Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Bossaerts, Liene"'
Autor:
Jensen, Anne Mette G., Raska, Jan, Fojtik, Petr, Monti, Giulia, Lunding, Melanie, Bartova, Simona, Pospisilova, Veronika, van der Lee, Sven J., Van Dongen, Jasper, Bossaerts, Liene, Van Broeckhoven, Christine, Dols-Icardo, Oriol, Lléo, Alberto, Bellini, Sonia, Ghidoni, Roberta, Hulsman, Marc, Petsko, Gregory A., Sleegers, Kristel, Bohaciakova, Dasa, Holstege, Henne
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 9/10/2024, Vol. 121 Issue 37, p1-12, 26p
Autor:
Bossaerts, Liene1 (AUTHOR), Cacace, Rita1 (AUTHOR), Van Broeckhoven, Christine1,2 (AUTHOR) christine.vanbroeckhoven@uantwerpen.vib.be
Publikováno v:
Molecular Neurodegeneration. 4/27/2022, Vol. 17 Issue 1, p1-12. 12p.
Autor:
Bossaerts, Liene1,2 (AUTHOR), Hendrickx Van de Craen, Elisabeth1,2,3 (AUTHOR), Cacace, Rita1,2 (AUTHOR), Asselbergh, Bob2,4 (AUTHOR), Van Broeckhoven, Christine1,2,5 (AUTHOR) christine.vanbroeckhoven@uantwerpen.vib.be
Publikováno v:
Acta Neuropathologica Communications. 3/31/2022, Vol. 10 Issue 1, p1-15. 15p.
Autor:
Bossaerts, Liene, Hens, Elisabeth, Hanseeuw, Bernard, Vandenberghe, Rik, Cras, Patrick, De Deyn, Peter P., Engelborghs, Sebastiaan, Van Broeckhoven, Christine
Publikováno v:
In Neurobiology of Aging October 2021 106:307-307
Akademický článek
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Autor:
Bossaerts, Liene, Hens, Elisabeth, Cacace, Rita, Hanseeuw, Bernard, Vandenberghe, Rik, Cras, Patrick, De Deyn, Peter Paul, Engelborghs, Sebastiaan, Van Broeckhoven, Christine
BACKGROUND: Initially, ABCA7 was associated with Alzheimer's disease (AD) in large genome-wide association studies. Targeted resequencing of ABCA7 suggested a role for rare premature termination codon (PTC) mutations. We observed loss of ABCA7 in PTC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::2c42fcb2574d2374bd62d26252cd4be1
https://biblio.vub.ac.be/vubir/rare-missense-mutations-and-compound-heterozygous-mutations-in-abca7-contribute-to-alzheimers-disease-in-belgian-patients(caf248e1-8e60-41f8-bb90-94d620525ca5).html
https://biblio.vub.ac.be/vubir/rare-missense-mutations-and-compound-heterozygous-mutations-in-abca7-contribute-to-alzheimers-disease-in-belgian-patients(caf248e1-8e60-41f8-bb90-94d620525ca5).html
Autor:
Bossaerts, Liene, Hendrickx Van de Craen, Elisabeth, Cacace, Rita, Asselbergh, Bob, Van Broeckhoven, Christine
Additional file 1: Supplementary material and methods.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::227ef606a96be99e4d64df6fef091b23
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
Molecular neurodegeneration
BackgroundAlzheimer’s disease (AD) is the leading cause of dementia, clinically characterized by memory deficits and progressive cognitive decline. Despite decades of research effective therapies are lacking, and a large part of the genetic heritab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3cf1b2225781d7928df7dc87fbd7032
https://pubmed.ncbi.nlm.nih.gov/35477481
https://pubmed.ncbi.nlm.nih.gov/35477481
Autor:
Hens, Elisabeth, Bossaerts, Liene, Sieben, Anne, Engelborghs, Sebastiaan, Vermeiren, Yannick, Hanseeuw, Bernard, Vandenberghe, Rik, De Deyn, Peter, Cras, Patrick, Van Broeckhoven, Christine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::507f25649cea27b2da1645ca242a5029
https://biblio.vub.ac.be/vubir/genotypephenotype-data-of-rare-abca7-missense-mutations-in-belgian-alzheimers-disease-patients(0ed5676e-f1e4-4757-a428-e9798c4b5091).html
https://biblio.vub.ac.be/vubir/genotypephenotype-data-of-rare-abca7-missense-mutations-in-belgian-alzheimers-disease-patients(0ed5676e-f1e4-4757-a428-e9798c4b5091).html