Gourdon G - Search Results

1

Molecular, physiological, and motor performance defects in DMSXL mice carrying >1,000 CTG repeats from the human DM1 locus.

Huguet A, Medja F, Nicole A, Vignaud A, Guiraud-Dogan C, Ferry A, Decostre V, Hogrel JY, Metzger F, Hoeflich A, Baraibar M, Gomes-Pereira M, Puymirat J, Bassez G, Furling D, Munnich A, Gourdon G. Huguet A, et al. Among authors: gourdon g. PLoS Genet. 2012;8(11):e1003043. doi: 10.1371/journal.pgen.1003043. Epub 2012 Nov 29. PLoS Genet. 2012. PMID: 23209425 Free PMC article.

2

Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice.

Gourdon G, Radvanyi F, Lia AS, Duros C, Blanche M, Abitbol M, Junien C, Hofmann-Radvanyi H. Gourdon G, et al. Nat Genet. 1997 Feb;15(2):190-2. doi: 10.1038/ng0297-190. Nat Genet. 1997. PMID: 9020847

3

Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacities.

Lia AS, Seznec H, Hofmann-Radvanyi H, Radvanyi F, Duros C, Saquet C, Blanche M, Junien C, Gourdon G. Lia AS, et al. Among authors: gourdon g. Hum Mol Genet. 1998 Aug;7(8):1285-91. doi: 10.1093/hmg/7.8.1285. Hum Mol Genet. 1998. PMID: 9668171

4

Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability.

Seznec H, Lia-Baldini AS, Duros C, Fouquet C, Lacroix C, Hofmann-Radvanyi H, Junien C, Gourdon G. Seznec H, et al. Among authors: gourdon g. Hum Mol Genet. 2000 May 1;9(8):1185-94. doi: 10.1093/hmg/9.8.1185. Hum Mol Genet. 2000. PMID: 10767343

5

Defective satellite cells in congenital myotonic dystrophy.

Furling D, Coiffier L, Mouly V, Barbet JP, St Guily JL, Taneja K, Gourdon G, Junien C, Butler-Browne GS. Furling D, et al. Among authors: gourdon g. Hum Mol Genet. 2001 Sep 15;10(19):2079-87. doi: 10.1093/hmg/10.19.2079. Hum Mol Genet. 2001. PMID: 11590125

6

Mice transgenic for the human myotonic dystrophy region with expanded CTG repeats display muscular and brain abnormalities.

Seznec H, Agbulut O, Sergeant N, Savouret C, Ghestem A, Tabti N, Willer JC, Ourth L, Duros C, Brisson E, Fouquet C, Butler-Browne G, Delacourte A, Junien C, Gourdon G. Seznec H, et al. Among authors: gourdon g. Hum Mol Genet. 2001 Nov 1;10(23):2717-26. doi: 10.1093/hmg/10.23.2717. Hum Mol Genet. 2001. PMID: 11726559

7

MSH2-dependent germinal CTG repeat expansions are produced continuously in spermatogonia from DM1 transgenic mice.

Savouret C, Garcia-Cordier C, Megret J, te Riele H, Junien C, Gourdon G. Savouret C, et al. Among authors: gourdon g. Mol Cell Biol. 2004 Jan;24(2):629-37. doi: 10.1128/MCB.24.2.629-637.2004. Mol Cell Biol. 2004. PMID: 14701736 Free PMC article.

8

Analysis of CTG repeats using DM1 model mice.

Savouret C, Junien C, Gourdon G. Savouret C, et al. Among authors: gourdon g. Methods Mol Biol. 2004;277:185-97. doi: 10.1385/1-59259-804-8:185. Methods Mol Biol. 2004. PMID: 15201457

9

Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice.

Foiry L, Dong L, Savouret C, Hubert L, te Riele H, Junien C, Gourdon G. Foiry L, et al. Among authors: gourdon g. Hum Genet. 2006 Jun;119(5):520-6. doi: 10.1007/s00439-006-0164-7. Epub 2006 Mar 22. Hum Genet. 2006. PMID: 16552576

10

CTG trinucleotide repeat "big jumps": large expansions, small mice.

Gomes-Pereira M, Foiry L, Nicole A, Huguet A, Junien C, Munnich A, Gourdon G. Gomes-Pereira M, et al. Among authors: gourdon g. PLoS Genet. 2007 Apr 6;3(4):e52. doi: 10.1371/journal.pgen.0030052. Epub 2007 Feb 22. PLoS Genet. 2007. PMID: 17411343 Free PMC article.

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