Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Anita Bonne"'
Autor:
Lutgarde Govaerts, Nicoline Hoogerbrugge, Eugène T P Verwiel, Eveline J. Kamping, Eric F.P.M. Schoenmakers, Roland P. Kuiper, Evelyne Lerut, Lilian Vreede, Eamonn R. Maher, Femke van Erp, Anita Bonne, Lianne van Kempen, Maria Debiec-Rychter, Ad Geurts van Kessel, Ramprasath Venkatachalam, Chris Ricketts
Publikováno v:
Cancer Genetics and Cytogenetics, 195, 105-11
Cancer Genetics and Cytogenetics, 195, 2, pp. 105-11
Cancer Genetics & Cytogenetics, 195(2), 105-111. Elsevier Inc.
Cancer Genetics and Cytogenetics, 195, 2, pp. 105-11
Cancer Genetics & Cytogenetics, 195(2), 105-111. Elsevier Inc.
Contains fulltext : 81144.pdf (Publisher’s version ) (Closed access) FBXW7 (alias CDC4) is a p53-dependent tumor suppressor gene that exhibits mutations or deletions in a variety of human tumors. Mutation or deletion of the FBXW7 gene has been asso
Autor:
J.M.M. Gijtenbeek, Bram Jacobs, Jacques W.M. Lenders, Pieter Wesseling, Anita Bonne, Benno Küsters, Judith W. M. Jeuken, Sandra H.E. Boots-Sprenger
Publikováno v:
Diagnostic Molecular Pathology, 14, 2, pp. 115-20
Diagnostic Molecular Pathology, 14, 115-20
Diagnostic Molecular Pathology, 14, 115-20
Contains fulltext : 48831.pdf (Publisher’s version ) (Closed access) Von Hippel-Lindau (VHL) disease is an autosomal dominant tumor syndrome, in which hemangioblastomas (HBs), clear cell renal cell carcinomas (RCCs), and pheochromocytomas are the m
Autor:
Vaclav Zidek, V. Bila, Hein A. van Lith, Bert F. M. Van Zutphen, Vlastimil Kostka, Michal Pravenec, Anita Bonne, Alena Musilova, Drahomira Krenova, Maria den Bieman, Vladimir Kren, G. F. Gillissen
Publikováno v:
Biochemical Genetics. 41:77-89
The amplified fragment length polymorphism (AFLP) technique has been used to enhance marker density in a large set of recombinant inbred strains (H x B and B x H) derived from a spontaneously hypertensive rat (SHR/OlaIpcv) and a Brown-Norway (BN.lx/C
Autor:
G. F. Gillissen, Michal Pravenec, Thomas Kreitler, Hein A. van Lith, Anita Bonne, Claudia Gosele, Vladimir Kren, Maria den Bieman, Bert F. M. Van Zutphen
Publikováno v:
Molecular Biology Reports. 30:173-176
The fatty acid binding protein 6 gene (Fabp6) codes for ileal lipid binding protein. After sequencing of rat Fabp6, the gene was localized in a radiation hybrid (RH) map on chromosome 10. An intronless Fabp6 segment was found in four related rat inbr
Autor:
A. C. Beynen, Anita Bonne, L.F.M. van Zutphen, B.A. van Oost, I.D. de Wolf, H.A. van Lith, X.M. Fielmich-Bouman
Publikováno v:
Experimental Biology and Medicine. 227:529-534
Significant differences in liver copper content have been observed between rat inbred strains. To define loci controlling this trait, the offspring (n = 190) from an (LEW/OlaHsd × BC/CpbU) F2-intercross was genetically analyzed. From each F2animal,
Publikováno v:
Cytogenetic and Genome Research. 97:183-186
Several genes involved in biosynthesis, transport or metabolism of cholesterol have been localized on rat chromosomes by using a radiation hybrid (RH) panel. The genes, coding for squalene epoxidase (Sqle), mevalonate kinase (Mvk), and farnesyl dipho
Autor:
Marie Jáchymová, Vladimir Kren, Hein A. van Lith, M Pravenec, Bert F. M. Van Zutphen, Drahomira Krenova, Milada Sladká, Blanka Míková, Yun-Fai Chris Lau, N. Qi, Vaclav Zidek, Anita Bonne, Elizabeth St. Lezin, Karel Horky
Publikováno v:
Hypertension. 37:1147-1152
Abstract —Previous studies with chromosome-Y consomic strains of spontaneously hypertensive rats (SHR) and Wistar-Kyoto rats suggest that a quantitative trait locus for blood pressure regulation exists on chromosome Y. To test this hypothesis in th
Publikováno v:
DNA Sequence. 12:285-287
Part of the nucleotide sequence of the Lipg gene in the rat was established using primers based on the mRNA sequence described in the mouse. The rat intron sequence served as a template for designing primers for the specific amplification of rat Lipg
Autor:
Lilian Vreede, Marc J. Eleveld, Corine Jansen, Conny M.A. van Ravenswaaij, Anita Bonne, Danielle Bodmer, Eric F.P.M. Schoenmakers, Ferake van Erp, Roland P. Kuiper, Nicoline Hoogerbrugge, Ger J. A. Arkesteijn, Ad Geurts van Kessel
Publikováno v:
Cancer Genetics and Cytogenetics, 179, 1, pp. 11-8
Cancer Genetics and Cytogenetics, 179(1), 11-18. ELSEVIER SCIENCE INC
Cancer Genetics and Cytogenetics, 179, 11-8
Cancer Genetics and Cytogenetics, 179(1), 11-18. ELSEVIER SCIENCE INC
Cancer Genetics and Cytogenetics, 179, 11-8
Contains fulltext : 52260.pdf (Publisher’s version ) (Closed access) Our group and others had previously developed a high throughput procedure to map translocation breakpoints using chromosome flow sorting in conjunction with microarray-based compa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e130d871183c3a0a8729b52684cd8c2
https://hdl.handle.net/2066/52260
https://hdl.handle.net/2066/52260
Autor:
Nanna Møller Sørensen, Morten Kobaek-Larsen, Anita Bonne, Bert van Zutphen, Claus Fenger, Karsten Kristiansen, Merel Ritskes-Hoitinga
Publikováno v:
University of Southern Denmark
The aim of the study reported here was to investigate whether the azoxymethane (AOM)-induced colon cancer rat model mimics the human situation with regard to microsatellite stability, changes in expression of beta-catenin, and/or changes in the seque