Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Arne IJpma"'
Autor:
Marie Beth van Egmond, Gabriele Spini, Onno van der Galien, Arne IJpma, Thijs Veugen, Wessel Kraaij, Alex Sangers, Thomas Rooijakkers, Peter Langenkamp, Bart Kamphorst, Natasja van de L’Isle, Milena Kooij-Janic
Publikováno v:
BMC Medical Informatics and Decision Making, Vol 21, Iss 1, Pp 1-16 (2021)
Abstract Background Recent developments in machine learning have shown its potential impact for clinical use such as risk prediction, prognosis, and treatment selection. However, relevant data are often scattered across different stakeholders and the
Externí odkaz:
https://doaj.org/article/8b263a8d1f5744b1a5839a1725efb851
Autor:
Arne IJpma, Zongsheng He, Dianne Vreeken, Daphne Heijsman, Hence J.M. Verhagen, Jorg De Bruijn, Sander Ten Raa, Hennie T. Bruggenwirth, Jolien W. Roos-Hesselink, Jos A. Bekkers, Danny Huylebroeck, John W.M. Creemers, Danielle Majoor-Krakauer
Publikováno v:
AORTA.
Autor:
Nathalie P. de Wagenaar, Timo L.M. ten Hagen, Danielle Majoor-Krakauer, Ingrid van der Pluijm, Arne IJpma, Joyce Burger, Hui Liu, Nicole van Vliet, Jeroen Essers, Alessandra Maugeri, Kak K. Yeung, Natalija Bogunovic, Dimitra Micha, Hence J.M. Verhagen
Publikováno v:
Burger, J, Bogunovic, N, de Wagenaar, N P, Liu, H, van Vliet, N, IJpma, A, Maugeri, A, Micha, D, Verhagen, H J M, Ten Hagen, T L M, Majoor-Krakauer, D, van der Pluijm, I, Essers, J & Yeung, K K 2021, ' Molecular phenotyping and functional assessment of smooth muscle-like cells with pathogenic variants in aneurysm genes ACTA2, MYH11, SMAD3 and FBN1 ', Human Molecular Genetics, vol. 30, no. 23, pp. 2286-2299 . https://doi.org/10.1093/hmg/ddab190
Human Molecular Genetics
Human Molecular Genetics, 30(23), 2286-2299. Oxford University Press
Human Molecular Genetics
Human Molecular Genetics, 30(23), 2286-2299. Oxford University Press
Aortic aneurysms (AAs) are pathological dilatations of the aorta. Pathogenic variants in genes encoding for proteins of the contractile machinery of vascular smooth muscle cells (VSMCs), genes encoding proteins of the transforming growth factor beta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::420d12b6b72536ee5cb8cc7cb77fbc75
https://research.vumc.nl/en/publications/15fd6bf7-89f7-4cdf-b65a-509ac7b80c0a
https://research.vumc.nl/en/publications/15fd6bf7-89f7-4cdf-b65a-509ac7b80c0a
Autor:
K.M. van de Luijtgaarden, L Te Riet, H.J.M. Verhagen, Joyce Burger, I. van der Pluijm, Arne IJpma, P.M. van Heijningen, Ellen V. Rouwet, Jeroen Essers, Danielle Majoor-Krakauer
Publikováno v:
Journal of Cardiovascular Development and Disease
Volume 6
Issue 4
Journal of Cardiovascular Development and Disease, Vol 6, Iss 4, p 38 (2019)
Journal of Cardiovascular Development and Disease, 6(4):38. Multidisciplinary Digital Publishing Institute (MDPI)
Volume 6
Issue 4
Journal of Cardiovascular Development and Disease, Vol 6, Iss 4, p 38 (2019)
Journal of Cardiovascular Development and Disease, 6(4):38. Multidisciplinary Digital Publishing Institute (MDPI)
Abdominal aortic aneurysms (AAA), are usually asymptomatic until rupture causes fatal bleeding, posing a major vascular health problem. AAAs are associated with advanced age, male gender, and cardiovascular risk factors (e.g. hypertension and smoking
Autor:
Katherine C MacKenzie, Marco Metzger, Nikhil Thapar, Arne IJpma, Robert M.W. Hofstra, Dipa Natarajan, Bart J. L. Eggen, Yunia Sribudiani, Alan J. Burns, Duco Schriemer, Ellen Binder
Publikováno v:
Developmental Biology, 416(1), 255-265. ACADEMIC PRESS INC ELSEVIER SCIENCE
Developmental Biology, 416(1), 255-265. Elsevier Inc.
Developmental Biology, 416(1), 255-265. Elsevier Inc.
The enteric nervous system (ENS) is required for peristalsis of the gut and is derived from Enteric Neural Crest Cells (ENCCs). During ENS development, the RET receptor tyrosine kinase plays a critical role in the proliferation and survival of ENCCs,
Publikováno v:
British Journal of Dermatology, 173(6), 1536-1539. Wiley-Blackwell Publishing Ltd
British journal of dermatology, 173(6), 1536-1539. Wiley-Blackwell
British journal of dermatology, 173(6), 1536-1539. Wiley-Blackwell
Currently available biologics for psoriasis target the function of TNF-α, IL-17A or IL-12/23 and include etanercept (anti-TNF receptor fusion protein), adalimumab and infliximab (anti-TNFα antibodies), anti-IL-17(receptor) molecules and ustekinumab
Autor:
Paige Anderson, Brian J. Peter, Emily M LeProust, Anne Bergstrom Lucas, Maithreyan Srinivasan, Bo Curry, Anniek De Witte, Michael Ruvolo, Arne Ijpma, Stephanie Fulmer-Smentek, Jayati Ghosh, Arjun Vadapalli, Nick Sampas, Ashutosh Ashutosh, Paula Costa
Publikováno v:
Cancer Research. 72:5095-5095
Advances in cancer research have greatly benefited from high resolution copy number (CN) measurements provided by oligo array Comparative Genomic Hybridization (aCGH). The addition of single nucleotide polymorphism (SNP) measurements to CGH microarra
Autor:
Daphne Heijsman, Hence J.M. Verhagen, Koen M. van de Luijtgaarden, Marjan M. Weiss, Hennie T. Brüggenwirth, Alessandra Maugeri, Arne IJpma, Danielle Majoor-Krakauer
Publikováno v:
Human Genetics, 134(8), 881-893. Springer-Verlag
Human Genetics, 134(8), 881-893. Springer Verlag
Human Genetics
van de Luijtgaarden, K M, Heijsman, D, Maugeri, A, Weiss, M M, Verhagen, H J M, Ijpma, A, Bruggenwirth, H T & Majoor-Krakauer, D 2015, ' First genetic analysis of aneurysm genes in familial and sporadic abdominal aortic aneurysm ', Human Genetics, vol. 134, no. 8, pp. 881-893 . https://doi.org/10.1007/s00439-015-1567-0
Human Genetics, 134(8), 881-893. Springer Verlag
Human Genetics
van de Luijtgaarden, K M, Heijsman, D, Maugeri, A, Weiss, M M, Verhagen, H J M, Ijpma, A, Bruggenwirth, H T & Majoor-Krakauer, D 2015, ' First genetic analysis of aneurysm genes in familial and sporadic abdominal aortic aneurysm ', Human Genetics, vol. 134, no. 8, pp. 881-893 . https://doi.org/10.1007/s00439-015-1567-0
Genetic causes for abdominal aortic aneurysm (AAA) have not been identified and the role of genes associated with familial thoracic aneurysms in AAA has not been explored. We analyzed nine genes associated with familial thoracic aortic aneurysms, the