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Mirella Filocamo

Showing results (71-80 of 103) with videos related to

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Molecular Pharmacology|January 16, 2003
Basic fibroblast growth factor activates endothelial nitric-oxide synthase in CHO-K1 cells via the activation of ceramide synthesisTullio Florio, Sara Arena, Alessandra Pattarozzi, et al.
Annals of the New York Academy of Sciences|December 18, 2002
Nitric oxide production stimulated by the basic fibroblast growth factor requires the synthesis of ceramideSara Arena, Alessandra Pattarozzi, Stefano Thellung, et al.
Neurogenetics|January 14, 2020
Changes in global gene expression indicate disordered autophagy, apoptosis and inflammatory processes and downregulation of cytoskeletal signalling and neuronal development in patients with Niemann-Pick C diseaseKatarzyna Hetmańczyk-Sawicka, Roksana Iwanicka-Nowicka, Anna Fogtman, et al.
Scientific Reports|April 17, 2019
Gene expression profile in patients with Gaucher disease indicates activation of inflammatory processesAgnieszka Ługowska, Katarzyna Hetmańczyk-Sawicka, Roksana Iwanicka-Nowicka, et al.
Human Mutation|January 16, 2007
GM1 gangliosidosis: molecular analysis of nine patients and development of an RT-PCR assay for GLB1 gene expression profilingAnna Caciotti, Maria Alice Donati, Elena Procopio, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 24, 2012
First pilot newborn screening for four lysosomal storage diseases in an Italian region: identification and analysis of a putative causative mutation in the GBA geneSilvia Paciotti, Emanuele Persichetti, Severo Pagliardini, et al.
Scientific Reports|January 29, 2021
Predicting the probability of Gaucher disease in subjects with splenomegaly and thrombocytopeniaIrene Motta, Dario Consonni, Marina Stroppiano, et al.
Orphanet Journal of Rare Diseases|February 5, 2013
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in ItalyFilippo Maria Santorelli, Barbara Garavaglia, Francesco Cardona, et al.
Annals of Human Genetics|October 16, 2010
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activitiesTiziana Bachetti, Eleonora Di Zanni, Francesca Lantieri, et al.
Neurogenetics|March 3, 2009
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian patients: identification and structural modeling of novel mutationsTatiana Fancello, Andrea Dardis, Camillo Rosano, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
Molecular Pharmacology|January 16, 2003
Basic fibroblast growth factor activates endothelial nitric-oxide synthase in CHO-K1 cells via the activation of ceramide synthesisTullio Florio, Sara Arena, Alessandra Pattarozzi, et al.
Annals of the New York Academy of Sciences|December 18, 2002
Nitric oxide production stimulated by the basic fibroblast growth factor requires the synthesis of ceramideSara Arena, Alessandra Pattarozzi, Stefano Thellung, et al.
Neurogenetics|January 14, 2020
Changes in global gene expression indicate disordered autophagy, apoptosis and inflammatory processes and downregulation of cytoskeletal signalling and neuronal development in patients with Niemann-Pick C diseaseKatarzyna Hetmańczyk-Sawicka, Roksana Iwanicka-Nowicka, Anna Fogtman, et al.
Scientific Reports|April 17, 2019
Gene expression profile in patients with Gaucher disease indicates activation of inflammatory processesAgnieszka Ługowska, Katarzyna Hetmańczyk-Sawicka, Roksana Iwanicka-Nowicka, et al.
Human Mutation|January 16, 2007
GM1 gangliosidosis: molecular analysis of nine patients and development of an RT-PCR assay for GLB1 gene expression profilingAnna Caciotti, Maria Alice Donati, Elena Procopio, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 24, 2012
First pilot newborn screening for four lysosomal storage diseases in an Italian region: identification and analysis of a putative causative mutation in the GBA geneSilvia Paciotti, Emanuele Persichetti, Severo Pagliardini, et al.
Scientific Reports|January 29, 2021
Predicting the probability of Gaucher disease in subjects with splenomegaly and thrombocytopeniaIrene Motta, Dario Consonni, Marina Stroppiano, et al.
Orphanet Journal of Rare Diseases|February 5, 2013
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in ItalyFilippo Maria Santorelli, Barbara Garavaglia, Francesco Cardona, et al.
Annals of Human Genetics|October 16, 2010
A novel polymorphic AP-1 binding element of the GFAP promoter is associated with different allelic transcriptional activitiesTiziana Bachetti, Eleonora Di Zanni, Francesca Lantieri, et al.
Neurogenetics|March 3, 2009
Molecular analysis of NPC1 and NPC2 gene in 34 Niemann-Pick C Italian patients: identification and structural modeling of novel mutationsTatiana Fancello, Andrea Dardis, Camillo Rosano, et al.
Pageof 11