L. Tagliavacca

发表

Progressively impaired proteasomal capacity during terminal plasma cell differentiation

P. Cascio, S. Masciarelli, A. Fra, 2006, The EMBO journal.

Biosynthesis, assembly and secretion of coagulation factor VIII.

R. Kaufman, M. Swaroop, S. Pipe, 1997, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Expression of Mutant or Cytosolic PrP in Transgenic Mice and Cells Is Not Associated with Endoplasmic Reticulum Stress or Proteasome Dysfunction

G. Forloni, M. Salmona, R. Chiesa, 2011, PloS one.

In vivo up-regulation of the unfolded protein response after hypoxia.

L. Tagliavacca, M. Samaja, A. Caretti, 2012, Biochimica et biophysica acta.

The Making of a Professional Secretory Cell: Architectural and Functional Changes in the ER during B Lymphocyte Plasma Cell Differentiation

R. Sitia, A. Mezghrani, Elena Ruffato, 2003, Biological chemistry.

Synthesis and structural characterization of the dilactone derivative of GD1a ganglioside.

S. Sonnino, G. Fronza, R. Bassi, 1988, Carbohydrate research.

Dihydroceramide delays cell cycle G1/S transition via activation of ER stress and induction of autophagy.

R. Ghidoni, J. Casas, G. Fabriàs, 2012, The international journal of biochemistry & cell biology.

ATP-dependent dissociation of non-disulfide-linked aggregates of coagulation factor VIII is a rate-limiting step for secretion.

R. Kaufman, L. Tagliavacca, Q. Wang, 2000, Biochemistry.

Inhibitors to Factor VIII in a Family with Mild Hemophilia: Molecular Characterization and Response to Factor VIII and Desmopressin

P. Mannucci, E. Santagostino, A. Gringeri, 1995, Thrombosis and Haemostasis.

Evaluation of an Adenoviral Vector Encoding Full-Length Human Factor VIII in Hemophiliac Mice

R. Kaufman, M. Kaleko, S. Connelly, 1999, Thrombosis and Haemostasis.

First Report on UK Database of Haemophilia B Mutations and Pedigrees

P. Green, S. Saad, F. Giannelli, 1994, Thrombosis and Haemostasis.

Carrier detection and prenatal diagnosis of hemophilia A: 5-years experience at a hemophilia center

E. Sacchi, P. Mannucci, L. Tagliavacca, 1992, International journal of clinical & laboratory research.

Two chimaeric transcription units result from an inversion breaking intron 1 of the factor VIII gene and a region reportedly affected by reciprocal translocations in T-cell leukaemia.

P. Green, P. Giangrande, F. Giannelli, 1996, Human molecular genetics.

Identification and Functional Requirement of Cu(I) and Its Ligands within Coagulation Factor VIII*

R. Kaufman, L. Tagliavacca, W. Dunham, 1997, The Journal of Biological Chemistry.

L1CAM and its cell-surface mutants: new mechanisms and effects relevant to the physiology and pathology of neural cells

J. Meldolesi, L. Tagliavacca, F. Colombo, 2012, Journal of neurochemistry.

Induction of cell cycle arrest and DNA damage by the HDAC inhibitor panobinostat (LBH589) and the lipid peroxidation end product 4-hydroxynonenal in prostate cancer cells.

Song Liu, P. Atadja, Dan Wang, 2011, Free radical biology & medicine.

THE PROTEOSTASIS OF THE ENDOPLASMIC RETICULUM AND THE ACTIVATION OF THE UNFOLDED PROTEIN RESPONSE PATHWAY IN VIVO

L. Tagliavacca, Maria Luisa Villa, 2010 .

Carrier detection and feasibility of prenatal diagnosis of hemophilia B by multiplex polymerase chain reaction

E. Sacchi, P. Mannucci, L. Tagliavacca, 1993, International journal of clinical & laboratory research.

Analysis of the haemophilia A mutation in sporadic patients registered at the Royal London Hospital and their families

P. Green, B. Colvin, F. Giannelli, 1997, Haemophilia : the official journal of the World Federation of Hemophilia.