Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Morgane Boillot"'
Autor:
Monica J. S. Nadler, Weipang Chang, Ekim Ozkaynak, Yuda Huo, Yi Nong, Morgane Boillot, Mark Johnson, Antonio Moreno, Matthew P. Anderson
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-17 (2023)
Human-specific SINE-VNTR-Alu (SVA) retrotransposons in neurodevelopmental genes CDK5RAP2 and SCN8A repress their expression to delay neuronal maturation. SVA-lncRNA AK057321 binds these SVAs to release gene repression and drive neuronal maturation.
Externí odkaz:
https://doaj.org/article/aca25956f52c469ba5776582c1a9a221
Autor:
Yi Nong, David C. Stoppel, Mark A. Johnson, Morgane Boillot, Jelena Todorovic, Jason Shen, Xinyu Zhou, Monica J.S. Nadler, Carrie Rodriguez, Yuda Huo, Ikue Nagakura, Ekkehard M. Kasper, Matthew P. Anderson
The circuit origins of aggression in autism spectrum disorder remain undefined. Here we reportTac1-expressing glutamatergic neurons in ventrolateral division of ventromedial hypothalamus (VMHvl) drive intermale aggression. Aggression is increased due
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::84ec27f9fcad416baf49fe38a5e3b53d
https://doi.org/10.1101/2023.02.28.530462
https://doi.org/10.1101/2023.02.28.530462
Autor:
Morgane Boillot
AGRP (agouti-related neuropeptide) expressing inhibitory neurons sense caloric needs of an animal to coordinate homeostatic feeding. Recent evidence suggests that AGRP neurons also suppress competing actions and motivations to mediate adaptive behavi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec11d926b02188beb8809a5c2209a3a1
https://europepmc.org/articles/PMC6668212/
https://europepmc.org/articles/PMC6668212/
Autor:
Léa Rodriguez, Fabrice Usseglio, Michaël Russier, Morgane Boillot, Fahamoe Youssouf, Norah Boumedine-Guignon, Mickaël Zbili, Christine Formisano-Tréziny, Michael Seagar, María J. Benítez, Marion Sangiardi, Laure Fronzaroli-Molinieres, Stéphanie Baulac, Olivier Caillard, Juan José Garrido, Yves Maulet, Marina De San Feliciano, Dominique Debanne, Oussama El Far
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America
Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2017, 114 (29), pp.7719-7724. ⟨10.1073/pnas.1618656114⟩
Proceedings of the National Academy of Sciences of the United States of America, 2017, 114 (29), pp.7719-7724. ⟨10.1073/pnas.1618656114⟩
Digital.CSIC. Repositorio Institucional del CSIC
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Proceedings of the National Academy of Sciences of the United States of America, National Academy of Sciences, 2017, 114 (29), pp.7719-7724. ⟨10.1073/pnas.1618656114⟩
Proceedings of the National Academy of Sciences of the United States of America, 2017, 114 (29), pp.7719-7724. ⟨10.1073/pnas.1618656114⟩
Digital.CSIC. Repositorio Institucional del CSIC
instname
© The Author(s).
Autosomal dominant epilepsy with auditory features results from mutations in leucine-rich glioma-inactivated 1 (LGI1), a soluble glycoprotein secreted by neurons. Animal models of LGI1 depletion display spontaneous seizures, ho
Autosomal dominant epilepsy with auditory features results from mutations in leucine-rich glioma-inactivated 1 (LGI1), a soluble glycoprotein secreted by neurons. Animal models of LGI1 depletion display spontaneous seizures, ho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f623ed8dbbc0511470554df8022dc0f5
https://www.hal.inserm.fr/inserm-01708767
https://www.hal.inserm.fr/inserm-01708767
Autor:
Stéphanie Baulac, Eric LeGuern, Morgane Boillot, Chun-Yao Lee, Camille Allene, Nathalie Rouach
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2016, 6, pp.21769. ⟨10.1038/srep21769⟩
Scientific Reports, 2016, 6, pp.21769. ⟨10.1038/srep21769⟩
Scientific Reports, Nature Publishing Group, 2016, 6, pp.21769. ⟨10.1038/srep21769⟩
Scientific Reports, 2016, 6, pp.21769. ⟨10.1038/srep21769⟩
The secreted leucine-rich glioma inactivated 1 (LGI1) protein is an important actor for human seizures of both genetic and autoimmune etiology: mutations in LGI1 cause inherited temporal lobe epilepsy, while LGI1 is involved in antibody-mediated ence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::632b5a95ab6ab53e328f251f70fddfe9
