Ten years of HPV vaccination in the Netherlands: current evidence and future challenges in HPV-related disease prevention

Autor: V. Qendri, T. M. Schurink-Van ’t Klooster, J. A. Bogaards, J. Berkhof

Publikováno v: Expert Review of Vaccines, Vol 17, Iss 12, Pp 1093-1104 (2018)

Introduction: Girls-only vaccination against human papillomavirus (HPV) type 16 and 18 was implemented in the Netherlands in 2009. Despite the evidence of the efficacy against precancerous lesions, cross-protection induced by the vaccine and a greate

Externí odkaz: https://doaj.org/article/445ae3e7f6564acd9d4a08abf8a46a5b

Work and oxygen consumption of isolated right ventricular papillary muscle in experimental pulmonary hypertension

Autor: Willem J. van der Laarse, Sylvia J. P. Bogaards, Ingrid Schalij, Anton Vonk Noordegraaf, Frédéric M. Vaz, Duncan van Groen

Publikováno v: Journal of Physiology, 600(20), 4465-4484. Wiley-Blackwell
van der Laarse, W J, Bogaards, S J P, Schalij, I, Noordegraaf, A V, Vaz, F M & van Groen, D 2022, ' Work and oxygen consumption of isolated right ventricular papillary muscle in experimental pulmonary hypertension ', Journal of Physiology, vol. 600, no. 20, pp. 4465-4484 . https://doi.org/10.1113/JP282991
Journal of physiology, 600(20), 4465-4484. Wiley-Blackwell

SummaryRight-sided myocardial mechanical efficiency (work output/metabolic energy input) in pulmonary hypertension can be severely reduced. We determined the contribution of intrinsic myocardial determinants of efficiency using papillary muscle prepa

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3538a0cf3edfb5496833f98a84b98e65
https://doi.org/10.1101/2021.12.30.474521

COVID-19 is associated with distinct myopathic features in the diaphragm of critically ill patients

Autor: Marloes van den Berg, Stefan Conijn, Yeszamin Onderwater, Sylvia J. P. Bogaards, Zhong-Hua Shi, Pedro Espinosa, Marianna Bugiani, Martijn van de Locht, Hans van der Hoeven, Leo M. A. Heunks, Coen A.C. Ottenheijm, Diewertje I Bink, Reinier A Boon

Publikováno v: BMJ open respiratory research, 8
BMJ open respiratory research, 8, 1
Shi, Z, Bogaards, S J P, Conijn, S, Onderwater, Y, Espinosa, P, Bink, D I, van den Berg, M, van de Locht, M, Bugiani, M, van der Hoeven, H, Boon, R A, Heunks, L & Ottenheijm, C A C 2021, ' COVID-19 is associated with distinct myopathic features in the diaphragm of critically ill patients ', BMJ Open Respiratory Research, vol. 8, no. 1, e001052 . https://doi.org/10.1136/bmjresp-2021-001052
BMJ Open Respiratory Research
BMJ Open Respiratory Research, Vol 8, Iss 1 (2021)
BMJ Open Respiratory Research, 8(1):e001052. BMJ Publishing Group

IntroductionThe diaphragm is the main muscle of inspiration, and its dysfunction contributes to adverse clinical outcomes in critically ill patients. We recently reported the infiltration of SARS-CoV-2, and the development of fibrosis, in the diaphra

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0adeeb1936b7f67f9611f1e9c0d0c82e
http://hdl.handle.net/2066/238748

KBTBD13 is an actin-binding protein that modulates muscle kinetics

Autor: Leonardo Nogara, Saskia Lassche, Jonne Doorduin, Norma B. Romero, Benno Küsters, Tamar E. Sztal, Baziel G.M. van Engelen, Balázs Kiss, Stefan Conijn, Josine M. de Winter, Coen A.C. Ottenheijm, Weikang Ma, Georg Ramm, Viola Oorschot, Joery P. Molenaar, Shengyi Shen, Christopher N. Johnson, Richard J. Rodenburg, Bert Blaauw, Robbert van der Pijl, Henk Granzier, Thomas E. Hall, Ken Campbell, Frank Li, Thomas C. Irving, Alan H. Beggs, Michaela Yuen, Reinier A. Boon, Manuela Marabita, Menne van Willigenburg, Esmee S.B. Van Kleef, Noelia Lozano-Vidal, Sylvia J. P. Bogaards, Robert J. Bryson-Richardson, Avnika A. Ruparelia, Dilson E. Rassier, Martijn van de Locht, Edoardo Malfatti, Malin Persson, Zherui Xiong, Nicol C. Voermans

Publikováno v: Journal of Clinical Investigation
Journal of Clinical Investigation, American Society for Clinical Investigation, 2020, 130 (2), pp.754-767. ⟨10.1172/JCI124000⟩
Journal of Clinical Investigation, 130, 2, pp. 754-767
J Clin Invest
Journal of Clinical Investigation, 130(2), 754-767. The American Society for Clinical Investigation
de Winter, J M, Molenaar, J P, Yuen, M, van der Pijl, R, Shen, S, Conijn, S, van de Locht, M, Willigenburg, M, Bogaards, S J P, van Kleef, E S, Lassche, S, Persson, M, Rassier, D E, Sztal, T E, Ruparelia, A A, Oorschot, V, Ramm, G, Hall, T E, Xiong, Z, Johnson, C N, Li, F, Kiss, B, Lozano-Vidal, N, Boon, R A, Marabita, M, Nogara, L, Blaauw, B, Rodenburg, R J, Küsters, B, Doorduin, J, Beggs, A H, Granzier, H, Campbell, K, Ma, W, Irving, T, Malfatti, E, Romero, N B, Bryson-Richardson, R J, van Engelen, B G M, Voermans, N C & Ottenheijm, C A C 2020, ' KBTBD13 is an actin-binding protein that modulates muscle kinetics ', Journal of Clinical Investigation, vol. 130, no. 2, pp. 754-767 . https://doi.org/10.1172/JCI124000
Journal of clinical investigation, 130(2), 754-767. The American Society for Clinical Investigation
Journal of Clinical Investigation, 130, 754-767

International audience; The mechanisms that modulate the kinetics of muscle relaxation are critically important for muscle function. A prime example of the impact of impaired relaxation kinetics is nemaline myopathy caused by mutations in KBTBD13 (NE

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8814b2daabcdfb84373f75468712d908
http://hdl.handle.net/11577/3321703

Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1 -related nemaline myopathy (NEM3)

Autor: Edoardo Malfatti, Dilson E. Rassier, Nigel F. Clarke, Stefan Conijn, Weikang Ma, Norma B. Romero, Malin Persson, Albert Kalganov, Sylvia J. P. Bogaards, Igor Kovacevic, Ger J.M. Stienen, Johan Lindqvist, Alan H. Beggs, Michaela Yuen, Josine M. de Winter, Barbara Joureau, Coen A.C. Ottenheijm, Thomas C. Irving

Publikováno v: Annals of Neurology. 83:269-282

Objective Nemaline myopathy (NM) is one of the most common congenital nondystrophic myopathies and is characterized by muscle weakness, often from birth. Mutations in ACTA1 are a frequent cause of NM (ie, NEM3). ACTA1 encodes alpha-actin 1, the main

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3e9f59fc6a136827a2033dd5f5d9bf0d
https://doi.org/10.1002/ana.25144