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Francesca Pantaleoni

Showing results (11-20 of 49) with videos related to

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Journal of Cellular and Molecular Medicine|October 13, 2009
Zoledronic acid repolarizes tumour-associated macrophages and inhibits mammary carcinogenesis by targeting the mevalonate pathwayMarta Coscia, Elena Quaglino, Manuela Iezzi, et al.
Molecular Genetics and Metabolism|November 20, 2013
Decreased bone mineral density in Costello syndromeChiara Leoni, David A Stevenson, Lucilla Martini, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutationsChristian P Kratz, Giuseppe Zampino, Marjolein Kriek, et al.
American Journal of Medical Genetics. Part A|January 13, 2009
Cognitive profile of disorders associated with dysregulation of the RAS/MAPK signaling cascadeLaura Cesarini, Paolo Alfieri, Francesca Pantaleoni, et al.
European Journal of Human Genetics : EJHG|January 22, 2009
Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype-phenotype correlationsMaria Lisa Dentici, Anna Sarkozy, Francesca Pantaleoni, et al.
American Journal of Medical Genetics. Part A|June 23, 2021
Broadening the phenotypic spectrum of Beta3GalT6-associated phenotypesChiara Leoni, Marta Tedesco, Francesca Clementina Radio, et al.
American Journal of Human Genetics|June 15, 2006
Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotypeClaudio Carta, Francesca Pantaleoni, Gianfranco Bocchinfuso, et al.
Behavior Genetics|January 29, 2011
Long term memory profile of disorders associated with dysregulation of the RAS-MAPK signaling cascadePaolo Alfieri, Laura Cesarini, Maria Mallardi, et al.
European Journal of Human Genetics : EJHG|April 14, 2023
Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variantsManuela Priolo, Erika Zara, Francesca Clementina Radio, et al.
Human Mutation|April 9, 2017
Aberrant HRAS transcript processing underlies a distinctive phenotype within the RASopathy clinical spectrumFrancesca Pantaleoni, Dorit Lev, Ion C Cirstea, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Journal of Cellular and Molecular Medicine|October 13, 2009
Zoledronic acid repolarizes tumour-associated macrophages and inhibits mammary carcinogenesis by targeting the mevalonate pathwayMarta Coscia, Elena Quaglino, Manuela Iezzi, et al.
Molecular Genetics and Metabolism|November 20, 2013
Decreased bone mineral density in Costello syndromeChiara Leoni, David A Stevenson, Lucilla Martini, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
Craniosynostosis in patients with Noonan syndrome caused by germline KRAS mutationsChristian P Kratz, Giuseppe Zampino, Marjolein Kriek, et al.
American Journal of Medical Genetics. Part A|January 13, 2009
Cognitive profile of disorders associated with dysregulation of the RAS/MAPK signaling cascadeLaura Cesarini, Paolo Alfieri, Francesca Pantaleoni, et al.
European Journal of Human Genetics : EJHG|January 22, 2009
Spectrum of MEK1 and MEK2 gene mutations in cardio-facio-cutaneous syndrome and genotype-phenotype correlationsMaria Lisa Dentici, Anna Sarkozy, Francesca Pantaleoni, et al.
American Journal of Medical Genetics. Part A|June 23, 2021
Broadening the phenotypic spectrum of Beta3GalT6-associated phenotypesChiara Leoni, Marta Tedesco, Francesca Clementina Radio, et al.
American Journal of Human Genetics|June 15, 2006
Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotypeClaudio Carta, Francesca Pantaleoni, Gianfranco Bocchinfuso, et al.
Behavior Genetics|January 29, 2011
Long term memory profile of disorders associated with dysregulation of the RAS-MAPK signaling cascadePaolo Alfieri, Laura Cesarini, Maria Mallardi, et al.
European Journal of Human Genetics : EJHG|April 14, 2023
Clinical profiling of MRD48 and functional characterization of two novel pathogenic RAC1 variantsManuela Priolo, Erika Zara, Francesca Clementina Radio, et al.
Human Mutation|April 9, 2017
Aberrant HRAS transcript processing underlies a distinctive phenotype within the RASopathy clinical spectrumFrancesca Pantaleoni, Dorit Lev, Ion C Cirstea, et al.
Pageof 5