Wirth B - Search Results

1

Plastin 3 is upregulated in iPSC-derived motoneurons from asymptomatic SMN1-deleted individuals.

Heesen L, Peitz M, Torres-Benito L, Hölker I, Hupperich K, Dobrindt K, Jungverdorben J, Ritzenhofen S, Weykopf B, Eckert D, Hosseini-Barkooie SM, Storbeck M, Fusaki N, Lonigro R, Heller R, Kye MJ, Brüstle O, Wirth B. Heesen L, et al. Among authors: wirth b. Cell Mol Life Sci. 2016 May;73(10):2089-104. doi: 10.1007/s00018-015-2084-y. Epub 2015 Nov 16. Cell Mol Life Sci. 2016. PMID: 26573968 Free PMC article.

2

Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.

Sun Y, Grimmler M, Schwarzer V, Schoenen F, Fischer U, Wirth B. Sun Y, et al. Among authors: wirth b. Hum Mutat. 2005 Jan;25(1):64-71. doi: 10.1002/humu.20111. Hum Mutat. 2005. PMID: 15580564

3

Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy number.

Wirth B, Brichta L, Schrank B, Lochmüller H, Blick S, Baasner A, Heller R. Wirth B, et al. Hum Genet. 2006 May;119(4):422-8. doi: 10.1007/s00439-006-0156-7. Epub 2006 Mar 1. Hum Genet. 2006. PMID: 16508748

4

In vivo activation of SMN in spinal muscular atrophy carriers and patients treated with valproate.

Brichta L, Holker I, Haug K, Klockgether T, Wirth B. Brichta L, et al. Among authors: wirth b. Ann Neurol. 2006 Jun;59(6):970-5. doi: 10.1002/ana.20836. Ann Neurol. 2006. PMID: 16607616 Clinical Trial.

5

The benzamide M344, a novel histone deacetylase inhibitor, significantly increases SMN2 RNA/protein levels in spinal muscular atrophy cells.

Riessland M, Brichta L, Hahnen E, Wirth B. Riessland M, et al. Among authors: wirth b. Hum Genet. 2006 Aug;120(1):101-10. doi: 10.1007/s00439-006-0186-1. Epub 2006 May 25. Hum Genet. 2006. PMID: 16724231

6

In vitro and ex vivo evaluation of second-generation histone deacetylase inhibitors for the treatment of spinal muscular atrophy.

Hahnen E, Eyüpoglu IY, Brichta L, Haastert K, Tränkle C, Siebzehnrübl FA, Riessland M, Hölker I, Claus P, Romstöck J, Buslei R, Wirth B, Blümcke I. Hahnen E, et al. Among authors: wirth b. J Neurochem. 2006 Jul;98(1):193-202. doi: 10.1111/j.1471-4159.2006.03868.x. J Neurochem. 2006. PMID: 16805808 Free article.

7

Spinal muscular atrophy: from gene to therapy.

Wirth B, Brichta L, Hahnen E. Wirth B, et al. Semin Pediatr Neurol. 2006 Jun;13(2):121-31. doi: 10.1016/j.spen.2006.06.008. Semin Pediatr Neurol. 2006. PMID: 17027862 Review.

8

Spinal muscular atrophy and therapeutic prospects.

Wirth B, Brichta L, Hahnen E. Wirth B, et al. Prog Mol Subcell Biol. 2006;44:109-32. doi: 10.1007/978-3-540-34449-0_6. Prog Mol Subcell Biol. 2006. PMID: 17076267

9

Nonsense-mediated messenger RNA decay of survival motor neuron 1 causes spinal muscular atrophy.

Brichta L, Garbes L, Jedrzejowska M, Grellscheid SN, Holker I, Zimmermann K, Wirth B. Brichta L, et al. Among authors: wirth b. Hum Genet. 2008 Mar;123(2):141-53. doi: 10.1007/s00439-007-0455-7. Epub 2008 Jan 3. Hum Genet. 2008. PMID: 18172693

10

Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy.

Oprea GE, Kröber S, McWhorter ML, Rossoll W, Müller S, Krawczak M, Bassell GJ, Beattie CE, Wirth B. Oprea GE, et al. Among authors: wirth b. Science. 2008 Apr 25;320(5875):524-7. doi: 10.1126/science.1155085. Science. 2008. PMID: 18440926 Free PMC article.

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