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pro vyhledávání: '"L. Inge"'
Akademický článek
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Publikováno v:
The Journal of Mathematical Behavior. 46:289-302
The Virginia Mathematics Specialist Initiative (VMSI) is an ongoing collaborative effort among all components of the mathematics and mathematics education community of Virginia spanning more than two and a half decades. This paper describes the use o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e1dc63f7883948626461672a0653a2d
https://doi.org/10.1016/j.jmathb.2016.12.003
https://doi.org/10.1016/j.jmathb.2016.12.003
Publikováno v:
2019 IEEE 25th International Symposium for Design and Technology in Electronic Packaging (SIITME).
Simulation of waterfall in nature can be done using a fluid level control system in a pool. This system is made of two mini-pools at a height of 50 cm from each other. The water monitoring system consists of a control and control board that reads the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb0cee2566d81649ada40e801607c432
https://doi.org/10.1109/siitme47687.2019.8990826
https://doi.org/10.1109/siitme47687.2019.8990826
Akademický článek
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Autor:
Rebekkah J. Hitti-Malin, Daan M. Panneman, Zelia Corradi, Erica G. M. Boonen, Galuh Astuti, Claire-Marie Dhaenens, Heidi Stöhr, Bernhard H. F. Weber, Dror Sharon, Eyal Banin, Marianthi Karali, Sandro Banfi, Tamar Ben-Yosef, Damjan Glavač, G. Jane Farrar, Carmen Ayuso, Petra Liskova, Lubica Dudakova, Marie Vajter, Monika Ołdak, Jacek P. Szaflik, Anna Matynia, Michael B. Gorin, Kati Kämpjärvi, Miriam Bauwens, Elfride De Baere, Carel B. Hoyng, Catherina H. Z. Li, Caroline C. W. Klaver, Chris F. Inglehearn, Kaoru Fujinami, Carlo Rivolta, Rando Allikmets, Jana Zernant, Winston Lee, Osvaldo L. Podhajcer, Ana Fakin, Jana Sajovic, Alaa AlTalbishi, Sandra Valeina, Gita Taurina, Andrea L. Vincent, Lisa Roberts, Raj Ramesar, Giovanna Sartor, Elena Luppi, Susan M. Downes, L. Ingeborgh van den Born, Terri L. McLaren, John N. De Roach, Tina M. Lamey, Jennifer A. Thompson, Fred K. Chen, Anna M. Tracewska, Smaragda Kamakari, Juliana Maria Ferraz Sallum, Hanno J. Bolz, Hülya Kayserili, Susanne Roosing, Frans P. M. Cremers
Publikováno v:
Biomolecules, Vol 14, Iss 3, p 367 (2024)
Inherited macular dystrophies (iMDs) are a group of genetic disorders, which affect the central region of the retina. To investigate the genetic basis of iMDs, we used single-molecule Molecular Inversion Probes to sequence 105 maculopathy-associated
Externí odkaz:
https://doaj.org/article/a59ac914048b4e7daf70faf03534c762
Publikováno v:
School Science and Mathematics. 112:310-324
This article describes the design and implementation of an assessment instrument for Numbers and Operations, the first course in a program to train elementary mathematics specialists. We briefly describe the course and its content, and then we elabor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75c1d60a7d20792cbcd4242590c3beb8
https://doi.org/10.1111/j.1949-8594.2012.00148.x
https://doi.org/10.1111/j.1949-8594.2012.00148.x
Autor:
Janine Reurink, Nicole Weisschuh, Alejandro Garanto, Adrian Dockery, L. Ingeborgh van den Born, Isabelle Fajardy, Lonneke Haer-Wigman, Susanne Kohl, Bernd Wissinger, G. Jane Farrar, Tamar Ben-Yosef, Fatma Kivrak Pfiffner, Wolfgang Berger, Marianna E. Weener, Lubica Dudakova, Petra Liskova, Dror Sharon, Manar Salameh, Ashley Offenheim, Elise Heon, Giorgia Girotto, Paolo Gasparini, Anna Morgan, Arthur A. Bergen, Jacoline B. ten Brink, Caroline C.W. Klaver, Lisbeth Tranebjærg, Nanna D. Rendtorff, Sascha Vermeer, Jeroen J. Smits, Ronald J.E. Pennings, Marco Aben, Jaap Oostrik, Galuh D.N. Astuti, Jordi Corominas Galbany, Hester Y. Kroes, Milan Phan, Wendy A.G. van Zelst-Stams, Alberta A.H.J. Thiadens, Joke B.G.M. Verheij, Mary J. van Schooneveld, Suzanne E. de Bruijn, Catherina H.Z. Li, Carel B. Hoyng, Christian Gilissen, Lisenka E.L.M. Vissers, Frans P.M. Cremers, Hannie Kremer, Erwin van Wijk, Susanne Roosing
Publikováno v:
HGG Advances, Vol 4, Iss 2, Pp 100181- (2023)
Summary: A significant number of individuals with a rare disorder such as Usher syndrome (USH) and (non-)syndromic autosomal recessive retinitis pigmentosa (arRP) remain genetically unexplained. Therefore, we assessed subjects suspected of USH2A-asso
Externí odkaz:
https://doaj.org/article/3a1d6bbbc0b84a3f9409fc1710e756ce
Autor:
L. Inge Wilms, Simon D. Nielsen
Publikováno v:
Frontiers in Psychology
Frontiers in Psychology, Vol 5 (2015)
Frontiers in Psychology, Vol 5 (2015)
We examined the effects of normal ageing on visual cognition in a sample of 112 healthy adults aged 60-75. A testbattery was designed to capture high-level measures of visual working memory and low-level measures of visuospatial attention and memory.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a64a3a803d8652cb8d8960d82a73cef
http://europepmc.org/articles/PMC4295434
http://europepmc.org/articles/PMC4295434
Autor:
J. Jason, K. L. Inge
Publikováno v:
Scandinavian Journal of Immunology. 53:259-267
To investigate whether human immunodeficiency virus (HIV)-1 and HIV-1 antigens modulate surface and cytoplasmic CD8 or CD3, as well as CD4, we used cell permeabilization reagents, surface/cytoplasmic fluorescent staining, multiparameter flow cytometr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::409894b9ce4855892bc449a0d6e85191
https://doi.org/10.1046/j.1365-3083.2001.00871.x
https://doi.org/10.1046/j.1365-3083.2001.00871.x
Autor:
Zeinab Fadaie, Laura Whelan, Tamar Ben-Yosef, Adrian Dockery, Zelia Corradi, Christian Gilissen, Lonneke Haer-Wigman, Jordi Corominas, Galuh D. N. Astuti, Laura de Rooij, L. Ingeborgh van den Born, Caroline C. W. Klaver, Carel B. Hoyng, Niamh Wynne, Emma S. Duignan, Paul F. Kenna, Frans P. M. Cremers, G. Jane Farrar, Susanne Roosing
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-11 (2021)
Abstract Inherited retinal diseases (IRDs) are a major cause of visual impairment. These clinically heterogeneous disorders are caused by pathogenic variants in more than 270 genes. As 30–40% of cases remain genetically unexplained following conven
Externí odkaz:
https://doaj.org/article/134ff20611604419a17d57355443d530