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Roberto Ravazzolo

Showing results (41-50 of 135) with videos related to

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Human Mutation|September 21, 2006
A common variant located in the 3'UTR of the RET gene is associated with protection from Hirschsprung diseasePaola Griseri, Francesca Lantieri, Francesca Puppo, et al.
International Journal of Molecular Medicine|September 12, 2006
The immediate upstream sequence of the mouse Ret gene controls tissue-specific expression in transgenic micePaola Zordan, Sara Tavella, Antonella Brizzolara, et al.
Pathogenetics|December 3, 2008
Transfection of the mutant MYH9 cDNA reproduces the most typical cellular phenotype of MYH9-related disease in different cell linesEmanuele Panza, Monica Marini, Alessandro Pecci, et al.
Molecular Pharmacology|April 25, 2007
Structure-activity relationship of 1,4-dihydropyridines as potentiators of the cystic fibrosis transmembrane conductance regulator chloride channelNicoletta Pedemonte, Davide Boido, Oscar Moran, et al.
American Journal of Respiratory Cell and Molecular Biology|April 23, 2013
Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosisAmbra Gianotti, Raffaella Melani, Emanuela Caci, et al.
Clinical Immunology (Orlando, Fla.)|January 14, 2009
Association of alleles at polymorphic sites in the Osteopontin encoding gene in young type 1 diabetic patientsRenato Marciano, Giuseppe D'Annunzio, Nicola Minuto, et al.
The Biochemical Journal|January 13, 2006
The TLX2 homeobox gene is a transcriptional target of PHOX2B in neural-crest-derived cellsSilvia Borghini, Tiziana Bachetti, Monica Fava, et al.
Proceedings of the American Thoracic Society|August 23, 2005
Effect of inflammatory stimuli on airway ion transportLuis J V Galietta, Chiara Folli, Emanuela Caci, et al.
Orphanet Journal of Rare Diseases|September 20, 2013
Identification and characterization of regulatory elements in the promoter of ACVR1, the gene mutated in Fibrodysplasia Ossificans ProgressivaFrancesca Giacopelli, Serena Cappato, Laura Tonachini, et al.
FEBS Letters|July 19, 2002
Cell-line specific chromatin acetylation at the Sox10-Pax3 enhancer site modulates the RET proto-oncogene expressionFrancesca Puppo, Paola Griseri, Mirco Fanelli, et al.
Pageof 14

Showing results (41-50 of 135) with videos related to

Sort By:
Pageof 14
Human Mutation|September 21, 2006
A common variant located in the 3'UTR of the RET gene is associated with protection from Hirschsprung diseasePaola Griseri, Francesca Lantieri, Francesca Puppo, et al.
International Journal of Molecular Medicine|September 12, 2006
The immediate upstream sequence of the mouse Ret gene controls tissue-specific expression in transgenic micePaola Zordan, Sara Tavella, Antonella Brizzolara, et al.
Pathogenetics|December 3, 2008
Transfection of the mutant MYH9 cDNA reproduces the most typical cellular phenotype of MYH9-related disease in different cell linesEmanuele Panza, Monica Marini, Alessandro Pecci, et al.
Molecular Pharmacology|April 25, 2007
Structure-activity relationship of 1,4-dihydropyridines as potentiators of the cystic fibrosis transmembrane conductance regulator chloride channelNicoletta Pedemonte, Davide Boido, Oscar Moran, et al.
American Journal of Respiratory Cell and Molecular Biology|April 23, 2013
Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosisAmbra Gianotti, Raffaella Melani, Emanuela Caci, et al.
Clinical Immunology (Orlando, Fla.)|January 14, 2009
Association of alleles at polymorphic sites in the Osteopontin encoding gene in young type 1 diabetic patientsRenato Marciano, Giuseppe D'Annunzio, Nicola Minuto, et al.
The Biochemical Journal|January 13, 2006
The TLX2 homeobox gene is a transcriptional target of PHOX2B in neural-crest-derived cellsSilvia Borghini, Tiziana Bachetti, Monica Fava, et al.
Proceedings of the American Thoracic Society|August 23, 2005
Effect of inflammatory stimuli on airway ion transportLuis J V Galietta, Chiara Folli, Emanuela Caci, et al.
Orphanet Journal of Rare Diseases|September 20, 2013
Identification and characterization of regulatory elements in the promoter of ACVR1, the gene mutated in Fibrodysplasia Ossificans ProgressivaFrancesca Giacopelli, Serena Cappato, Laura Tonachini, et al.
FEBS Letters|July 19, 2002
Cell-line specific chromatin acetylation at the Sox10-Pax3 enhancer site modulates the RET proto-oncogene expressionFrancesca Puppo, Paola Griseri, Mirco Fanelli, et al.
Pageof 14