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Human Mutation
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September 21, 2006
A common variant located in the 3'UTR of the RET gene is associated with protection from Hirschsprung disease
Paola 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 mice
Paola 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 lines
Emanuele 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 channel
Nicoletta 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 fibrosis
Ambra 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 patients
Renato 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 cells
Silvia Borghini, Tiziana Bachetti, Monica Fava, et al.
Proceedings of the American Thoracic Society
|
August 23, 2005
Effect of inflammatory stimuli on airway ion transport
Luis 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 Progressiva
Francesca 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 expression
Francesca Puppo, Paola Griseri, Mirco Fanelli, et al.
Page
of 14
Search research articles
Search
Showing results (41-50 of 135) with videos related to
Sort By:
Page
of 14
Human Mutation
|
September 21, 2006
A common variant located in the 3'UTR of the RET gene is associated with protection from Hirschsprung disease
Paola 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 mice
Paola 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 lines
Emanuele 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 channel
Nicoletta 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 fibrosis
Ambra 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 patients
Renato 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 cells
Silvia Borghini, Tiziana Bachetti, Monica Fava, et al.
Proceedings of the American Thoracic Society
|
August 23, 2005
Effect of inflammatory stimuli on airway ion transport
Luis 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 Progressiva
Francesca 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 expression
Francesca Puppo, Paola Griseri, Mirco Fanelli, et al.
Page
of 14