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Daniela Iaconis

Showing results (1-10 of 30) with videos related to

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Human Molecular Genetics|February 21, 2020
The HOPS complex subunit VPS39 controls ciliogenesis through autophagyDaniela Iaconis, Claudia Crina, Simona Brillante, et al.
Journal of Cheminformatics|June 9, 2023
ProfhEX: AI-based platform for small molecules liability profilingFilippo Lunghini, Anna Fava, Vincenzo Pisapia, et al.
Molecular Medicine Reports|April 12, 2011
Disruption of the IQSEC2 transcript in a female with X;autosome translocation t(X;20)(p11.2;q11.2) and a phenotype resembling X-linked infantile spasms (ISSX) syndromeManuela Morleo, Daniela Iaconis, David Chitayat, et al.
Human Molecular Genetics|May 7, 2010
Kidney-specific inactivation of Ofd1 leads to renal cystic disease associated with upregulation of the mTOR pathwayAlessandro Zullo, Daniela Iaconis, Adriano Barra, et al.
Molecules (Basel, Switzerland)|March 27, 2025
Integrating Surface Plasmon Resonance and Docking Analysis for Mechanistic Insights of Tryptase InhibitorsAlessia Porta, Candida Manelfi, Carmine Talarico, et al.
Tissue & Cell|June 1, 2020
The centrosomal/basal body protein OFD1 is required for microtubule organization and cell cycle progressionMariaevelina Alfieri, Daniela Iaconis, Roberta Tammaro, et al.
Viruses|October 29, 2025
SARS-CoV-2 Entry Can Be Mimicked in <i>C. elegans</i> Expressing Human ACE2: A New Tool for Pharmacological StudiesMargherita Romeo, Sara Baroni, Maria Monica Barzago, et al.
Human Molecular Genetics|November 1, 2016
Oral-facial-digital syndrome type I cells exhibit impaired DNA repair; unanticipated consequences of defective OFD1 outside of the cilia networkIga Abramowicz, Gillian Carpenter, Mariaevelina Alfieri, et al.
American Journal of Human Genetics|October 13, 2006
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndromeIsabella Wimplinger, Manuela Morleo, Georg Rosenberger, et al.
Antioxidants (Basel, Switzerland)|September 28, 2021
L-Methionine Protects against Oxidative Stress and Mitochondrial Dysfunction in an In Vitro Model of Parkinson's DiseaseMariano Catanesi, Laura Brandolini, Michele d'Angelo, et al.
Pageof 3

Showing results (1-10 of 30) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|February 21, 2020
The HOPS complex subunit VPS39 controls ciliogenesis through autophagyDaniela Iaconis, Claudia Crina, Simona Brillante, et al.
Journal of Cheminformatics|June 9, 2023
ProfhEX: AI-based platform for small molecules liability profilingFilippo Lunghini, Anna Fava, Vincenzo Pisapia, et al.
Molecular Medicine Reports|April 12, 2011
Disruption of the IQSEC2 transcript in a female with X;autosome translocation t(X;20)(p11.2;q11.2) and a phenotype resembling X-linked infantile spasms (ISSX) syndromeManuela Morleo, Daniela Iaconis, David Chitayat, et al.
Human Molecular Genetics|May 7, 2010
Kidney-specific inactivation of Ofd1 leads to renal cystic disease associated with upregulation of the mTOR pathwayAlessandro Zullo, Daniela Iaconis, Adriano Barra, et al.
Molecules (Basel, Switzerland)|March 27, 2025
Integrating Surface Plasmon Resonance and Docking Analysis for Mechanistic Insights of Tryptase InhibitorsAlessia Porta, Candida Manelfi, Carmine Talarico, et al.
Tissue & Cell|June 1, 2020
The centrosomal/basal body protein OFD1 is required for microtubule organization and cell cycle progressionMariaevelina Alfieri, Daniela Iaconis, Roberta Tammaro, et al.
Viruses|October 29, 2025
SARS-CoV-2 Entry Can Be Mimicked in <i>C. elegans</i> Expressing Human ACE2: A New Tool for Pharmacological StudiesMargherita Romeo, Sara Baroni, Maria Monica Barzago, et al.
Human Molecular Genetics|November 1, 2016
Oral-facial-digital syndrome type I cells exhibit impaired DNA repair; unanticipated consequences of defective OFD1 outside of the cilia networkIga Abramowicz, Gillian Carpenter, Mariaevelina Alfieri, et al.
American Journal of Human Genetics|October 13, 2006
Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndromeIsabella Wimplinger, Manuela Morleo, Georg Rosenberger, et al.
Antioxidants (Basel, Switzerland)|September 28, 2021
L-Methionine Protects against Oxidative Stress and Mitochondrial Dysfunction in an In Vitro Model of Parkinson's DiseaseMariano Catanesi, Laura Brandolini, Michele d'Angelo, et al.
Pageof 3