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G Novelli

Showing results (271-280 of 330) with videos related to

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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 29, 2009
Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patientsF Rinaldi, A Botta, L Vallo, et al.
Transplantation Proceedings|September 27, 2005
Molecular adsorbent recirculating system treatment for acute hepatic failure in patients with hepatitis B undergoing chemotherapy for non-Hodgkin's lymphomaG Novelli, M Rossi, G Ferretti, et al.
Human Genetics|March 1, 1988
Multilocus analysis of the fragile X syndromeW T Brown, A Gross, C Chan, et al.
Neurobiology of Disease|August 30, 2011
Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissuesF Rinaldi, C Terracciano, V Pisani, et al.
Transplantation Proceedings|June 11, 2010
Clinical results of treatment of postsurgical endotoxin-mediated sepsis with polymyxin-B direct hemoperfusionG Novelli, G Ferretti, L Poli, et al.
Transplantation Proceedings|June 8, 2006
Intractable pruritus in patients with hepatitis C virusG Novelli, M Rossi, L Poli, et al.
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.
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.
Lupus|November 24, 2016
A polymorphism upstream MIR1279 gene is associated with pericarditis development in Systemic Lupus Erythematosus and contributes to definition of a genetic risk profile for this complicationC Ciccacci, C Perricone, C Politi, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|February 10, 2009
"The Linosa Study": epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolateA Bellia, E Giardina, D Lauro, et al.
Pageof 33

Showing results (271-280 of 330) with videos related to

Sort By:
Pageof 33
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|May 29, 2009
Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patientsF Rinaldi, A Botta, L Vallo, et al.
Transplantation Proceedings|September 27, 2005
Molecular adsorbent recirculating system treatment for acute hepatic failure in patients with hepatitis B undergoing chemotherapy for non-Hodgkin's lymphomaG Novelli, M Rossi, G Ferretti, et al.
Human Genetics|March 1, 1988
Multilocus analysis of the fragile X syndromeW T Brown, A Gross, C Chan, et al.
Neurobiology of Disease|August 30, 2011
Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissuesF Rinaldi, C Terracciano, V Pisani, et al.
Transplantation Proceedings|June 11, 2010
Clinical results of treatment of postsurgical endotoxin-mediated sepsis with polymyxin-B direct hemoperfusionG Novelli, G Ferretti, L Poli, et al.
Transplantation Proceedings|June 8, 2006
Intractable pruritus in patients with hepatitis C virusG Novelli, M Rossi, L Poli, et al.
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.
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.
Lupus|November 24, 2016
A polymorphism upstream MIR1279 gene is associated with pericarditis development in Systemic Lupus Erythematosus and contributes to definition of a genetic risk profile for this complicationC Ciccacci, C Perricone, C Politi, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|February 10, 2009
"The Linosa Study": epidemiological and heritability data of the metabolic syndrome in a Caucasian genetic isolateA Bellia, E Giardina, D Lauro, et al.
Pageof 33