Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Lotte Van Den Heuvel"'
Autor:
Shalini S. Nayak, Pauline E. Schneeberger, Siddaramappa J. Patil, Karegowda M. Arun, Pujar V. Suresh, Viralam S. Kiran, Sateesh Siddaiah, Shreesha Maiya, Shrikanth K. Venkatachalagupta, Neethukrishna Kausthubham, Fanny Kortüm, Isabella Rau, Alexandra Wey-Fabrizius, Lotte Van Den Heuvel, Josephina Meester, Lut Van Laer, Anju Shukla, Bart Loeys, Katta M. Girisha, Kerstin Kutsche
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Marfan syndrome and related disorders are a group of heritable connective tissue disorders and share many clinical features that involve cardiovascular, skeletal, craniofacial, ocular, and cutaneous abnormalities. The majority of affected in
Externí odkaz:
https://doaj.org/article/f21f727d6c214802940b31d4975ffaa6
Autor:
Ilse Van Gucht, Alice Krebsova, Birgitte Rode Diness, Steven Laga, Dave Adlam, Marlies Kempers, Nilesh J. Samani, Tom R. Webb, Ania A. Baranowska, Lotte Van Den Heuvel, Melanie Perik, Ilse Luyckx, Nils Peeters, Pavel Votypka, Milan Macek, Josephina Meester, Lut Van Laer, Aline Verstraeten, Bart L. Loeys
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 13, p 7111 (2021)
Thoracic aortic aneurysm and dissection (TAAD) is a major cause of cardiovascular morbidity and mortality. Loss-of-function variants in LOX, encoding the extracellular matrix crosslinking enzyme lysyl oxidase, have been reported to cause familial TAA
Externí odkaz:
https://doaj.org/article/e25f439b79014f749dedd56b5f5649ef
Publikováno v:
Cerebrovascular Diseases.
Introduction: The CYP2C19 enzyme converts clopidogrel into an active metabolite. Carriers of CYP2C19 loss-of-function (LOF) variants with a history of ischemic stroke or transient ischemic attack (TIA) using clopidogrel may have a higher risk of recu
Autor:
Abdulrahman Almesned, Dorien Schepers, Mehran Beiraghi Toosi, Zuhair N. Al-Hassnan, Jill A. Rosenfeld, Erin M. Miller, Hassan Mottaghi Moghaddam Shahri, Maaike Alaerts, Melanie Perik, Desiderio Rodrigues, Aline Verstraeten, Reza Maroofian, Silke Peeters, Cédric H. G. Neutel, Ilse Luyckx, Nicole Revencu, Jenny C. Taylor, Jarl Bastianen, Isabel Pintelon, Henry Houlden, Matteo P. Ferla, Erik Fransen, Kayal Vijayakumar, Lut Van Laer, Anthony R. Dallosso, Mandy Vermont, Isabelle Maystadt, Lotte Van Den Heuvel, Thierry Sluysmans, David Murphy, K. Nicole Weaver, Paria Najarzadeh Torbati, Jotte Rodrigues Bento, Amber Begtrup, Maggie Williams, Ilse Van Gucht, Maaike Bastiaansen, Ashish Chikermane, Gangadhara Bharmappanavara, Alistair T. Pagnamenta, Bart Loeys, Joe Davis Velchev, Julie Evans, Josephina A.N. Meester, Narges Hashemi, Julie Vogt, Pieter-Jan Guns
Publikováno v:
The American Journal of Human Genetics
American Journal of Human Genetics, 108, 1115-1125
American Journal of Human Genetics, 108, 6, pp. 1115-1125
Am J Hum Genet
The American journal of human genetics
American Journal of Human Genetics, 108, 1115-1125
American Journal of Human Genetics, 108, 6, pp. 1115-1125
Am J Hum Genet
The American journal of human genetics
Importin 8, encoded by IPO8, is a ubiquitously expressed member of the importin-beta protein family that translocates cargo molecules such as proteins, RNAs, and ribonucleoprotein complexes into the nucleus in a RanGTP-dependent manner. Current knowl
Autor:
Lotte Van Den Heuvel, Josephina Meester, Silke Peeters, Romain Alderweireldt, Aline Verstraeten, Paul Coucke, Bart Loeys
Publikováno v:
AORTA.
