Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Gert van Cappellen"'
1
Synaptic vesicle dynamic changes in a model of fragile X
Autor: Jantine A. C. Broek, Sabine Bahn, Elize D. Haasdijk, Rob Willemsen, Heleen M van 't Spijker, Sureyya Ozcan, Zhanmin Lin, Adriaan B. Houtsmuller, H. Martijn de Gruiter, David Cox, Gert van Cappellen, Chris I. De Zeeuw
Publikováno v: Molecular Autism, 7. BioMed Central Ltd.
Molecular Autism
Molecular Autism, 7. BioMed Central
Background Fragile X syndrome (FXS) is a single-gene disorder that is the most common heritable cause of intellectual disability and the most frequent monogenic cause of autism spectrum disorders (ASD). FXS is caused by an expansion of trinucleotide
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::008fcd2235abf94ccafe9437488e661d
https://doi.org/10.1186/s13229-016-0080-1
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2
Transporters involved in the hepatic uptake of (99m)Tc-mebrofenin and indocyanine green
Autor: Michal Heger, Bruno Stieger, Gert van Cappellen, Gerd A. Kullak-Ublick, Stephanie Häusler, Rolf Hesselmann, Thomas M. van Gulik, Tessa M van Ginhoven, Wilmar de Graaf, Roelof J. Bennink
Publikováno v: Journal of hepatology
Journal of Hepatology, 54(4), 738-745. Elsevier
Journal of hepatology, 54(4), 738-745. Elsevier
Background & Aims: (99m)Tc-mebrofenin hepatobiliary scintigraphy (HBS) and the indocyanine green (ICG) clearance test are used for the assessment of hepatic function before and after liver surgery. The hepatic uptake of (99m)Tc-mebrofenin and ICG is
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2571a13dd7e404534e1ef878e5ec7ae1
http://www.ncbi.nlm.nih.gov/pubmed/21163547
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3
Transport kinetics of FMRP containing the I304N mutation of severe fragile X syndrome in neurites of living rat PC12 cells
Autor: Sandra van 't Padje, Ben A. Oostra, Mariëtte Schrier, Gert van Cappellen, Maria Rife, Lies-Anne Severijnen, Surya A. Reis, Rob Willemsen
Publikováno v: Experimental Neurology, 189, 343-353. Academic Press
Lack of fragile X mental retardation protein (FMRP) causes the fragile X syndrome, a common form of inherited mental retardation. The syndrome usually results from the expansion of a CGG repeat in the FMR1 gene with consequent transcriptional silenci
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b849cc80b81b70c760b3f979e32215f
https://pure.eur.nl/en/publications/8be8df22-db38-407d-aa98-5c35bcdd4ab4
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4
Centrosomes split in the presence of impaired DNA integrity during mitosis
Autor: Willy Lemstra, Gert van Cappellen, Ody C. M. Sibon, Engbert H. Blaauw, Harm H. Kampinga, Henderika M.J. Hut
Publikováno v: Molecular Biology of the Cell, 14, 1993-2004. American Society for Cell Biology
Molecular Biology of the Cell, 14(5), 1993-2004. AMER SOC CELL BIOLOGY
A well-established function of centrosomes is their role in accomplishing a successful mitosis that gives rise to a pair of identical daughter cells. We recently showed that DNA replication defects and DNA damage in Drosophila embryos trigger centros
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71aac21c17ad6851c53ec0d6cf1a63ca
https://doi.org/10.1091/mbc.e02-08-0510
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5
Visualization of Microtubule Growth in Cultured Neurons via the Use of EB3-GFP (End-Binding Protein 3-Green Fluorescent Protein)
Autor: Anna Akhmanova, Gert van Cappellen, Gideon Lansbergen, Tatiana Stepanova, Niels Galjart, Chris I. De Zeeuw, Jenny Slemmer, Frank Grosveld, Casper C. Hoogenraad, Bjorn R. Dortland
Publikováno v: Journal of Neuroscience, 23(7), 2655-2664. Society for Neuroscience
Several microtubule binding proteins, including CLIP-170 (cytoplasmic linker protein-170), CLIP-115, and EB1 (end-binding protein 1), have been shown to associate specifically with the ends of growing microtubules in non-neuronal cells, thereby regul
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfbd42746eca854616ff017949e77d9f
https://doi.org/10.1523/jneurosci.23-07-02655.2003
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6
Loss of HR6B Ubiquitin-Conjugating Activity Results in Damaged Synaptonemal Complex Structure and Increased Crossing-Over Frequency during the Male Meiotic Prophase
Autor: Jan H.J. Hoeijmakers, Evelyne Wassenaar, Jos W. Hoogerbrugge, J. T. M. Vreeburg, Willy M. Baarends, Gert van Cappellen, J. Anton Grootegoed, M. P. Ooms, Henk P. Roest
Publikováno v: Molecular and Cellular Biology, 23(4), 1151-1162. American Society for Microbiology
The ubiquitin-conjugating enzymes HR6A and HR6B are the two mammalian homologs of Saccharomyces cerevisiae RAD6. In yeast, RAD6 plays an important role in postreplication DNA repair and in sporulation. HR6B knockout mice are viable, but spermatogenes
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60b406f37e251351f2eb235027dfe54d
https://doi.org/10.1128/mcb.23.4.1151-1162.2003
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7
Transport of Fragile X Mental Retardation Protein via Granules in Neurites of PC12 Cells
Autor: Lies-Anne Severijnen, Ben A. Oostra, Yolanda De Diego Otero, Rob Willemsen, Gert van Cappellen, Mariëtte Schrier
Publikováno v: Molecular and Cellular Biology, 22(23), 8332-8341. American Society for Microbiology
Lack of fragile X mental retardation protein (FMRP) causes fragile X syndrome, a common form of inherited mental retardation. FMRP is an RNA binding protein thought to be involved in translation efficiency and/or trafficking of certain mRNAs. Recentl
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba44743af8224bb3091382005ad2b457
https://doi.org/10.1128/mcb.22.23.8332-8341.2002
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