Zobrazeno 1 - 10
of 90
pro vyhledávání: '"Janssen, Manoe J."'
Publikováno v:
In Trends in Molecular Medicine July 2021 27(7):673-686
Autor:
Janssen, Manoe J., Nieskens, Tom T.G., Steevels, Tessa A.M., Caetano-Pinto, Pedro, den Braanker, Dirk, Mulder, Melissa, Ponstein, Yolanda, Jones, Shaun, Masereeuw, Rosalinde, den Besten, Cathaline, Wilmer, Martijn J.
Publikováno v:
In Molecular Therapy - Nucleic Acids 6 December 2019 18:298-307
Akademický článek
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Autor:
Genderen, Anne Metje van, G Valverde, Marta, Capendale, Pamela E, Kersten, Valerie, Sendino Garví, Elena, Schuurmans, Carl C L, Ruelas, Marina, Soeiro, Joana T, Tang, Guosheng, Janssen, Manoe J, Jansen, Jitske, Mihăilă, Silvia M, Vermonden, Tina, Zhang, Y Shrike, Masereeuw, Rosalinde
Despite the increasing incidence of kidney-related diseases, we are still far from understanding the underlying mechanisms of these diseases and their progression. This lack of understanding is partly because of a poor replication of the diseasesin v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______101::23d9547998b11624587ca5acb8272600
https://dspace.library.uu.nl/handle/1874/423078
https://dspace.library.uu.nl/handle/1874/423078
Autor:
García Valverde, Marta, Ferreira Faria, João, Sendino Garví, Elena, Janssen, Manoe J, Masereeuw, Rosalinde, Mihaila, Silvia, Afd Pharmacology, Pharmacology
Publikováno v:
Pediatric Nephrology, 37(12), 2985. Springer Verlag
Chronic kidney disease (CKD) is a major healthcare burden that takes a toll on the quality of life of many patients. Emerging evidence indicates that a substantial proportion of these patients carry a genetic defect that contributes to their disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae7b4889c1006e63edfae85824386146
https://zenodo.org/record/7620710
https://zenodo.org/record/7620710
Akademický článek
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Autor:
Garví, Elena Sendino, Masereeuw, Rosalinde, Janssen, Manoe J., Afd Pharmacology, Pharmacology
Publikováno v:
Cells, 11(1), 1. Multidisciplinary Digital Publishing Institute (MDPI)
Cells, Vol 11, Iss 177, p 177 (2022)
Cells
Cells; Volume 11; Issue 1; Pages: 177
Cells, Vol 11, Iss 177, p 177 (2022)
Cells
Cells; Volume 11; Issue 1; Pages: 177
Nephropathic cystinosis is a rare and severe disease caused by disruptions in the CTNS gene. Cystinosis is characterized by lysosomal cystine accumulation, vesicle trafficking impairment, oxidative stress, and apoptosis. Additionally, cystinotic pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5cd248e360d06fc44af08af1101bd95
https://dspace.library.uu.nl/handle/1874/421317
https://dspace.library.uu.nl/handle/1874/421317
Autor:
Taranta, Anna, elmonem, mohamed a, Bellomo, Francesco, Leo, Ester De, Boenzi, Sara, Janssen, Manoe J., Jamalpoor, Amer, Cairoli, Sara, Pastore, Anna, Stefanis, Cristiano De, Colucci, Manuela, Rega, Laura R., giovannoni, isabella, Francalanci, Paola, Heuvel, Lambertus P. van den, Dionisi-Vici, Carlo, Goffredo, Bianca M., Masereeuw, Rosalinde, Levtchenko, Elena, Emma, Francesco, Afd Pharmacology, Pharmacology
Publikováno v:
Cells, 10
Cells, 10(12), 1. Multidisciplinary Digital Publishing Institute (MDPI)
Cells; Volume 10; Issue 12; Pages: 3294
Cells, Vol 10, Iss 3294, p 3294 (2021)
Cells
Cells, 10, 12
Cells, 10(12), 1. Multidisciplinary Digital Publishing Institute (MDPI)
Cells; Volume 10; Issue 12; Pages: 3294
Cells, Vol 10, Iss 3294, p 3294 (2021)
Cells
Cells, 10, 12
Nephropathic cystinosis is a rare disease caused by mutations of the CTNS gene that encodes for cystinosin, a lysosomal cystine/H+ symporter. The disease is characterized by early-onset chronic kidney failure and progressive development of extra-rena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd93ce0aab0f9f430f8fb0eeafadd2b2
https://lirias.kuleuven.be/handle/20.500.12942/687163
https://lirias.kuleuven.be/handle/20.500.12942/687163
Autor:
G. Valverde, Marta, Faria, João, Sendino Garví, Elena, Janssen, Manoe J., Masereeuw, Rosalinde, Mihăilă, Silvia M.
Publikováno v:
Pediatric Nephrology; Dec2022, Vol. 37 Issue 12, p2985-2996, 12p, 2 Diagrams
Akademický článek
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