Autor:
Josephina A.N. Meester, Silke Peeters, Lotte Van Den Heuvel, Geert Vandeweyer, Erik Fransen, Elizabeth Cappella, Harry C. Dietz, Geoffrey Forbus, Bruce D. Gelb, Elizabeth Goldmuntz, Arvind Hoskoppal, Andrew P. Landstrom, Teresa Lee, Seema Mital, Shaine Morris, Aaron K. Olson, Marjolijn Renard, Dan M. Roden, Michael N. Singh, Elif Seda Selamet Tierney, Justin T. Tretter, Sara L. Van Driest, Marcia Willing, Aline Verstraeten, Lut Van Laer, Ronald V. Lacro, Bart L. Loeys
Publikováno v:
Genetics in medicine
Genetics in Medicine, 24, 1045-1053
Genetics in Medicine, 24, 5, pp. 1045-1053
Genetics in Medicine, 24, 1045-1053
Genetics in Medicine, 24, 5, pp. 1045-1053
PURPOSE In a large cohort of 373 pediatric patients with Marfan syndrome (MFS) with a severe cardiovascular phenotype, we explored the proportion of patients with MFS with a pathogenic FBN1 variant and analyzed whether the type/location of FBN1 varia
Autor:
Lotte van den Heuvel, Patrik Rönnbäck
Publikováno v:
Fisheries Research. 258:106519
Recreational anglers collectively spend a great amount of time on fishing activities. While being out fishing, these anglers perceive various components of aquatic ecosystems, allowing them to accumulate knowledge of the ecological status of the syst
Publikováno v:
Journal of Outdoor Recreation and Tourism. 39:100549
The incorporation of theories and methods from tourism research in recreational fisheries research is not common practice, despite many parallels between the two research fields. Adopting a tourism perspective could contribute to our understanding of
Autor:
Malgorzata Blicharska, Janez Susnik, Sara Masia, Lotte van den Heuvel, Thomas Grabs, Claudia Teutschbein
Global change is a growing problem, governed by demographic, economic and climatological drivers. Such developments are leading to an increasing demand for natural resources. Traditionally, management of products and services from water, energy, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acdbf1bcd4a4426cb7baf57c811db76b
https://doi.org/10.5194/egusphere-egu2020-18681
https://doi.org/10.5194/egusphere-egu2020-18681
Autor:
Alice Krebsová, Aline Verstraeten, Steven Laga, Tom R. Webb, Melanie Perik, Josephina A.N. Meester, Milan Macek, Pavel Votypka, Dave Adlam, Birgitte Rode Diness, Bart Loeys, Ilse Van Gucht, Lotte Van Den Heuvel, Nils Peeters, Ania A Baranowska, Nilesh J. Samani, Lut Van Laer, Ilse Luyckx, Marlies Kempers
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, 22
Volume 22
Issue 13
International Journal of Molecular Sciences, Vol 22, Iss 7111, p 7111 (2021)
International journal of molecular sciences
International Journal of Molecular Sciences, 22, 13
Van Gucht, I, Krebsova, A, Diness, B R, Laga, S, Adlam, D, Kempers, M, Samani, N J, Webb, T R, Baranowska, A A, Van Den Heuvel, L, Perik, M, Luyckx, I, Peeters, N, Votypka, P, Macek, M, Meester, J, Van Laer, L, Verstraeten, A & Loeys, B L 2021, ' Novel lox variants in five families with aortic/arterial aneurysm and dissection with variable connective tissue findings ', International Journal of Molecular Sciences, vol. 22, no. 13, 7111 . https://doi.org/10.3390/ijms22137111
International Journal of Molecular Sciences, 22
Volume 22
Issue 13
International Journal of Molecular Sciences, Vol 22, Iss 7111, p 7111 (2021)
International journal of molecular sciences
International Journal of Molecular Sciences, 22, 13
Van Gucht, I, Krebsova, A, Diness, B R, Laga, S, Adlam, D, Kempers, M, Samani, N J, Webb, T R, Baranowska, A A, Van Den Heuvel, L, Perik, M, Luyckx, I, Peeters, N, Votypka, P, Macek, M, Meester, J, Van Laer, L, Verstraeten, A & Loeys, B L 2021, ' Novel lox variants in five families with aortic/arterial aneurysm and dissection with variable connective tissue findings ', International Journal of Molecular Sciences, vol. 22, no. 13, 7111 . https://doi.org/10.3390/ijms22137111
Thoracic aortic aneurysm and dissection (TAAD) is a major cause of cardiovascular morbidity and mortality. Loss-of-function variants in LOX, encoding the extracellular matrix crosslinking enzyme lysyl oxidase, have been reported to cause familial TAA