanoma research (01.04.2010)
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Journal Article
Targeted-capture massively-parallel sequencing enables robust detection of clinically informative mutations from formalin-fixed tumours
Wong, Stephen Q, Li, Jason, Salemi, Renato, Sheppard, Karen E, Do, Hongdo, Tothill, Richard W, McArthur, Grant A, Dobrovic, Alexander
Published in Scientific reports (13.12.2013)
Published in Scientific reports (13.12.2013)
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Journal Article
NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency
Kirby, Denise M., Salemi, Renato, Sugiana, Canny, Ohtake, Akira, Parry, Lee, Bell, Katrina M., Kirk, Edwin P., Boneh, Avihu, Taylor, Robert W., Dahl, Hans-Henrik M., Ryan, Michael T., Thorburn, David R.
Published in The Journal of clinical investigation (15.09.2004)
Published in The Journal of clinical investigation (15.09.2004)
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Journal Article
Mutations in KIT occur at low frequency in melanomas arising from anatomical sites associated with chronic and intermittent sun exposure: KIT mutations in cutaneous melanoma
Handolias, Despina, Salemi, Renato, Murray, William, Tan, Angela, Liu, Wendy, Viros, Amaya, Dobrovic, Alexander, Kelly, John, McArthur, Grant A.
Published in Pigment cell and melanoma research (01.04.2010)
Published in Pigment cell and melanoma research (01.04.2010)
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Journal Article
401: Alpers Syndrome with POLG mutations: clinical, EEG and radiological features
Hunter, Matthew, Mackay, Mark T, Peters, Heidi, Salemi, Renato, Thorburn, David
Published in Journal of clinical neuroscience (01.03.2008)
Published in Journal of clinical neuroscience (01.03.2008)
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Journal Article
Functional glucocorticoid receptors in the mesonephros of the ovine fetus
Peers, Arianne, Hantzis, Vicky, Dodic, Miodrag, Koukoulas, Irene, Gibson, Angela, Baird, Rebecca, Salemi, Renato, Wintour, E. Marelyn
Published in Kidney international (01.02.2001)
Published in Kidney international (01.02.2001)
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