Zobrazeno 1 - 10 of 23 pro vyhledávání: '"Marcel Mulder"'
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On the electrochemistry of an anode stack for all-solid-state 3D-integrated batteries
Autor: Johan Hendrik Klootwijk, T. van Dongen, Petrus H. L. Notten, Marcel Mulder, Loïc Baggetto, J.F.M. Oudenhoven, M.H.J.M. de Croon, Rogier Adrianus Henrica Niessen
Publikováno v: Journal of Power Sources, 189(1), 402-410. Elsevier
This paper will report on the electrochemical and material characterization of a potential planar anode stack for all-solid-state 3D-integrated batteries. The first element of the stack is the silicon substrate. On top of silicon, a Li diffusion barr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e09021224e43a354ced2fd70f763735
https://doi.org/10.1016/j.jpowsour.2008.07.076
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3
The human leukocyte antigen region and colorectal cancer risk
Autor: Jan H. Kleibeuker, Marijke Niens, Elisabeth G.E. de Vries, Robert M.W. Hofstra, Marcel Mulder, Rolf H. Sijmons, Gerrit van der Steege, Gerard J. te Meerman, Mirjam M. de Jong, Marcel Bruinenberg, Winette T. A. van der Graaf, Michael Schaapveld, Ilja M. Nolte
Publikováno v: DISEASES OF THE COLON & RECTUM, 48(2), 303-306. LIPPINCOTT WILLIAMS & WILKINS
PURPOSE: Recently, we found a certain haplotype in the human leukocyte antigen Class III subregion to be associated with breast cancer. Epidemiologic studies have shown that breast cancer and colorectal cancer have several risk factors in common. In
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::731b45a80ccdccd9b24b5540dfefd201
https://research.rug.nl/en/publications/772a625a-d397-4450-b808-d2544064392c
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4
Analysis of Cell-Stabilizing Additives in Low-Density Polyethylene Foams Using Low-Frequency Dielectric Spectroscopy
Autor: Warner J. Nauta, Matthias Wessling, Paul A. M. Steeman, Ronald H. S. Jansen, Marcel Mulder, C. Bostoen, J.N. Barsema
Publikováno v: Macromolecules, 36(18), 6817-6823. American Chemical Society
Addition of low amounts of additives is necessary to guarantee dimensional stability of low-density flexible polyethylene foam after extrusion. It is expected that the additives form a layer on the foam cell walls. However, the physical phenomena res
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f65c745378c44f2c6e63a54e1933fa4
https://doi.org/10.1021/ma025947v
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5
Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy
Autor: Tessa Homfray, Jeroen F. van der Heijden, Hennie Bikker, Marcel Mulder, Jan D. H. Jongbloed, Anneke M. van Mil, Judith A. Groeneweg, Arthur A.M. Wilde, Arjan C. Houweling, J. Peter van Tintelen, Jan G. Post, Richard N.W. Hauer, Jasper J. van der Smagt, Amber Ummels, Dennis Dooijes, Arif Elvan
Publikováno v: Heart rhythm, 11(11), 2010-2017. Elsevier
Heart Rhythm, 11(11), 2010-2017. Elsevier
Groeneweg, J A, Ummels, A, Mulder, M, Bikker, H, van der Smagt, J J, van Mil, A M, Homfray, T, Post, J G, Elvan, A, van der Heijden, J F, Houweling, A C, Jongbloed, J D, Wilde, A A, van Tintelen, J, Hauer, R N & Dooijes, D 2014, ' Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy ', Heart Rhythm, vol. 11, no. 11, pp. 2010-2017 . https://doi.org/10.1016/j.hrthm.2014.07.041
Heart Rhythm, 11(11), 2010-2017. ELSEVIER SCIENCE INC
Heart Rhythm, 11(11), 2010-2017
BACKGROUND Interpretation of genetic screening results in arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) often is difficult. Pathogenicity of variants with uncertain clinical significance may be predicted by software algorithms. H
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13dd7fd5a0b6045b169ddd54a0a2901a
https://pubmed.ncbi.nlm.nih.gov/25087486
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6
