Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Johannes Aerts"'
Autor:
Or Cabasso, Sumit Paul, Gali Maor, Metsada Pasmanik-Chor, Wouter Kallemeijn, Johannes Aerts, Mia Horowitz
Publikováno v:
Cells, Vol 10, Iss 3, p 630 (2021)
Human GBA1 encodes lysosomal acid β-glucocerebrosidase (GCase), which hydrolyzes cleavage of the beta-glucosidic linkage of glucosylceramide (GlcCer). Mutations in this gene lead to reduced GCase activity, accumulation of glucosylceramide and glucos
Externí odkaz:
https://doaj.org/article/1a3b960c9e94479e8bff3c7edfa4213b
Autor:
Panagiota Papadopoulou, Rianne van der Pol, Niek van Hilten, Mohammad-Amin Moradi, Maria Ferraz, Johannes aerts, Nico Sommerdijk, Jelger Risselada, agur sevink, alexander kros
The membrane-protein interface in lipid nanoparticles (LNPs) is important for their in vivo behavior. Better understanding may assist to evolve current drug delivery methods to more precise, cell- or tissue-specific nanomedicine. Previously, we demon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca77f637721583ef08b0570f8b8c2312
https://doi.org/10.26434/chemrxiv-2023-9q9wh-v2
https://doi.org/10.26434/chemrxiv-2023-9q9wh-v2
Autor:
Isidro Arévalo-Vargas, Laura López de Frutos, Irene Serrano Gonzalo, Carlos Lahoz, Pilar Mozas, Pilar Giraldo, Maria J. Ferraz, Johannes Aerts
Publikováno v:
Molecular Genetics and Metabolism. 138:107005
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c98b8362554260c322a9b1d812370c0a
https://doi.org/10.1016/j.ymgme.2022.107005
https://doi.org/10.1016/j.ymgme.2022.107005
Publikováno v:
ResearcherID
Acta paediatrica (Oslo, Norway, 94(Suppl. 447). Wiley-Blackwell
Acta paediatrica (Oslo, Norway, 94(Suppl. 447). Wiley-Blackwell
The value of biomarkers in the clinical management of lysosomal storage diseases is best illustrated by the present use of plasma chitotriosidase levels in the diagnosis and monitoring of Gaucher disease. The enzyme chitotriosidase is specifically pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c74fc5bf09185d3642640843dd003f5
https://doi.org/10.1080/08035320510028094
https://doi.org/10.1080/08035320510028094
Autor:
Johannes Aerts
Publikováno v:
JAMA: The Journal of the American Medical Association. 275:548-553
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::340e992f185b12ba18dc4270452d5aea
https://doi.org/10.1001/jama.275.7.548
https://doi.org/10.1001/jama.275.7.548
Publikováno v:
International review of cytology. A survey of cell biology. Volume 252, 71-128
STARTPAGE=71;ENDPAGE=128;TITLE=International review of cytology. A survey of cell biology. Volume 252
ResearcherID
STARTPAGE=71;ENDPAGE=128;TITLE=International review of cytology. A survey of cell biology. Volume 252
ResearcherID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7490e62db85fb2b3dd8a33aa4c36138b
https://pure.amc.nl/en/publications/the-biology-of-the-gaucher-cell-the-cradle-of-human-chitinases(d6b6a0f9-3709-4a72-bb01-c69acdac98fc).html
https://pure.amc.nl/en/publications/the-biology-of-the-gaucher-cell-the-cradle-of-human-chitinases(d6b6a0f9-3709-4a72-bb01-c69acdac98fc).html
Publikováno v:
American journal of clinical pathology, 122(3), 359-369. American Society of Clinical Pathologists
American Journal of Clinical Pathology, 122, 359-369. Oxford University Press
ResearcherID
American Journal of Clinical Pathology, 122, 359-369. Oxford University Press
ResearcherID
Although the existence of anti-inflammatory alternatively activated macrophages (aamphi) has been accepted widely based on in vitro studies, their in. vivo location, phenotype, and function still are debated. Gaucher disease (GD) is caused by a genet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::332f30b4f2690b7076f09907e8ebced1
https://pure.amc.nl/en/publications/gaucher-cells-demonstrate-a-distinct-macrophage-phenotype-and-resemble-alternatively-activated-macrophages(c0921b35-bc7a-4eac-b1f7-617dd3e9facc).html
https://pure.amc.nl/en/publications/gaucher-cells-demonstrate-a-distinct-macrophage-phenotype-and-resemble-alternatively-activated-macrophages(c0921b35-bc7a-4eac-b1f7-617dd3e9facc).html
Autor:
M.F.G. Johannes Aerts, Dave Speijer, D. Blom, Wilma G. Donker-Koopman, Anneke Strijland, Gabor E. Linthorst
Publikováno v:
American journal of human genetics, 72(1), 23-31. Cell Press
American Journal of Human Genetics, 72, 23-31. Cell Press
ResearcherID
American Journal of Human Genetics, 72, 23-31. Cell Press
ResearcherID
For more than a decade, protein-replacement therapy has been employed successfully for the treatment of Gaucher disease. Recently, a comparable therapy has become available for the related lipid-storage disorder Fabry disease. Two differently produce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38a11303d0a641ae55063baa743f7360
https://europepmc.org/articles/PMC420010/
https://europepmc.org/articles/PMC420010/