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203 results

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Page 1
Synaptopodin and 4 novel genes identified in primary sensory neurons.
Verpoorten N, Verhoeven K, Weckx S, Jacobs A, Serneels S, Del Favero J, Ceuterick C, Van Bockstaele DR, Berneman ZN, Van den Bosch L, Robberecht W, Nobbio L, Schenone A, Dessaud E, deLapeyrière O, Huylebroeck D, Zwijsen A, De Jonghe P, Timmerman V. Verpoorten N, et al. Among authors: del favero j. Mol Cell Neurosci. 2005 Nov;30(3):316-25. doi: 10.1016/j.mcn.2005.07.005. Epub 2005 Sep 1. Mol Cell Neurosci. 2005. PMID: 16139508
novoSNP, a novel computational tool for sequence variation discovery.
Weckx S, Del-Favero J, Rademakers R, Claes L, Cruts M, De Jonghe P, Van Broeckhoven C, De Rijk P. Weckx S, et al. Among authors: del favero j. Genome Res. 2005 Mar;15(3):436-42. doi: 10.1101/gr.2754005. Genome Res. 2005. PMID: 15741513 Free PMC article.
SNPbox: a modular software package for large-scale primer design.
Weckx S, De Rijk P, Van Broeckhoven C, Del-Favero J. Weckx S, et al. Among authors: del favero j. Bioinformatics. 2005 Feb 1;21(3):385-7. doi: 10.1093/bioinformatics/bti006. Epub 2004 Sep 3. Bioinformatics. 2005. PMID: 15347573
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS.
Gijselinck I, Sleegers K, Engelborghs S, Robberecht W, Martin JJ, Vandenberghe R, Sciot R, Dermaut B, Goossens D, van der Zee J, De Pooter T, Del-Favero J, Santens P, De Jonghe P, De Deyn PP, Van Broeckhoven C, Cruts M. Gijselinck I, et al. Among authors: del favero j. Neurobiol Aging. 2009 Aug;30(8):1329-31. doi: 10.1016/j.neurobiolaging.2007.11.002. Epub 2008 Jan 10. Neurobiol Aging. 2009. PMID: 18068872
SNPbox: web-based high-throughput primer design from gene to genome.
Weckx S, De Rijk P, Van Broeckhoven C, Del-Favero J. Weckx S, et al. Among authors: del favero j. Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W170-2. doi: 10.1093/nar/gkh369. Nucleic Acids Res. 2004. PMID: 15215373 Free PMC article.
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample.
Rademakers R, Cruts M, Sleegers K, Dermaut B, Theuns J, Aulchenko Y, Weckx S, De Pooter T, Van den Broeck M, Corsmit E, De Rijk P, Del-Favero J, van Swieten J, van Duijn CM, Van Broeckhoven C. Rademakers R, et al. Among authors: del favero j. Am J Hum Genet. 2005 Oct;77(4):643-52. doi: 10.1086/491749. Epub 2005 Aug 30. Am J Hum Genet. 2005. PMID: 16175510 Free PMC article.
De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy.
Claes L, Ceulemans B, Audenaert D, Smets K, Löfgren A, Del-Favero J, Ala-Mello S, Basel-Vanagaite L, Plecko B, Raskin S, Thiry P, Wolf NI, Van Broeckhoven C, De Jonghe P. Claes L, et al. Among authors: del favero j. Hum Mutat. 2003 Jun;21(6):615-21. doi: 10.1002/humu.10217. Hum Mutat. 2003. PMID: 12754708
203 results