Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Tiziana Bachetti

Showing results (31-40 of 84) with videos related to

Pageof 9
Sort By:
Oncogene|March 1, 2005
PHOX2B mutations and genetic predisposition to neuroblastomaPatrizia Perri, Tiziana Bachetti, Luca Longo, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 26, 2009
The ADMA/DDAH pathway regulates VEGF-mediated angiogenesisLorna R Fiedler, Tiziana Bachetti, James Leiper, et al.
Journal of Molecular and Cellular Cardiology|November 4, 2004
Co-expression and modulation of neuronal and endothelial nitric oxide synthase in human endothelial cellsTiziana Bachetti, Laura Comini, Salvatore Curello, et al.
Cells|December 24, 2021
Functional Conservation and Genetic Divergence of Chordate Glycinergic Neurotransmission: Insights from Amphioxus Glycine TransportersMatteo Bozzo, Simone Costa, Valentina Obino, et al.
Frontiers in Genetics|December 24, 2021
Parental Somatic Mosaicism Uncovers Inheritance of an Apparently <i>De Novo GFAP</i> MutationAlice Grossi, Federico Morelli, Marco Di Duca, 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.
Frontiers in Genetics|April 7, 2022
Corrigendum: Parental Somatic Mosaicism Uncovers Inheritance of an Apparently De Novo GFAP MutationAlice Grossi, Federico Morelli, Marco Di Duca, et al.
Physiological Genomics|September 8, 2005
Comparative genomic sequence analysis coupled to chromatin immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locusFrancesca Puppo, Marco Musso, Doroti Pirulli, et al.
European Heart Journal|December 24, 2004
Ischaemia-reperfusion injury activates matrix metalloproteinases in the human heartManoj M Lalu, Evasio Pasini, Costas J Schulze, et al.
Human Mutation|November 4, 2017
Structural and functional differences in PHOX2B frameshift mutations underlie isolated or syndromic congenital central hypoventilation syndromeSimona Di Lascio, Roberta Benfante, Eleonora Di Zanni, et al.
Pageof 9

Showing results (31-40 of 84) with videos related to

Sort By:
Pageof 9
Oncogene|March 1, 2005
PHOX2B mutations and genetic predisposition to neuroblastomaPatrizia Perri, Tiziana Bachetti, Luca Longo, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|September 26, 2009
The ADMA/DDAH pathway regulates VEGF-mediated angiogenesisLorna R Fiedler, Tiziana Bachetti, James Leiper, et al.
Journal of Molecular and Cellular Cardiology|November 4, 2004
Co-expression and modulation of neuronal and endothelial nitric oxide synthase in human endothelial cellsTiziana Bachetti, Laura Comini, Salvatore Curello, et al.
Cells|December 24, 2021
Functional Conservation and Genetic Divergence of Chordate Glycinergic Neurotransmission: Insights from Amphioxus Glycine TransportersMatteo Bozzo, Simone Costa, Valentina Obino, et al.
Frontiers in Genetics|December 24, 2021
Parental Somatic Mosaicism Uncovers Inheritance of an Apparently <i>De Novo GFAP</i> MutationAlice Grossi, Federico Morelli, Marco Di Duca, 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.
Frontiers in Genetics|April 7, 2022
Corrigendum: Parental Somatic Mosaicism Uncovers Inheritance of an Apparently De Novo GFAP MutationAlice Grossi, Federico Morelli, Marco Di Duca, et al.
Physiological Genomics|September 8, 2005
Comparative genomic sequence analysis coupled to chromatin immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locusFrancesca Puppo, Marco Musso, Doroti Pirulli, et al.
European Heart Journal|December 24, 2004
Ischaemia-reperfusion injury activates matrix metalloproteinases in the human heartManoj M Lalu, Evasio Pasini, Costas J Schulze, et al.
Human Mutation|November 4, 2017
Structural and functional differences in PHOX2B frameshift mutations underlie isolated or syndromic congenital central hypoventilation syndromeSimona Di Lascio, Roberta Benfante, Eleonora Di Zanni, et al.
Pageof 9