Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Grazia Saturno
Observed names:
G. Saturno,
G.S. Saturno,
Grazia S Saturno
Observed institutions:
Institute of Cancer Research,
Cancer Research UK,
University of Manchester,
Nerviano Medical Sciences,
Cancer Research UK Manchester Institute,
Fondazione IRCCS Istituto Nazionale dei Tumori
show all 6
OpenAlex ID:
A5111489266
Targeting the LOX/hypoxia axis reverses many of the features that make pancreatic cancer deadly: inhibition of LOX abrogates metastasis and enhances drug efficacy
2015
·
Bryan W Miller
, Jennifer P Morton
, et al.
·
EMBO Molecular Medicine
·
299
PDF
Application of Sequencing, Liquid Biopsies, and Patient-Derived Xenografts for Personalized Medicine in Melanoma
2015
·
Maria Romina Girotti
, Gabriela Gremel
, et al.
·
Cancer Discovery
·
235
Paradox-Breaking RAF Inhibitors that Also Target SRC Are Effective in Drug-Resistant BRAF Mutant Melanoma
2014
·
Maria Romina Girotti
, Filipa Lopes
, et al.
·
Cancer Cell
·
218
PDF
BRAF Inhibitors Induce Metastasis in RAS Mutant or Inhibitor-Resistant Melanoma Cells by Reactivating MEK and ERK Signaling
2014
·
Berta Sanchez-Laorden
, Amaya Viros
, et al.
·
Science Signaling
·
131
Lysyl oxidase drives tumour progression by trapping EGF receptors at the cell surface
2017
·
HaoRan Tang
, Leo Leung
, et al.
·
Nature Communications
·
93
PDF
Anti-metastatic Inhibitors of Lysyl Oxidase (LOX): Design and Structure–Activity Relationships
2019
·
Leo Leung
, Dan Niculescu-Duvaz
, et al.
·
Journal of Medicinal Chemistry
·
77
Whole-genome sequencing reveals complex mechanisms of intrinsic resistance to BRAF inhibition
2014
·
S. Turajlic
, S.J. Furney
, et al.
·
Annals of Oncology
·
68
PDF
An in vivo and in vitro comparison of CYP induction in rat liver and intestine using slices and quantitative RT-PCR
2004
·
Marcella Martignoni
, Ruben de Kanter
, et al.
·
Chemico-Biological Interactions
·
64
No longer an untreatable disease: How targeted and immunotherapies have changed the management of melanoma patients
2014
·
Maria Romina Girotti
, Grazia Saturno
, et al.
·
Molecular Oncology
·
49
PDF
Combining TRAIL with PI3 Kinase or HSP90 inhibitors enhances apoptosis in colorectal cancer cells via suppression of survival signaling
2013
·
Grazia Saturno
, Melanie Valenti
, et al.
·
Oncotarget
·
39
PDF
An in vivo and in vitro comparison of CYP gene induction in mice using liver slices and quantitative RT-PCR
2005
·
Marcella Martignoni
, Ruben de Kanter
, et al.
·
Toxicology in Vitro
·
25
Selective modulation of ER-? by estradiol and xenoestrogens in human breast cancer cell lines
2003
·
V. Cappelletti
, G. Saturno
, et al.
·
Cellular and Molecular Life Sciences
·
24
The paradox-breaking panRAF plus SRC family kinase inhibitor, CCT3833, is effective in mutant KRAS-driven cancers
2020
·
G. Saturno
, F. Lopes
, et al.
·
Annals of Oncology
·
21
PDF
Assessing and managing toxicities induced by kinase inhibitors.
2007
·
Raffaella E Castoldi
, Giulia Pennella
, et al.
·
PubMed
·
17
Expression of Serine/Threonine Protein-Kinases and Related Factors in Normal Monkey and Human Retinas: The Mechanistic Understanding of a CDK2 Inhibitor Induced Retinal Toxicity
2007
·
Grazia Saturno
, Manuela Pesenti
, et al.
·
Toxicologic Pathology
·
16
PDF
Paradox-Breaking RAF Inhibitors that Also Target SRC Are Effective in Drug-Resistant BRAF Mutant Melanoma
2017
·
Maria Romina Girotti
, Filipa Lopes
, et al.
·
Cancer Cell
·
9
PDF
Abstract LB_A12: Initial results from 2 Phase I studies of NMS-03305293, a selective PARP1 inhibitor
2023
·
Marjolein Geurts
, Dorothee Gramatzki
, et al.
·
Molecular Cancer Therapeutics
·
6
Abstract 1615: NMS-812, a novel potent PERK inhibitor that also inhibits GCN2, exhibits strong anti-tumor activity as single agent and in combination in preclinical models
2023
·
Claudia Perrera
, Maurizio Pulici
, et al.
·
Cancer Research
·
5
Therapeutic efficacy of the paradox-breaking panRAF and SRC drug CCT3833/BAL3833 in KRAS-driven cancer models
2016
·
G. Saturno
, F. Lopes
, et al.
·
European Journal of Cancer
·
5
Discovery and optimization of 4-pyrazolyl-2-aminopyrimidine derivatives as potent spleen tyrosine kinase (SYK) inhibitors
2024
·
Giovanni Cervi
, Roberto D'Alessio
, et al.
·
European Journal of Medicinal Chemistry
·
4
NMS-173, a potent, covalent second generation IDH1/IDH2 inhibitor
2022
·
P. Magnaghi
, F. Casuscelli
, et al.
·
European Journal of Cancer
·
3
Abstract LB-212: Therapeutic efficacy of the paradox-breaking panRAF and SRC drug CCT3833/BAL3833 in KRAS-driven cancer models
2016
·
Grazia Saturno
, Filipa Lopes
, et al.
·
Cancer Research
·
2
Abstract 4167: Ultraviolet radiation cooperates with individual oncogenes to drive melanomagenesis through distinct molecular mechanisms
2016
·
Amaya Viros
, Malin Pedersen
, et al.
·
Cancer Research
·
1
Application of sequencing, liquid biopsies and patient-derived xenografts for personalized medicine in melanoma
2016
·
M.R. Girotti
, G. Gremel
, et al.
·
European Journal of Cancer
·
1
Abstract 3704: Novel panRAF inhibitors active in melanomas that are resistant to BRAF-selective, or BRAF-selective/MEK inhibitor combinations
2014
·
Maria R. Girotti
, Filipa Lopes
, et al.
·
Cancer Research
·
1
Show more works
View as search
Works count:
49
Citation count:
1,413
H-index:
15
I10-index:
15
Year
Topic
Type