Jablonka S - Search Results

1

C9ORF72 interaction with cofilin modulates actin dynamics in motor neurons.

Sivadasan R, Hornburg D, Drepper C, Frank N, Jablonka S, Hansel A, Lojewski X, Sterneckert J, Hermann A, Shaw PJ, Ince PG, Mann M, Meissner F, Sendtner M. Sivadasan R, et al. Among authors: jablonka s. Nat Neurosci. 2016 Dec;19(12):1610-1618. doi: 10.1038/nn.4407. Epub 2016 Oct 10. Nat Neurosci. 2016. PMID: 27723745 Free article.

2

The role of SMN in spinal muscular atrophy.

Jablonka S, Rossoll W, Schrank B, Sendtner M. Jablonka S, et al. J Neurol. 2000 Mar;247 Suppl 1:I37-42. doi: 10.1007/s004150050555. J Neurol. 2000. PMID: 10795885 Review.

3

Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?

Rossoll W, Kröning AK, Ohndorf UM, Steegborn C, Jablonka S, Sendtner M. Rossoll W, et al. Among authors: jablonka s. Hum Mol Genet. 2002 Jan 1;11(1):93-105. doi: 10.1093/hmg/11.1.93. Hum Mol Genet. 2002. PMID: 11773003

4

Gene targeting of Gemin2 in mice reveals a correlation between defects in the biogenesis of U snRNPs and motoneuron cell death.

Jablonka S, Holtmann B, Meister G, Bandilla M, Rossoll W, Fischer U, Sendtner M. Jablonka S, et al. Proc Natl Acad Sci U S A. 2002 Jul 23;99(15):10126-31. doi: 10.1073/pnas.152318699. Epub 2002 Jun 28. Proc Natl Acad Sci U S A. 2002. PMID: 12091709 Free PMC article.

5

Missense mutation in the tubulin-specific chaperone E (Tbce) gene in the mouse mutant progressive motor neuronopathy, a model of human motoneuron disease.

Bommel H, Xie G, Rossoll W, Wiese S, Jablonka S, Boehm T, Sendtner M. Bommel H, et al. Among authors: jablonka s. J Cell Biol. 2002 Nov 25;159(4):563-9. doi: 10.1083/jcb.200208001. J Cell Biol. 2002. PMID: 12446740 Free PMC article.

6

Molecular and cellular basis of spinal muscular atrophy.

Jablonka S, Sendtner M. Jablonka S, et al. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):144-9. doi: 10.1080/14660820310011296. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003. PMID: 13129800 Review.

7

Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons.

Rossoll W, Jablonka S, Andreassi C, Kröning AK, Karle K, Monani UR, Sendtner M. Rossoll W, et al. Among authors: jablonka s. J Cell Biol. 2003 Nov 24;163(4):801-12. doi: 10.1083/jcb.200304128. Epub 2003 Nov 17. J Cell Biol. 2003. PMID: 14623865 Free PMC article.

8

Axonal defects in mouse models of motoneuron disease.

Jablonka S, Wiese S, Sendtner M. Jablonka S, et al. J Neurobiol. 2004 Feb 5;58(2):272-86. doi: 10.1002/neu.10313. J Neurobiol. 2004. PMID: 14704958

9

Characterization of Ighmbp2 in motor neurons and implications for the pathomechanism in a mouse model of human spinal muscular atrophy with respiratory distress type 1 (SMARD1).

Grohmann K, Rossoll W, Kobsar I, Holtmann B, Jablonka S, Wessig C, Stoltenburg-Didinger G, Fischer U, Hübner C, Martini R, Sendtner M. Grohmann K, et al. Among authors: jablonka s. Hum Mol Genet. 2004 Sep 15;13(18):2031-42. doi: 10.1093/hmg/ddh222. Epub 2004 Jul 21. Hum Mol Genet. 2004. PMID: 15269181

10

Bag1 is essential for differentiation and survival of hematopoietic and neuronal cells.

Götz R, Wiese S, Takayama S, Camarero GC, Rossoll W, Schweizer U, Troppmair J, Jablonka S, Holtmann B, Reed JC, Rapp UR, Sendtner M. Götz R, et al. Among authors: jablonka s. Nat Neurosci. 2005 Sep;8(9):1169-78. doi: 10.1038/nn1524. Epub 2005 Aug 21. Nat Neurosci. 2005. PMID: 16116448 Free PMC article.

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