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Items: 1 to 20 of 106

1.

pY RNA1-s2: a highly retina-enriched small RNA that selectively binds to Matrin 3 (Matr3).

Yamazaki F, Kim HH, Lau P, Hwang CK, Iuvone PM, Klein D, Clokie SJ.

PLoS One. 2014 Feb 18;9(2):e88217. doi: 10.1371/journal.pone.0088217. eCollection 2014.

2.

Matrin 3 binds and stabilizes mRNA.

Salton M, Elkon R, Borodina T, Davydov A, Yaspo ML, Halperin E, Shiloh Y.

PLoS One. 2011;6(8):e23882. doi: 10.1371/journal.pone.0023882. Epub 2011 Aug 17.

3.

Characterization of the HIV-1 RNA associated proteome identifies Matrin 3 as a nuclear cofactor of Rev function.

Kula A, Guerra J, Knezevich A, Kleva D, Myers MP, Marcello A.

Retrovirology. 2011 Jul 20;8:60. doi: 10.1186/1742-4690-8-60.

4.

MATR3 disruption in human and mouse associated with bicuspid aortic valve, aortic coarctation and patent ductus arteriosus.

Quintero-Rivera F, Xi QJ, Keppler-Noreuil KM, Lee JH, Higgins AW, Anchan RM, Roberts AE, Seong IS, Fan X, Lage K, Lu LY, Tao J, Hu X, Berezney R, Gelb BD, Kamp A, Moskowitz IP, Lacro RV, Lu W, Morton CC, Gusella JF, Maas RL.

Hum Mol Genet. 2015 Apr 15;24(8):2375-89. doi: 10.1093/hmg/ddv004. Epub 2015 Jan 7.

5.

Nuclear poly(A) binding protein 1 (PABPN1) and Matrin3 interact in muscle cells and regulate RNA processing.

Banerjee A, Vest KE, Pavlath GK, Corbett AH.

Nucleic Acids Res. 2017 Oct 13;45(18):10706-10725. doi: 10.1093/nar/gkx786.

6.

Replication study of MATR3 in familial and sporadic amyotrophic lateral sclerosis.

Leblond CS, Gan-Or Z, Spiegelman D, Laurent SB, Szuto A, Hodgkinson A, Dionne-Laporte A, Provencher P, de Carvalho M, Orrù S, Brunet D, Bouchard JP, Awadalla P, Dupré N, Dion PA, Rouleau GA.

Neurobiol Aging. 2016 Jan;37:209.e17-209.e21. doi: 10.1016/j.neurobiolaging.2015.09.013. Epub 2015 Sep 28.

PMID:
26493020
7.

Matrin 3: chromosomal distribution and protein interactions.

Zeitz MJ, Malyavantham KS, Seifert B, Berezney R.

J Cell Biochem. 2009 Sep 1;108(1):125-33. doi: 10.1002/jcb.22234.

PMID:
19562669
8.

The transcription-splicing protein NonO/p54nrb and three NonO-interacting proteins bind to distal enhancer region and augment rhodopsin expression.

Yadav SP, Hao H, Yang HJ, Kautzmann MA, Brooks M, Nellissery J, Klocke B, Seifert M, Swaroop A.

Hum Mol Genet. 2014 Apr 15;23(8):2132-44. doi: 10.1093/hmg/ddt609. Epub 2013 Dec 2.

9.

Autosomal-dominant distal myopathy associated with a recurrent missense mutation in the gene encoding the nuclear matrix protein, matrin 3.

Senderek J, Garvey SM, Krieger M, Guergueltcheva V, Urtizberea A, Roos A, Elbracht M, Stendel C, Tournev I, Mihailova V, Feit H, Tramonte J, Hedera P, Crooks K, Bergmann C, Rudnik-Schöneborn S, Zerres K, Lochmüller H, Seboun E, Weis J, Beckmann JS, Hauser MA, Jackson CE.

Am J Hum Genet. 2009 Apr;84(4):511-8. doi: 10.1016/j.ajhg.2009.03.006. Epub 2009 Apr 2.

10.

Identification of novel nesprin-1 binding partners and cytoplasmic matrin-3 in processing bodies.

Rajgor D, Hanley JG, Shanahan CM.

Mol Biol Cell. 2016 Dec 1;27(24):3894-3902. Epub 2016 Oct 12.

11.

Matrin 3 and HIV Rev regulation of mRNA.

Dayton AI.

Retrovirology. 2011 Jul 20;8:62. doi: 10.1186/1742-4690-8-62.

12.

Crystal structure of human UP1, the domain of hnRNP A1 that contains two RNA-recognition motifs.

Xu RM, Jokhan L, Cheng X, Mayeda A, Krainer AR.

Structure. 1997 Apr 15;5(4):559-70.

13.
14.

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis.

Johnson JO, Pioro EP, Boehringer A, Chia R, Feit H, Renton AE, Pliner HA, Abramzon Y, Marangi G, Winborn BJ, Gibbs JR, Nalls MA, Morgan S, Shoai M, Hardy J, Pittman A, Orrell RW, Malaspina A, Sidle KC, Fratta P, Harms MB, Baloh RH, Pestronk A, Weihl CC, Rogaeva E, Zinman L, Drory VE, Borghero G, Mora G, Calvo A, Rothstein JD; ITALSGEN, Drepper C, Sendtner M, Singleton AB, Taylor JP, Cookson MR, Restagno G, Sabatelli M, Bowser R, Chiò A, Traynor BJ.

Nat Neurosci. 2014 May;17(5):664-666. doi: 10.1038/nn.3688. Epub 2014 Mar 30.

15.

Cooperative assembly of an hnRNP complex induced by a tissue-specific homolog of polypyrimidine tract binding protein.

Markovtsov V, Nikolic JM, Goldman JA, Turck CW, Chou MY, Black DL.

Mol Cell Biol. 2000 Oct;20(20):7463-79.

16.

Mutational analysis of MATR3 in Taiwanese patients with amyotrophic lateral sclerosis.

Lin KP, Tsai PC, Liao YC, Chen WT, Tsai CP, Soong BW, Lee YC.

Neurobiol Aging. 2015 May;36(5):2005.e1-4. doi: 10.1016/j.neurobiolaging.2015.02.008. Epub 2015 Feb 14.

PMID:
25771394
17.

The defective splicing caused by the ISCU intron mutation in patients with myopathy with lactic acidosis is repressed by PTBP1 but can be derepressed by IGF2BP1.

Nordin A, Larsson E, Holmberg M.

Hum Mutat. 2012 Mar;33(3):467-70. doi: 10.1002/humu.22002. Epub 2011 Dec 29.

PMID:
22125086
18.
19.

Accumulation of H/ACA snoRNPs depends on the integrity of the conserved central domain of the RNA-binding protein Nhp2p.

Henras A, Dez C, Noaillac-Depeyre J, Henry Y, Caizergues-Ferrer M.

Nucleic Acids Res. 2001 Jul 1;29(13):2733-46.

20.

Proteome-wide characterization of the RNA-binding protein RALY-interactome using the in vivo-biotinylation-pulldown-quant (iBioPQ) approach.

Tenzer S, Moro A, Kuharev J, Francis AC, Vidalino L, Provenzani A, Macchi P.

J Proteome Res. 2013 Jun 7;12(6):2869-84. doi: 10.1021/pr400193j. Epub 2013 May 6.

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