L. Mare

发表

Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms

G. Montalbano, R. Valli, B. Pressato, 2013, Molecular Cytogenetics.

Cytogenetic Monitoring in Shwachman-Diamond Syndrome: A Note on Clonal Progression and a Practical Warning

G. Montalbano, R. Valli, B. Pressato, 2015, Journal of pediatric hematology/oncology.

Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms

G. Montalbano, R. Valli, B. Pressato, 2013, Molecular Cytogenetics.

Deletion of chromosome 20 in bone marrow of patients with Shwachman‐Diamond syndrome, loss of the EIF6 gene and benign prognosis

G. Montalbano, R. Valli, B. Pressato, 2012, British journal of haematology.

The γ-secretase modulator CHF5074 restores memory and hippocampal synaptic plasticity in plaque-free Tg2576 mice.

G. Nisticó, A. Usiello, G. Forloni, 2011, Journal of Alzheimer's disease : JAD.

C-jun N-terminal Kinase Binding Domain– Dependent Phosphorylation of Mitogen-activated Protein Kinase Kinase 4 and Mitogen-activated Protein Kinase Kinase 7 and Balancing Cross-talk between C-jun N-terminal Kinase and Extracellular Signal-regulated Kinase Pathways in Cortical Neurons Article in Pres

M. Repici, M. Salmona, P. Nicod, 2022 .

Suppression of beta 1,3galactosyltransferase beta 3Gal-T5 in cancer cells reduces sialyl-Lewis a and enhances poly N-acetyllactosamines and sialyl-Lewis x on O-glycans.

L. Mare, M. Trinchera, 2004, European journal of biochemistry.

CA19.9 antigen circulating in the serum of colon cancer patients: where is it from?

L. Mare, R. Albertini, A. Caretti, 2013, The international journal of biochemistry & cell biology.

Comparative Analysis of Retroviral and Native Promoters Driving Expression of β1,3-Galactosyltransferase β3Gal-T5 in Human and Mouse Tissues*

L. Mare, M. Trinchera, 2007, Journal of Biological Chemistry.

Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes

F. Locatelli, M. Bernardo, G. Montalbano, 2012, Molecular Cytogenetics.

Clonal chromosome anomalies affecting FLI1 mimic inherited thrombocytopenia of the Paris‐Trousseau type

P. Noris, R. Valli, L. Mare, 2012, European journal of haematology.

APP1 Transcription Is Regulated by Inositol-phosphorylceramide Synthase 1-Diacylglycerol Pathway and Is Controlled by ATF2 Transcription Factor in Cryptococcus neoformans*

Maria Teresa Montagna, M. Del Poeta, M. Montagna, 2005, Journal of Biological Chemistry.

c-Jun N-terminal kinase binding domain–dependent phosphorylation of mitogen-activated protein kinase kinase 4 and mitogen-activated protein kinase kinase 7 and balancing cross-talk between c-Jun N-terminal kinase and extracellular signal-regulated kinase pathways in cortical neurons

L. Mare, T. Borsello, C. Ploia, 2009, Neuroscience.