Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marina, Ventayol Garcia"'
Autor:
Arnoud Boot, Jan Oosting, Saskia Doorn, Sarah Ouahoud, Marina Ventayol Garcia, Dina Ruano, Hans Morreau, Tom van Wezel
Publikováno v:
International Journal of Genomics, Vol 2019 (2019)
Allele-specific expression (ASE) is found in approximately 20-30% of human genes. During tumorigenesis, ASE changes due to somatic alterations that change the regulatory landscape. In colorectal cancer (CRC), many chromosomes show frequent gains or l
Externí odkaz:
https://doaj.org/article/0e9484ab60014c35b853523bf8762606
Autor:
Maria de la Puente, Kristiaan J. van der Gaag, Sabrina Ingold, Ewelina Pospiech, Catarina Xavier, Susan Walsh, Wojciech Branicki, Cordula Haas, Christopher Phillips, Walther Parson, Arwin Ralf, Marina Ventayol Garcia, Magdalena Kukla-Bartoszek, Ana Freire-Aradas, Manfred Kayser, Bailey Wills, Noah Herrick, Titia Sijen, Krystal Breslin
Publikováno v:
Forensic Science International: Genetics, 43:Unsp 102152. Elsevier Ireland Ltd
Forensic DNA Phenotyping (FDP) provides the ability to predict externally visible characteristics from minute amounts of crime scene DNA, which can help find unknown perpetrators who are typically unidentifiable via conventional forensic DNA profilin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7be73836568b3dcc626008c0d40858a8
https://www.zora.uzh.ch/id/eprint/178564/
https://www.zora.uzh.ch/id/eprint/178564/
Autor:
Dina Ruano, Arnoud Boot, Saskia Doorn, Hans Morreau, Tom van Wezel, Marina Ventayol Garcia, Jan Oosting, Sarah Ouahoud
Publikováno v:
International Journal of Genomics. HINDAWI LTD
International Journal of Genomics
International Journal of Genomics, Vol 2019 (2019)
International Journal of Genomics
International Journal of Genomics, Vol 2019 (2019)
Allele-specific expression (ASE) is found in approximately 20-30% of human genes. During tumorigenesis, ASE changes due to somatic alterations that change the regulatory landscape. In colorectal cancer (CRC), many chromosomes show frequent gains or l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::279757c9f6498eab72094c6938024398
http://hdl.handle.net/1887/121805
http://hdl.handle.net/1887/121805
Autor:
Arnoud, Boot, Jan, Oosting, Saskia, Doorn, Sarah, Ouahoud, Marina, Ventayol Garcia, Dina, Ruano, Hans, Morreau, Tom, van Wezel
Publikováno v:
International Journal of Genomics
Allele-specific expression (ASE) is found in approximately 20-30% of human genes. During tumorigenesis, ASE changes due to somatic alterations that change the regulatory landscape. In colorectal cancer (CRC), many chromosomes show frequent gains or l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::35c81af237513c922e1a71a96c8428f3
https://pubmed.ncbi.nlm.nih.gov/31093489
https://pubmed.ncbi.nlm.nih.gov/31093489
Autor:
Anne M.L. Jansen, Frederik J. Hes, Marina Ventayol Garcia, Stijn Crobach, Dina Ruano, Brendy E.W.M. van den Akker, Carli M. J. Tops, Tom van Wezel, Juul T. Wijnen, Hans Morreau, Willemina R. R. Geurts-Giele, Winand N.M. Dinjens, Maartje Nielsen
Publikováno v:
Gastroenterology, 152(3), 546
Gastroenterology, 152(3), 546-+. W.B. Saunders
Gastroenterology, 152(3), 546-+. W.B. Saunders
We investigated the presence and patterns of mosaicism in the APC gene in patients with colon neoplasms not associated with any other genetic variants; we performed deep sequence analysis of APC in at least 2 adenomas or carcinomas per patient. We id
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::051f0874001a5fc7990d4c97b2768144
https://hdl.handle.net/1887/116005
https://hdl.handle.net/1887/116005
Autor:
Carli M. J. Tops, Juul T. Wijnen, Frederik J. Hes, Encarna B. Gomez-Garcia, Tom G.W. Letteboer, Anne M.L. Jansen, Brendy E.W.M. van den Akker, Dina Ruano, Peter Devilee, Anja Wagner, Hans Morreau, Marina Ventayol Garcia, Tom van Wezel
Publikováno v:
European Journal of Human Genetics, 24(7), 1089-1092
European Journal of Human Genetics
European Journal of Human Genetics, 24(7), 1089-1092. Nature Publishing Group
European Journal of Human Genetics, 24(7), 1089. Nature Publishing Group
European Journal of Human Genetics
European Journal of Human Genetics, 24(7), 1089-1092. Nature Publishing Group
European Journal of Human Genetics, 24(7), 1089. Nature Publishing Group
Many suspected Lynch Syndrome (sLS) patients who lack mismatch repair (MMR) germline gene variants and MLH1 or MSH2 hypermethylation are currently explained by somatic MMR gene variants or, occasionally, by germline POLE variants. To further investig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f24ba1ca890ab6997926847796325c1
http://hdl.handle.net/1887/111860
http://hdl.handle.net/1887/111860
Autor:
Pieter S. Hiemstra, Marina Ventayol Garcia, Johan T. den Dunnen, Ken Kraaijeveld, Letty A. de Weger, Jeroen Frank, Henk P. J. Buermans
Publikováno v:
Molecular Ecology Resources, 15(1), 8-16
Pollen monitoring is an important and widely used tool in allergy research and creation of awareness in pollen-allergic patients. Current pollen monitoring methods are microscope-based, labour intensive and cannot identify pollen to the genus level i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05e8fb8c28fbe4c6cae45d83d0a9a57e
https://pubmed.ncbi.nlm.nih.gov/24893805
https://pubmed.ncbi.nlm.nih.gov/24893805