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Angeliki Louvi

Showing results (31-40 of 52) with videos related to

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Science Advances|June 10, 2026
Mice produce interneurons in the septum as a response to aversive experiences and antidepressant treatmentAikaterini Lampada, Chiara Rolando, Nigel Whittle, et al.
Scientific Reports|March 9, 2017
Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephalyParaskevi Sgourdou, Ketu Mishra-Gorur, Ichiko Saotome, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 19, 2008
Linking Notch signaling to ischemic strokeJoseph F Arboleda-Velasquez, Zhipeng Zhou, Hwa Kyoung Shin, et al.
Gut|March 3, 2016
Notch1 and Notch2 receptors regulate mouse and human gastric antral epithelial cell homoeostasisGail B Gifford, Elise S Demitrack, Theresa M Keeley, et al.
Journal of Neuroimmune Pharmacology : the Official Journal of the Society on Neuroimmune Pharmacology|April 18, 2016
B-Cell Depletion Reduces the Maturation of Cerebral Cavernous Malformations in Murine ModelsChangbin Shi, Robert Shenkar, Hussein A Zeineddine, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2011
Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel diseaseJoseph F Arboleda-Velasquez, Jan Manent, Jeong Hyun Lee, et al.
Developmental Cell|July 8, 2022
Interferon-γ resistance and immune evasion in glioma develop via Notch-regulated co-evolution of malignant and immune cellsElena Parmigiani, Robert Ivanek, Chiara Rolando, et al.
The New England Journal of Medicine|September 8, 2021
Somatic <i>PIK3CA</i> Mutations in Sporadic Cerebral Cavernous MalformationsMatthieu Peyre, Danielle Miyagishima, Franck Bielle, et al.
American Journal of Human Genetics|January 9, 2008
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersBetul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 30, 2013
Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegenerationKaya Bilguvar, Navneet K Tyagi, Cigdem Ozkara, et al.
Pageof 6

Showing results (31-40 of 52) with videos related to

Sort By:
Pageof 6
Science Advances|June 10, 2026
Mice produce interneurons in the septum as a response to aversive experiences and antidepressant treatmentAikaterini Lampada, Chiara Rolando, Nigel Whittle, et al.
Scientific Reports|March 9, 2017
Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephalyParaskevi Sgourdou, Ketu Mishra-Gorur, Ichiko Saotome, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 19, 2008
Linking Notch signaling to ischemic strokeJoseph F Arboleda-Velasquez, Zhipeng Zhou, Hwa Kyoung Shin, et al.
Gut|March 3, 2016
Notch1 and Notch2 receptors regulate mouse and human gastric antral epithelial cell homoeostasisGail B Gifford, Elise S Demitrack, Theresa M Keeley, et al.
Journal of Neuroimmune Pharmacology : the Official Journal of the Society on Neuroimmune Pharmacology|April 18, 2016
B-Cell Depletion Reduces the Maturation of Cerebral Cavernous Malformations in Murine ModelsChangbin Shi, Robert Shenkar, Hussein A Zeineddine, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2011
Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel diseaseJoseph F Arboleda-Velasquez, Jan Manent, Jeong Hyun Lee, et al.
Developmental Cell|July 8, 2022
Interferon-γ resistance and immune evasion in glioma develop via Notch-regulated co-evolution of malignant and immune cellsElena Parmigiani, Robert Ivanek, Chiara Rolando, et al.
The New England Journal of Medicine|September 8, 2021
Somatic <i>PIK3CA</i> Mutations in Sporadic Cerebral Cavernous MalformationsMatthieu Peyre, Danielle Miyagishima, Franck Bielle, et al.
American Journal of Human Genetics|January 9, 2008
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersBetul Bakkaloglu, Brian J O'Roak, Angeliki Louvi, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 30, 2013
Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegenerationKaya Bilguvar, Navneet K Tyagi, Cigdem Ozkara, et al.
Pageof 6