Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Calinda K. E. Dingenouts"'
Autor:
Calinda K E Dingenouts, Wineke Bakker, Kirsten Lodder, Karien C Wiesmeijer, Asja T Moerkamp, Janita A Maring, Helen M Arthur, Anke M Smits, Marie-José Goumans
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189805 (2017)
AimsHereditary Hemorrhagic Telangiectasia type-1 (HHT1) is a genetic vascular disorder caused by haploinsufficiency of the TGFβ co-receptor endoglin. Dysfunctional homing of HHT1 mononuclear cells (MNCs) towards the infarcted myocardium hampers card
Externí odkaz:
https://doaj.org/article/5e61c32fbfbc40819382bae5a8ae2141
Autor:
Anke M. Smits, Alwin de Jong, Margreet R. de Vries, Marie-José Goumans, Kondababu Kurakula, Kirsten Lodder, Paul H.A. Quax, Hans-Jurgen J. Mager, Karien C. Wiesmeijer, Calinda K. E. Dingenouts, Wineke Bakker
Publikováno v:
International Journal of Molecular Sciences, 22(4):2010, 1-19. Multidisciplinary Digital Publishing Institute (MDPI)
International Journal of Molecular Sciences
Volume 22
Issue 4
International Journal of Molecular Sciences, 22(4). MDPI
Bakker, W, Dingenouts, C K E, Lodder, K, Wiesmeijer, K C, de Jong, A, Kurakula, K, Mager, H J J, Smits, A M, de Vries, M R, Quax, P H A & Goumans, M J T H 2021, ' Bmp receptor inhibition enhances tissue repair in endoglin heterozygous mice ', International Journal of Molecular Sciences, vol. 22, no. 4, 2010, pp. 1-19 . https://doi.org/10.3390/ijms22042010
International Journal of Molecular Sciences, Vol 22, Iss 2010, p 2010 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 4
International Journal of Molecular Sciences, 22(4). MDPI
Bakker, W, Dingenouts, C K E, Lodder, K, Wiesmeijer, K C, de Jong, A, Kurakula, K, Mager, H J J, Smits, A M, de Vries, M R, Quax, P H A & Goumans, M J T H 2021, ' Bmp receptor inhibition enhances tissue repair in endoglin heterozygous mice ', International Journal of Molecular Sciences, vol. 22, no. 4, 2010, pp. 1-19 . https://doi.org/10.3390/ijms22042010
International Journal of Molecular Sciences, Vol 22, Iss 2010, p 2010 (2021)
Hereditary hemorrhagic telangiectasia type 1 (HHT1) is a severe vascular disorder caused by mutations in the TGFβ/BMP co-receptor endoglin. Endoglin haploinsufficiency results in vascular malformations and impaired neoangiogenesis. Furthermore, HHT1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6553fd9c02efe074d4d70e8093091f4
https://hdl.handle.net/1887/3214289
https://hdl.handle.net/1887/3214289
Autor:
Janita A. Maring, Emma A. Mol, Asja T. Moerkamp, Joost P.G. Sluijter, Karien C. Wiesmeijer, Calinda K. E. Dingenouts, Janine C. Deddens, Kirsten Lodder, Marie-José Goumans, Vera Verhage, Pieter Vader, Anke M. Smits
Publikováno v:
Journal of Cardiovascular Translational Research, 12(1), 5-17. SPRINGER
Journal of Cardiovascular Translational Research
Journal of Cardiovascular Translational Research
Cell transplantation studies have shown that injection of progenitor cells can improve cardiac function after myocardial infarction (MI). Transplantation of human cardiac progenitor cells (hCPCs) results in an increased ejection fraction, but surviva
Autor:
Thijs Berends, Asja T. Moerkamp, Noortje A.M. Bax, Calinda K. E. Dingenouts, Marie-José Goumans, Anke M. Smits, Kirsten Lodder, Hau Wan Leung, Stephanie Holst, Andre Choo
Publikováno v:
Stem Cells and Development, 26(21), 1552-1565. Mary Ann Liebert Inc.
Stem Cells and Development
Stem Cells and Development
The aim of stem cell therapy after cardiac injury is to replace damaged cardiac tissue. Human cardiac progenitor cells (CPCs) represent an interesting cell population for clinical strategies to treat cardiac disease and human CPC-specific antibodies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::291b69a60962c1bf8a771e752a587261
https://hdl.handle.net/1887/94813
https://hdl.handle.net/1887/94813
Autor:
Janita A. Maring, Anke M. Smits, Karien C. Wiesmeijer, Marie-José Goumans, Wineke Bakker, Helen M. Arthur, Calinda K. E. Dingenouts, Asja T. Moerkamp, Kirsten Lodder
Publikováno v:
PLoS ONE, Vol 12, Iss 12, p e0189805 (2017)
PLoS ONE
PLoS ONE, 12(12)
PLoS ONE
PLoS ONE, 12(12)
AimsHereditary Hemorrhagic Telangiectasia type-1 (HHT1) is a genetic vascular disorder caused by haploinsufficiency of the TGFβ co-receptor endoglin. Dysfunctional homing of HHT1 mononuclear cells (MNCs) towards the infarcted myocardium hampers card
Autor:
Asja T. Moerkamp, Thomas J van Brakel, Calinda K. E. Dingenouts, Marie-José Goumans, Esther Dronkers, Kirsten Lodder, Tessa van Herwaarden, Fredrik C. Tengström, Anke M. Smits
Publikováno v:
Stem Cell Research & Therapy
Stem Cell Research and Therapy, 7
Stem Cell Research and Therapy, 7
Background The epicardium, a cell layer covering the heart, plays an important role during cardiogenesis providing cardiovascular cell types and instructive signals, but becomes quiescent during adulthood. Upon cardiac injury the epicardium is activa
Publikováno v:
Frontiers in Genetics
Frontiers in Genetics, Vol 6 (2015)
Frontiers in Genetics, Vol 6 (2015)
Hereditary hemorrhagic telangiectasia (HHT) or Rendu–Osler–Weber disease is a rare genetic vascular disorder known for its endothelial dysplasia causing arteriovenous malformations and severe bleedings. HHT-1 and HHT-2 are the most prevalent vari
Autor:
J Yang, Patricia Green, D Danso-Abeam, Junbo Ge, X Yang, S Ding, L Xu, Claudia Monaco, M.J. Goumans, Calinda K. E. Dingenouts, Kirsten Lodder, Wineke Bakker, Michael E. Goddard, Christina Kassiteridi, Jennifer Cole, Inhye Park
Publikováno v:
Cardiovascular Research. 111:S83-S83
464 STAT4 deficiency exacerbates atherosclerosis by promoting mobilization of myeloid cells, polarization of M1 macrophages and formation of foam cells {#article-title-2} Background: Atherosclerosis (AS) is a chronic inflammatory disease of large and
Autor:
Peter ten Dijke, M.J. Goumans, C.J. Westerman, Repke J. Snijder, Pha Quax, H.J. Mager, M.R. de Vries, Calinda K. E. Dingenouts, Kirsten Lodder, Wineke Bakker
Publikováno v:
Cardiovascular Research. 103:S63.4-S63
Introduction: Endoglin is a co-receptor of Transforming Growth Factorβ (TGFβ) and is crucial for the formation of new blood vessels. Endoglin-haploinsuffiency is the leading cause of the severe vascular disease Hereditary hemorrhagic telangiectasia