Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Joachim De Schrijver"'
Autor:
Els M Gielis, Charlie Beirnaert, Amélie Dendooven, Pieter Meysman, Kris Laukens, Joachim De Schrijver, Steven Van Laecke, Wim Van Biesen, Marie-Paule Emonds, Benedicte Y De Winter, Jean-Louis Bosmans, Jurgen Del Favero, Daniel Abramowicz, Kristien J Ledeganck
Publikováno v:
PLoS ONE, Vol 13, Iss 12, p e0208207 (2018)
BackgroundAfter transplantation, cell-free DNA derived from the donor organ (ddcfDNA) can be detected in the recipient's circulation. We aimed to quantify ddcfDNA levels in plasma of kidney transplant recipients thereby investigating the kinetics of
Externí odkaz:
https://doaj.org/article/7e7af26579fd4a578bb50bfc39391899
Autor:
Kim De Leeneer, Joachim De Schrijver, Lieven Clement, Machteld Baetens, Steve Lefever, Sarah De Keulenaer, Wim Van Criekinge, Dieter Deforce, Filip Van Nieuwerburgh, Sofie Bekaert, Filip Pattyn, Bram De Wilde, Paul Coucke, Jo Vandesompele, Kathleen Claes, Jan Hellemans
Publikováno v:
PLoS ONE, Vol 6, Iss 9, p e25531 (2011)
Despite improvements in terms of sequence quality and price per basepair, Sanger sequencing remains restricted to screening of individual disease genes. The development of massively parallel sequencing (MPS) technologies heralded an era in which mole
Externí odkaz:
https://doaj.org/article/1c7ea325314c4c078c8c55e56b1d228f
Autor:
Akanksha Khare, Anne Bergstrom Lucas, Joachim de-Schrijver, Manjula Aliminati, Hanjun Shin, Linus Forsmark, Barbara Novak, Jeroen Crappe, Michael Ruvolo
Publikováno v:
Cancer Research. 82:2941-2941
Background: The current standard for genomic profiling of cancer tissues relies upon multiple technologies to aid in tumor characterization. Here we describe a comprehensive genomic profiling pan-cancer assay that detects single nucleotide polymorphi
Autor:
Kris Laukens, Joachim De Schrijver, Amélie Dendooven, Benedicte Y. De Winter, Els M. Gielis, Daniel Abramowicz, Marie-Paule Emonds, Wim Van Biesen, Pieter Meysman, Jean-Louis Bosmans, Steven Van Laecke, Kristien J. Ledeganck, Charlie Beirnaert, Jurgen Del Favero
Publikováno v:
Nephrology, dialysis, transplantation
Background After transplantation, cell-free deoxyribonucleic acid (DNA) derived from the donor organ (ddcfDNA) can be detected in the recipient’s circulation. We aimed to investigate the role of plasma ddcfDNA as biomarker for acute kidney rejectio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b125df7690f42a5f752933b0d42b089f
https://lirias.kuleuven.be/handle/123456789/658855
https://lirias.kuleuven.be/handle/123456789/658855
Autor:
Frederiek-Maarten Kerckhof, Pieter Van den Abbeele, Marc Bracke, Barbara Vanhoecke, Tom Van de Wiele, Charlotte Grootaert, Mireille Van Gele, Tine De Ryck, Joachim De Schrijver, Simon Swift, Laura Jaspaert
Publikováno v:
Applied Microbiology and Biotechnology. 98:6831-6846
Crosstalk between the human host and its microbiota is reported to influence various diseases such as mucositis. Fundamental research in this area is however complicated by the time frame restrictions during which host-microbe interactions can be stu
Autor:
Vera Wewer, Wim Van Criekinge, Nico De Storme, Peter Dörmann, Danny Geelen, Joachim De Schrijver
Publikováno v:
PLANT CELL
In sexually reproducing plants, the meiocyte-producing archesporal cell lineage is maintained at the diploid state to consolidate the formation of haploid gametes. In search of molecular factors that regulate this ploidy consistency, we isolated an A
Autor:
Tom Van de Wiele, Frederiek-Maarten Kerckhof, Joachim De Schrijver, Marc Bracke, Tine De Ryck, Barbara Vanhoecke, Tom Boterberg
Publikováno v:
JOURNAL OF NUCLEAR MEDICINE AND RADIATION THERAPY
The impact of irradiation on host-microbe crosstalk is still underexplored. By use of an in vitro oral mucosa model, we show an impact of irradiation on epithelial wound healing depending on the microbial composition and functionality. 454-pyrosequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::515e1c1d87c5694d50375117f22f01a1
https://hdl.handle.net/1854/LU-7017244
https://hdl.handle.net/1854/LU-7017244
Autor:
Guy Van Camp, Jean-Pierre Renard, Paul Coucke, Jan Hellemans, Dieter Deforce, Jo Vandesompele, Steve Lefever, Joachim De Schrijver, Wim Van Criekinge, Hendrik Van de Voorde, Filip Pattyn, Sarah De Keulenaer, Daisy Flamez, Mohammad Amin Tabatabaiefar, Bieke Scharlaken, Filip Van Nieuwerburgh, Sofie Bekaert
Publikováno v:
BMC MEDICAL GENOMICS
BMC Medical Genomics, Vol 5, Iss 1, p 17 (2012)
BMC Medical Genomics
BMC Medical Genomics, Vol 5, Iss 1, p 17 (2012)
BMC Medical Genomics
Background Hereditary hearing loss (HL) can originate from mutations in one of many genes involved in the complex process of hearing. Identification of the genetic defects in patients is currently labor intensive and expensive. While screening with S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34fa53bcb0817090c655f418eed5771c
https://biblio.ugent.be/publication/3070495/file/3070512
https://biblio.ugent.be/publication/3070495/file/3070512
Autor:
Anne De Paepe, Jan Hellemans, Joachim De Schrijver, Wim Van Criekinge, Kathleen Claes, Bruce Poppe, Kim De Leeneer, Machteld Baetens, Paul Coucke
Publikováno v:
Human Mutation
Human Mutation, Wiley, 2011, 32 (3), pp.335. ⟨10.1002/humu.21428⟩
Human Mutation, Wiley, 2011, 32 (3), pp.335. ⟨10.1002/humu.21428⟩
International audience; This study describes how the new massive parallel sequencing technology can be implemented in a diagnostic setting by proof of concept studies for the breast cancer susceptibility genes (BRCA1&2). Throughput was maximized by i
Autor:
Olivier Thas, Rafael A. Irizarry, Lieven Clement, Joachim De Schrijver, Wim Van Criekinge, Kristof De Beuf
Publikováno v:
BMC Bioinformatics
BMC Bioinformatics, Vol 13, Iss 1, p 303 (2012)
BMC BIOINFORMATICS
BMC Bioinformatics, Vol 13, Iss 1, p 303 (2012)
BMC BIOINFORMATICS
Background: 454 pyrosequencing is a commonly used massively parallel DNA sequencing technology with a wide variety of application fields such as epigenetics, metagenomics and transcriptomics. A well-known problem of this platform is its sensitivity t