Zobrazeno 1 - 10
of 11
pro vyhledávání: '"R F, Suijkerbuijk"'
Autor:
L. F. Johansson, E. N. de Boer, H. A. de Weerd, F. van Dijk, M. G. Elferink, G. H. Schuring-Blom, R. F. Suijkerbuijk, R. J. Sinke, G. J. te Meerman, R. H. Sijmons, M. A. Swertz, B. Sikkema-Raddatz
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-11 (2017)
Abstract Non-invasive prenatal testing (NIPT) of cell-free DNA in maternal plasma, which is a mixture of maternal DNA and a low percentage of fetal DNA, can detect fetal aneuploidies using massively parallel sequencing. Because of the low percentage
Externí odkaz:
https://doaj.org/article/50fe59706dee446cb5379772bb6c48fa
Preimplantation genetic diagnosis for X;autosome translocations: lessons from a case of misdiagnosis
Autor:
Jolande A. Land, E. C. Dul, van Conny Ravenswaaij-Arts, R. F. Suijkerbuijk, Edith Coonen, B. Reuters, J. van Echten-Arends
Publikováno v:
Human Reproduction, 28(11), 3141-3145. Oxford University Press
Preimplantation genetic diagnosis (PGD) is offered to couples carrying a reciprocal translocation in an attempt to increase their chance of phenotypically normal offspring. For the selection of embryos that are balanced for the translocation chromoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfa0daaf25527b4e1e74e6b759a8b910
https://research.rug.nl/en/publications/8a037700-6f3b-4529-aa4d-56854fdd58cc
https://research.rug.nl/en/publications/8a037700-6f3b-4529-aa4d-56854fdd58cc
Autor:
A, Simons, I M, Janssen, R F, Suijkerbuijk, R P, Veth, M, Pruszczynski, C A, Hulsbergen-van de Kaa, S, du Manoir, A, Geurts van Kessel
Publikováno v:
Genes, chromosomescancer. 20(2)
Comparative genomic hybridization analysis of a primary osteosarcoma and its metastasis revealed two regions of DNA amplification, one at 17p11.2-12 and one at 19q12-13. Subsequent representational difference analysis of the primary tumor resulted in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::aea9388eb70b73ec380fdef4a4c58eca
https://pubmed.ncbi.nlm.nih.gov/9331570
https://pubmed.ncbi.nlm.nih.gov/9331570
Reviews of chromosome studies in urological tumors. III. Cytogenetics and genes in testicular tumors
Publikováno v:
The Journal of urology. 155(5)
We reviewed available cytogenetic and molecular findings in testicular germ cell tumors, and their possible application to clinical, pathological and basic parameters.Findings in the literature on testicular germ cell tumors as well as those from our
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fd6ca11479b34aec93f033abe067a3a9
https://pubmed.ncbi.nlm.nih.gov/8627820
https://pubmed.ncbi.nlm.nih.gov/8627820
Autor:
D, Olde Weghuis, M E, Stoepker, B, de Leeuw, E, van den Berg, R F, Suijkerbuijk, W M, Molenaar, B, de Jong, A, Geurts van Kessel
Publikováno v:
Genes, chromosomescancer. 9(4)
The initial cytogenetic analysis of a biphasic synovial sarcoma revealed complex anomalies involving six different chromosomes: 46,Y,t(X;18;5;4)(p11;q11;p13;q12),t(2;5)(q35;q11). After fluorescence in situ hybridization (FISH) analysis, using chromos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ea7d41ba3b39cdbd2b0f229f5432c83
https://pubmed.ncbi.nlm.nih.gov/7519051
https://pubmed.ncbi.nlm.nih.gov/7519051
Autor:
T W, de Bruin, R M, Slater, R, Defferrari, A, Geurts van Kessel, R F, Suijkerbuijk, G, Jansen, B, de Jong, J W, Oosterhuis
Publikováno v:
Cancer research. 54(6)
We report the chromosomal characteristics of a recurrent pineal non-seminomatous germ cell tumor in a 16-year-old male patient. This non-seminomatous tumor had the following components: embryonal carcinoma, teratoma, yolk sac tumor, and trophoblastic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::a5cfcc4d60bdb7b3db67e31fe68e68af
https://pubmed.ncbi.nlm.nih.gov/8137260
https://pubmed.ncbi.nlm.nih.gov/8137260
Publikováno v:
Cytogenetics and cell genetics. 67(1)
The rat N-ras protooncogene has been assigned to chromosome 2q34 by fluorescence in situ hybridization on rat metaphase chromosomes. This was accomplished using two recently isolated genomic clones with a length of 8.2 and 4.1 kb.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::538c922a83218357fbf81518b6477968
https://pubmed.ncbi.nlm.nih.gov/8187546
https://pubmed.ncbi.nlm.nih.gov/8187546
Autor:
R. J. Sinke, B. de Leeuw, H. A. P. Janssen, D. Olde Weghuis, R. F. Suijkerbuijk, A. M. Meloni, S. Gilgenkrantz, W. Berger, H. H. Ropers, A. A. Sandberg, A. Geurts van Kessel
Publikováno v:
Human genetics. 92(3)
A series of thirteen different DNA markers was mapped relative to papillary renal cell carcinoma- and synovial sarcoma-associated translocation breakpoints in Xp11.2 using a panel of tumor-derived somatic cell hybrids in conjunction with Southern blo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82ca1acec291e9a3d5373fc7872f8252
https://pubmed.ncbi.nlm.nih.gov/8406438
https://pubmed.ncbi.nlm.nih.gov/8406438
Autor:
B, de Leeuw, R F, Suijkerbuijk, M, Balemans, R J, Sinke, B, de Jong, W M, Molenaar, A M, Meloni, A A, Sandberg, M, Geraghty, M, Hofker
Publikováno v:
Oncogene. 8(6)
In a previous study we localized the synovial sarcoma-associated t(X;18)(p11;q11) breakpoint within the ornithine aminotransferase-like 1 (OATL1) cluster on the X chromosome. This localization was delineated from both somatic cell hybrid and fluoresc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31b1cf47213f06c9cfab3dae003389f2
https://pubmed.ncbi.nlm.nih.gov/8389029
https://pubmed.ncbi.nlm.nih.gov/8389029
Autor:
B. De Leeuw, W. Berger, R. J. Sinke, R. F. Suijkerbuijk, S. Gilgenkrantz, M. T. Geraghty, D. Valle, A. P. Monaco, H. Lehrach, H. H. Ropers, A. Geurts Van Kessel
Publikováno v:
GENES CHROMOSOMES & CANCER, 6(3), 182-189. Wiley
A somatic cell hybrid containing the synovial sarcoma-associated t(X;18)(p11.2;q11.2) derivative (der(X)) chromosome was used to characterize the translocation breakpoint region on the X chromosome. By using Southern hybridization of DNA from this de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::510852df383fe001ba3ca1524e95c889
https://research.rug.nl/en/publications/c8803326-7ef3-4b56-a21a-8c651e0c1a62
https://research.rug.nl/en/publications/c8803326-7ef3-4b56-a21a-8c651e0c1a62