Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Régine Terracol"'
Publikováno v:
Journal of Cell Science
Journal of Cell Science, Company of Biologists, 2011, 124 (Pt 10), pp.1664-71. ⟨10.1242/jcs.081216⟩
Journal of Cell Science, Company of Biologists, 2011, 124 (Pt 10), pp.1664-71. ⟨10.1242/jcs.081216⟩
International audience; Unattached kinetochores generate an anaphase inhibitor, through the spindle assembly checkpoint (SAC), that allows cells more time to establish proper kinetochore-microtubule (K-MT) linkages and thus avoid aneuploidy. Mad1 is
Autor:
Roger E. Karess, Natacha Raich, Michael L. Goldberg, Régine Terracol, Byron C. Williams, Xavier Baudin, Lénaïg Défachelles
Publikováno v:
Chromosome Research
Chromosome Research, Springer Verlag, 2015, 23 (2), pp.333-42. ⟨10.1007/s10577-015-9472-x⟩
Chromosome Research, Springer Verlag, 2015, 23 (2), pp.333-42. ⟨10.1007/s10577-015-9472-x⟩
The presence or absence of Mad1 at kinetochores is a major determinant of spindle assembly checkpoint (SAC) activity, the surveillance mechanism that delays anaphase onset if one or more kinetochores remain unattached to spindle fibers. Among the fac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f591656afb0de8f159f6636380b3b0fd
https://hal.archives-ouvertes.fr/hal-01220965
https://hal.archives-ouvertes.fr/hal-01220965
Publikováno v:
Development. 130:3651-3662
Vri is closely related to bZIP transcription factors involved in growth or cell death. vri clonal and overexpression analyses revealed defects at the cellular level. vri clones in the adult cuticle contain smaller cells with atrophic bristles. The ph
Autor:
Régine Terracol, Hélène George
Publikováno v:
Genetics. 146:1345-1363
We report here the genetical and molecular characterization of a new Drosophila zygotic lethal locus, vrille (vri). vri alleles act not only as dominant maternal enhancers of embryonic dorsoventral patterning defects caused by easter and decapentaple
Publikováno v:
Mechanisms of Development
Mechanisms of Development, Elsevier, 1995, 49 (1-2), pp.83-95. ⟨10.1016/0925-4773(94)00305-7⟩
Mechanisms of Development, Elsevier, 1995, 49 (1-2), pp.83-95. ⟨10.1016/0925-4773(94)00305-7⟩
Genetic analyses of Drosophila oogenesis have revealed the central role of ovo , a gene required for differentiation of the female germline. A number of recessive ovo mutations also affect the shavenbaby (svb) function required for late embryo patter
Autor:
Régine Terracol, Elisabeth Guillemet, Thomas Preat, Claudie Lamour-Isnard, Denise Busson, Bernadette Limbourg-Bouchon, Hervé Tricoire, Pascal P. Thérond
Publikováno v:
Mechanisms of Development. 44:65-80
The Drosophila segment-polarity gene fused (fu) is required for pattern formation within embryonic segments and imaginal discs. We previously reported that the 5′ part of the fused gene is homologous to the catalytic domain of serine/threonine kina
Autor:
Sébastien Szuplewski, Régine Terracol
Publikováno v:
Genetics. 158(4)
Cytochrome c oxidase is the terminal enzyme of the mitochondrial electron transfer chain. In eukaryotes, the enzyme is composed of 3 mitochondrial DNA-encoded subunits and 7–10 (in mammals) nuclear DNA-encoded subunits. This enzyme has been extensi
Autor:
Régine Terracol, J A Lengyel
Publikováno v:
Genetics. 138(1)
We have discovered a new member of the class of genes controlling embryonic dorsoventral patterning. Mutants of the thick veins (tkv) gene have been described previously (as slater alleles) as embryonic lethal, lacking dorsal epidermis, but not as sh
Publikováno v:
Biology of the cell. 68(1)
In Drosophila melanogaster the tandemly arranged repetitive sequences coding for 18S and 28S rRNA are heterogenous at the level of the spacers between units and insertions that interrupt many 28S rRNA genes. This heterogeneity contrasts with the homo
Autor:
Régine Terracol
Publikováno v:
Molecular and General Genetics MGG. 208:168-176
In Drosophila melanogaster a partial loss of ribosomal genes leads to the bobbed phenotype. Magnification is a heritable increase in rDNA that may occur in males carrying a deleted X chromosome with a strong bobbed phenotype. The restriction patterns