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Your search keyword '"Scherpenisse M"' showing total 5 results
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5 results on '"Scherpenisse M"'

1. Expertpanelbeoordeling van (potentiële) risico’s en managementopties van invasieve exoten in nederland; inhoudelijke input voor het nederlandse standpunt over de plaatsing van soorten op eu-verordening 1143/2014

Author

Verbrugge, L.N.H., Hoop, L. de, Leuven, R.S.E.W., Aukema, R., Beringen, R., Creemers, R.C.M., Duinen, G.A. van, Hollander, H. Den, Scherpenisse, M., Spikmans, F., Turnhout, C.A.M. van, Wijnhoven, S., and Hullu, E. de

Subjects
GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries), Environmental Sciences
Abstract

Contains fulltext : 142445.pdf (Publisher’s version ) (Open Access) 54 p.

Published
2015

3. Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

Author

BONORA, ELENA, Lamb J. A., Barnby G., Sykes N., Moberly T., Beyer K. S., Klauck S. M., Poustka F., Battaglia A., Haracopos D., Pedersen L., Isager T., Eriksen G., Viskum B., Sorensen E. U., Brondum Nielsen K., Cotterill R., Engeland H., Jonge M., Kemner C., Steggehuis K., Scherpenisse M., Rutter M., Bolton P. F., Parr J. R., Poustka A., Bailey A. J., Monaco A. P., International Molecular Genetic Study of Austism Consortium, BACCHELLI, ELENA, BLASI, FRANCESCA, MAESTRINI, ELENA, Bonora E., Lamb J.A., Barnby G., Sykes N., Moberly T., Beyer K.S., Klauck S.M., Poustka F., Bacchelli E., Blasi F., Maestrini E., Battaglia A., Haracopos D., Pedersen L., Isager T., Eriksen G., Viskum B., Sorensen E.U., Brondum-Nielsen K., Cotterill R., Engeland H., Jonge M., Kemner C., Steggehuis K., Scherpenisse M., Rutter M., Bolton P.F., Parr J.R., Poustka A., Bailey A.J., Monaco A.P., and International Molecular Genetic Study of Austism Consortium.

Abstract

Genetic studies have provided evidence for an autism susceptibility locus (AUTS1) on chromosome 7q. Screening for mutations in six genes mapping to 7q, CUTL1, SRPK2, SYPL, LAMB1, NRCAM and PTPRZ1 in 48 unrelated individuals with autism led to the identification of several new coding variants in the genes CUTL1, LAMB1 and PTPRZ1. Analysis of genetic variants provided evidence for association with autism for one of the new missense changes identified in LAMB1; this effect was stronger in a subgroup of affected male sibling pair families, implying a possible specific sex-related effect for this variant. Association was also detected for several polymorphisms in the promoter and untranslated region of NRCAM, suggesting that alterations in expression of this gene may be linked to autism susceptibility.

Published
2005

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