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Isabella Ceccherini

Showing results (41-50 of 180) 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.
Oncogene|March 1, 2005
PHOX2B mutations and genetic predisposition to neuroblastomaPatrizia Perri, Tiziana Bachetti, Luca Longo, et al.
Experimental Cell Research|July 24, 2018
Desogestrel down-regulates PHOX2B and its target genes in progesterone responsive neuroblastoma cellsSilvia Cardani, Simona Di Lascio, Debora Belperio, 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.
Journal of Neurology|November 16, 2007
Adult-onset Alexander disease : report on a familyPietro Balbi, Marco Seri, Isabella Ceccherini, et al.
Medicine|March 14, 2009
Hirschsprung disease and congenital anomalies of the kidney and urinary tract (CAKUT): a novel syndromic associationAlessio Pini Prato, Marco Musso, Isabella Ceccherini, et al.
European Journal of Human Genetics : EJHG|June 13, 2019
Current practices for the genetic diagnosis of autoinflammatory diseases: results of a European Molecular Genetics Quality Network SurveyDorota Rowczenio, Yael Shinar, Isabella Ceccherini, et al.
Pediatric Pulmonology|September 12, 2008
A novel missense mutation in the PHOX2B gene is associated with late onset central hypoventilation syndromeSara Parodi, Maria Pia Baglietto, Alessio Pini Prato, 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.
Pageof 18

Showing results (41-50 of 180) with videos related to

Sort By:
Pageof 18
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.
Oncogene|March 1, 2005
PHOX2B mutations and genetic predisposition to neuroblastomaPatrizia Perri, Tiziana Bachetti, Luca Longo, et al.
Experimental Cell Research|July 24, 2018
Desogestrel down-regulates PHOX2B and its target genes in progesterone responsive neuroblastoma cellsSilvia Cardani, Simona Di Lascio, Debora Belperio, 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.
Journal of Neurology|November 16, 2007
Adult-onset Alexander disease : report on a familyPietro Balbi, Marco Seri, Isabella Ceccherini, et al.
Medicine|March 14, 2009
Hirschsprung disease and congenital anomalies of the kidney and urinary tract (CAKUT): a novel syndromic associationAlessio Pini Prato, Marco Musso, Isabella Ceccherini, et al.
European Journal of Human Genetics : EJHG|June 13, 2019
Current practices for the genetic diagnosis of autoinflammatory diseases: results of a European Molecular Genetics Quality Network SurveyDorota Rowczenio, Yael Shinar, Isabella Ceccherini, et al.
Pediatric Pulmonology|September 12, 2008
A novel missense mutation in the PHOX2B gene is associated with late onset central hypoventilation syndromeSara Parodi, Maria Pia Baglietto, Alessio Pini Prato, 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.
Pageof 18