Rossoll W - Search Results

1

The role of SMN in spinal muscular atrophy.

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

2

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. Hum Mol Genet. 2002 Jan 1;11(1):93-105. doi: 10.1093/hmg/11.1.93. Hum Mol Genet. 2002. PMID: 11773003

3

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. 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.

4

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: rossoll w. 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

5

The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy.

Monani UR, Sendtner M, Coovert DD, Parsons DW, Andreassi C, Le TT, Jablonka S, Schrank B, Rossoll W, Prior TW, Morris GE, Burghes AH. Monani UR, et al. Among authors: rossoll w. Hum Mol Genet. 2000 Feb 12;9(3):333-9. doi: 10.1093/hmg/9.3.333. Hum Mol Genet. 2000. PMID: 10655541

6

Reduced survival motor neuron (Smn) gene dose in mice leads to motor neuron degeneration: an animal model for spinal muscular atrophy type III.

Jablonka S, Schrank B, Kralewski M, Rossoll W, Sendtner M. Jablonka S, et al. Among authors: rossoll w. Hum Mol Genet. 2000 Feb 12;9(3):341-6. doi: 10.1093/hmg/9.3.341. Hum Mol Genet. 2000. PMID: 10655542

7

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. Among authors: rossoll w. 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.

8

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: rossoll w. J Cell Biol. 2002 Nov 25;159(4):563-9. doi: 10.1083/jcb.200208001. J Cell Biol. 2002. PMID: 12446740 Free PMC article.

9

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: rossoll w. Nat Neurosci. 2005 Sep;8(9):1169-78. doi: 10.1038/nn1524. Epub 2005 Aug 21. Nat Neurosci. 2005. PMID: 16116448 Free PMC article.

10

The heterogeneous nuclear ribonucleoprotein-R is necessary for axonal beta-actin mRNA translocation in spinal motor neurons.

Glinka M, Herrmann T, Funk N, Havlicek S, Rossoll W, Winkler C, Sendtner M. Glinka M, et al. Among authors: rossoll w. Hum Mol Genet. 2010 May 15;19(10):1951-66. doi: 10.1093/hmg/ddq073. Epub 2010 Feb 18. Hum Mol Genet. 2010. PMID: 20167579

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