D'Hooge R - Search Results

1

Genotype-phenotype correlation in L1 associated diseases.

Fransen E, Van Camp G, D'Hooge R, Vits L, Willems PJ. Fransen E, et al. J Med Genet. 1998 May;35(5):399-404. doi: 10.1136/jmg.35.5.399. J Med Genet. 1998. PMID: 9610803 Free PMC article.

2

L1 knockout mice show dilated ventricles, vermis hypoplasia and impaired exploration patterns.

Fransen E, D'Hooge R, Van Camp G, Verhoye M, Sijbers J, Reyniers E, Soriano P, Kamiguchi H, Willemsen R, Koekkoek SK, De Zeeuw CI, De Deyn PP, Van der Linden A, Lemmon V, Kooy RF, Willems PJ. Fransen E, et al. Hum Mol Genet. 1998 Jun;7(6):999-1009. doi: 10.1093/hmg/7.6.999. Hum Mol Genet. 1998. PMID: 9580664

3

Transgenic mouse model for the fragile X syndrome.

Kooy RF, D'Hooge R, Reyniers E, Bakker CE, Nagels G, De Boulle K, Storm K, Clincke G, De Deyn PP, Oostra BA, Willems PJ. Kooy RF, et al. Am J Med Genet. 1996 Aug 9;64(2):241-5. doi: 10.1002/(SICI)1096-8628(19960809)64:2<241::AID-AJMG1>3.0.CO;2-X. Am J Med Genet. 1996. PMID: 8844056

4

Long-term potentiation in the hippocampus of fragile X knockout mice.

Godfraind JM, Reyniers E, De Boulle K, D'Hooge R, De Deyn PP, Bakker CE, Oostra BA, Kooy RF, Willems PJ. Godfraind JM, et al. Am J Med Genet. 1996 Aug 9;64(2):246-51. doi: 10.1002/(SICI)1096-8628(19960809)64:2<246::AID-AJMG2>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8844057

5

Effect of genetic background on acoustic startle response in fragile X knockout mice.

Errijgers V, Fransen E, D'Hooge R, De Deyn PP, Kooy RF. Errijgers V, et al. Genet Res (Camb). 2008 Aug;90(4):341-5. doi: 10.1017/S0016672308009415. Genet Res (Camb). 2008. PMID: 18840308

6

Mildly impaired water maze performance in male Fmr1 knockout mice.

D'Hooge R, Nagels G, Franck F, Bakker CE, Reyniers E, Storm K, Kooy RF, Oostra BA, Willems PJ, De Deyn PP. D'Hooge R, et al. Neuroscience. 1997 Jan;76(2):367-76. doi: 10.1016/s0306-4522(96)00224-2. Neuroscience. 1997. PMID: 9015322

7

CALL interrupted in a patient with non-specific mental retardation: gene dosage-dependent alteration of murine brain development and behavior.

Frints SG, Marynen P, Hartmann D, Fryns JP, Steyaert J, Schachner M, Rolf B, Craessaerts K, Snellinx A, Hollanders K, D'Hooge R, De Deyn PP, Froyen G. Frints SG, et al. Hum Mol Genet. 2003 Jul 1;12(13):1463-74. doi: 10.1093/hmg/ddg165. Hum Mol Genet. 2003. PMID: 12812975

8

TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions.

Rooms L, Reyniers E, Scheers S, van Luijk R, Wauters J, Van Aerschot L, Callaerts-Vegh Z, D'Hooge R, Mengus G, Davidson I, Courtens W, Kooy RF. Rooms L, et al. Eur J Hum Genet. 2006 Oct;14(10):1090-6. doi: 10.1038/sj.ejhg.5201674. Epub 2006 Jun 14. Eur J Hum Genet. 2006. PMID: 16773126

9

Restoring the phenotype of fragile X syndrome: insight from the mouse model.

Gantois I, Bakker CE, Reyniers E, Willemsen R, D'Hooge R, De Deyn PP, Oostra BA, Kooy RF. Gantois I, et al. Curr Mol Med. 2001 Sep;1(4):447-55. doi: 10.2174/1566524013363492. Curr Mol Med. 2001. PMID: 11899089 Review.

10

Placebos in clinical practice and research.

De Deyn PP, D'Hooge R. De Deyn PP, et al. J Med Ethics. 1996 Jun;22(3):140-6. doi: 10.1136/jme.22.3.140. J Med Ethics. 1996. PMID: 8798935 Free PMC article. Review.

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