http://europepmc.org/articles/PMC4754946
http://europepmc.org/articles/PMC4754946
Autor:
Stéphanie Baulac, Morgane Boillot
Publikováno v:
Journal of Neuroscience Methods
Journal of Neuroscience Methods, 2015, 260, pp.132-143. ⟨10.1016/j.jneumeth.2015.06.003⟩
Journal of Neuroscience Methods, Elsevier, 2015, 260, pp.132-143. ⟨10.1016/j.jneumeth.2015.06.003⟩
Journal of Neuroscience Methods, 2015, 260, pp.132-143. ⟨10.1016/j.jneumeth.2015.06.003⟩
Journal of Neuroscience Methods, Elsevier, 2015, 260, pp.132-143. ⟨10.1016/j.jneumeth.2015.06.003⟩
International audience; Focal epilepsies were for a long time thought to be acquired disorders secondary to cerebral lesions. However, the important role of genetic factors in focal epilepsies is now well established. Several focal epilepsy syndromes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5443d0d2bed0fa3d15a920a56c3a273
https://hal.sorbonne-universite.fr/hal-01166902/document
https://hal.sorbonne-universite.fr/hal-01166902/document
Autor:
Virginie Lambrecq, Stéphanie Baulac, Saeko Ishida, Katia Hardies, Federico Zara, Sarah Weckhuysen, Olivier Dulac, Isabelle An-Gourfinkel, Michel Baulac, Morgane Boillot, Mailys Daniau, Fabienne Picard, Carlo Minetti, Michele Iacomino, Rima Nabbout, Eric LeGuern, Mélanie Morin-Brureau, Pasquale Striano
Publikováno v:
Neurology Genetics
Neurology Genetics, American Academy of Neurology, 2015, 1 (4), pp.e35. ⟨10.1212/NXG.0000000000000035⟩
Neurology : Genetics
Neurology: Genetics
Neurology: Genetics, Vol. 1, No 4 (2015) P. e35
Neurology Genetics, 2015, 1 (4), pp.e35. ⟨10.1212/NXG.0000000000000035⟩
Neurology: Genetics, 2015, 1 (4), pp.e35. <10.1212/NXG.0000000000000035>
Neurology Genetics, American Academy of Neurology, 2015, 1 (4), pp.e35. ⟨10.1212/NXG.0000000000000035⟩
Neurology : Genetics
Neurology: Genetics
Neurology: Genetics, Vol. 1, No 4 (2015) P. e35
Neurology Genetics, 2015, 1 (4), pp.e35. ⟨10.1212/NXG.0000000000000035⟩
Neurology: Genetics, 2015, 1 (4), pp.e35. <10.1212/NXG.0000000000000035>
International audience; Objective: To identify the genetic cause in a large family with febrile seizures (FS) and temporal lobe epilepsy (TLE) and subsequently search for additional mutations in a cohort of 107 families with FS, with or without epile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1935ddd76d96577cefc3f650305f1f18
http://hdl.handle.net/11567/841167
http://hdl.handle.net/11567/841167
Autor:
Jérôme Garrigue, Eric LeGuern, Morgane Boillot, Benoit Martin, Richard B. Miles, Vincent Navarro, Elise Marsan, Matthew P. Anderson, Béatrice Dufresnois, Katia Lehongre, Ekim Ozkaynak, Stéphanie Baulac, Saeko Ishida, Clément Huneau
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, Oxford University Press (OUP), 2014, 137 (11), pp.2984-2996. ⟨10.1093/brain/awu259⟩
Brain-A Journal of Neurology, 2014, 137 (11), pp.2984-2996. ⟨10.1093/brain/awu259⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2014, 137 (11), pp.2984-2996. ⟨10.1093/brain/awu259⟩
Brain-A Journal of Neurology, 2014, 137 (11), pp.2984-2996. ⟨10.1093/brain/awu259⟩
Leucin-rich, glioma inactivated 1 (LGI1) is a secreted protein linked to human seizures of both genetic and autoimmune aetiology. Mutations in the LGI1 gene are responsible for autosomal dominant temporal lobe epilepsy with auditory features, whereas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b758d9689618a6e558bcf9ad93ea4c8
https://europepmc.org/articles/PMC4208469/
https://europepmc.org/articles/PMC4208469/
Autor:
Masatsugu Ueda, Naohiro Fumoto, Akio Ikeda, Tomoji Mashimo, Stéphanie Baulac, Morgane Boillot, Saeko Ishida, Toshihiro Aoto, Akiko Takizawa, Ryosuke Takahashi, Tadao Serikawa, Yukihiro Ohno, Mitsuru Kuwamura, Eric LeGuern
Publikováno v:
Human Molecular Genetics; Vol 21
Mutations of the leucine-rich glioma-inactivated 1 (LGI1) gene cause an autosomal dominant partial epilepsy with auditory features also known as autosomal-dominant lateral temporal lobe epilepsy. LGI1 is also the main antigen present in sera and cere
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a2f0c6ce5aee5a2a671303e36ea61e6
https://pubmed.ncbi.nlm.nih.gov/22589250
https://pubmed.ncbi.nlm.nih.gov/22589250