Jablonka S - Search Results

1

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.

2

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: jablonka s. Hum Mol Genet. 2000 Feb 12;9(3):333-9. doi: 10.1093/hmg/9.3.333. Hum Mol Genet. 2000. PMID: 10655541

3

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. Hum Mol Genet. 2000 Feb 12;9(3):341-6. doi: 10.1093/hmg/9.3.341. Hum Mol Genet. 2000. PMID: 10655542

4

Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy.

Jablonka S, Bandilla M, Wiese S, Bühler D, Wirth B, Sendtner M, Fischer U. Jablonka S, et al. Hum Mol Genet. 2001 Mar 1;10(5):497-505. doi: 10.1093/hmg/10.5.497. Hum Mol Genet. 2001. PMID: 11181573

5

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

6

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.

7

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.

8

A transgene carrying an A2G missense mutation in the SMN gene modulates phenotypic severity in mice with severe (type I) spinal muscular atrophy.

Monani UR, Pastore MT, Gavrilina TO, Jablonka S, Le TT, Andreassi C, DiCocco JM, Lorson C, Androphy EJ, Sendtner M, Podell M, Burghes AH. Monani UR, et al. Among authors: jablonka s. J Cell Biol. 2003 Jan 6;160(1):41-52. doi: 10.1083/jcb.200208079. Epub 2003 Jan 6. J Cell Biol. 2003. PMID: 12515823 Free PMC article.

9

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.

10

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.

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