Froyen G - Search Results

1

Rer1p maintains ciliary length and signaling by regulating γ-secretase activity and Foxj1a levels.

Jurisch-Yaksi N, Rose AJ, Lu H, Raemaekers T, Munck S, Baatsen P, Baert V, Vermeire W, Scales SJ, Verleyen D, Vandepoel R, Tylzanowski P, Yaksi E, de Ravel T, Yost HJ, Froyen G, Arrington CB, Annaert W. Jurisch-Yaksi N, et al. Among authors: froyen g. J Cell Biol. 2013 Mar 18;200(6):709-20. doi: 10.1083/jcb.201208175. Epub 2013 Mar 11. J Cell Biol. 2013. PMID: 23479743 Free PMC article.

2

Microdeletion of the escape genes KDM5C and IQSEC2 in a girl with severe intellectual disability and autistic features.

Fieremans N, Van Esch H, de Ravel T, Van Driessche J, Belet S, Bauters M, Froyen G. Fieremans N, et al. Among authors: froyen g. Eur J Med Genet. 2015 May;58(5):324-7. doi: 10.1016/j.ejmg.2015.03.003. Epub 2015 Apr 7. Eur J Med Genet. 2015. PMID: 25858702

3

Partial duplications of the ATRX gene cause the ATR-X syndrome.

Thienpont B, de Ravel T, Van Esch H, Van Schoubroeck D, Moerman P, Vermeesch JR, Fryns JP, Froyen G, Lacoste C, Badens C, Devriendt K. Thienpont B, et al. Among authors: froyen g. Eur J Hum Genet. 2007 Oct;15(10):1094-7. doi: 10.1038/sj.ejhg.5201878. Epub 2007 Jun 20. Eur J Hum Genet. 2007. PMID: 17579672

4

Sporadic male patients with intellectual disability: contribution of X-chromosome copy number variants.

Isrie M, Froyen G, Devriendt K, de Ravel T, Fryns JP, Vermeesch JR, Van Esch H. Isrie M, et al. Among authors: froyen g. Eur J Med Genet. 2012 Nov;55(11):577-85. doi: 10.1016/j.ejmg.2012.05.005. Epub 2012 May 30. Eur J Med Genet. 2012. PMID: 22659343

5

Granulocyte chemotactic protein-2 and related CXC chemokines: from gene regulation to receptor usage.

Van Damme J, Wuyts A, Froyen G, Van Coillie E, Struyf S, Billiau A, Proost P, Wang JM, Opdenakker G. Van Damme J, et al. Among authors: froyen g. J Leukoc Biol. 1997 Nov;62(5):563-9. doi: 10.1002/jlb.62.5.563. J Leukoc Biol. 1997. PMID: 9365109 Review.

6

NXF5, a novel member of the nuclear RNA export factor family, is lost in a male patient with a syndromic form of mental retardation.

Jun L, Frints S, Duhamel H, Herold A, Abad-Rodrigues J, Dotti C, Izaurralde E, Marynen P, Froyen G. Jun L, et al. Among authors: froyen g. Curr Biol. 2001 Sep 18;11(18):1381-91. doi: 10.1016/s0960-9822(01)00419-5. Curr Biol. 2001. PMID: 11566096 Free article.

7

Generation and characterization of an Nxf7 knockout mouse to study NXF5 deficiency in a patient with intellectual disability.

Vanmarsenille L, Verbeeck J, Belet S, Roebroek AJ, Van de Putte T, Nevelsteen J, Callaerts-Vegh Z, D'Hooge R, Marynen P, Froyen G. Vanmarsenille L, et al. Among authors: froyen g. PLoS One. 2013 May 13;8(5):e64144. doi: 10.1371/journal.pone.0064144. Print 2013. PLoS One. 2013. PMID: 23675524 Free PMC article.

8

The mitochondrial solute carrier SLC25A5 at Xq24 is a novel candidate gene for non-syndromic intellectual disability.

Vandewalle J, Bauters M, Van Esch H, Belet S, Verbeeck J, Fieremans N, Holvoet M, Vento J, Spreiz A, Kotzot D, Haberlandt E, Rosenfeld J, Andrieux J, Delobel B, Dehouck MB, Devriendt K, Fryns JP, Marynen P, Goldstein A, Froyen G. Vandewalle J, et al. Among authors: froyen g. Hum Genet. 2013 Oct;132(10):1177-85. doi: 10.1007/s00439-013-1322-3. Epub 2013 Jun 20. Hum Genet. 2013. PMID: 23783460

9

Telomere length homeostasis and telomere position effect on a linear human artificial chromosome are dictated by the genetic background.

Weuts A, Voet T, Verbeeck J, Lambrechts N, Wirix E, Schoonjans L, Danloy S, Marynen P, Froyen G. Weuts A, et al. Among authors: froyen g. Nucleic Acids Res. 2012 Dec;40(22):11477-89. doi: 10.1093/nar/gks926. Epub 2012 Oct 11. Nucleic Acids Res. 2012. PMID: 23066103 Free PMC article.

10

A novel fragile X syndrome mutation reveals a conserved role for the carboxy-terminus in FMRP localization and function.

Okray Z, de Esch CE, Van Esch H, Devriendt K, Claeys A, Yan J, Verbeeck J, Froyen G, Willemsen R, de Vrij FM, Hassan BA. Okray Z, et al. Among authors: froyen g. EMBO Mol Med. 2015 Apr;7(4):423-37. doi: 10.15252/emmm.201404576. EMBO Mol Med. 2015. PMID: 25693964 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

98 results

Search Page

Filters