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G Novelli

Showing results (181-190 of 330) with videos related to

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Annali Italiani Di Chirurgia|January 1, 1991
[The role of endoscopy in the hemorrhagic complications of gastroduodenal ulcer]A Scamporrino, U De Petris, G Novelli, et al.
American Journal of Human Genetics|January 1, 1995
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patientsB Mercier, C Verlingue, W Lissens, et al.
Cellular and Molecular Life Sciences : CMLS|November 2, 2005
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatmentM Columbaro, C Capanni, E Mattioli, et al.
Biochemistry and Molecular Biology International|April 17, 1999
Cellular uptake and delivery monitoring of liposome/DNA complexes during in vitro transfection of CFTR geneA L Serafino, G Novelli, S Di Sario, et al.
La Clinica Terapeutica|December 31, 1985
[Comparative evaluation in the treatment of arterial hypertension between prolonged-action clonidine and atenolol]M La Vecchia, G Vergara, G Iannuzzi, et al.
Clinical and Experimental Immunology|June 26, 2016
Polymorphisms in STAT-4, IL-10, PSORS1C1, PTPN2 and MIR146A genes are associated differently with prognostic factors in Italian patients affected by rheumatoid arthritisC Ciccacci, P Conigliaro, C Perricone, et al.
American Journal of Medical Genetics|April 1, 1990
Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney DiseaseP Mandich, G Restagno, G Novelli, et al.
American Journal of Medical Genetics|February 13, 2001
Exclusion of the elastin gene in the pathogenesis of Costello syndromeC Tandoi, A Botta, G Fini, et al.
Mutation Research|September 1, 1989
Identification of 4 ataxia telangiectasia cell lines hypersensitive to gamma-irradiation but not to hydrogen peroxideO Cantoni, P Sestili, M Fiorilli, et al.
Neurogenetics|May 17, 2001
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonatesA De Luca, M Rizzardi, I Torrente, et al.
Pageof 33

Showing results (181-190 of 330) with videos related to

Sort By:
Pageof 33
Annali Italiani Di Chirurgia|January 1, 1991
[The role of endoscopy in the hemorrhagic complications of gastroduodenal ulcer]A Scamporrino, U De Petris, G Novelli, et al.
American Journal of Human Genetics|January 1, 1995
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patientsB Mercier, C Verlingue, W Lissens, et al.
Cellular and Molecular Life Sciences : CMLS|November 2, 2005
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatmentM Columbaro, C Capanni, E Mattioli, et al.
Biochemistry and Molecular Biology International|April 17, 1999
Cellular uptake and delivery monitoring of liposome/DNA complexes during in vitro transfection of CFTR geneA L Serafino, G Novelli, S Di Sario, et al.
La Clinica Terapeutica|December 31, 1985
[Comparative evaluation in the treatment of arterial hypertension between prolonged-action clonidine and atenolol]M La Vecchia, G Vergara, G Iannuzzi, et al.
Clinical and Experimental Immunology|June 26, 2016
Polymorphisms in STAT-4, IL-10, PSORS1C1, PTPN2 and MIR146A genes are associated differently with prognostic factors in Italian patients affected by rheumatoid arthritisC Ciccacci, P Conigliaro, C Perricone, et al.
American Journal of Medical Genetics|April 1, 1990
Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney DiseaseP Mandich, G Restagno, G Novelli, et al.
American Journal of Medical Genetics|February 13, 2001
Exclusion of the elastin gene in the pathogenesis of Costello syndromeC Tandoi, A Botta, G Fini, et al.
Mutation Research|September 1, 1989
Identification of 4 ataxia telangiectasia cell lines hypersensitive to gamma-irradiation but not to hydrogen peroxideO Cantoni, P Sestili, M Fiorilli, et al.
Neurogenetics|May 17, 2001
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonatesA De Luca, M Rizzardi, I Torrente, et al.
Pageof 33