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Items: 1 to 20 of 212

1.

SMN tudor domain structure and its interaction with the Sm proteins.

Selenko P, Sprangers R, Stier G, Bühler D, Fischer U, Sattler M.

Nat Struct Biol. 2001 Jan;8(1):27-31.

PMID:
11135666
2.

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
3.
4.

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
5.

Definition of domain boundaries and crystallization of the SMN Tudor domain.

Sprangers R, Selenko P, Sattler M, Sinning I, Groves MR.

Acta Crystallogr D Biol Crystallogr. 2003 Feb;59(Pt 2):366-8. Epub 2003 Jan 23.

PMID:
12554955
7.

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.

8.

Determinants of the interaction of the spinal muscular atrophy disease protein SMN with the dimethylarginine-modified box H/ACA small nucleolar ribonucleoprotein GAR1.

Whitehead SE, Jones KW, Zhang X, Cheng X, Terns RM, Terns MP.

J Biol Chem. 2002 Dec 13;277(50):48087-93. Epub 2002 Sep 19.

9.

The Ewing's sarcoma protein interacts with the Tudor domain of the survival motor neuron protein.

Young PJ, Francis JW, Lince D, Coon K, Androphy EJ, Lorson CL.

Brain Res Mol Brain Res. 2003 Nov 6;119(1):37-49.

PMID:
14597228
10.

Distinct domains of the spinal muscular atrophy protein SMN are required for targeting to Cajal bodies in mammalian cells.

Renvoisé B, Khoobarry K, Gendron MC, Cibert C, Viollet L, Lefebvre S.

J Cell Sci. 2006 Feb 15;119(Pt 4):680-92. Epub 2006 Jan 31.

11.
12.

The SMN complex: an assembly machine for RNPs.

Battle DJ, Kasim M, Yong J, Lotti F, Lau CK, Mouaikel J, Zhang Z, Han K, Wan L, Dreyfuss G.

Cold Spring Harb Symp Quant Biol. 2006;71:313-20. Review.

PMID:
17381311
13.

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.

14.

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.

15.

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.

16.

Analysis of mutations in the tudor domain of the survival motor neuron protein SMN.

Mohaghegh P, Rodrigues NR, Owen N, Ponting CP, Le TT, Burghes AH, Davies KE.

Eur J Hum Genet. 1999 Jul;7(5):519-25.

17.

Tudor reign.

MacKenzie AE, Gendron NH.

Nat Struct Biol. 2001 Jan;8(1):13-5. No abstract available.

PMID:
11135659
18.

The Gemin6-Gemin7 heterodimer from the survival of motor neurons complex has an Sm protein-like structure.

Ma Y, Dostie J, Dreyfuss G, Van Duyne GD.

Structure. 2005 Jun;13(6):883-92.

19.

A comprehensive interaction map of the human survival of motor neuron (SMN) complex.

Otter S, Grimmler M, Neuenkirchen N, Chari A, Sickmann A, Fischer U.

J Biol Chem. 2007 Feb 23;282(8):5825-33. Epub 2006 Dec 18.

20.

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

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