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Items: 1 to 20 of 188

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.

Essential role for the tudor domain of SMN in spliceosomal U snRNP assembly: implications for spinal muscular atrophy.

Bühler D, Raker V, Lührmann R, Fischer U.

Hum Mol Genet. 1999 Dec;8(13):2351-7.

PMID:
10556282
5.

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.

6.

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.

7.

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.

8.

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.

9.

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.

PMID:
11181573
10.
12.

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
13.
14.

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.

Hum Mol Genet. 2002 Jan 1;11(1):93-105.

PMID:
11773003
15.

Direct interaction of the spinal muscular atrophy disease protein SMN with the small nucleolar RNA-associated protein fibrillarin.

Jones KW, Gorzynski K, Hales CM, Fischer U, Badbanchi F, Terns RM, Terns MP.

J Biol Chem. 2001 Oct 19;276(42):38645-51. Epub 2001 Aug 16.

16.

Depletion of SMN by RNA interference in HeLa cells induces defects in Cajal body formation.

Girard C, Neel H, Bertrand E, Bordonné R.

Nucleic Acids Res. 2006 May 31;34(10):2925-32. Print 2006.

17.

Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis.

Carrel TL, McWhorter ML, Workman E, Zhang H, Wolstencroft EC, Lorson C, Bassell GJ, Burghes AH, Beattie CE.

J Neurosci. 2006 Oct 25;26(43):11014-22.

18.

The SMN complex is associated with snRNPs throughout their cytoplasmic assembly pathway.

Massenet S, Pellizzoni L, Paushkin S, Mattaj IW, Dreyfuss G.

Mol Cell Biol. 2002 Sep;22(18):6533-41.

19.

A role for complexes of survival of motor neurons (SMN) protein with gemins and profilin in neurite-like cytoplasmic extensions of cultured nerve cells.

Sharma A, Lambrechts A, Hao le T, Le TT, Sewry CA, Ampe C, Burghes AH, Morris GE.

Exp Cell Res. 2005 Sep 10;309(1):185-97.

PMID:
15975577
20.

The role of the SMN gene in proximal spinal muscular atrophy.

Lefebvre S, Bürglen L, Frézal J, Munnich A, Melki J.

Hum Mol Genet. 1998;7(10):1531-6. Review.

PMID:
9735373

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