Laggerbauer B - Search Results

1

Evidence that fragile X mental retardation protein is a negative regulator of translation.

Laggerbauer B, Ostareck D, Keidel EM, Ostareck-Lederer A, Fischer U. Laggerbauer B, et al. Hum Mol Genet. 2001 Feb 15;10(4):329-38. doi: 10.1093/hmg/10.4.329. Hum Mol Genet. 2001. PMID: 11157796

2

Tdrd3 is a novel stress granule-associated protein interacting with the Fragile-X syndrome protein FMRP.

Linder B, Plöttner O, Kroiss M, Hartmann E, Laggerbauer B, Meister G, Keidel E, Fischer U. Linder B, et al. Among authors: laggerbauer b. Hum Mol Genet. 2008 Oct 15;17(20):3236-46. doi: 10.1093/hmg/ddn219. Epub 2008 Jul 28. Hum Mol Genet. 2008. PMID: 18664458

3

Characterization of a nuclear 20S complex containing the survival of motor neurons (SMN) protein and a specific subset of spliceosomal Sm proteins.

Meister G, Bühler D, Laggerbauer B, Zobawa M, Lottspeich F, Fischer U. Meister G, et al. Among authors: laggerbauer b. Hum Mol Genet. 2000 Aug 12;9(13):1977-86. doi: 10.1093/hmg/9.13.1977. Hum Mol Genet. 2000. PMID: 10942426

4

Systemic splicing factor deficiency causes tissue-specific defects: a zebrafish model for retinitis pigmentosa.

Linder B, Dill H, Hirmer A, Brocher J, Lee GP, Mathavan S, Bolz HJ, Winkler C, Laggerbauer B, Fischer U. Linder B, et al. Among authors: laggerbauer b. Hum Mol Genet. 2011 Jan 15;20(2):368-77. doi: 10.1093/hmg/ddq473. Epub 2010 Nov 3. Hum Mol Genet. 2011. PMID: 21051334

5

IGHMBP2 is a ribosome-associated helicase inactive in the neuromuscular disorder distal SMA type 1 (DSMA1).

Guenther UP, Handoko L, Laggerbauer B, Jablonka S, Chari A, Alzheimer M, Ohmer J, Plöttner O, Gehring N, Sickmann A, von Au K, Schuelke M, Fischer U. Guenther UP, et al. Among authors: laggerbauer b. Hum Mol Genet. 2009 Apr 1;18(7):1288-300. doi: 10.1093/hmg/ddp028. Epub 2009 Jan 20. Hum Mol Genet. 2009. PMID: 19158098

6

Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy.

Winkler C, Eggert C, Gradl D, Meister G, Giegerich M, Wedlich D, Laggerbauer B, Fischer U. Winkler C, et al. Among authors: laggerbauer b. Genes Dev. 2005 Oct 1;19(19):2320-30. doi: 10.1101/gad.342005. Genes Dev. 2005. PMID: 16204184 Free PMC article.

7

SMNrp is an essential pre-mRNA splicing factor required for the formation of the mature spliceosome.

Meister G, Hannus S, Plöttner O, Baars T, Hartmann E, Fakan S, Laggerbauer B, Fischer U. Meister G, et al. Among authors: laggerbauer b. EMBO J. 2001 May 1;20(9):2304-14. doi: 10.1093/emboj/20.9.2304. EMBO J. 2001. PMID: 11331595 Free PMC article.

8

Spinal muscular atrophy: the RNP connection.

Eggert C, Chari A, Laggerbauer B, Fischer U. Eggert C, et al. Among authors: laggerbauer b. Trends Mol Med. 2006 Mar;12(3):113-21. doi: 10.1016/j.molmed.2006.01.005. Epub 2006 Feb 13. Trends Mol Med. 2006. PMID: 16473550

9

Identification of a PRPF4 loss-of-function variant that abrogates U4/U6.U5 tri-snRNP integration and is associated with retinitis pigmentosa.

Linder B, Hirmer A, Gal A, Rüther K, Bolz HJ, Winkler C, Laggerbauer B, Fischer U. Linder B, et al. Among authors: laggerbauer b. PLoS One. 2014 Nov 10;9(11):e111754. doi: 10.1371/journal.pone.0111754. eCollection 2014. PLoS One. 2014. PMID: 25383878 Free PMC article.

10

An evolutionarily conserved U5 snRNP-specific protein is a GTP-binding factor closely related to the ribosomal translocase EF-2.

Fabrizio P, Laggerbauer B, Lauber J, Lane WS, Lührmann R. Fabrizio P, et al. Among authors: laggerbauer b. EMBO J. 1997 Jul 1;16(13):4092-106. doi: 10.1093/emboj/16.13.4092. EMBO J. 1997. PMID: 9233818 Free PMC article.

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