The ubiquitin-activating enzyme E1-like protein in lung cancer cell lines
Autor: Klaas Kok, Soesja W. Hu, Pamela M.J. McLaughlin, Marcel H. J. Ruiters, Charles H.C.M. Buys, Marcel Mulder, Marja G. L. Brinker, Wijnand Helfrich, Lou F. M. H. de Leij
Publikováno v: International Journal of Cancer. 85:871-876
The UBE1L gene isolated from the chromosome 3p21 region has an extremely reduced level of mRNA in lung cancer. Sequence analysis showed a 45% homology to the human ubiquitin-activating enzyme E1 at the amino acid level. To further characterize the pr
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1a3be4234aaa8ca196163e767c1b778e
https://doi.org/10.1002/(sici)1097-0215(20000315)85:6<871::aid-ijc22>3.0.co
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7
Elektronická kniha
Basic Principles of Membrane Technology
Autor: Marcel Mulder
III. 2 Preparation of synthetic membranes 72 III. 3 Phase inversion membranes 75 III. 3. 1 Preparation by evaporation 76 III. 3. 2 Precipitation. from the vapour phase 76 III. 3. 3 Precipitation by controlled evaporation 76 Thermal precipitation 76 I
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8
No association between the Arg201Gly polymorphism of the DCC gene and colorectal cancer
Autor: G. J. Te Meerman, W.T.A. van der Graaf, M M de Jong, R. M. W. Hofstra, Marcel Bruinenberg, Michael Schaapveld, Ilja M. Nolte, Jan H. Kleibeuker, E.G.E. de Vries, G van der Steege, Rolf H. Sijmons, Marcel Mulder
Publikováno v: Digestive and Liver Disease, 36(12), 821-823. ELSEVIER SCIENCE INC
Background and aims. In one small study, the DCC Arg201Gly polymorphism has been observed more frequently in colorectal cancer cases compared with controls. We wondered whether these results could be replicated in a much larger study.Methodology. The
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3905f33009cb2b2146f7a240dcc983a9
https://doi.org/10.1016/j.dld.2004.07.011
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9
Search for copy number alterations in the MEFV gene using multiplex ligation probe amplification, experience from three diagnostic centres
Autor: Cécile Ritorre, Laurent Philibert, Claire de la Chapelle, Marielle E. van Gijn, Sylvie Grandemange, Johannes K Ploos van Amstel, Joost Frenkel, Michiel van der Wielen, Marjolein Kriek, Stéphan Soler, Marcel Mulder, Egbert Bakker, Isabelle Touitou
Publikováno v: European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2008, 16 (11), pp.1404-1406. ⟨10.1038/ejhg.2008.135⟩
Familial mediterranean fever (FMF) is a hereditary autoinflammatory autosomal recessive disease caused by mutations in the MEFV gene. Despite the identification of many disease associated MEFV mutations, often the clinical diagnosis cannot be genetic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d8111f69e61d1997f5fa8fc1d09f03c
https://pubmed.ncbi.nlm.nih.gov/18648395
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10
Colorectal cancer and the CHEK2 1100delC mutation
Autor: Gerrit van der Steege, Renee C. Niessen, Elisabeth G.E. de Vries, Gerard J. te Meerman, Jan H. Kleibeuker, Rolf H. Sijmons, Maran J.W. Berends, Robert M.W. Hofstra, Mirjam M. de Jong, Marcel Bruinenberg, Winette T. A. van der Graaf, Michael Schaapveld, Ilja M. Nolte, Marcel Mulder
Publikováno v: GENES CHROMOSOMES & CANCER, 43(4), 377-382. Wiley
The CHEK2 1100delC mutation was recently identified as a low-penetrance breast cancer susceptibility allele. The mutation occurred more frequently in families with clustering of breast and colorectal cancers (CRCs) than in families with clustering of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::085dc8f944afdce8e0848667ed6edbad
https://research.rug.nl/en/publications/5c554f3a-96c9-4871-9651-e23efe0f9373
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