Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Frédéric M, Coquelle"'
Publikováno v:
BMC Research Notes, Vol 13, Iss 1, Pp 1-6 (2020)
Abstract Objective Most eukaryotic cells contain microtubule filaments, which play central roles in intra-cellular organization. However, microtubule networks have a wide variety of architectures from one cell type and organism to another. Nonetheles
Externí odkaz:
https://doaj.org/article/72b60021ec034b089ccf9dc335a6d4a9
Autor:
Arthur T. Molines, Jessica Marion, Salem Chabout, Laetitia Besse, Jim P. Dompierre, Grégory Mouille, Frédéric M. Coquelle
Publikováno v:
Biology Open, Vol 7, Iss 8 (2018)
Microtubules are involved in plant development and adaptation to their environment, but the sustaining molecular mechanisms remain elusive. Microtubule-end-binding 1 (EB1) proteins participate in directional root growth in Arabidopsis thaliana. Howev
Externí odkaz:
https://doaj.org/article/f6b99c769a7348b6964ecfa7d5ba1c7f
Autor:
Océane Anezo, Laura Duciel, Koushik Mandal, David Gentien, Simon Saule, Nathalie Planque, Frédéric M. Coquelle, Jean-Baptiste Manneville, Cécile Laurent
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2019, 9 (1), pp.2990. ⟨10.1038/s41598-019-39643-y⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-13 (2019)
Scientific Reports, Nature Publishing Group, 2019, 9 (1), pp.2990. ⟨10.1038/s41598-019-39643-y⟩
Scientific Reports, Vol 9, Iss 1, Pp 1-13 (2019)
Uveal melanoma (UM) is an aggressive tumor in which approximately 50% of patients develop metastasis. Expression of the PTP4A3 gene, encoding a phosphatase, is predictive of poor patient survival. PTP4A3 expression in UM cells increases their migrati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99e93c0e987ce0dd81d692274240ed74
https://hal.archives-ouvertes.fr/hal-02332471
https://hal.archives-ouvertes.fr/hal-02332471
Autor:
Frédéric M. Coquelle, Laetitia Besse, Jim Dompierre, Salem Chabout, Grégory Mouille, Jessica Marion, Arthur T. Molines
Publikováno v:
Biology Open
Biology Open, Royal Society, 2018, 7 (8), pp.UNSP bio030510. ⟨10.1242/bio.030510⟩
Biology Open 8 (7), 1-10. (2018)
Biology Open, Vol 7, Iss 8 (2018)
Biology Open, 2018, 7 (8), pp.UNSP bio030510. ⟨10.1242/bio.030510⟩
Biology Open, Royal Society, 2018, 7 (8), pp.UNSP bio030510. ⟨10.1242/bio.030510⟩
Biology Open 8 (7), 1-10. (2018)
Biology Open, Vol 7, Iss 8 (2018)
Biology Open, 2018, 7 (8), pp.UNSP bio030510. ⟨10.1242/bio.030510⟩
Microtubules are involved in plant development and adaptation to their environment, but the sustaining molecular mechanisms remain elusive. Microtubule-end-binding 1 (EB1) proteins participate in directional root growth in Arabidopsis thaliana. Howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d41ae46f380d6a3c0e557bc40443565
https://hal.archives-ouvertes.fr/hal-02182309/document
https://hal.archives-ouvertes.fr/hal-02182309/document
Autor:
Frédéric M. Coquelle, Simon Bossi, Heather McLean, Raoudha Dammak, Marie-Ange Richard, Paulette Decottignies, Christelle Cadilhac, Thomas Bessiron, Solenne Chardonnet, Pierre Le Maréchal, Fabrice Ango, Cathy Isaura Ramos, Hervé Daniel, Céline Boursier, Catherine Berrier
Publikováno v:
Neuropharmacology
Neuropharmacology, Elsevier, 2017, 121, pp.247-260. ⟨10.1016/j.neuropharm.2017.04.036⟩
Neuropharmacology, Elsevier, 2017, 121, pp.247-260. 〈10.1016/j.neuropharm.2017.04.036〉
Neuropharmacology, 2017, 121, pp.247-260. ⟨10.1016/j.neuropharm.2017.04.036⟩
Neuropharmacology, Elsevier, 2017, 121, pp.247-260. ⟨10.1016/j.neuropharm.2017.04.036⟩
Neuropharmacology, Elsevier, 2017, 121, pp.247-260. 〈10.1016/j.neuropharm.2017.04.036〉
Neuropharmacology, 2017, 121, pp.247-260. ⟨10.1016/j.neuropharm.2017.04.036⟩
International audience; In cerebellar cortex, mGlu4 receptors located on parallel fibers play an essential role in normal motor function, but the molecular mechanisms involved are not yet completely understood. Using a strategy combining biochemical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f55656f16fb2b81ff17933f10d169dd
https://hal.archives-ouvertes.fr/hal-01571666
https://hal.archives-ouvertes.fr/hal-01571666
Autor:
Solenne, Chardonnet, Thomas, Bessiron, Cathy Isaura, Ramos, Raoudha, Dammak, Marie-Ange, Richard, Céline, Boursier, Christelle, Cadilhac, Frédéric M, Coquelle, Simon, Bossi, Fabrice, Ango, Pierre, Le Maréchal, Paulette, Decottignies, Catherine, Berrier, Heather, McLean, Hervé, Daniel
Publikováno v:
Neuropharmacology. 121
In cerebellar cortex, mGlu
Publikováno v:
Biochemical Society Transactions
Biochemical Society Transactions, Portland Press, 2009, 37 (Pt 5), pp.997-1001. ⟨10.1042/BST0370997⟩
Biochemical Society Transactions, 2009, 37 (Pt 5), pp.997-1001. ⟨10.1042/BST0370997⟩
Biochemical Society Transactions, Portland Press, 2009, 37 (Pt 5), pp.997-1001. ⟨10.1042/BST0370997⟩
Biochemical Society Transactions, 2009, 37 (Pt 5), pp.997-1001. ⟨10.1042/BST0370997⟩
International audience; +TIPs (plus-end tracking proteins) are an increasing group of molecules that localize preferentially to the end of growing microtubules. +TIPs regulate microtubule dynamics and contribute to the organization of the microtubula
Autor:
Sven Bergmann, Frédéric M. Coquelle, Irit Orr, Naama Barkai, Orly Reiner, Yehuda Brody, Sharon G. Wolf, Gregor Eichele, Daniela Bar-El, Tamar Sapir, Talia Levy
Publikováno v:
Cell Cycle. 5:976-983
The doublecortin-like (DCX) domains serve as protein-interaction platforms. DCX tandem domains appear in the product of the X-linked doublecortin (DCX) gene, in retinitis pigmentosa-1 (RP1), as well as in other gene products. Mutations in the human D
Autor:
Orly Reiner, Frédéric M. Coquelle
Publikováno v:
CMLS Cellular and Molecular Life Sciences. 62:425-434
Proper human brain formation is dependent upon the integrated activity of multiple genes. Malfunctioning of key proteins results in brain developmental abnormalities. Mutation(s) in the LIS1 gene or the X-linked gene doublecortin (DCX) results in a s
Autor:
Orly Reiner, Michal Caspi, Cynthia Koifman, Junken Aoki, Jan De Mey, Hiroyuki Arai, Frédéric M. Coquelle, Talia Levy
Publikováno v:
Journal of Biological Chemistry. 278:38740-38748
Mutations in one allele of the human LIS1 gene cause a severe brain malformation, lissencephaly. Although most LIS1 mutations involve deletions, several point mutations with a single amino acid alteration were described. Patients carrying these mutat