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2003 | 1 |
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Page 1
Human and mouse VEGFA-amplified hepatocellular carcinomas are highly sensitive to sorafenib treatment.
Cancer Discov. 2014 Jun;4(6):730-43. doi: 10.1158/2159-8290.CD-13-0782. Epub 2014 Mar 31.
Cancer Discov. 2014.
PMID: 24687604
Mutation spectrum in HNPCC in the Israeli population.
Goldberg Y, Porat RM, Kedar I, Shochat C, Sagi M, Eilat A, Mendelson S, Hamburger T, Nissan A, Hubert A, Kadouri L, Pikarski E, Lerer I, Abeliovich D, Bercovich D, Peretz T.
Goldberg Y, et al. Among authors: porat rm.
Fam Cancer. 2008;7(4):309-17. doi: 10.1007/s10689-008-9191-y. Epub 2008 Apr 4.
Fam Cancer. 2008.
PMID: 18389388
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An Ashkenazi founder mutation in the MSH6 gene leading to HNPCC.
Goldberg Y, Porat RM, Kedar I, Shochat C, Galinsky D, Hamburger T, Hubert A, Strul H, Kariiv R, Ben-Avi L, Savion M, Pikarsky E, Abeliovich D, Bercovich D, Lerer I, Peretz T.
Goldberg Y, et al. Among authors: porat rm.
Fam Cancer. 2010 Jun;9(2):141-50. doi: 10.1007/s10689-009-9298-9.
Fam Cancer. 2010.
PMID: 19851887
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NF-kappaB functions as a tumour promoter in inflammation-associated cancer.
Pikarsky E, Porat RM, Stein I, Abramovitch R, Amit S, Kasem S, Gutkovich-Pyest E, Urieli-Shoval S, Galun E, Ben-Neriah Y.
Pikarsky E, et al. Among authors: porat rm.
Nature. 2004 Sep 23;431(7007):461-6. doi: 10.1038/nature02924. Epub 2004 Aug 25.
Nature. 2004.
PMID: 15329734
Free article.
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Tissue oxygen levels control astrocyte movement and differentiation in developing retina.
Zhang Y, Porat RM, Alon T, Keshet E, Stone J.
Zhang Y, et al. Among authors: porat rm.
Brain Res Dev Brain Res. 1999 Dec 10;118(1-2):135-45. doi: 10.1016/s0165-3806(99)00140-6.
Brain Res Dev Brain Res. 1999.
PMID: 10611512
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Specific induction of tie1 promoter by disturbed flow in atherosclerosis-prone vascular niches and flow-obstructing pathologies.
Porat RM, Grunewald M, Globerman A, Itin A, Barshtein G, Alhonen L, Alitalo K, Keshet E.
Porat RM, et al.
Circ Res. 2004 Feb 20;94(3):394-401. doi: 10.1161/01.RES.0000111803.92923.D6. Epub 2003 Dec 11.
Circ Res. 2004.
PMID: 14670840
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Homozygosity of MSH2 c.1906G-->C germline mutation is associated with childhood colon cancer, astrocytoma and signs of Neurofibromatosis type I.
Toledano H, Goldberg Y, Kedar-Barnes I, Baris H, Porat RM, Shochat C, Bercovich D, Pikarsky E, Lerer I, Yaniv I, Abeliovich D, Peretz T.
Toledano H, et al. Among authors: porat rm.
Fam Cancer. 2009;8(3):187-94. doi: 10.1007/s10689-008-9227-3. Epub 2008 Dec 20.
Fam Cancer. 2009.
PMID: 19101824
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