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Patrizia De Marco

Showing results (41-50 of 96) with videos related to

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Biomedical Materials (Bristol, England)|June 14, 2017
Graphene oxide improves the biocompatibility of collagen membranes in an in vitro model of human primary gingival fibroblastsPatrizia De Marco, Susi Zara, Marianna De Colli, et al.
Journal of Human Genetics|July 12, 2002
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian populationPatrizia De Marco, Maria Grazia Calevo, Anna Moroni, et al.
Human Molecular Genetics|April 4, 2017
Scribble1 plays an important role in the pathogenesis of neural tube defects through its mediating effect of Par-3 and Vangl1/2 localizationFares Kharfallah, Marie Claude Guyot, Abdul Rahman El Hassan, et al.
Gene|January 14, 2014
Identification of a novel mouse Dbl proto-oncogene splice variant: evidence that SEC14 domain is involved in GEF activity regulationMarzia Ognibene, Cristina Vanni, Fabiola Blengio, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 6, 2011
Maternal periconceptional factors affect the risk of spina bifida-affected pregnancies: an Italian case-control studyPatrizia De Marco, Elisa Merello, Maria Grazia Calevo, et al.
European Journal of Human Genetics : EJHG|April 4, 2003
Reduced folate carrier polymorphism (80A-->G) and neural tube defectsPatrizia De Marco, Maria Grazia Calevo, Anna Moroni, et al.
European Journal of Human Genetics : EJHG|May 18, 2017
Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type I reveals candidate genes for cranio-facial developmentElisa Merello, Lorenzo Tattini, Alberto Magi, et al.
Orphanet Journal of Rare Diseases|February 5, 2015
Cost effective assay choice for rare disease study designsDesmond D Campbell, Robert M Porsch, Stacey S Cherny, et al.
Human Mutation|March 26, 2009
Novel mutations in VANGL1 in neural tube defectsZoha Kibar, Ciprian M Bosoi, Megan Kooistra, et al.
Reviews in Medical Virology|July 10, 2026
West Nile Neuroinvasive Disease: Current Management, Emerging Therapies and Future Clinical Trial PrioritiesAmbrogio Curtolo, Dimitra Kontogiannis, Tommaso Ascoli Bartoli, et al.
Pageof 10

Showing results (41-50 of 96) with videos related to

Sort By:
Pageof 10
Biomedical Materials (Bristol, England)|June 14, 2017
Graphene oxide improves the biocompatibility of collagen membranes in an in vitro model of human primary gingival fibroblastsPatrizia De Marco, Susi Zara, Marianna De Colli, et al.
Journal of Human Genetics|July 12, 2002
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian populationPatrizia De Marco, Maria Grazia Calevo, Anna Moroni, et al.
Human Molecular Genetics|April 4, 2017
Scribble1 plays an important role in the pathogenesis of neural tube defects through its mediating effect of Par-3 and Vangl1/2 localizationFares Kharfallah, Marie Claude Guyot, Abdul Rahman El Hassan, et al.
Gene|January 14, 2014
Identification of a novel mouse Dbl proto-oncogene splice variant: evidence that SEC14 domain is involved in GEF activity regulationMarzia Ognibene, Cristina Vanni, Fabiola Blengio, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|January 6, 2011
Maternal periconceptional factors affect the risk of spina bifida-affected pregnancies: an Italian case-control studyPatrizia De Marco, Elisa Merello, Maria Grazia Calevo, et al.
European Journal of Human Genetics : EJHG|April 4, 2003
Reduced folate carrier polymorphism (80A-->G) and neural tube defectsPatrizia De Marco, Maria Grazia Calevo, Anna Moroni, et al.
European Journal of Human Genetics : EJHG|May 18, 2017
Exome sequencing of two Italian pedigrees with non-isolated Chiari malformation type I reveals candidate genes for cranio-facial developmentElisa Merello, Lorenzo Tattini, Alberto Magi, et al.
Orphanet Journal of Rare Diseases|February 5, 2015
Cost effective assay choice for rare disease study designsDesmond D Campbell, Robert M Porsch, Stacey S Cherny, et al.
Human Mutation|March 26, 2009
Novel mutations in VANGL1 in neural tube defectsZoha Kibar, Ciprian M Bosoi, Megan Kooistra, et al.
Reviews in Medical Virology|July 10, 2026
West Nile Neuroinvasive Disease: Current Management, Emerging Therapies and Future Clinical Trial PrioritiesAmbrogio Curtolo, Dimitra Kontogiannis, Tommaso Ascoli Bartoli, et al.
Pageof 10