Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lynn Supply"'
Autor:
Edith Bonnin, Pauline Cabochette, Alessandro Filosa, Ramona Jühlen, Shoko Komatsuzaki, Mohammed Hezwani, Achim Dickmanns, Valérie Martinelli, Marjorie Vermeersch, Lynn Supply, Nuno Martins, Laurence Pirenne, Gianina Ravenscroft, Marcus Lombard, Sarah Port, Christiane Spillner, Sandra Janssens, Ellen Roets, Jo Van Dorpe, Martin Lammens, Ralph H Kehlenbach, Ralf Ficner, Nigel G Laing, Katrin Hoffmann, Benoit Vanhollebeke, Birthe Fahrenkrog
Publikováno v:
PLoS Genetics, Vol 14, Iss 12, p e1007845 (2018)
Nucleoporins build the nuclear pore complex (NPC), which, as sole gate for nuclear-cytoplasmic exchange, is of outmost importance for normal cell function. Defects in the process of nucleocytoplasmic transport or in its machinery have been frequently
Externí odkaz:
https://doaj.org/article/88c96d3ae2aa45ddb907f5a735313301
Autor:
Ellen Roets, Ralf Ficner, Marcus Lombard, Alessandro Filosa, Pauline Cabochette, Martin Lammens, Nuno Martins, Christiane Spillner, Birthe Fahrenkrog, Achim Dickmanns, Nigel G. Laing, Marjorie Vermeersch, Sarah A. Port, Shoko Komatsuzaki, Lynn Supply, Ralph H. Kehlenbach, Valérie Martinelli, Benoit Vanhollebeke, Mohammed Hezwani, Katrin Hoffmann, Gianina Ravenscroft, Sandra Janssens, Jo Van Dorpe, Edith Bonnin, Ramona Juehlen, Laurence Pirenne
Nucleoporins build the nuclear pore complex (NPC), which, as sole gate for nuclear-cytoplasmic exchange, are of outmost importance for normal cell function. Defects in the process of nucleocytoplasmic transport or in its machinery have been frequentl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::586e7deecb389bd780e0af35818f2925
AAV9 delivered bispecific nanobody attenuates amyloid burden in the gelsolin amyloidosis mouse model
Autor:
Adriaan Verhelle, Lynn Supply, Thierry Vandendriessche, Olivier Zwaenepoel, Marinee K Chuah, Cindy Peleman, Jan Gettemans, Tony Lahoutte, Nisha Nair, Nick Devoogdt, Wim Derave, Inge Everaert, Wouter Van Overbeke, Jo Van Dorpe
Publikováno v:
ResearcherID
Gelsolin amyloidosis is a dominantly inherited, incurable type of amyloidosis. A single point mutation in the gelsolin gene (G654A is most common) results in the loss of a Ca2+ binding site in the second gelsolin domain. Consequently, this domain par
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dec09a43eab319b7c3e4e92b447c4c5
https://hdl.handle.net/20.500.14017/864eadef-40ed-4e81-aefe-4f9bebb9cd4a
https://hdl.handle.net/20.500.14017/864eadef-40ed-4e81-aefe-4f9bebb9cd4a