Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Lisanne E. Wisse"'
Autor:
Lauria Claeys, Lidiia Zhytnik, Laura Ventura, Lisanne E. Wisse, Elisabeth M. W. Eekhoff, Gerard Pals, Nathalie Bravenboer, Vivi M. Heine, Dimitra Micha
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 6, p 3417 (2024)
(1) Mesenchymal stem cells (MSCs) are a valuable cell model to study the bone pathology of Osteogenesis Imperfecta (OI), a rare genetic collagen-related disorder characterized by bone fragility and skeletal dysplasia. We aimed to generate a novel OI
Externí odkaz:
https://doaj.org/article/f8229f0bdcb648eab2dbc260c8792f45
Autor:
Lauria Claeys, Lidiia Zhytnik, Lisanne E. Wisse, Huib W. van Essen, E. Marelise W. Eekhoff, Gerard Pals, Nathalie Bravenboer, Dimitra Micha
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionOsteogenesis Imperfecta is a rare genetic connective tissue disorder, characterized by skeletal dysplasia and fragile bones. Currently only two mouse models have been reported for haploinsufficient (HI) mild Osteogenesis Imperfecta (OI);
Externí odkaz:
https://doaj.org/article/96b8e8cb8e5b4cdfbc5c3e11a5af583c
Autor:
Ruben D. de Ruiter, Lisanne E. Wisse, Ton Schoenmaker, Maqsood Yaqub, Gonzalo Sánchez-Duffhues, E. Marelise W. Eekhoff, Dimitra Micha
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 3, p 2299 (2023)
Fibrodysplasia ossificans progressiva (FOP) is a catastrophic, ultra-rare disease of heterotopic ossification caused by genetic defects in the ACVR1 gene. The mutant ACVR1 receptor, when triggered by an inflammatory process, leads to heterotopic ossi
Externí odkaz:
https://doaj.org/article/f9c43e69ef2c4e53ab14cf513164ae1a
Autor:
Truus E. M. Abbink, Lisanne E. Wisse, Ermelinda Jaku, Michiel J. Thiecke, Daniel Voltolini‐González, Hein Fritsen, Sander Bobeldijk, Timo J. terBraak, Emiel Polder, Nienke L. Postma, Marianna Bugiani, Eduard A. Struijs, Mark Verheijen, Nina Straat, Sophie van derSluis, Adri A. M. Thomas, Douwe Molenaar, Marjo S. van derKnaap
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 8, Pp 1407-1422 (2019)
Abstract Objective Vanishing white matter (VWM) is a fatal, stress‐sensitive leukodystrophy that mainly affects children and is currently without treatment. VWM is caused by recessive mutations in eukaryotic initiation factor 2B (eIF2B) that is cru
Externí odkaz:
https://doaj.org/article/bc70e13747d84b12b5b25ba59f4dcbfe
Autor:
Inna Slynko, Stephanie Nguyen, Eline M. C. Hamilton, Lisanne E. Wisse, Iwan J. P. deEsch, Chris deGraaf, John B. Bruning, Christopher G. Proud, Truus E. M. Abbink, Marjo S. van derKnaap
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Abstract Background Vanishing white matter (VWM) is a leukodystrophy, caused by recessive mutations in eukaryotic initiation factor 2B (eIF2B)‐subunit genes (EIF2B1–EIF2B5); 80% are missense mutations. Clinical severity is highly variable, with a
Externí odkaz:
https://doaj.org/article/c5d9110157154fc9adce3ee143db795c
Autor:
Lisanne E. Wisse, Renske Penning, Esther A. Zaal, Carola G. M. van Berkel, Timo J. ter Braak, Emiel Polder, Justin W. Kenney, Christopher G. Proud, Celia R. Berkers, Maarten A. F. Altelaar, Dave Speijer, Marjo S. van der Knaap, Truus E. M. Abbink
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 11 (2017)
Vanishing white matter (VWM) is a leukodystrophy with predominantly early-childhood onset. Affected children display various neurological signs, including ataxia and spasticity, and die early. VWM patients have bi-allelic mutations in any of the five
Externí odkaz:
https://doaj.org/article/a9b90c5610104ba2a6d226daf4f5408c
Autor:
Eline M.C. Hamilton, Stephanie Nguyen, Chris de Graaf, Iwan J. P. de Esch, Christopher G. Proud, John B. Bruning, Lisanne E. Wisse, Marjo S. van der Knaap, Inna Slynko, Truus Em Abbink
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Molecular Genetics and Genomic Medicine, 9(3):e1593, 1-15. John Wiley and Sons Inc.
Molecular Genetics and Genomic Medicine, 9(3):e1593. John Wiley and Sons Inc.
