Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Regis Giet"'
Publikováno v:
Journal of Cell Science
Journal of Cell Science, 2022, 135 (9), ⟨10.1242/jcs.259344⟩
Journal of Cell Science, 2022, 135 (9), ⟨10.1242/jcs.259344⟩
Proper mitotic spindle orientation depends on the correct anchorage of astral microtubules to the cortex. It relies on the remodeling of the cell cortex, a process not fully understood. Annexin A2 (Anx2; also known as ANXA2) is a protein known to be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25e33be674048cc7de57f34d85732c08
https://hal.science/hal-03630005
https://hal.science/hal-03630005
Autor:
Alexandre Thomas, Régis Giet
Publikováno v:
STAR Protocols, Vol 3, Iss 3, Pp 101493- (2022)
Summary: Drosophila neural stem cells (NSCs) divide asymmetrically to generate siblings of different sizes. This model system has proved helpful in deciphering the contribution of polarity cues and the mitotic spindle in asymmetric cell division. Her
Externí odkaz:
https://doaj.org/article/78acab6b987045b9b43bca86dc99f2ec
Autor:
Emmanuel Gallaud, Laurent Richard-Parpaillon, Laetitia Bataillé, Aude Pascal, Mathieu Métivier, Vincent Archambault, Régis Giet
Publikováno v:
PLoS Genetics, Vol 18, Iss 4, p e1010145 (2022)
The maintenance of a restricted pool of asymmetrically dividing stem cells is essential for tissue homeostasis. This process requires the control of mitotic progression that ensures the accurate chromosome segregation. In addition, this event is coup
Externí odkaz:
https://doaj.org/article/9c5a51037ed44bd5852710ef4f3b144b
Publikováno v:
Biomolecules, Vol 9, Iss 1, p 28 (2019)
Accurate chromosome segregation requires the perfect spatiotemporal rearrangement of the cellular cytoskeleton. Isolated more than two decades ago from Drosophila, Aurora A is a widespread protein kinase that plays key roles during cell division. Num
Externí odkaz:
https://doaj.org/article/1f723f1cd70e47a9a3c79205a0370f52
Autor:
Charlotte Mouden, Marie de Tayrac, Christèle Dubourg, Sophie Rose, Wilfrid Carré, Houda Hamdi-Rozé, Marie-Claude Babron, Linda Akloul, Bénédicte Héron-Longe, Sylvie Odent, Valérie Dupé, Régis Giet, Véronique David
Publikováno v:
PLoS ONE, Vol 10, Iss 2, p e0117418 (2015)
Holoprosencephaly (HPE) is a frequent congenital malformation of the brain characterized by impaired forebrain cleavage and midline facial anomalies. Heterozygous mutations in 14 genes have been identified in HPE patients that account for only 30% of
Externí odkaz:
https://doaj.org/article/64dc7400317b48858eaf50a81f960129
Publikováno v:
PLoS ONE, Vol 6, Iss 1, p e14600 (2011)
BACKGROUND: CDK11(p58) is a mitotic protein kinase, which has been shown to be required for different mitotic events such as centrosome maturation, chromatid cohesion and cytokinesis. METHODOLOGY/PRINCIPAL FINDINGS: In addition to these previously de
Externí odkaz:
https://doaj.org/article/35c9613e8b92401a860ec2653f884133