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Genomics|Features|Gene Therapy

Gene Therapy

Genome Editing: New Scientific Medical Frontier - January 23, 2015

Genome editing-based HIV therapies.
Gu WG. Trends Biotechnol. 2015 Jan 15.

Strategies for cloning and manipulating natural and synthetic chromosomes.
Karas BJ, et al. Chromosome Res. 2015 Jan 18

The impact of CRISPR-Cas9 on target identification and validation.
Moore JD. Drug Discov Today. 2015 Jan 5

Beyond traditional pharmacology: new tools and approaches.
Gurevich EV, Gurevich VV. Br J Pharmacol. 2015 Jan 9.

Unraveling the potential of CRISPR-Cas9 for gene therapy.
Barrangou R, May AP. Expert Opin Biol Ther. 2014 Dec 23:1-4

One-shot, one cure with genome editing for dyslipidemia.
Gupta RM. Circ Cardiovasc Genet. 2014 Dec;7(6):967-8

Correction of a genetic disease by CRISPR-Cas9-mediated gene editing in mouse spermatogonial stem cells.
Wu Y, et al. Cell Res. 2015 Jan;25(1):67-79

CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites.
Lee MC, et al. Genome Med. 2014 Aug 26;6(8):63

Genome editing. The new frontier of genome engineering with CRISPR-Cas9.
Doudna JA, et al. Science. 2014 Nov 28;346(6213):1258096.

Genome editing for human gene therapy.
Meissner TB, et al. Methods Enzymol. 2014;546:273-95

Genome editing: a tool for research and therapy: targeted genome editing hits the clinic.
Lombardo A, et al. Nat Med. 2014 Oct;20(10):1101-3

Genome editing: a tool for research and therapy: towards a functional understanding of variants for molecular diagnostics using genome editing.
Tsai SQ, et al. Nat Med. 2014 Oct;20(10):1103-4

Call for debate on human genome editing, by Dr Philippa Brice, PHG Foundation, Jan 22

Gene Therapy & Gene Editing: Recent Insights - October 16, 2014

In hopes of fixing faulty genes, one scientist starts with the basics, by Joe Palca, National Public Radio, Oct 13

Advances in CRISPR genome-editing, PHG Foundation, Oct 7

CRISPR-Cas9 knockin mice for genome editing and cancer modeling.
Platt RJ, et al. Cell. 2014 Oct 9;159(2):440-55.

Sequence-specific antimicrobials using efficiently delivered RNA-guided nucleases
Citorik RJ, et al. Nat Biotechnol. 2014 Sep 21.

Exploiting CRISPR-Cas nucleases to produce sequence-specific antimicrobials.
Bikard D, et al. Nat Biotechnol. 2014 Oct 5.

RNA-directed gene editing specifically eradicates latent and prevents new HIV-1 infection
Hu W, et al.  PNAS, Jul 21, 2014.

Genome editing cuts out HIV
Grens K. The Scientist, Jul 21, 2014.

Gene researchers work to engineer HIV-resistant cells 
Hampton T. JAMA, Jul 9, 2014.

Gene editing of CCR5 in autologous CD4 T cells of persons infected with HIV
Tebas P, et al. N Engl J Med. 2014 Mar 6;370(10):901-10.

Promising results from HIV gene editing therapy, PHG Foundation, Mar 10