C Bordignon
Overview
Explore the profile of C Bordignon including associated specialties, affiliations and a list of published articles.
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Articles
96
Citations
1960
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Recent Articles
1.
Noviello M, Forcina A, Veronica V, Crocchiolo R, Stanghellini M, Carrabba M, et al.
Bone Marrow Transplant
. 2015 Jun;
50(9):1262-4.
PMID: 26076126
No abstract available.
2.
Bonini C, Peccatori J, Stanghellini M, Vago L, Bondanza A, Cieri N, et al.
Bone Marrow Transplant
. 2015 Jun;
50 Suppl 2:S67-71.
PMID: 26039212
Hematopoietic SCT (HSCT) from HLA haploidentical family donors is a promising therapy for high-risk hematological malignancies. In the past 15 years at San Raffaele Scientific Institute, we investigated several transplant...
3.
Crucitti L, Crocchiolo R, Toffalori C, Mazzi B, Greco R, Signori A, et al.
Leukemia
. 2014 Nov;
29(5):1143-52.
PMID: 25371177
Genomic loss of the mismatched human leukocyte antigen (HLA) is a recently described mechanism of leukemia immune escape and relapse after allogeneic hematopoietic stem cell transplantation (HSCT). Here we first...
4.
Peccatori J, Forcina A, Clerici D, Crocchiolo R, Vago L, Stanghellini M, et al.
Leukemia
. 2014 Jun;
29(2):396-405.
PMID: 24897508
Hematopoietic stem cell transplantation (HSCT) from human leukocyte antigen (HLA) haploidentical family donors is a promising therapeutic option for high-risk hematologic malignancies. Here we explored in 121 patients, mostly with...
5.
Di Matteo P, Hackl C, Jedeszko C, Valentinis B, Bordignon C, Traversari C, et al.
Br J Cancer
. 2013 Jul;
109(2):360-9.
PMID: 23828516
Background: Administration of certain chemotherapy drugs at the maximum tolerated dose, vascular-disrupting agents (VDAs) and irradiation can induce mobilisation and tumour homing of proangiogenic bone marrow-derived cells (BMDCs). Increases in...
6.
Zucali P, Simonelli M, de Vincenzo F, Lorenzi E, Perrino M, Bertossi M, et al.
Br J Cancer
. 2012 Nov;
108(1):58-63.
PMID: 23169299
Background: NGR-hTNF exploits the peptide asparagine-glycine-arginine (NGR) for selectively targeting tumour necrosis factor (TNF) to CD13-overexpressing tumour vessels. Maximum-tolerated dose (MTD) of NGR-hTNF was previously established at 45 μg m(-2)...
7.
Lorusso D, Scambia G, Amadio G, Di Legge A, Pietragalla A, De Vincenzo R, et al.
Br J Cancer
. 2012 May;
107(1):37-42.
PMID: 22644293
Background: The NGR-hTNF (asparagine-glycine-arginine-human tumour necrosis factor) is able to promote antitumour immune responses and to improve the intratumoural doxorubicin uptake by selectively damaging tumour blood vessels. Methods: Patients progressing...
8.
Mammoliti S, Andretta V, Bennicelli E, Caprioni F, Comandini D, Fornarini G, et al.
Ann Oncol
. 2010 Sep;
22(4):973-978.
PMID: 20855468
Background: asparagine-glycine-arginine-human tumour necrosis factor (NGR-hTNF), an agent selectively damaging the tumour vasculature, showed a biphasic dose-response curve in preclinical models. Previous phase I trials of NGR-hTNF indicated 0.8 and...
9.
Santoro A, Pressiani T, Citterio G, Donadoni G, Pozzi F, Rimassa L, et al.
Br J Cancer
. 2010 Aug;
103(6):837-44.
PMID: 20717115
Background: Hepatocellular carcinoma (HCC) is a highly vascularised and poor-prognosis tumour. NGR-hTNF is a vascular-targeting agent consisting of human tumour necrosis factor-alpha fused to the tumour-homing peptide NGR, which is...
10.
Mastaglio S, Stanghellini M, Bordignon C, Bondanza A, Ciceri F, Bonini C
Gene Ther
. 2010 May;
17(11):1309-17.
PMID: 20508597
Graft-versus-host disease (GvHD) is one of the major complications of allogeneic hematopoietic stem cell transplantation, an otherwise highly effective therapeutic modality for patients affected by hematological diseases. The main inducers...