Sendtner M - Search Results

1

Hot-spot KIF5A mutations cause familial ALS.

Brenner D, Yilmaz R, Müller K, Grehl T, Petri S, Meyer T, Grosskreutz J, Weydt P, Ruf W, Neuwirth C, Weber M, Pinto S, Claeys KG, Schrank B, Jordan B, Knehr A, Günther K, Hübers A, Zeller D, Kubisch C, Jablonka S, Sendtner M, Klopstock T, de Carvalho M, Sperfeld A, Borck G, Volk AE, Dorst J, Weis J, Otto M, Schuster J, Del Tredici K, Braak H, Danzer KM, Freischmidt A, Meitinger T, Strom TM, Ludolph AC, Andersen PM, Weishaupt JH; German ALS network MND-NET. Brenner D, et al. Among authors: sendtner m. Brain. 2018 Mar 1;141(3):688-697. doi: 10.1093/brain/awx370. Brain. 2018. PMID: 29342275 Free PMC article.

2

Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos.

Schrank B, Götz R, Gunnersen JM, Ure JM, Toyka KV, Smith AG, Sendtner M. Schrank B, et al. Among authors: sendtner m. Proc Natl Acad Sci U S A. 1997 Sep 2;94(18):9920-5. doi: 10.1073/pnas.94.18.9920. Proc Natl Acad Sci U S A. 1997. PMID: 9275227 Free PMC article.

3

Potential implications of a ciliary neurotrophic factor gene mutation in a German population of patients with motor neuron disease.

Giess R, Goetz R, Schrank B, Ochs G, Sendtner M, Toyka K. Giess R, et al. Among authors: sendtner m. Muscle Nerve. 1998 Feb;21(2):236-8. doi: 10.1002/(sici)1097-4598(199802)21:2<236::aid-mus12>3.0.co;2-#. Muscle Nerve. 1998. PMID: 9466600

4

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

5

The role of SMN in spinal muscular atrophy.

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

6

Motoneuron cell death and neurotrophic factors: basic models for development of new therapeutic strategies in ALS.

Beck M, Karch C, Wiese S, Sendtner M. Beck M, et al. Among authors: sendtner m. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001 Mar;2 Suppl 1:S55-68. Amyotroph Lateral Scler Other Motor Neuron Disord. 2001. PMID: 11465926 Review.

7

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

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: sendtner m. 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

Molecular and cellular basis of spinal muscular atrophy.

Jablonka S, Sendtner M. Jablonka S, et al. Among authors: sendtner m. 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: sendtner m. 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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