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Anne Joutel

Showing results (41-50 of 74) with videos related to

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Human Molecular Genetics|March 3, 2007
The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivoMarie Monet, Valérie Domenga, Barbara Lemaire, et al.
Annals of Neurology|July 18, 2018
Notch3<sup>ECD</sup> immunotherapy improves cerebrovascular responses in CADASIL miceLamia Ghezali, Carmen Capone, Céline Baron-Menguy, et al.
Brain : a Journal of Neurology|March 19, 2009
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domainMarie Monet-Leprêtre, Boris Bardot, Barbara Lemaire, et al.
Annals of Neurology|February 3, 2004
Clinical features of cerebral cavernous malformations patients with KRIT1 mutationsChristian Denier, Pierre Labauge, Laurent Brunereau, et al.
Brain Pathology (Zurich, Switzerland)|October 18, 2014
CADASIL and CARASILSaara Tikka, Marc Baumann, Maija Siitonen, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2021
PIP<sub>2</sub> corrects cerebral blood flow deficits in small vessel disease by rescuing capillary Kir2.1 activityFabrice Dabertrand, Osama F Harraz, Masayo Koide, et al.
Nature Communications|September 2, 2024
Neurovascular coupling and CO<sub>2</sub> interrogate distinct vascular regulationsMarine Tournissac, Emmanuelle Chaigneau, Sonia Pfister, et al.
Cardiovascular Research|May 5, 2018
Understanding the role of the perivascular space in cerebral small vessel diseaseRosalind Brown, Helene Benveniste, Sandra E Black, et al.
Stroke|January 30, 2025
Impaired Resting-State Functional Connectivity in Cerebral Autosomal-Dominant Arteriopathy, Subcortical Infarcts, and Leukoencephalopathy Mutant MiceSanem Aslihan Aykan, James Han Lai, Kazutaka Sugimoto, et al.
Annals of Neurology|December 10, 2015
Reducing Timp3 or vitronectin ameliorates disease manifestations in CADASIL miceCarmen Capone, Emmanuel Cognat, Lamia Ghezali, et al.
Pageof 8

Showing results (41-50 of 74) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|March 3, 2007
The archetypal R90C CADASIL-NOTCH3 mutation retains NOTCH3 function in vivoMarie Monet, Valérie Domenga, Barbara Lemaire, et al.
Annals of Neurology|July 18, 2018
Notch3<sup>ECD</sup> immunotherapy improves cerebrovascular responses in CADASIL miceLamia Ghezali, Carmen Capone, Céline Baron-Menguy, et al.
Brain : a Journal of Neurology|March 19, 2009
Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domainMarie Monet-Leprêtre, Boris Bardot, Barbara Lemaire, et al.
Annals of Neurology|February 3, 2004
Clinical features of cerebral cavernous malformations patients with KRIT1 mutationsChristian Denier, Pierre Labauge, Laurent Brunereau, et al.
Brain Pathology (Zurich, Switzerland)|October 18, 2014
CADASIL and CARASILSaara Tikka, Marc Baumann, Maija Siitonen, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 20, 2021
PIP<sub>2</sub> corrects cerebral blood flow deficits in small vessel disease by rescuing capillary Kir2.1 activityFabrice Dabertrand, Osama F Harraz, Masayo Koide, et al.
Nature Communications|September 2, 2024
Neurovascular coupling and CO<sub>2</sub> interrogate distinct vascular regulationsMarine Tournissac, Emmanuelle Chaigneau, Sonia Pfister, et al.
Cardiovascular Research|May 5, 2018
Understanding the role of the perivascular space in cerebral small vessel diseaseRosalind Brown, Helene Benveniste, Sandra E Black, et al.
Stroke|January 30, 2025
Impaired Resting-State Functional Connectivity in Cerebral Autosomal-Dominant Arteriopathy, Subcortical Infarcts, and Leukoencephalopathy Mutant MiceSanem Aslihan Aykan, James Han Lai, Kazutaka Sugimoto, et al.
Annals of Neurology|December 10, 2015
Reducing Timp3 or vitronectin ameliorates disease manifestations in CADASIL miceCarmen Capone, Emmanuel Cognat, Lamia Ghezali, et al.
Pageof 8