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M Fiorini

Showing results (51-60 of 246) with videos related to

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Journal of Immunology (Baltimore, Md. : 1950)|July 22, 1998
Monocytes from Wiskott-Aldrich patients display reduced chemotaxis and lack of cell polarization in response to monocyte chemoattractant protein-1 and formyl-methionyl-leucyl-phenylalanineR Badolato, S Sozzani, F Malacarne, et al.
Molecular Medicine (Cambridge, Mass.)|June 20, 2000
X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative GroupV Moschese, P Orlandi, A Plebani, et al.
Neurology|May 11, 2005
Phosphorylated 14-3-3zeta protein in the CSF of neuroleptic-treated patientsG Zanusso, M Fiorini, A Farinazzo, et al.
Human Genetics|September 12, 2000
Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphismR F Schumacher, P Mella, R Badolato, et al.
British Journal of Haematology|June 20, 1998
Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)G S Wengler, S Giliani, M Fiorini, et al.
British Journal of Anaesthesia|May 8, 2013
Heart-fatty acid-binding and tau proteins relate to brain injury severity and long-term outcome in subarachnoid haemorrhage patientsE R Zanier, T Zoerle, M Fiorini, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysisS Giliani, M Fiorini, P Mella, et al.
Human Mutation|January 1, 1997
Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemiaI Vorechovský, L Luo, J M Hertz, et al.
Clinical Immunology (Orlando, Fla.)|May 4, 2000
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterizationP Mella, L Imberti, D Brugnoni, et al.
Immunological Reviews|February 24, 2001
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, C Mazza, et al.
Pageof 25

Showing results (51-60 of 246) with videos related to

Sort By:
Pageof 25
Journal of Immunology (Baltimore, Md. : 1950)|July 22, 1998
Monocytes from Wiskott-Aldrich patients display reduced chemotaxis and lack of cell polarization in response to monocyte chemoattractant protein-1 and formyl-methionyl-leucyl-phenylalanineR Badolato, S Sozzani, F Malacarne, et al.
Molecular Medicine (Cambridge, Mass.)|June 20, 2000
X-chromosome inactivation and mutation pattern in the Bruton's tyrosine kinase gene in patients with X-linked agammaglobulinemia. Italian XLA Collaborative GroupV Moschese, P Orlandi, A Plebani, et al.
Neurology|May 11, 2005
Phosphorylated 14-3-3zeta protein in the CSF of neuroleptic-treated patientsG Zanusso, M Fiorini, A Farinazzo, et al.
Human Genetics|September 12, 2000
Complete genomic organization of the human JAK3 gene and mutation analysis in severe combined immunodeficiency by single-strand conformation polymorphismR F Schumacher, P Mella, R Badolato, et al.
British Journal of Haematology|June 20, 1998
Mutation analysis by a non-radioactive single-strand conformation polymorphism assay in nine families with X-linked severe combined immunodeficiency (SCIDX1)G S Wengler, S Giliani, M Fiorini, et al.
British Journal of Anaesthesia|May 8, 2013
Heart-fatty acid-binding and tau proteins relate to brain injury severity and long-term outcome in subarachnoid haemorrhage patientsE R Zanier, T Zoerle, M Fiorini, et al.
Prenatal Diagnosis|March 12, 1999
Prenatal molecular diagnosis of Wiskott-Aldrich syndrome by direct mutation analysisS Giliani, M Fiorini, P Mella, et al.
Human Mutation|January 1, 1997
Mutation pattern in the Bruton's tyrosine kinase gene in 26 unrelated patients with X-linked agammaglobulinemiaI Vorechovský, L Luo, J M Hertz, et al.
Clinical Immunology (Orlando, Fla.)|May 4, 2000
Development of autologous T lymphocytes in two males with X-linked severe combined immune deficiency: molecular and cellular characterizationP Mella, L Imberti, D Brugnoni, et al.
Immunological Reviews|February 24, 2001
Of genes and phenotypes: the immunological and molecular spectrum of combined immune deficiency. Defects of the gamma(c)-JAK3 signaling pathway as a modelL D Notarangelo, S Giliani, C Mazza, et al.
Pageof 25