daniela tavian
daniela tavian
Associate Professor of Biochemistry, UniversitÓ Cattolica (Milano)
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Expression of urokinase-type plasminogen activator (u-PA), u-PA receptor and tissue-type PA messenger RNAs in human hepatocellular carcinoma
G De Petro, D Tavian, A Copeta, N Portolani, ...
Cancer Reaserch, 2234-2239, 1998
u‐PA and c‐MET mRNA expression is co‐ordinately enhanced while hepatocyte growth factor mRNA is down‐regulated in human hepatocellular carcinoma
D Tavian, G De Petro, A Benetti, N Portolani, SM Giulini, S Barlati
International journal of cancer 87 (5), 644-649, 2000
RT-PCR detection of fibronectin EDA+ and EDB+ mRNA isoforms: molecular markers for hepatocellular carcinoma
D Tavian, G De Petro, M Colombi, N Portolani, SM Giulini, R Gardella, ...
International Journal of Cancer, 1994
Contribution of novel ATGL missense mutations to the clinical phenotype of NLSD-M: a strikingly low amount of lipase activity may preserve cardiac function
D Tavian, S Missaglia, C Redaelli, EM Pennisi, G Invernici, ...
Human molecular genetics 21 (24), 5318-5328, 2012
Clinical and genetic characterization of Chanarin-Dorfman syndrome patients: first report of large deletions in the ABHD5 gene
C Redaelli, RA Coleman, L Moro, C Dacou-Voutetakis, SM Elsayed, ...
Orphanet journal of rare diseases 5 (1), 1-11, 2010
Early exposure to alcohol leads to permanent impairment of dendritic excitability in neocortical pyramidal neurons
A Granato, LM Palmer, A De Giorgio, D Tavian, ME Larkum
Journal of neuroscience 32 (4), 1377-1382, 2012
Harm avoidance moderates the influence of serotonin transporter gene variants on treatment outcome in bipolar patients
L Mandelli, M Mazza, G Martinotti, M Di Nicola, D Tavian, E Colombo, ...
Journal of affective disorders 119 (1-3), 205-209, 2009
Recent insights into genotype–phenotype relationships in patients with Rett syndrome using a fine grain scale
RA Fabio, B Colombo, S Russo, F Cogliati, M Masciadri, S Foglia, ...
Research in Developmental Disabilities 35 (11), 2976-2986, 2014
Neutral lipid storage diseases as cellular model to study lipid droplet function
S Missaglia, RA Coleman, A Mordente, D Tavian
Cells 8 (2), 187, 2019
Topoisomerases and anthracyclines: recent advances and perspectives in anticancer therapy and prevention of cardiotoxicity
A Mordente, E Meucci, G EttoreMartorana, D Tavian, A Silvestrini
Current medicinal chemistry 24 (15), 1607-1626, 2017
Coordinated sumoylation and ubiquitination modulate EGF induced EGR1 expression and stability
AG Manente, G Pinton, D Tavian, G Lopez-Rodas, E Brunelli, L Moro
PloS one 6 (10), e25676, 2011
Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients
EM Pennisi, M Arca, E Bertini, C Bruno, D Cassandrini, A D’amico, ...
Orphanet journal of rare diseases 12 (1), 1-10, 2017
Novel missense mutations in PNPLA2 causing late onset and clinical heterogeneity of neutral lipid storage disease with myopathy in three siblings
S Missaglia, E Tasca, C Angelini, L Moro, D Tavian
Molecular Genetics and Metabolism 115 (2-3), 110-117, 2015
Improved cytochemical method for detecting Jordans’ bodies in neutral lipid storage diseases
D Tavian, R Colombo
Journal of clinical pathology 60 (8), 956-958, 2007
Social stress regulation in 4-month-old infants: contribution of maternal social engagement and infants'5-HTTLPR genotype
R Montirosso, L Provenzi, D Tavian, F Morandi, A Bonanomi, S Missaglia, ...
Early human development 91 (3), 173-179, 2015
Genetic mutations in adipose triglyceride lipase and myocardial up-regulation of peroxisome proliferated activated receptor-γ in patients with triglyceride depositá…
K Hirano, T Tanaka, Y Ikeda, S Yamaguchi, N Zaima, K Kobayashi, ...
Biochemical and biophysical research communications 443 (2), 574-579, 2014
Nanotechnology advances in brain tumors: the state of the art
G Invernici, S Cristini, G Alessandri, S E Navone, L Canzi, D Tavian, ...
Recent patents on anti-cancer drug discovery 6 (1), 58-69, 2011
Matrix assembly induction and cell migration and invasion inhibition by a 13-amino acid fibronectin peptide
M Colombi, N Zoppi, G De Petro, E Marchina, R Gardella, D Tavian, ...
Journal of Biological Chemistry 278 (16), 14346-14355, 2003
Heterogeneous Phenotypes in Lipid Storage Myopathy Due to ETFDH Gene Mutations
C Angelini, D Tavian, S Missaglia
JIMD Reports, Volume 38, 33-40, 2017
Severe steatohepatitis in a patient with a rare neutral lipid storage disorder due to ABDH5 mutation
A Ronchetti, D Prati, MG Pezzotta, D Tavian, R Colombo, F Callea, A Colli
Journal of hepatology 49 (3), 474-477, 2008
Il sistema al momento non pu˛ eseguire l'operazione. Riprova pi¨ tardi.
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