Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Slot, R. van 't"'
Autor:
Martin, J.E., Broen, J.C., Carmona, F.D., Teruel, M., Simeon, C.P., Vonk, M.C., Slot, R. van 't, Rodriguez-Rodriguez, L., Vicente, E., Fonollosa, V., Ortego-Centeno, N., Gonzalez-Gay, M.A., Garcia-Hernandez, F.J., Pena, P.G. de la, Carreira, P., Voskuyl, A.E., Schuerwegh, A.J., Riel, P.L.C.M. van, Kreuter, A., Witte, T., Riemekasten, G., Airo, P., Scorza, R., Lunardi, C., Hunzelmann, N., Distler, J.H.W., Beretta, L., Laar, J. van, Chee, M.M., Worthington, J., Herrick, A., Denton, C., Tan, F.K., Arnett, F.C., Assassi, S., Fonseca, C., Mayes, M.D., Radstake, T.R.D.J., Koeleman, B.P.C., Martin, J., Spanish Schleroderma Grp
Publikováno v:
Human Molecular Genetics, 21, 2825-35
Digital.CSIC. Repositorio Institucional del CSIC
instname
Human Molecular Genetics, 21(12), 2825-2835
Human Molecular Genetics, 21, 12, pp. 2825-35
Human Molecular Genetics, 21(12), 2825-2835. Oxford University Press
Martin, J E, Broen, J C, Carmona, F D, Teruel, M, Simeon, C P, Vonk, M C, van't Slot, R, Rodriguez-Rodriguez, L, Vicente, E, Fonollosa, V, Ortego-Centeno, N, Gonzalez-Gay, M A, Garcia-Hernandez, F J, de la Pena, P G, Carreira, P, Voskuyl, A E, Schuerwegh, A J, van Riel, P L C M, Kreuter, A, Witte, T, Riemekasten, G, Airo, P, Scorza, R, Lunardi, C, Hunzelmann, N, Distler, J H W, Beretta, L, van Laar, J, Chee, M M, Worthington, J, Herrick, A, Denton, C, Tan, F K, Arnett, F C, Assassi, S, Fonseca, C, Mayes, M D, Radstake, T R D J, Koeleman, B P C & Martin, J 2012, ' Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up ', Human Molecular Genetics, vol. 21, no. 12, pp. 2825-2835 . https://doi.org/10.1093/hmg/dds099
Digital.CSIC. Repositorio Institucional del CSIC
instname
Human Molecular Genetics, 21(12), 2825-2835
Human Molecular Genetics, 21, 12, pp. 2825-35
Human Molecular Genetics, 21(12), 2825-2835. Oxford University Press
Martin, J E, Broen, J C, Carmona, F D, Teruel, M, Simeon, C P, Vonk, M C, van't Slot, R, Rodriguez-Rodriguez, L, Vicente, E, Fonollosa, V, Ortego-Centeno, N, Gonzalez-Gay, M A, Garcia-Hernandez, F J, de la Pena, P G, Carreira, P, Voskuyl, A E, Schuerwegh, A J, van Riel, P L C M, Kreuter, A, Witte, T, Riemekasten, G, Airo, P, Scorza, R, Lunardi, C, Hunzelmann, N, Distler, J H W, Beretta, L, van Laar, J, Chee, M M, Worthington, J, Herrick, A, Denton, C, Tan, F K, Arnett, F C, Assassi, S, Fonseca, C, Mayes, M D, Radstake, T R D J, Koeleman, B P C & Martin, J 2012, ' Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up ', Human Molecular Genetics, vol. 21, no. 12, pp. 2825-2835 . https://doi.org/10.1093/hmg/dds099
Systemic sclerosis (SSc) is complex autoimmune disease affecting the connective tissue; influenced by genetic and environmental components. Recently, we performed the first successful genome-wide association study (GWAS) of SSc. Here, we perform a la
Autor:
Radstake, T.R.D.J., Gorlova, O., Rueda, B., Martin, J.E., Alizadeh, B.Z., Palomino-Morales, R., Coenen, M., Vonk, M.C., Voskuyl, A.E., Schuerwegh, A.J., Broen, J.C.A., Riel, P.L.C.M. van, Slot, R. van 't, Italiaander, A., Ophoff, R.A., Riemekasten, G., Hunzelmann, N., Simeon, C.P., Ortego-Centeno, N., Gonzalez-Gay, M.A., Gonzalez-Escribano, M.F., Airo, P., Laar, J. van, Herrick, A., Worthington, J., Hesselstrand, R., Smith, V., Keyser, F. de, Houssiau, F., Chee, M.M., Madhok, R., Shiels, P., Westhovens, R., Kreuter, A., Kiener, H., Baere, E. de, Witte, T.J.M. de, Padykov, L., Klareskog, L., Beretta, L., Scorza, R., Lie, B.A., Hoffmann-Vold, A.M., Carreira, P., Varga, J., Hinchcliff, M., Gregersen, P.K., Lee, A.T., Ying, J., Han, Y., Weng, S.F., Amos, C.I., Wigley, F.M., Hummers, L., Nelson, J.L., Agarwal, S.K., Assassi, S., Gourh, P., Tan, F.K., Koeleman, B.P., Arnett, F.C., Martin, J., Mayes, M.D.
Publikováno v:
Nature Genetics, 43, 5, pp. 499-499
Nature Genetics, 43, 499-499
Nature Genetics, 43, 499-499
Contains fulltext : 97765.pdf (Publisher’s version ) (Closed access) 01 mei 2010
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::37616f38c73fac7edf8bbc3396861cb4
https://hdl.handle.net/2066/97765
https://hdl.handle.net/2066/97765
Autor:
Wapenaar, M.C., Monsuur, A.J., Poell, J., Slot, R. van 't, Meijer, J.W.R., Meijer, G.A., Mulder, C.J., Mearin, M.L., Wijmenga, C.
Publikováno v:
Immunogenetics, 59(5), 349. Springer
The gene family of serine protease inhibitors of the Kazal type (SPINK) are functional and positional candidate genes for celiac disease (CD). Our aim was to assess the gut mucosal gene expression and genetic association of SPINK1, -2, -4, and -5 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::51203b107ac80e147f0d2008a2c8266b
https://dspace.library.uu.nl/handle/1874/23744
https://dspace.library.uu.nl/handle/1874/23744