Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Paal Skyt Andersen"'
Autor:
Márcia Melo Medeiros, Anna Cäcilia Ingham, Line Møller Nanque, Claudino Correia, Marc Stegger, Paal Skyt Andersen, Ane Baerent Fisker, Christine Stabell Benn, Miguel Lanaspa, Henrique Silveira, Patrícia Abrantes
Publikováno v:
Frontiers in Microbiology, Vol 13 (2022)
After the eradication of polio infection, the plan is to phase-out the live-attenuated oral polio vaccine (OPV). Considering the protective non-specific effects (NSE) of OPV on unrelated pathogens, the withdrawal may impact child health negatively. W
Externí odkaz:
https://doaj.org/article/604ed65265904cc3ad50ca25d3af8b7a
Autor:
Elaine R. Nimmo, Jack Satsangi, Colin Veal, Christopher G. Mathew, I. Vind, Peder Fode, Pia S. Munkholm, Edward J. Hollox, Natalie J. Prescott, John C. Mansfield, Paal Skyt Andersen, Shamik Polley
Publikováno v:
Polley, S, Prescott, N, Nimmo, E, Veal, C, Vind, I, Munkholm, P, Fode, P, Mansfield, J, Skyt Andersen, P, Satsangi, J, G Mathew, C & Hollox, E J 2016, ' Copy number variation of scavenger-receptor cysteine-rich domains within DMBT1 and Crohn's disease ', European journal of human genetics : EJHG . https://doi.org/10.1038/ejhg.2015.280
Polley, S, Prescott, N, Nimmo, E, Veal, C, Vind, I, Munkholm, P, Fode, P, Mansfield, J, Skyt Andersen, P, Satsangi, J, Matthew, C G & Hollox, E J 2016, ' Copy number variation of scavenger-receptor cysteine-rich domains within DMBT1 and Crohn's disease ', European Journal of Human Genetics . https://doi.org/10.1038/ejhg.2015.280
European Journal of Human Genetics
Polley, S, Prescott, N, Nimmo, E, Veal, C, Vind, I, Munkholm, P, Fode, P, Mansfield, J, Skyt Andersen, P, Satsangi, J, Matthew, C G & Hollox, E J 2016, ' Copy number variation of scavenger-receptor cysteine-rich domains within DMBT1 and Crohn's disease ', European Journal of Human Genetics . https://doi.org/10.1038/ejhg.2015.280
European Journal of Human Genetics
Previous work has shown that the gene DMBT1, which encodes a large secreted epithelial glycoprotein known as salivary agglutinin, gp340, hensin or muclin, is an innate immune defence protein that binds bacteria. A deletion variant of DMBT1 has been p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a1cd17bf71a1d8099ae198def90afc0
https://kclpure.kcl.ac.uk/ws/files/46527839/ejhg2015280a.pdf
https://kclpure.kcl.ac.uk/ws/files/46527839/ejhg2015280a.pdf
Autor:
Paal Skyt Andersen, Reinhard Ullmann, Christina Cintin, Rodney M. J. Cotterill, Ole Mors, Astrid M. Vicente, Niels Tommerup, Marlene Briciet Lauritsen, Iben Bache, Claes Lundsteen, Karen Friis Henriksen, Thomas Rosenberg, Zeynep Tümer, Karen Brøndum-Nielsen, Guiomar Oliveira, Hans Eiberg, Morten Møller, Hans-Hilger Ropers, Mette Gilling
Publikováno v:
Gilling, M, Lauritsen, M B, Møller, M, Henriksen, K F, Vicente, A, Oliveira, G, Cintin, C, Eiberg, H, Andersen, P S, Mors, O, Rosenberg, T, Brøndum-Nielsen, K, Cotterill, R M J, Lundsteen, C, Ropers, H-H, Ullmann, R, Bache, I, Tümer, Z & Tommerup, N 2008, ' A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia. ', European Journal of Human Genetics, vol. 16, no. 3, pp. 312-9 . https://doi.org/10.1038/sj.ejhg.5201985
Udgivelsesdato: 2008-Mar Autism spectrum disorders (ASDs) are a heterogeneous group of disorders with unknown aetiology. Even though ASDs are suggested to be among the most heritable complex disorders, only a few reproducible mutations leading to sus