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P Vezzoni

Showing results (51-60 of 100) with videos related to

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Tumori|February 28, 1986
Alkaline phosphatase and gamma glutamyltranspeptidase in human lymphomasS Spinazzè, M A Vezzoni, M Murone, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 11, 2012
Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implicationsA Pangrazio, M E Caldana, N Lo Iacono, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
N-terminal RAG1 frameshift mutations in Omenn's syndrome: internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domainsS Santagata, C A Gomez, C Sobacchi, et al.
Gene Therapy|June 6, 1998
In vitro and in vivo antisense-mediated growth inhibition of a mammary adenocarcinoma from MMTV-neu transgenic miceM G Sacco, O Barbieri, D Piccini, et al.
Diagnostic Immunology|January 1, 1986
The contribution of molecular biology in the diagnosis of human lymphomasP Vezzoni, G Cairo, M R Pozzi, et al.
Human Mutation|January 1, 1994
A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosisA Ferlini, M C Patrosso, M Repetto, et al.
Genomics|September 1, 1994
Genomic organization of the human VP16 accessory protein, a housekeeping gene (HCFC1) mapping to Xq28A Frattini, S Faranda, E Redolfi, et al.
DNA and Cell Biology|January 9, 1999
Identification of CXorf1, a novel intronless gene in Xq27.3, expressed in human hippocampusE Redolfi, C Montagna, S Mumm, et al.
Cancer Gene Therapy|August 11, 2001
Growth of human melanoma xenografts is suppressed by systemic angiostatin gene therapyM Rodolfo, E M Catò, S Soldati, et al.
Biochemical and Biophysical Research Communications|June 30, 1993
Type 2 vasopressin receptor gene, the gene responsible nephrogenic diabetes insipidus, maps to Xq28 close to the LICAM geneA Frattini, I Zucchi, A Villa, et al.
Pageof 10

Showing results (51-60 of 100) with videos related to

Sort By:
Pageof 10
Tumori|February 28, 1986
Alkaline phosphatase and gamma glutamyltranspeptidase in human lymphomasS Spinazzè, M A Vezzoni, M Murone, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|January 11, 2012
Autosomal recessive osteopetrosis: report of 41 novel mutations in the TCIRG1 gene and diagnostic implicationsA Pangrazio, M E Caldana, N Lo Iacono, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 20, 2000
N-terminal RAG1 frameshift mutations in Omenn's syndrome: internal methionine usage leads to partial V(D)J recombination activity and reveals a fundamental role in vivo for the N-terminal domainsS Santagata, C A Gomez, C Sobacchi, et al.
Gene Therapy|June 6, 1998
In vitro and in vivo antisense-mediated growth inhibition of a mammary adenocarcinoma from MMTV-neu transgenic miceM G Sacco, O Barbieri, D Piccini, et al.
Diagnostic Immunology|January 1, 1986
The contribution of molecular biology in the diagnosis of human lymphomasP Vezzoni, G Cairo, M R Pozzi, et al.
Human Mutation|January 1, 1994
A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosisA Ferlini, M C Patrosso, M Repetto, et al.
Genomics|September 1, 1994
Genomic organization of the human VP16 accessory protein, a housekeeping gene (HCFC1) mapping to Xq28A Frattini, S Faranda, E Redolfi, et al.
DNA and Cell Biology|January 9, 1999
Identification of CXorf1, a novel intronless gene in Xq27.3, expressed in human hippocampusE Redolfi, C Montagna, S Mumm, et al.
Cancer Gene Therapy|August 11, 2001
Growth of human melanoma xenografts is suppressed by systemic angiostatin gene therapyM Rodolfo, E M Catò, S Soldati, et al.
Biochemical and Biophysical Research Communications|June 30, 1993
Type 2 vasopressin receptor gene, the gene responsible nephrogenic diabetes insipidus, maps to Xq28 close to the LICAM geneA Frattini, I Zucchi, A Villa, et al.
Pageof 10