M. Deganuto

发表

Start sites of bidirectional DNA synthesis at the human lamin B2 origin.

M. Giacca, S. Riva, G. Biamonti, 2000, Science.

APE1/Ref-1 Interacts with NPM1 within Nucleoli and Plays a Role in the rRNA Quality Control Process

A. Leonardi, A. Scaloni, C. Vascotto, 2009, Molecular and Cellular Biology.

Nucleophosmin is overexpressed in thyroid tumors.

G. Tell, I. Paron, C. di Loreto, 2010, Biochemical and biophysical research communications.

Altered intracellular redox status in Gaucher disease fibroblasts and impairment of adaptive response against oxidative stress

G. Tell, B. Bembi, M. Kelley, 2007, Journal of cellular physiology.

First pilot newborn screening for four lysosomal storage diseases in an Italian region: identification and analysis of a putative causative mutation in the GBA gene.

T. Beccari, C. Rosano, B. Bembi, 2012, Clinica chimica acta; international journal of clinical chemistry.

Role of LIMP‐2 in the intracellular trafficking of β‐glucosidase in different human cellular models

B. Bembi, M. Deganuto, A. Sechi, 2015, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Efficacy of multidisciplinary approach in the treatment of two cases of nonclassical infantile glycogenosis type II

B. Bembi, M. Deganuto, M. G. Pittis, 2003, Journal of Inherited Metabolic Disease.

Bisphosphonates activate nucleotide receptors signaling and induce the expression of Hsp90 in osteoblast-like cell lines.

G. Tell, M. Deganuto, A. Pines, 2006, Bone.

Bilirubin-induced cell toxicity involves PTEN activation through an APE1/Ref-1-dependent pathway

C. Vascotto, G. Tell, J. Ostrow, 2007, Journal of Molecular Medicine.

Cerebrospinal Fluid Lysosomal Enzymes and Alpha-Synuclein in Parkinson's Disease

P. Calabresi, M. Onofrj, L. Bonanni, 2014, Movement disorders : official journal of the Movement Disorder Society.

A proteomic approach to the bilirubin‐induced toxicity in neuronal cells reveals a protective function of DJ‐1 protein

Stefano Gustincich, Andrea Scaloni, Giovanni Renzone, 2010, Proteomics.

Glycogenosis type II: identification and expression of three novel mutations in the acid alpha-glucosidase gene causing the infantile form of the disease.

B. Bembi, M. Deganuto, M. G. Pittis, 2004, Molecular genetics and metabolism.

Functional analysis of 11 novel GBA alleles

C. Rosano, B. Bembi, S. Grossi, 2013, European Journal of Human Genetics.

Genome‐wide analysis and proteomic studies reveal APE1/Ref‐1 multifunctional role in mammalian cells

G. Taglialatela, D. Delneri, A. Scaloni, 2009, Proteomics.

Identification of four novel mutations in the alpha glucosidase gene in five Italian patients with infantile onset glycogen storage disease type II

B. Bembi, M. Deganuto, M. Candusso, 2003, American journal of medical genetics. Part A.

Identification and functional characterization of five novel mutant alleles in 58 Italian patients with Gaucher disease type 1

K. Vlahovicek, B. Bembi, M. Filocamo, 2005, Human mutation.

APE1/Ref-1 regulates PTEN expression mediated by Egr-1

S. Gustincich, C. Vascotto, G. Tell, 2008, Free radical research.

A proteomic approach to the bilirubin‐induced toxicity in neuronal cells reveals a protective function of DJ‐1 protein

S. Gustincich, A. Scaloni, G. Tell, 2010, Proteomics.