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Results: 1 to 20 of 165

Similar articles for PubMed (Select 9323129)

2.

The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis.

Fischer U, Liu Q, Dreyfuss G.

Cell. 1997 Sep 19;90(6):1023-9.

3.

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.

Hum Mutat. 2005 Jan;25(1):64-71.

PMID:
15580564
4.

Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems.

Charroux B, Pellizzoni L, Perkinson RA, Shevchenko A, Mann M, Dreyfuss G.

J Cell Biol. 1999 Dec 13;147(6):1181-94.

5.
6.

The survival of motor neurons protein determines the capacity for snRNP assembly: biochemical deficiency in spinal muscular atrophy.

Wan L, Battle DJ, Yong J, Gubitz AK, Kolb SJ, Wang J, Dreyfuss G.

Mol Cell Biol. 2005 Jul;25(13):5543-51.

7.

A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing.

Pellizzoni L, Kataoka N, Charroux B, Dreyfuss G.

Cell. 1998 Nov 25;95(5):615-24.

8.

SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins.

Pellizzoni L, Charroux B, Dreyfuss G.

Proc Natl Acad Sci U S A. 1999 Sep 28;96(20):11167-72.

9.

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.

Hum Mol Genet. 2000 Aug 12;9(13):1977-86.

10.

Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli.

Charroux B, Pellizzoni L, Perkinson RA, Yong J, Shevchenko A, Mann M, Dreyfuss G.

J Cell Biol. 2000 Mar 20;148(6):1177-86.

11.

The spinal muscular atrophy disease gene product, SMN: A link between snRNP biogenesis and the Cajal (coiled) body.

Carvalho T, Almeida F, Calapez A, Lafarga M, Berciano MT, Carmo-Fonseca M.

J Cell Biol. 1999 Nov 15;147(4):715-28.

12.

Gemin8 is a novel component of the survival motor neuron complex and functions in small nuclear ribonucleoprotein assembly.

Carissimi C, Saieva L, Baccon J, Chiarella P, Maiolica A, Sawyer A, Rappsilber J, Pellizzoni L.

J Biol Chem. 2006 Mar 24;281(12):8126-34. Epub 2006 Jan 24.

13.

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.

Hum Mol Genet. 2001 Mar 1;10(5):497-505.

14.

SMN, the product of the spinal muscular atrophy gene, binds preferentially to dimethylarginine-containing protein targets.

Friesen WJ, Massenet S, Paushkin S, Wyce A, Dreyfuss G.

Mol Cell. 2001 May;7(5):1111-7.

15.
17.

Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs.

Gabanella F, Butchbach ME, Saieva L, Carissimi C, Burghes AH, Pellizzoni L.

PLoS One. 2007 Sep 26;2(9):e921.

18.

Subcellular distribution of survival motor neuron (SMN) protein: possible involvement in nucleocytoplasmic and dendritic transport.

Béchade C, Rostaing P, Cisterni C, Kalisch R, La Bella V, Pettmann B, Triller A.

Eur J Neurosci. 1999 Jan;11(1):293-304.

PMID:
9987032
20.
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