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Francesca Vitelli

Showing results (1-10 of 11) with videos related to

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Trends in Genetics : TIG|October 31, 2003
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?Francesca Vitelli, Antonio Baldini
Genesis (New York, N.Y. : 2000)|March 3, 2009
Gain of function of Tbx1 affects pharyngeal and heart development in the mouseFrancesca Vitelli, Tuong Huynh, Antonio Baldini
Journal of Molecular and Cellular Cardiology|September 3, 2010
Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8Francesca Vitelli, Gabriella Lania, Tuong Huynh, et al.
Advances in Biochemical Engineering/Biotechnology|March 15, 2017
Gene TherapyBarb Thorne, Ryan Takeya, Francesca Vitelli, et al.
Human Molecular Genetics|April 25, 2002
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathwaysFrancesca Vitelli, Masae Morishima, Ilaria Taddei, et al.
Human Molecular Genetics|August 13, 2003
TBX1 is required for inner ear morphogenesisFrancesca Vitelli, Antonella Viola, Masae Morishima, et al.
Developmental Biology|May 16, 2006
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutantsFrancesca Vitelli, Zhen Zhang, Tuong Huynh, et al.
Development (Cambridge, England)|September 12, 2002
A genetic link between Tbx1 and fibroblast growth factor signalingFrancesca Vitelli, Ilaria Taddei, Masae Morishima, et al.
Developmental Biology|April 25, 2009
Early thyroid development requires a Tbx1-Fgf8 pathwayGabriella Lania, Zhen Zhang, Tuong Huynh, et al.
Development (Cambridge, England)|November 15, 2005
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery developmentZhen Zhang, Fabiana Cerrato, Huansheng Xu, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Trends in Genetics : TIG|October 31, 2003
Generating and modifying DiGeorge syndrome-like phenotypes in model organisms: is there a common genetic pathway?Francesca Vitelli, Antonio Baldini
Genesis (New York, N.Y. : 2000)|March 3, 2009
Gain of function of Tbx1 affects pharyngeal and heart development in the mouseFrancesca Vitelli, Tuong Huynh, Antonio Baldini
Journal of Molecular and Cellular Cardiology|September 3, 2010
Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: genetic evidence of impaired tissue response to Fgf8Francesca Vitelli, Gabriella Lania, Tuong Huynh, et al.
Advances in Biochemical Engineering/Biotechnology|March 15, 2017
Gene TherapyBarb Thorne, Ryan Takeya, Francesca Vitelli, et al.
Human Molecular Genetics|April 25, 2002
Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathwaysFrancesca Vitelli, Masae Morishima, Ilaria Taddei, et al.
Human Molecular Genetics|August 13, 2003
TBX1 is required for inner ear morphogenesisFrancesca Vitelli, Antonella Viola, Masae Morishima, et al.
Developmental Biology|May 16, 2006
Fgf8 expression in the Tbx1 domain causes skeletal abnormalities and modifies the aortic arch but not the outflow tract phenotype of Tbx1 mutantsFrancesca Vitelli, Zhen Zhang, Tuong Huynh, et al.
Development (Cambridge, England)|September 12, 2002
A genetic link between Tbx1 and fibroblast growth factor signalingFrancesca Vitelli, Ilaria Taddei, Masae Morishima, et al.
Developmental Biology|April 25, 2009
Early thyroid development requires a Tbx1-Fgf8 pathwayGabriella Lania, Zhen Zhang, Tuong Huynh, et al.
Development (Cambridge, England)|November 15, 2005
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery developmentZhen Zhang, Fabiana Cerrato, Huansheng Xu, et al.
Pageof 2