Strähle U - Search Results

1

The use of zebrafish mutants to identify secondary target effects of acetylcholine esterase inhibitors.

Behra M, Etard C, Cousin X, Strähle U. Behra M, et al. Among authors: strahle u. Toxicol Sci. 2004 Feb;77(2):325-33. doi: 10.1093/toxsci/kfh020. Epub 2003 Dec 2. Toxicol Sci. 2004. PMID: 14657522

2

Acetylcholinesterase is required for neuronal and muscular development in the zebrafish embryo.

Behra M, Cousin X, Bertrand C, Vonesch JL, Biellmann D, Chatonnet A, Strähle U. Behra M, et al. Among authors: strahle u. Nat Neurosci. 2002 Feb;5(2):111-8. doi: 10.1038/nn788. Nat Neurosci. 2002. PMID: 11753420

3

Mutation in the delta-subunit of the nAChR suppresses the muscle defects caused by lack of Dystrophin.

Etard C, Behra M, Ertzer R, Fischer N, Jesuthasan S, Blader P, Geisler R, Strähle U. Etard C, et al. Among authors: strahle u. Dev Dyn. 2005 Dec;234(4):1016-25. doi: 10.1002/dvdy.20592. Dev Dyn. 2005. PMID: 16245342 Free article.

4

The UCS factor Steif/Unc-45b interacts with the heat shock protein Hsp90a during myofibrillogenesis.

Etard C, Behra M, Fischer N, Hutcheson D, Geisler R, Strähle U. Etard C, et al. Among authors: strahle u. Dev Biol. 2007 Aug 1;308(1):133-43. doi: 10.1016/j.ydbio.2007.05.014. Epub 2007 May 18. Dev Biol. 2007. PMID: 17586488 Free article.

5

Are there non-catalytic functions of acetylcholinesterases? Lessons from mutant animal models.

Cousin X, Strähle U, Chatonnet A. Cousin X, et al. Among authors: strahle u. Bioessays. 2005 Feb;27(2):189-200. doi: 10.1002/bies.20153. Bioessays. 2005. PMID: 15666354

6

Lack of Apobec2-related proteins causes a dystrophic muscle phenotype in zebrafish embryos.

Etard C, Roostalu U, Strähle U. Etard C, et al. Among authors: strahle u. J Cell Biol. 2010 May 3;189(3):527-39. doi: 10.1083/jcb.200912125. J Cell Biol. 2010. PMID: 20440001 Free PMC article.

7

Novel IQCE variations confirm its role in postaxial polydactyly and cause ciliary defect phenotype in zebrafish.

Estrada-Cuzcano A, Etard C, Delvallée C, Stoetzel C, Schaefer E, Scheidecker S, Geoffroy V, Schneider A, Studer F, Mattioli F, Chennen K, Sigaudy S, Plassard D, Poch O, Piton A, Strahle U, Muller J, Dollfus H. Estrada-Cuzcano A, et al. Among authors: strahle u. Hum Mutat. 2020 Jan;41(1):240-254. doi: 10.1002/humu.23924. Epub 2019 Oct 17. Hum Mutat. 2020. PMID: 31549751

8

Dystrophin and Dp71, two products of the DMD gene, show a different pattern of expression during embryonic development in zebrafish.

Bolaños-Jiménez F, Bordais A, Behra M, Strähle U, Sahel J, Rendón A. Bolaños-Jiménez F, et al. Among authors: strahle u. Mech Dev. 2001 Apr;102(1-2):239-41. doi: 10.1016/s0925-4773(01)00310-0. Mech Dev. 2001. PMID: 11287201 Free article.

9

Glycolysis supports embryonic muscle growth by promoting myoblast fusion.

Tixier V, Bataillé L, Etard C, Jagla T, Weger M, Daponte JP, Strähle U, Dickmeis T, Jagla K. Tixier V, et al. Among authors: strahle u. Proc Natl Acad Sci U S A. 2013 Nov 19;110(47):18982-7. doi: 10.1073/pnas.1301262110. Epub 2013 Nov 4. Proc Natl Acad Sci U S A. 2013. PMID: 24191061 Free PMC article.

10

A mutation in VPS15 (PIK3R4) causes a ciliopathy and affects IFT20 release from the cis-Golgi.

Stoetzel C, Bär S, De Craene JO, Scheidecker S, Etard C, Chicher J, Reck JR, Perrault I, Geoffroy V, Chennen K, Strähle U, Hammann P, Friant S, Dollfus H. Stoetzel C, et al. Among authors: strahle u. Nat Commun. 2016 Nov 24;7:13586. doi: 10.1038/ncomms13586. Nat Commun. 2016. PMID: 27882921 Free PMC article.

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