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Items: 6

1.

MHC universal cells survive in an allogeneic environment after incompatible transplantation.

Figueiredo C, Wedekind D, Müller T, Vahlsing S, Horn PA, Seltsam A, Blasczyk R.

Biomed Res Int. 2013;2013:796046. doi: 10.1155/2013/796046. Epub 2013 Oct 9.

2.

An adenoviral vector-based expression and delivery system for the inhibition of wild-type adenovirus replication by artificial microRNAs.

Ibrišimović M, Kneidinger D, Lion T, Klein R.

Antiviral Res. 2013 Jan;97(1):10-23. doi: 10.1016/j.antiviral.2012.10.008. Epub 2012 Nov 2.

3.

Drug Targeting of alpha-Synuclein Oligomerization in Synucleinopathies.

Outeiro TF, Kazantsev A.

Perspect Medicin Chem. 2008 Apr 10;2:41-9.

4.

AAV vector-mediated RNAi of mutant huntingtin expression is neuroprotective in a novel genetic rat model of Huntington's disease.

Franich NR, Fitzsimons HL, Fong DM, Klugmann M, During MJ, Young D.

Mol Ther. 2008 May;16(5):947-56. doi: 10.1038/mt.2008.50. Epub 2008 Mar 25.

5.

Therapeutic application of RNAi: is mRNA targeting finally ready for prime time?

Grimm D, Kay MA.

J Clin Invest. 2007 Dec;117(12):3633-41. Review.

6.

In vivo gene delivery in the retina using polyethylenimine.

Liao HW, Yau KW.

Biotechniques. 2007 Mar;42(3):285-6, 288. No abstract available.

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