Meuleman J - Search Results

1

A single amino acid substitution (Cys249Trp) in Crb1 causes retinal degeneration and deregulates expression of pituitary tumor transforming gene Pttg1.

van de Pavert SA, Meuleman J, Malysheva A, Aartsen WM, Versteeg I, Tonagel F, Kamphuis W, McCabe CJ, Seeliger MW, Wijnholds J. van de Pavert SA, et al. Among authors: meuleman j. J Neurosci. 2007 Jan 17;27(3):564-73. doi: 10.1523/JNEUROSCI.3496-06.2007. J Neurosci. 2007. PMID: 17234588 Free PMC article.

2

Crumbs homologue 1 in polarity and blindness.

Meuleman J, van de Pavert SA, Wijnholds J. Meuleman J, et al. Biochem Soc Trans. 2004 Nov;32(Pt 5):828-30. doi: 10.1042/BST0320828. Biochem Soc Trans. 2004. PMID: 15494026 Review.

3

Crumbs homologue 1 is required for maintenance of photoreceptor cell polarization and adhesion during light exposure.

van de Pavert SA, Kantardzhieva A, Malysheva A, Meuleman J, Versteeg I, Levelt C, Klooster J, Geiger S, Seeliger MW, Rashbass P, Le Bivic A, Wijnholds J. van de Pavert SA, et al. Among authors: meuleman j. J Cell Sci. 2004 Aug 15;117(Pt 18):4169-77. doi: 10.1242/jcs.01301. J Cell Sci. 2004. PMID: 15316081

4

Pals1/Mpp5 is required for correct localization of Crb1 at the subapical region in polarized Muller glia cells.

van Rossum AG, Aartsen WM, Meuleman J, Klooster J, Malysheva A, Versteeg I, Arsanto JP, Le Bivic A, Wijnholds J. van Rossum AG, et al. Among authors: meuleman j. Hum Mol Genet. 2006 Sep 15;15(18):2659-72. doi: 10.1093/hmg/ddl194. Epub 2006 Aug 2. Hum Mol Genet. 2006. PMID: 16885194

5

Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3.

Irobi J, Nelis E, Meuleman J, Venken K, De Jonghe P, Van Broeckhoven C, Timmerman V. Irobi J, et al. Among authors: meuleman j. Ann Hum Genet. 2001 Nov;65(Pt 6):517-29. doi: 10.1017/S0003480001008910. Ann Hum Genet. 2001. PMID: 11851982

6

Molecular genetics of inherited peripheral neuropathies: who are the actors?

Meuleman J, Timmerman V, Nelis E, De Jonghe P. Meuleman J, et al. Acta Neurol Belg. 2000 Sep;100(3):171-80. Acta Neurol Belg. 2000. PMID: 11098291 Review.

7

Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA).

Meuleman J, Kuhlenbäumer G, Audenaert D, Hünermund G, Hor H, Young P, Stögbauer F, Ringelstein EB, Van Broeckhoven C, De Jonghe P, Timmerman V. Meuleman J, et al. Hum Genet. 2001 May;108(5):390-3. doi: 10.1007/s004390100510. Hum Genet. 2001. PMID: 11409865

8

Caspr1/Paranodin/Neurexin IV is most likely not a common disease-causing gene for inherited peripheral neuropathies.

Venken K, Meuleman J, Irobi J, Ceuterick C, Martini R, De Jonghe P, Timmerman V. Venken K, et al. Among authors: meuleman j. Neuroreport. 2001 Aug 8;12(11):2609-14. doi: 10.1097/00001756-200108080-00063. Neuroreport. 2001. PMID: 11496158

9

Hereditary neuralgic amyotrophy.

Meuleman J, Timmerman V, Van Broeckhoven C, De Jonghe P. Meuleman J, et al. Neurogenetics. 2001 Jul;3(3):115-8. doi: 10.1007/s100480100109. Neurogenetics. 2001. PMID: 11523561 Review.

10

Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA).

Kuhlenbaeumer G, Meuleman J, Schirmacher A, Stoegbauer F, Ringelstein EB, Wehnert M, Hoeltzenbein M, Broeckhoven CV, Timmerman V. Kuhlenbaeumer G, et al. Among authors: meuleman j. Ann Hum Genet. 1998 Sep;62(Pt 5):397-400. doi: 10.1046/j.1469-1809.1998.6250397.x. Ann Hum Genet. 1998. PMID: 10088036

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