Hanauer A - Search Results

1

The Coffin-Lowry syndrome-associated protein RSK2 is implicated in calcium-regulated exocytosis through the regulation of PLD1.

Zeniou-Meyer M, Liu Y, Béglé A, Olanich ME, Hanauer A, Becherer U, Rettig J, Bader MF, Vitale N. Zeniou-Meyer M, et al. Among authors: hanauer a. Proc Natl Acad Sci U S A. 2008 Jun 17;105(24):8434-9. doi: 10.1073/pnas.0710676105. Epub 2008 Jun 11. Proc Natl Acad Sci U S A. 2008. PMID: 18550821 Free PMC article.

2

The Coffin-Lowry syndrome-associated protein RSK2 regulates neurite outgrowth through phosphorylation of phospholipase D1 (PLD1) and synthesis of phosphatidic acid.

Ammar MR, Humeau Y, Hanauer A, Nieswandt B, Bader MF, Vitale N. Ammar MR, et al. Among authors: hanauer a. J Neurosci. 2013 Dec 11;33(50):19470-9. doi: 10.1523/JNEUROSCI.2283-13.2013. J Neurosci. 2013. PMID: 24336713 Free PMC article.

3

PLD1 participates in BDNF-induced signalling in cortical neurons.

Ammar MR, Thahouly T, Hanauer A, Stegner D, Nieswandt B, Vitale N. Ammar MR, et al. Among authors: hanauer a. Sci Rep. 2015 Oct 6;5:14778. doi: 10.1038/srep14778. Sci Rep. 2015. PMID: 26437780 Free PMC article.

4

Coffin-Lowry syndrome.

Pereira PM, Schneider A, Pannetier S, Heron D, Hanauer A. Pereira PM, et al. Among authors: hanauer a. Eur J Hum Genet. 2010 Jun;18(6):627-33. doi: 10.1038/ejhg.2009.189. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888300 Free PMC article. Review.

5

Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome.

Delaunoy JP, Dubos A, Marques Pereira P, Hanauer A. Delaunoy JP, et al. Among authors: hanauer a. Clin Genet. 2006 Aug;70(2):161-6. doi: 10.1111/j.1399-0004.2006.00660.x. Clin Genet. 2006. PMID: 16879200

6

The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient.

Marques Pereira P, Heron D, Hanauer A. Marques Pereira P, et al. Among authors: hanauer a. Hum Genet. 2007 Dec;122(5):541-3. doi: 10.1007/s00439-007-0424-1. Epub 2007 Aug 24. Hum Genet. 2007. PMID: 17717706

7

Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin-Lowry syndrome.

Morice E, Farley S, Poirier R, Dallerac G, Chagneau C, Pannetier S, Hanauer A, Davis S, Vaillend C, Laroche S. Morice E, et al. Among authors: hanauer a. Neurobiol Dis. 2013 Oct;58:156-68. doi: 10.1016/j.nbd.2013.05.016. Epub 2013 Jun 3. Neurobiol Dis. 2013. PMID: 23742761

8

Rsk-2 activity is necessary for epidermal growth factor-induced phosphorylation of CREB protein and transcription of c-fos gene.

De Cesare D, Jacquot S, Hanauer A, Sassone-Corsi P. De Cesare D, et al. Among authors: hanauer a. Proc Natl Acad Sci U S A. 1998 Oct 13;95(21):12202-7. doi: 10.1073/pnas.95.21.12202. Proc Natl Acad Sci U S A. 1998. PMID: 9770464 Free PMC article.

9

Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior.

Poirier R, Jacquot S, Vaillend C, Soutthiphong AA, Libbey M, Davis S, Laroche S, Hanauer A, Welzl H, Lipp HP, Wolfer DP. Poirier R, et al. Among authors: hanauer a. Behav Genet. 2007 Jan;37(1):31-50. doi: 10.1007/s10519-006-9116-1. Epub 2006 Oct 11. Behav Genet. 2007. PMID: 17033934 Free article.

10

Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome.

Zeniou M, Gattoni R, Hanauer A, Stévenin J. Zeniou M, et al. Among authors: hanauer a. Nucleic Acids Res. 2004 Feb 18;32(3):1214-23. doi: 10.1093/nar/gkh272. Print 2004. Nucleic Acids Res. 2004. PMID: 14973203 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

114 results

Search Page

Filters