Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Dieter De Coninck"'
Autor:
Sien De Koster, Moniek Ringenier, Basil Britto Xavier, Christine Lammens, Dieter De Coninck, Katrien De Bruyne, Klaas Mensaert, Marjolein Kluytmans-van den Bergh, Jan Kluytmans, Jeroen Dewulf, Herman Goossens, on behalf of the i-4-1-Health Study Group
Publikováno v:
Frontiers in Microbiology, Vol 14 (2023)
BackgroundThe increasing number of infections caused by Escherichia coli resistant to clinically important antibiotics is a global concern for human and animal health. High overall levels of extended-spectrum beta-lactamase (ESBL)-producing and cipro
Externí odkaz:
https://doaj.org/article/9a2ae29d379948eda5ecb2775f152e26
Autor:
Bibi C. G. C. Slingerland, Margreet C. Vos, Willeke Bras, René F. Kornelisse, Dieter De Coninck, Alex van Belkum, Irwin K. M. Reiss, Wil H. F. Goessens, Corné H. W. Klaassen, Nelianne J. Verkaik
Publikováno v:
Antimicrobial Resistance and Infection Control, Vol 9, Iss 1, Pp 1-7 (2020)
Abstract Background Neonatal Staphylococcus aureus (S. aureus) bacteremia is an important cause of morbidity and mortality. In this study, we examined whether methicillin-susceptible S. aureus (MSSA) transmission and genetic makeup contribute to the
Externí odkaz:
https://doaj.org/article/fb19f1ffadd048cbabc1607791e81e32
Autor:
Lieselot Deleye, Yannick Gansemans, Dieter De Coninck, Filip Van Nieuwerburgh, Dieter Deforce
Publikováno v:
PLoS ONE, Vol 13, Iss 4, p e0196334 (2018)
Single Gene Disorders (SGD) are still routinely diagnosed using PCR-based assays that need to be developed and validated for each individual disease-specific gene fragment. The TruSight One sequencing panel currently covers 12 Mb of genomic content,
Externí odkaz:
https://doaj.org/article/b9fb13ddc3c24b17adcfaff67a3f5420
Autor:
Paul H. M. Savelkoul, Lieke B. van Alphen, Klaas Mensaert, Dieter De Coninck, Herman Goossens, Christian J. P. A. Hoebe, Natascha Perales Selva, Christine Lammens, Sien De Koster, Casper Jamin, Stefanie van Koeveringe, Katrien De Bruyne
Publikováno v:
Microbial Genomics, 7(7):000567. Microbiology Society
Microbial Genomics
Microbial Genomics
Whole-genome sequencing (WGS) is becoming the de facto standard for bacterial typing and outbreak surveillance of resistant bacterial pathogens. However, interoperability for WGS of bacterial outbreaks is poorly understood. We hypothesized that harmo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5caf27a9ac2ebcd188bfea9d39dc54e5
https://cris.maastrichtuniversity.nl/en/publications/31c5aaa4-a369-4a10-8f63-42f8fcee33ce
https://cris.maastrichtuniversity.nl/en/publications/31c5aaa4-a369-4a10-8f63-42f8fcee33ce
Autor:
Dieter De Coninck, A. Van Soom, Mina Popovic, E Sutherland, Björn Heindryckx, J Van de Sompele, M Van der Jeught, Laurentijn Tilleman, G Duggal, P. De Sutter, S M Chuva de Sousa Lopes, Jasin Taelman, Pieter Mestdagh, Sylvie Lierman, Björn Menten, Dieter Deforce, F. Van Nieuwerburgh, Luc Peelman, Sharat Warrier
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-10 (2017)
Nature Communications
NATURE COMMUNICATIONS
Nature Communications, 8
Nature Communications
NATURE COMMUNICATIONS
Nature Communications, 8
Until recently, human embryonic stem cells (hESCs) were shown to exist in a state of primed pluripotency, while mouse embryonic stem cells (mESCs) display a naive or primed pluripotent state. Here we show the rapid conversion of in-house-derived prim
Autor:
Yannick Gansemans, Senne Cornelis, Dieter Deforce, Filip Van Nieuwerburgh, Maarten Dhaenens, Christophe Van Neste, Dieter De Coninck, Sander Willems, Bart J. G. Broeckx
Publikováno v:
Forensic Science International: Genetics. 26:e14-e16
Autor:
Yannick Gansemans, Filip Van Nieuwerburgh, Lieselot Deleye, Dieter De Coninck, Dieter Deforce
Publikováno v:
PLoS ONE
PLoS ONE, Vol 13, Iss 4, p e0196334 (2018)
PLOS ONE
PLoS ONE, Vol 13, Iss 4, p e0196334 (2018)
PLOS ONE
Single Gene Disorders (SGD) are still routinely diagnosed using PCR-based assays that need to be developed and validated for each individual disease-specific gene fragment. The TruSight One sequencing panel currently covers 12 Mb of genomic content,
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1712
Shallow whole genome sequencing has recently been introduced for genome-wide detection of chromosomal copy number alterations (CNAs) in preimplantation genetic diagnosis (PGD), using only 4-7 trophectoderm cells biopsied from day-5 embryos. This chap
Publikováno v:
Methods in Molecular Biology ISBN: 9781493975129
Shallow whole genome sequencing has recently been introduced for genome-wide detection of chromosomal copy number alterations (CNAs) in preimplantation genetic diagnosis (PGD), using only 4-7 trophectoderm cells biopsied from day-5 embryos. This chap
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b4f3e9e015f2b6e703f24a196ef3012
https://doi.org/10.1007/978-1-4939-7514-3_3
https://doi.org/10.1007/978-1-4939-7514-3_3
Autor:
Michael E. Pfrender, Jana Asselman, Karel A.C. De Schamphelaere, Dieter De Coninck, Eline Beert, Luisa Orsini, Ellen Decaestecker, Colin R. Janssen
Publikováno v:
ENVIRONMENTAL SCIENCE & TECHNOLOGY
Little is known about the influence that environmental stressors may have on genome-wide methylation patterns, and to what extent epigenetics may be involved in environmental stress response. Yet, studies of methylation patterns under stress could pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc4e57f09614f4ef503e3c43a75b0eeb
https://lirias.kuleuven.be/handle/123456789/561757
https://lirias.kuleuven.be/handle/123456789/561757