Ségalat L - Search Results

1

Caenorhabditis elegans as a chemical screening tool for the study o f neuromuscular disorders. Manual and semi-automated methods.

Giacomotto J, Ségalat L, Carre-Pierrat M, Gieseler K. Giacomotto J, et al. Among authors: segalat l. Methods. 2012 Jan;56(1):103-13. doi: 10.1016/j.ymeth.2011.10.010. Epub 2011 Oct 21. Methods. 2012. PMID: 22041718

2

Chemical genetics unveils a key role of mitochondrial dynamics, cytochrome c release and IP3R activity in muscular dystrophy.

Giacomotto J, Brouilly N, Walter L, Mariol MC, Berger J, Ségalat L, Becker TS, Currie PD, Gieseler K. Giacomotto J, et al. Among authors: segalat l. Hum Mol Genet. 2013 Nov 15;22(22):4562-78. doi: 10.1093/hmg/ddt302. Epub 2013 Jun 25. Hum Mol Genet. 2013. PMID: 23804750

3

Prednisone reduces muscle degeneration in dystrophin-deficient Caenorhabditis elegans.

Gaud A, Simon JM, Witzel T, Carre-Pierrat M, Wermuth CG, Ségalat L. Gaud A, et al. Among authors: segalat l. Neuromuscul Disord. 2004 Jun;14(6):365-70. doi: 10.1016/j.nmd.2004.02.011. Neuromuscul Disord. 2004. PMID: 15145337

4

Blocking of striated muscle degeneration by serotonin in C. elegans.

Carre-Pierrat M, Mariol MC, Chambonnier L, Laugraud A, Heskia F, Giacomotto J, Ségalat L. Carre-Pierrat M, et al. Among authors: segalat l. J Muscle Res Cell Motil. 2006;27(3-4):253-8. doi: 10.1007/s10974-006-9070-9. Epub 2006 Jun 22. J Muscle Res Cell Motil. 2006. PMID: 16791712

5

High-throughput screening and small animal models, where are we?

Giacomotto J, Ségalat L. Giacomotto J, et al. Among authors: segalat l. Br J Pharmacol. 2010 May;160(2):204-16. doi: 10.1111/j.1476-5381.2010.00725.x. Br J Pharmacol. 2010. PMID: 20423335 Free PMC article. Review.

6

Overexpression of dystrobrevin delays locomotion defects and muscle degeneration in a dystrophin-deficient Caenorhabditis elegans.

Gieseler K, Grisoni K, Mariol MC, Ségalat L. Gieseler K, et al. Among authors: segalat l. Neuromuscul Disord. 2002 May;12(4):371-7. doi: 10.1016/s0960-8966(01)00330-3. Neuromuscul Disord. 2002. PMID: 12062255

7

The SLO-1 BK channel of Caenorhabditis elegans is critical for muscle function and is involved in dystrophin-dependent muscle dystrophy.

Carre-Pierrat M, Grisoni K, Gieseler K, Mariol MC, Martin E, Jospin M, Allard B, Ségalat L. Carre-Pierrat M, et al. Among authors: segalat l. J Mol Biol. 2006 Apr 28;358(2):387-95. doi: 10.1016/j.jmb.2006.02.037. Epub 2006 Feb 28. J Mol Biol. 2006. PMID: 16527307

8

Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans.

Gieseler K, Grisoni K, Ségalat L. Gieseler K, et al. Among authors: segalat l. Curr Biol. 2000 Sep 21;10(18):1092-7. doi: 10.1016/s0960-9822(00)00691-6. Curr Biol. 2000. PMID: 10996789 Free article.

9

Dystrobrevin requires a dystrophin-binding domain to function in Caenorhabditis elegans.

Grisoni K, Gieseler K, Ségalat L. Grisoni K, et al. Among authors: segalat l. Eur J Biochem. 2002 Mar;269(6):1607-12. doi: 10.1046/j.1432-1327.2002.02780.x. Eur J Biochem. 2002. PMID: 11895430 Free article.

10

In vitro interactions of Caenorhabditis elegans dystrophin with dystrobrevin and syntrophin.

Gieseler K, Abdel-Dayem M, Ségalat L. Gieseler K, et al. Among authors: segalat l. FEBS Lett. 1999 Nov 12;461(1-2):59-62. doi: 10.1016/s0014-5793(99)01421-0. FEBS Lett. 1999. PMID: 10561496 Free article.

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