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Simona Coppola

Showing results (11-20 of 25) with videos related to

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FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 4, 2004
Glutathione depletion up-regulates Bcl-2 in BSO-resistant cellsMaria D'Alessio, Claudia Cerella, Carla Amici, et al.
The Journal of Allergy and Clinical Immunology|February 14, 2022
Mutations at the C-terminus of CDC42 cause distinct hematopoietic and autoinflammatory disordersSimona Coppola, Antonella Insalaco, Erika Zara, et al.
Cancer Gene Therapy|March 6, 2004
GSH depletion enhances adenoviral bax-induced apoptosis in lung cancer cellsTsuyoshi Honda, Simona Coppola, Lina Ghibelli, et al.
International Journal of Molecular Sciences|March 14, 2026
A Novel Heterozygous <i>ARL3</i> Variant in Non-Syndromic Retinitis Pigmentosa: Clinical and Functional CharacterizationEmilia Stellacci, Lucia Ziccardi, Alessandro Bruselles, 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.
Frontiers in Immunology|March 21, 2022
Pro Nerve Growth Factor and Its Receptor p75NTR Activate Inflammatory Responses in Synovial Fibroblasts: A Novel Targetable Mechanism in ArthritisLuciapia Farina, Gaetana Minnone, Stefano Alivernini, et al.
Nature Communications|November 16, 2024
Autoinflammatory patients with Golgi-trapped CDC42 exhibit intracellular trafficking defects leading to STING hyperactivation and ER stressAlberto Iannuzzo, Selket Delafontaine, Rana El Masri, et al.
Human Molecular Genetics|May 21, 2019
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathyMarialetizia Motta, Lena Sagi-Dain, Oliver H F Krumbach, et al.
Human Molecular Genetics|February 22, 2014
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotypePamela Magini, Tommaso Pippucci, I-Chun Tsai, et al.
European Journal of Human Genetics : EJHG|January 8, 2026
Newly identified ARF3 variants strengthen the causal link between Golgi fragmentation and brain malformationsValentina Muto, Giulia Fasano, Francesca Clementina Radio, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 4, 2004
Glutathione depletion up-regulates Bcl-2 in BSO-resistant cellsMaria D'Alessio, Claudia Cerella, Carla Amici, et al.
The Journal of Allergy and Clinical Immunology|February 14, 2022
Mutations at the C-terminus of CDC42 cause distinct hematopoietic and autoinflammatory disordersSimona Coppola, Antonella Insalaco, Erika Zara, et al.
Cancer Gene Therapy|March 6, 2004
GSH depletion enhances adenoviral bax-induced apoptosis in lung cancer cellsTsuyoshi Honda, Simona Coppola, Lina Ghibelli, et al.
International Journal of Molecular Sciences|March 14, 2026
A Novel Heterozygous <i>ARL3</i> Variant in Non-Syndromic Retinitis Pigmentosa: Clinical and Functional CharacterizationEmilia Stellacci, Lucia Ziccardi, Alessandro Bruselles, 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.
Frontiers in Immunology|March 21, 2022
Pro Nerve Growth Factor and Its Receptor p75NTR Activate Inflammatory Responses in Synovial Fibroblasts: A Novel Targetable Mechanism in ArthritisLuciapia Farina, Gaetana Minnone, Stefano Alivernini, et al.
Nature Communications|November 16, 2024
Autoinflammatory patients with Golgi-trapped CDC42 exhibit intracellular trafficking defects leading to STING hyperactivation and ER stressAlberto Iannuzzo, Selket Delafontaine, Rana El Masri, et al.
Human Molecular Genetics|May 21, 2019
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathyMarialetizia Motta, Lena Sagi-Dain, Oliver H F Krumbach, et al.
Human Molecular Genetics|February 22, 2014
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotypePamela Magini, Tommaso Pippucci, I-Chun Tsai, et al.
European Journal of Human Genetics : EJHG|January 8, 2026
Newly identified ARF3 variants strengthen the causal link between Golgi fragmentation and brain malformationsValentina Muto, Giulia Fasano, Francesca Clementina Radio, et al.
Pageof 3