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A Pizzuti

Showing results (91-100 of 117) with videos related to

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Human Molecular Genetics|February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromeA Pizzuti, G Novelli, A Ratti, et al.
Genomics|February 28, 1998
Human NRD convertase: a highly conserved metalloendopeptidase expressed at specific sites during development and in adult tissuesP Fumagalli, M Accarino, A Egeo, et al.
Molecular Genetics and Metabolism|June 25, 1999
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndromeA Pizzuti, G Novelli, A Ratti, et al.
Journal of Medical Genetics|September 10, 2003
Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromesA Sarkozy, E Conti, D Seripa, et al.
Science (New York, N.Y.)|March 16, 1992
An unstable triplet repeat in a gene related to myotonic muscular dystrophyY H Fu, A Pizzuti, R G Fenwick, et al.
Diabetes|September 10, 1999
A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistanceA Pizzuti, L Frittitta, A Argiolas, et al.
Science (New York, N.Y.)|April 9, 1993
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophyY H Fu, D L Friedman, S Richards, et al.
Kidney International|January 1, 1997
Hepatitis G virus infection in hemodialysis patientsM Sampietro, S Badalamenti, G Graziani, et al.
Minerva Cardioangiologica|May 13, 1998
[Natriuretic peptides and the heart. Critical review and application]G Baralis, E Antonielli, A Pizzuti, et al.
Cell|May 31, 1991
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeA J Verkerk, M Pieretti, J S Sutcliffe, et al.
Pageof 12

Showing results (91-100 of 117) with videos related to

Sort By:
Pageof 12
Human Molecular Genetics|February 1, 1997
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndromeA Pizzuti, G Novelli, A Ratti, et al.
Genomics|February 28, 1998
Human NRD convertase: a highly conserved metalloendopeptidase expressed at specific sites during development and in adult tissuesP Fumagalli, M Accarino, A Egeo, et al.
Molecular Genetics and Metabolism|June 25, 1999
Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndromeA Pizzuti, G Novelli, A Ratti, et al.
Journal of Medical Genetics|September 10, 2003
Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromesA Sarkozy, E Conti, D Seripa, et al.
Science (New York, N.Y.)|March 16, 1992
An unstable triplet repeat in a gene related to myotonic muscular dystrophyY H Fu, A Pizzuti, R G Fenwick, et al.
Diabetes|September 10, 1999
A polymorphism (K121Q) of the human glycoprotein PC-1 gene coding region is strongly associated with insulin resistanceA Pizzuti, L Frittitta, A Argiolas, et al.
Science (New York, N.Y.)|April 9, 1993
Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophyY H Fu, D L Friedman, S Richards, et al.
Kidney International|January 1, 1997
Hepatitis G virus infection in hemodialysis patientsM Sampietro, S Badalamenti, G Graziani, et al.
Minerva Cardioangiologica|May 13, 1998
[Natriuretic peptides and the heart. Critical review and application]G Baralis, E Antonielli, A Pizzuti, et al.
Cell|May 31, 1991
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndromeA J Verkerk, M Pieretti, J S Sutcliffe, et al.
Pageof 12