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Showing results (91-100 of 100) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|December 21, 2004
Gene expression profiles of epithelial cells microscopically isolated from a breast-invasive ductal carcinoma and a nodal metastasisI Zucchi, E Mento, V A Kuznetsov, et al.
Molecular and Cellular Biology|July 13, 2000
Mutations in conserved regions of the predicted RAG2 kelch repeats block initiation of V(D)J recombination and result in primary immunodeficienciesC A Gomez, L M Ptaszek, A Villa, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2001
Proteomic dissection of dome formation in a mammary cell line: role of tropomyosin-5b and maspinI Zucchi, L Bini, R Valaperta, et al.
Blood|February 3, 1998
Development of autologous, oligoclonal, poorly functioning T lymphocytes in a patient with autosomal recessive severe combined immunodeficiency caused by defects of the Jak3 tyrosine kinaseD Brugnoni, L D Notarangelo, A Sottini, et al.
Nature Genetics|July 11, 2000
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosisA Frattini, P J Orchard, C Sobacchi, et al.
Molecular and Cellular Biology|June 8, 2001
Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein familyB W Richter, S S Mir, L J Eiben, et al.
Blood|November 14, 1997
Structural and functional basis for JAK3-deficient severe combined immunodeficiencyF Candotti, S A Oakes, J A Johnston, et al.
Advances in Genetics|October 19, 2000
Primary immunodeficiency mutation databasesM Vihinen, F X Arredondo-Vega, J L Casanova, et al.
Human Molecular Genetics|September 5, 2001
The mutational spectrum of human malignant autosomal recessive osteopetrosisC Sobacchi, A Frattini, P Orchard, et al.
Blood|January 3, 2001
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentationsA Villa, C Sobacchi, L D Notarangelo, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2004
Gene expression profiles of epithelial cells microscopically isolated from a breast-invasive ductal carcinoma and a nodal metastasisI Zucchi, E Mento, V A Kuznetsov, et al.
Molecular and Cellular Biology|July 13, 2000
Mutations in conserved regions of the predicted RAG2 kelch repeats block initiation of V(D)J recombination and result in primary immunodeficienciesC A Gomez, L M Ptaszek, A Villa, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 2, 2001
Proteomic dissection of dome formation in a mammary cell line: role of tropomyosin-5b and maspinI Zucchi, L Bini, R Valaperta, et al.
Blood|February 3, 1998
Development of autologous, oligoclonal, poorly functioning T lymphocytes in a patient with autosomal recessive severe combined immunodeficiency caused by defects of the Jak3 tyrosine kinaseD Brugnoni, L D Notarangelo, A Sottini, et al.
Nature Genetics|July 11, 2000
Defects in TCIRG1 subunit of the vacuolar proton pump are responsible for a subset of human autosomal recessive osteopetrosisA Frattini, P J Orchard, C Sobacchi, et al.
Molecular and Cellular Biology|June 8, 2001
Molecular cloning of ILP-2, a novel member of the inhibitor of apoptosis protein familyB W Richter, S S Mir, L J Eiben, et al.
Blood|November 14, 1997
Structural and functional basis for JAK3-deficient severe combined immunodeficiencyF Candotti, S A Oakes, J A Johnston, et al.
Advances in Genetics|October 19, 2000
Primary immunodeficiency mutation databasesM Vihinen, F X Arredondo-Vega, J L Casanova, et al.
Human Molecular Genetics|September 5, 2001
The mutational spectrum of human malignant autosomal recessive osteopetrosisC Sobacchi, A Frattini, P Orchard, et al.
Blood|January 3, 2001
V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentationsA Villa, C Sobacchi, L D Notarangelo, et al.
Pageof 10