Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bart De Cat"'
Autor:
Bart De Cat, Guido David
Publikováno v:
Seminars in Cell & Developmental Biology. 12:117-125
Glypicans are proteins with very characteristic structures that are substituted with heparan sulfate and that are linked to the cell surface via glycosylphosphatidylinositol. The modular structure of the glypicans has been highly conserved throughout
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::300c3aa1483bd88ed35f628c956ed807
https://doi.org/10.1006/scdb.2000.0240
https://doi.org/10.1006/scdb.2000.0240
Autor:
S Frints, Bernhard Weidle, Guido David, Sin -Ya Muyldermans, Bart De Cat, Jean-Pierre Fryns, Mark Veugelers, Gunter Reekmans, Neiva Magdalena, Connie Schrander-Stumpel, Nathalie Delande, Eric Legius
Publikováno v:
Human Molecular Genetics. 9:1321-1328
Simpson-Golabi-Behmel syndrome (SGBS) is an X-linked syndrome characterized by pre- and postnatal overgrowth (gigantism), which clinically resembles the autosomal Beckwith-Wiedemann syndrome (BWS). Deletions and translocations involving the glypican-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::406706a85f28e6db801991a53fb4a93d
https://doi.org/10.1093/hmg/9.9.1321
https://doi.org/10.1093/hmg/9.9.1321
Autor:
Willem Van de Ven, Marc Gewillig, Hilde Peeters, Kristin Verschueren, Danny Huylebroeck, Ann Schellens, Hélène Pendeville, John W. Belmont, Jean-Pierre Fryns, Marianne Voz, Koenraad Devriendt, Bernard Peers, Bernard Thienpont, Guido David, Bart De Cat
Publikováno v:
Human molecular genetics. 15(22)
Remarkable progress has been made in understanding the molecular mechanisms underlying left-right asymmetry in vertebrate animal models but little is known on left-right axis formation in humans. Previously, we identified SESN1 (also known as PA26) a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29799bfeda87b84b1c1579fe40f935dd
https://pubmed.ncbi.nlm.nih.gov/17038485
https://pubmed.ncbi.nlm.nih.gov/17038485
Autor:
Bernadette Vanderschueren, Gisèle Degeest, Christien Coomans, Bart De Cat, Frédéric Biemar, Bernard Peers, John W.M. Creemers, Guido David, Sin -Ya Muyldermans
Publikováno v:
The Journal of Cell Biology
Glypican (GPC)-3 inhibits cell proliferation and regulates cell survival during development. This action is demonstrated by GPC3 loss-of-function mutations in humans and mice. Here, we show that the GPC3 core protein is processed by a furinlike conve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::484239fb37dee17900038bcc5395af15
http://www.jcb.org/cgi/pmidlookup?view=long&pmid=14610063
http://www.jcb.org/cgi/pmidlookup?view=long&pmid=14610063
Autor:
Jean-Pierre Fryns, Mark Veugelers, Peter Marynen, Bart De Cat, Guido David, Ines Bonk, Nathalie Delande, Joris Vermeesch, Carl Esselens
Publikováno v:
Matrix biology : journal of the International Society for Matrix Biology. 20(5-6)
The glypicans compose a family of glycosylphosphatidylinositol-anchored heparan sulfate proteoglycans that may play a role in the control of cell division and growth regulation. So far, six members (GPC1-6) of this family are known in vertebrates. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41a9a12297141b0ef13fcc77b323bfab
https://pubmed.ncbi.nlm.nih.gov/11566272
https://pubmed.ncbi.nlm.nih.gov/11566272
Autor:
Helga Ceulemans, Anne-Marie Bruystens, Guido David, Bart De Cat, Peter Marynen, Christien Coomans, Joachim Dürr, Joris Vermeesch, Mark Veugelers
Publikováno v:
The Journal of biological chemistry. 274(38)
The glypicans compose a family of glycosylphosphatidylinositol-anchored heparan sulfate proteoglycans. Mutations in dally, a gene encoding a Drosophila glypican, and in GPC3, the gene for human glypican-3, implicate glypicans in the control of cell g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ff2b4a310c56e54933ed92aea2ef2a3
https://pubmed.ncbi.nlm.nih.gov/10480909
https://pubmed.ncbi.nlm.nih.gov/10480909