Zobrazeno 1 - 10
of 160
pro vyhledávání: '"Te Meerman, G.j."'
Autor:
Oostenbrug, L.E., Nolte, I.M., Oosterom, E., van der Steege, G., te Meerman, G.J., van Dullemen, H.M., Drenth, J.P.H., de Jong, D.J., van der Linde, K., Jansen, P.L.M., Kleibeuker, J.H.
Publikováno v:
In Digestive and Liver Disease 2006 38(11):834-845
Autor:
de Jong, M.M., te Meerman, G.J., van der Graaf, W.T.A., de Vries, E.G.E., Nolte, I.M., Mulder, M.J., Bruinenberg, M., van der Steege, G., Schaapveld, M., Sijmons, R.H., Hofstra, R.M.W., Kleibeuker, J.H. *
Publikováno v:
In Digestive and Liver Disease 2004 36(12):821-823
Publikováno v:
In Neurobiology of Disease 2003 14(3):602-618
During pregnancy, cell-free DNA (cfDNA) in maternal blood encompasses a small percentage of cell-free fetal DNA (cffDNA), an easily accessible source for determination of fetal disease status in risk families through non-invasive procedures. In case
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::c759ad2732bae6537beb9da5debc14dd
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3085733
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3085733
Publikováno v:
In Theriogenology 1999 52(8):1281-1293
Akademický článek
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0001: ANALYSIS OF THE ENTIRE HLA REGION IN SUSCEPTIBILITY FOR CERVICAL CANCER: A COMPREHENSIVE STUDY
Autor:
van der Zee, A.G., Nolte, I.J., Zoodsma, M., Schipper, M., Ter Steege, G., Oosterom, E., de Vries, E.G., Te Meerman, G.J.
Publikováno v:
In International Journal of Gynecological Cancer September 2005 15 Supplement 2:51-51
Inheritance mode of multiple sclerosis: the effect of HLA class II alleles is stronger than additive
Autor:
Boon, M., Nolte, I.m., Bruinenberg, M., Spijker, G.t., Terpstra, Marin, Raelson, J., De Keyser, Jacques, Zwanikken, C.p., Hulsbeek, M., Hofstra, R.m., Buys, C.h., Te Meerman, G.j.
We previously identified on chromosome 6 an interval of 51 kb as the most likely interval in the HLA region for a disease-susceptibility locus for multiple sclerosis (MS). The interval was located between markers G511525 and D6S1666 and identified by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::8f6e96cd1c89f58bae3e842633861f55
https://hdl.handle.net/20.500.14017/af813904-1917-4754-8e07-423f0f2e8e00
https://hdl.handle.net/20.500.14017/af813904-1917-4754-8e07-423f0f2e8e00
Autor:
Nolte, I.m., Bruinenberg, M., Spijker, G.t., Terpstra, Marin, De Keyser, Jacques, Zwanikken, C.p., Hulsbeek, M., Hofstra, R.m., Buys, C.h., Te Meerman, G.j., Boon, Maartje, Raelson, J.
Multiple sclerosis (MS) is a complex disease that is partly genetic in origin. Although an association of MS with specific human leukocyte antigen (HLA) types has been known for almost 30 years, the nature of this relationship has remained unclear. F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3848::46f28fd9d627b582a490fac009c84da8
https://biblio.vub.ac.be/vubir/mapping-of-a-susceptibility-gene-for-multiple-sclerosis-to-the-51-kb-interval-between-g511525-and-d6s1666-using-a-new-method-of-haplotype-sharing-analysis(2459e628-2a66-488c-b090-f52e1620bd93).html
https://biblio.vub.ac.be/vubir/mapping-of-a-susceptibility-gene-for-multiple-sclerosis-to-the-51-kb-interval-between-g511525-and-d6s1666-using-a-new-method-of-haplotype-sharing-analysis(2459e628-2a66-488c-b090-f52e1620bd93).html
Akademický článek
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