Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Davina Tondeleir"'
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e85608 (2014)
The mouse genome consists of six functional actin genes of which the expression patterns are temporally and spatially regulated during development and in the adult organism. Deletion of beta-actin in mouse is lethal during embryonic development, alth
Externí odkaz:
https://doaj.org/article/fd7038d6a93e47f2bf1f930b4a4766e0
Autor:
Davina Tondeleir, Benjamin Drogat, Karolina Slowicka, Karima Bakkali, Sonia Bartunkova, Steven Goossens, Jody J Haigh, Christophe Ampe
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e67855 (2013)
The functions of actin family members during development are poorly understood. To investigate the role of beta-actin in mammalian development, a beta-actin knockout mouse model was used. Homozygous beta-actin knockout mice are lethal at embryonic da
Externí odkaz:
https://doaj.org/article/0d2e3a226c0c47fc879db4237039b521
Autor:
Olivier Debeir, Karima Bakkali, Drieke Vandamme, Christophe Ampe, Matthias Müller, Veronique Jonckheere, Boris Hinz, Marianne Lemaistre, Kris Gevaert, Joël Vandekerckhove, Niklaas Colaert, Evy Timmerman, Davy Waterschoot, An Staes, Christine Decaestecker, Davina Tondeleir, Thierry Doll, Anja Lambrechts
Publikováno v:
Molecular & cellular proteomics, 11 (8
Vertebrate nonmuscle cells express two actin isoforms: cytoplasmic β- and γ-actin. Because of the presence and localized translation of β-actin at the leading edge, this isoform is generally accepted to specifically generate protrusive forces for
Publikováno v:
Cell Motility and the Cytoskeleton. 66:798-815
The dynamic actin cytoskeleton, consisting of six actin isoforms in mammals and a variety of actin binding proteins is essential for all developmental processes and for the viability of the adult organism. Actin isoform specific functions have been p
Autor:
Sonia Bartunkova, Jody J. Haigh, Christophe Ampe, Davina Tondeleir, Karima Bakkali, Benjamin Drogat, Steven Goossens, Karolina Slowicka
Publikováno v:
PloS one, 8 (6
PLoS ONE, Vol 8, Iss 6, p e67855 (2013)
PLoS ONE
PLOS ONE
PLoS ONE, Vol 8, Iss 6, p e67855 (2013)
PLoS ONE
PLOS ONE
The functions of actin family members during development are poorly understood. To investigate the role of beta-actin in mammalian development, a beta-actin knockout mouse model was used. Homozygous beta-actin knockout mice are lethal at embryonic da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f217be9a538a7ff0ae0a4cf33634233
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/168374
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/168374
Publikováno v:
eLS
Actin is an evolutionary conserved molecule that self assembles into long polymers. These filaments form the building block of the actin cytoskeleton. This system is one of the main engines enabling cell motility processes. In muscle cells stable act
Autor:
Christophe Ampe, Veronique Jonckheere, Anja Lambrechts, Joël Vandekerckhove, Davina Tondeleir, Karima Bakkali, Matthias Müller, Davy Waterschoot
Publikováno v:
Developmental Biology. 331(2)
Publikováno v:
PLoS ONE, Vol 9, Iss 1, p e85608 (2014)
PLOS ONE
PLoS ONE
PLOS ONE
PLoS ONE
The mouse genome consists of six functional actin genes of which the expression patterns are temporally and spatially regulated during development and in the adult organism. Deletion of beta-actin in mouse is lethal during embryonic development, alth
Autor:
Davy Waterschoot, Davina Tondeleir, Bruno Constantin, Ellen Lambert, Drieke Vandamme, Laura M. Machesky, Joël Vandekerckhove, Heidi Rommelaere, Christophe Ampe
Publikováno v:
BMC Research Notes
BMC Research Notes, BioMed Central, 2009, 2, pp.40. ⟨10.1186/1756-0500-2-40⟩
BMC RESEARCH NOTES
BMC Research Notes, Vol 2, Iss 1, p 40 (2009)
BMC Research Notes, BioMed Central, 2009, 2, pp.40. ⟨10.1186/1756-0500-2-40⟩
BMC RESEARCH NOTES
BMC Research Notes, Vol 2, Iss 1, p 40 (2009)
Background Nemaline myopathy is a neuromuscular disorder characterized by the presence of nemaline bodies in patient muscles. 20% of the cases are associated with α-skeletal muscle actin mutations. We previously showed that actin mutations can cause