Slynko, I, Nguyen, S, Hamilton, E M C, Wisse, L E, de Esch, I J P, de Graaf, C, Bruning, J B, Proud, C G, Abbink, T E M & van der Knaap, M S 2021, ' Vanishing white matter : Eukaryotic initiation factor 2B model and the impact of missense mutations ', Molecular Genetics and Genomic Medicine, vol. 9, no. 3, e1593, pp. 1-15 . https://doi.org/10.1002/mgg3.1593
Slynko, I, Nguyen, S, Hamilton, E M C, Wisse, L E, de Esch, I J P, de Graaf, C, Bruning, J B, Proud, C G, Abbink, T E M & van der Knaap, M S 2021, ' Vanishing white matter : Eukaryotic initiation factor 2B model and the impact of missense mutations ', Molecular Genetics and Genomic Medicine, vol. 9, no. 3, e1593 . https://doi.org/10.1002/mgg3.1593
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Molecular Genetics and Genomic Medicine, 9(3):e1593, 1-15. John Wiley and Sons Inc.
Molecular Genetics and Genomic Medicine, 9(3):e1593. John Wiley and Sons Inc.
Slynko, I, Nguyen, S, Hamilton, E M C, Wisse, L E, de Esch, I J P, de Graaf, C, Bruning, J B, Proud, C G, Abbink, T E M & van der Knaap, M S 2021, ' Vanishing white matter : Eukaryotic initiation factor 2B model and the impact of missense mutations ', Molecular Genetics and Genomic Medicine, vol. 9, no. 3, e1593, pp. 1-15 . https://doi.org/10.1002/mgg3.1593
Slynko, I, Nguyen, S, Hamilton, E M C, Wisse, L E, de Esch, I J P, de Graaf, C, Bruning, J B, Proud, C G, Abbink, T E M & van der Knaap, M S 2021, ' Vanishing white matter : Eukaryotic initiation factor 2B model and the impact of missense mutations ', Molecular Genetics and Genomic Medicine, vol. 9, no. 3, e1593 . https://doi.org/10.1002/mgg3.1593
Background Vanishing white matter (VWM) is a leukodystrophy, caused by recessive mutations in eukaryotic initiation factor 2B (eIF2B)‐subunit genes (EIF2B1–EIF2B5); 80% are missense mutations. Clinical severity is highly variable, with a strong,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::016af327f62ae4cca37228683e8873df
https://doi.org/10.1002/mgg3.1593
https://doi.org/10.1002/mgg3.1593
Autor:
Yuanyuan Ma, Jasmijn M. Rootlieb, Lisanne E. Wisse, Laura v. Huizen, Ludo v. Haasterecht, Dimitra Micha, Elisabeth M. Eekhoff, Peter Kloen, Thomas Rustemeyer, Marie L. Groot
Publikováno v:
Unconventional Optical Imaging III.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae37731619957adc63b56a3396f4f1d0
https://doi.org/10.1117/12.2632796
https://doi.org/10.1117/12.2632796
Autor:
Truus Em Abbink, Abdellatif Bakkali, Christopher D. Morrison, Denise Visser, Timo J. ter Braak, E.A. Struys, Marjo S van der Knaap, Lisanne E. Wisse
Publikováno v:
Nutritional Neuroscience, 25(6), 1219-1230. Maney Publishing
Wisse, L E, Visser, D, ter Braak, T J, Bakkali, A, Struys, E A, Morrison, C D, van der Knaap, M S & Abbink, T E M 2022, ' Isocaloric low protein diet in a mouse model for vanishing white matter does not impact ISR deregulation in brain, but reveals ISR deregulation in liver ', Nutritional Neuroscience, vol. 25, no. 6, pp. 1219-1230 . https://doi.org/10.1080/1028415X.2020.1846356
Wisse, L E, Visser, D, ter Braak, T J, Bakkali, A, Struys, E A, Morrison, C D, van der Knaap, M S & Abbink, T E M 2020, ' Isocaloric low protein diet in a mouse model for vanishing white matter does not impact ISR deregulation in brain, but reveals ISR deregulation in liver ', Nutritional neuroscience . https://doi.org/10.1080/1028415X.2020.1846356
Nutritional neuroscience. Maney Publishing
Wisse, L E, Visser, D, ter Braak, T J, Bakkali, A, Struys, E A, Morrison, C D, van der Knaap, M S & Abbink, T E M 2022, ' Isocaloric low protein diet in a mouse model for vanishing white matter does not impact ISR deregulation in brain, but reveals ISR deregulation in liver ', Nutritional Neuroscience, vol. 25, no. 6, pp. 1219-1230 . https://doi.org/10.1080/1028415X.2020.1846356
