Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Marcel Mannens"'
Autor:
Judith Ensink, Taylor Keding, Peter Henneman, Andrea Venema, Ligia Papale, Reid Alisch, Yousha Westerman, Guido van Wingen, Jasper Zantvoord, Christel Middeldorp, Marcel Mannens, Ryan Herringa, Ramón Lindauer
Recent findings in neuroimaging and epigenetics offer important insights into brain structures and biological pathways of altered gene expression associated with posttraumatic stress disorder (PTSD). However, it is unknown to what extent epigenetic m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01f3d1a88125b31b13adbae64cbe972a
https://doi.org/10.21203/rs.3.rs-87419/v1
https://doi.org/10.21203/rs.3.rs-87419/v1
Autor:
Marcel Mannens
Publikováno v:
OBM Genetics, 3(2)
Mannens, M 2019, ' Epigenetics is here to stay ', OBM Genetics, vol. 3, no. 2 . https://doi.org/10.21926/obm.genet.1902075
OBM Genetics, 3(2). LIDSEN Publishing Inc
Mannens, M 2019, ' Epigenetics is here to stay ', OBM Genetics, vol. 3, no. 2 . https://doi.org/10.21926/obm.genet.1902075
OBM Genetics, 3(2). LIDSEN Publishing Inc
Autor:
Marcel Mannens
Publikováno v:
Encyclopedia of Cancer ISBN: 9783642278419
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7ca71c2ddbd299400aeda19233eb3b2
https://doi.org/10.1007/978-3-662-46875-3_575
https://doi.org/10.1007/978-3-662-46875-3_575
Autor:
Ian J.J.P. Heding, Alasdair C. Ivens, Jeff Wilson, Mark Strivens, Simon Gregory, Jan M.N. Hoovers, Marcel Mannens, Bert Redeker, David Porteous, Veronica van Heyningen, Peter F.R. Little
Publikováno v:
Genomics, 13(1), 89-94. Academic Press Inc.
We describe progress in a continuing project aimed at the generation of an overlapping cosmid DNA clone map of the short arm of human chromosome 11. The automated procedures used to prepare DNA samples and the computerized data collection and recordi
Autor:
Benjamin Tycko, Marcel Mannens
Publikováno v:
Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics ISBN: 0470849746
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c4936304a831a57429718b4dc06fe13
https://doi.org/10.1002/047001153x.g103213
https://doi.org/10.1002/047001153x.g103213
Autor:
Judy Fantes, Bert Redeker, Matthew Breen, Shelagh Boyle, John Brown, Judy Fletcher, Sinead Jones, Wendy Bickmore, Yoshimitsu Fukushima, Marcel Mannens, Sarah Danes, Veronica van Heyningen, Isabel Hanson
Publikováno v:
Human molecular genetics, 4(3), 415-422. Oxford University Press
Current evidence suggests that aniridia (absence of iris) is caused by loss of function of one copy of the PAX6 gene, which maps to 11p13. We present the further characterisation of two aniridia pedigrees in which the disease segregates with chromoso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c459ec43295d1d4c37ec0574fa0d64c9
https://pure.amc.nl/en/publications/aniridiaassociated-cytogenetic-rearrangements-suggest-that-a-position-effect-may-cause-the-mutant-phenotype(72f731fc-3bfb-4f7b-ac39-94e5e1501a70).html
https://pure.amc.nl/en/publications/aniridiaassociated-cytogenetic-rearrangements-suggest-that-a-position-effect-may-cause-the-mutant-phenotype(72f731fc-3bfb-4f7b-ac39-94e5e1501a70).html
Autor:
Marcel Mannens
Publikováno v:
Trends in Genetics. 11:418-419
Autor:
Xiaofeng Hu, Astrid Plomp, Theo Gorgels, Jacoline Ten Brink, Willem Loves, Marcel Mannens, Paulus T.V.M. De Jong, Arthur A.B. Bergen
Publikováno v:
Genetic Testing; Fall2004, Vol. 8 Issue 3, p292-300, 9p
Autor:
Aam Wilde, Marieke W. Veldkamp, Mte Bink-Boelkens, Connie R. Bezzina, van den Maarten Berg, van Irene Langen, M.M.A.M. (Marcel) Mannens, JW Viersma, G Tan-Sindhunata, M. B. Rook, AH van der Hout, Alex V. Postma
Publikováno v:
Europe PubMed Central
Abstract —Mutations in SCN5A , the gene encoding the cardiac Na + channel, have been identified in 2 distinct diseases associated with sudden death: one form of the long-QT syndrome (LQT 3 ) and the Brugada syndrome. We have screened SCN5A in a lar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f34e1e1b118331fe21fd6f1694f6470
http://europepmc.org/abstract/med/10590249
http://europepmc.org/abstract/med/10590249