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Results: 10

Related Articles by Review for PubMed (Select 18839960)

1.

DcpS as a therapeutic target for spinal muscular atrophy.

Singh J, Salcius M, Liu SW, Staker BL, Mishra R, Thurmond J, Michaud G, Mattoon DR, Printen J, Christensen J, Bjornsson JM, Pollok BA, Kiledjian M, Stewart L, Jarecki J, Gurney ME.

ACS Chem Biol. 2008 Nov 21;3(11):711-22. doi: 10.1021/cb800120t.

2.

Decapping Scavenger (DcpS) enzyme: advances in its structure, activity and roles in the cap-dependent mRNA metabolism.

Milac AL, Bojarska E, Wypijewska del Nogal A.

Biochim Biophys Acta. 2014 Jun;1839(6):452-62. doi: 10.1016/j.bbagrm.2014.04.007. Epub 2014 Apr 15. Review.

PMID:
24742626
3.

Therapeutics development for spinal muscular atrophy.

Sumner CJ.

NeuroRx. 2006 Apr;3(2):235-45. Review.

4.

DcpS, a general modulator of cap-binding protein-dependent processes?

Bail S, Kiledjian M.

RNA Biol. 2008 Oct-Dec;5(4):216-9. Epub 2008 Oct 9. Review.

6.

Spinal muscular atrophy: state-of-the-art and therapeutic perspectives.

Wirth B.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2002 Jun;3(2):87-95. Review.

PMID:
12215230
7.

Therapeutics that directly increase SMN expression to treat spinal muscular atrophy.

Shababi M, Mattis VB, Lorson CL.

Drug News Perspect. 2010 Oct;23(8):475-82. doi: 10.1358/dnp.2010.23.8.1507295. Review.

PMID:
21031163
8.

Spinal muscular atrophy: mechanisms and therapeutic strategies.

Lorson CL, Rindt H, Shababi M.

Hum Mol Genet. 2010 Apr 15;19(R1):R111-8. doi: 10.1093/hmg/ddq147. Epub 2010 Apr 13. Review.

9.

Genetic testing and risk assessment for spinal muscular atrophy (SMA).

Ogino S, Wilson RB.

Hum Genet. 2002 Dec;111(6):477-500. Epub 2002 Oct 3. Review.

PMID:
12436240
10.

Is RNA manipulation a viable therapy for spinal muscular atrophy?

Horne C, Young PJ.

J Neurol Sci. 2009 Dec 15;287(1-2):27-31. doi: 10.1016/j.jns.2009.08.055. Epub 2009 Sep 15. Review.

PMID:
19758605
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