Wisse, L E, Visser, D, ter Braak, T J, Bakkali, A, Struys, E A, Morrison, C D, van der Knaap, M S & Abbink, T E M 2020, ' Isocaloric low protein diet in a mouse model for vanishing white matter does not impact ISR deregulation in brain, but reveals ISR deregulation in liver ', Nutritional neuroscience . https://doi.org/10.1080/1028415X.2020.1846356
Nutritional neuroscience. Maney Publishing
Objective: Vanishing white matter (VWM) is a genetic brain white matter disorder caused by mutations in eIF2B. eIF2B is central in the integrated stress response (ISR), during which its activity is inhibited by various cellular stresses. VWM is a chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69606f844515c8da945dafdc9f16b2b7
https://research.vu.nl/en/publications/4c62cd7f-455d-47fb-9f85-1730c766f395
https://research.vu.nl/en/publications/4c62cd7f-455d-47fb-9f85-1730c766f395
Autor:
Sander Bobeldijk, Mark H. G. Verheijen, Adri A. M. Thomas, Douwe Molenaar, Eduard A. Struijs, Marianna Bugiani, Timo J. ter Braak, Nienke L. Postma, Truus Em Abbink, Lisanne E. Wisse, Daniel Voltolini-González, Emiel Polder, Sophie van der Sluis, Michiel J. Thiecke, Ermelinda Jaku, Marjo S. van der Knaap, Hein Fritsen, Nina Straat
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 6, Iss 8, Pp 1407-1422 (2019)
Abbink, T E M, Wisse, L E, Jaku, E, Thiecke, M J, Voltolini-González, D, Fritsen, H, Bobeldijk, S, ter Braak, T J, Polder, E, Postma, N L, Bugiani, M, Struijs, E A, Verheijen, M, Straat, N, van der Sluis, S, Thomas, A A M, Molenaar, D & van der Knaap, M S 2019, ' Vanishing white matter: deregulated integrated stress response as therapy target ', Annals of Clinical and Translational Neurology, vol. 6, no. 8, pp. 1407-1422 . https://doi.org/10.1002/acn3.50826
Abbink, T E M, Wisse, L E, Jaku, E, Thiecke, M J, Voltolini-González, D, Fritsen, H, Bobeldijk, S, ter Braak, T J, Polder, E, Postma, N L, Bugiani, M, Struijs, E A, Verheijen, M, Straat, N, van der Sluis, S, Thomas, A A M, Molenaar, D & van der Knaap, M S 2019, ' Vanishing white matter : deregulated integrated stress response as therapy target ', Annals of Clinical and Translational Neurology, vol. 6, no. 8, pp. 1407-1422 . https://doi.org/10.1002/acn3.50826
Annals of Clinical and Translational Neurology, 6(8), 1407-1422. John Wiley and Sons Ltd
Annals of Clinical and Translational Neurology
Abbink, T E M, Wisse, L E, Jaku, E, Thiecke, M J, Voltolini-González, D, Fritsen, H, Bobeldijk, S, ter Braak, T J, Polder, E, Postma, N L, Bugiani, M, Struijs, E A, Verheijen, M, Straat, N, van der Sluis, S, Thomas, A A M, Molenaar, D & van der Knaap, M S 2019, ' Vanishing white matter: deregulated integrated stress response as therapy target ', Annals of Clinical and Translational Neurology, vol. 6, no. 8, pp. 1407-1422 . https://doi.org/10.1002/acn3.50826
Abbink, T E M, Wisse, L E, Jaku, E, Thiecke, M J, Voltolini-González, D, Fritsen, H, Bobeldijk, S, ter Braak, T J, Polder, E, Postma, N L, Bugiani, M, Struijs, E A, Verheijen, M, Straat, N, van der Sluis, S, Thomas, A A M, Molenaar, D & van der Knaap, M S 2019, ' Vanishing white matter : deregulated integrated stress response as therapy target ', Annals of Clinical and Translational Neurology, vol. 6, no. 8, pp. 1407-1422 . https://doi.org/10.1002/acn3.50826
Annals of Clinical and Translational Neurology, 6(8), 1407-1422. John Wiley and Sons Ltd
Annals of Clinical and Translational Neurology
Objective: Vanishing white matter (VWM) is a fatal, stress-sensitive leukodystrophy that mainly affects children and is currently without treatment. VWM is caused by recessive mutations in eukaryotic initiation factor 2B (eIF2B) that is crucial for i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc38ffb7fe3629e60ea3de02637fcbd1
https://doi.org/10.1002/acn3.50826
https://doi.org/10.1002/acn3.50826