Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marie-Jo Masse"'
Publikováno v:
Microsc Res Tech
Microsc Res Tech, 2006, 69 (11), pp.933-9. ⟨10.1002/jemt.20370⟩
Microsc Res Tech, 2006, 69 (11), pp.933-9. ⟨10.1002/jemt.20370⟩
International audience; Fluorescent protein-based FRET is a powerful method for visualizing protein-protein interactions and biochemical reactions in living cells. It can be difficult, however, to avoid photobleaching when observing fluorescent cells
Publikováno v:
Journal of Virology. 74:474-482
The UL25 gene of pseudorabies virus (PrV) can encode a protein of about 57 kDa which is well conserved among herpesviruses. The UL25 protein of herpes simplex virus type 1 is a capsid constituent involved in virus penetration and capsid maturation. T
Autor:
Marie Jo Masse, Xuan Nguyen, Brigitte Simonet, Sybille Dezélée, Patrice Vende, Françoise Bras, Anne Flamand
Publikováno v:
Virus Research. 42:27-39
The genomes of pseudorabies virus (PrV) and of herpes simplex virus type 1 (HSV1) are colinear, excepting an inversion in the unique long region, of which one extremity resides within the BamHI fragment 9. This fragment (4088 bp) encodes the counterp
Autor:
Maïté Coppey-Moisan, Marie-Jo Masse, Nicolas Audugó, Hervé Lalucque, Jean Claude Mével, Marc Tramier, Sergi Padilla-Parra
Publikováno v:
Biophysical Journal. 96(3)
Quantification of protein-protein interactions in living cells by using a fluorescent-protein based FRET approach is a powerful method, especially combined with Fluorescence Lifetime Imaging Microscopy (FLIM), since the fluorescent lifetime does not
Autor:
Myriam Allioux-Guérin, Jean-Claude Mevel, Delphine Icard-Arcizet, François Gallet, Maïté Coppey-Moisan, Christiane Durieux, Marc Tramier, Sylvie Hénon, Marie-Jo Masse
Publikováno v:
Biophysical Journal
Biophysical Journal, Biophysical Society, 2008, 96 (1), pp.238-247. ⟨10.1529/biophysj.108.134627⟩
Biophysical Journal, Biophysical Society, 2009, 96 (1), pp.238-247
Biophysical Journal, Biophysical Society, 2008, epub ahead of print. ⟨10.1529/biophysj.108.134627⟩
Biophysical Journal, Biophysical Society, 2008, 96 (1), pp.238-247. ⟨10.1529/biophysj.108.134627⟩
Biophysical Journal, Biophysical Society, 2009, 96 (1), pp.238-247
Biophysical Journal, Biophysical Society, 2008, epub ahead of print. ⟨10.1529/biophysj.108.134627⟩
International audience; We investigate the dynamic response of single cells to weak and local rigidities, applied at controlled adhesion sites. Using multiple latex beads functionalized with fibronectin and trapped each in its own optical trap, we st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::353b7b6206326d780bf0be549ee93673
https://hal.archives-ouvertes.fr/hal-00339221
https://hal.archives-ouvertes.fr/hal-00339221
Publikováno v:
Journal of virology. 73(12)
Glycoproteins gM and gN are conserved throughout the herpesviruses but are dispensable for viral replication in cell cultures. To assay for a function of these proteins in infection of an animal, deletion mutants of pseudorabies virus lacking gM or g
Autor:
Sybille Dezélée, Xuan Nguyen, Anne Flamand, Marie Jo Masse, Françoise Bras, Patrice Vende, Brigitte Simonet
Publikováno v:
Virus research. 60(1)
The genome of pseudorabies virus (PrV) is collinear with the herpes simplex virus type 1 (HSV1) genome, except for an inversion in the unique long region, the right extremity of which resides within the BamHI fragment 9 and the left within the BamHI