Howe S - Search Results

1

Vps33b is crucial for structural and functional hepatocyte polarity.

Hanley J, Dhar DK, Mazzacuva F, Fiadeiro R, Burden JJ, Lyne AM, Smith H, Straatman-Iwanowska A, Banushi B, Virasami A, Mills K, Lemaigre FP, Knisely AS, Howe S, Sebire N, Waddington SN, Paulusma CC, Clayton P, Gissen P. Hanley J, et al. Among authors: howe s. J Hepatol. 2017 May;66(5):1001-1011. doi: 10.1016/j.jhep.2017.01.001. Epub 2017 Jan 9. J Hepatol. 2017. PMID: 28082148 Free PMC article.

2

Lentiviral vectors can be used for full-length dystrophin gene therapy.

Counsell JR, Asgarian Z, Meng J, Ferrer V, Vink CA, Howe SJ, Waddington SN, Thrasher AJ, Muntoni F, Morgan JE, Danos O. Counsell JR, et al. Sci Rep. 2017 Mar 17;7:44775. doi: 10.1038/srep44775. Sci Rep. 2017. PMID: 28303972 Free PMC article.

3

The differentiation and engraftment potential of mouse hematopoietic stem cells is maintained after bio-electrospray.

Bartolovic K, Mongkoldhumrongkul N, Waddington SN, Jayasinghe SN, Howe SJ. Bartolovic K, et al. Analyst. 2010 Jan;135(1):157-64. doi: 10.1039/b917813a. Epub 2009 Nov 13. Analyst. 2010. PMID: 20024196

4

Perinatal gene transfer to the liver.

McKay TR, Rahim AA, Buckley SM, Ward NJ, Chan JK, Howe SJ, Waddington SN. McKay TR, et al. Curr Pharm Des. 2011;17(24):2528-41. doi: 10.2174/138161211797247541. Curr Pharm Des. 2011. PMID: 21774770 Free PMC article. Review.

5

Lentiviral vectors can be used for full-length dystrophin gene therapy.

Counsell JR, Asgarian Z, Meng J, Ferrer V, Vink CA, Howe SJ, Waddington SN, Thrasher AJ, Muntoni F, Morgan JE, Danos O. Counsell JR, et al. Sci Rep. 2017 Mar 6;7(1):79. doi: 10.1038/s41598-017-00152-5. Sci Rep. 2017. PMID: 28250438 Free PMC article.

6

Eliminating HIV-1 Packaging Sequences from Lentiviral Vector Proviruses Enhances Safety and Expedites Gene Transfer for Gene Therapy.

Vink CA, Counsell JR, Perocheau DP, Karda R, Buckley SMK, Brugman MH, Galla M, Schambach A, McKay TR, Waddington SN, Howe SJ. Vink CA, et al. Mol Ther. 2017 Aug 2;25(8):1790-1804. doi: 10.1016/j.ymthe.2017.04.028. Epub 2017 May 24. Mol Ther. 2017. PMID: 28550974 Free PMC article.

7

Gene delivery of a mutant TGFβ3 reduces markers of scar tissue formation after cutaneous wounding.

Waddington SN, Crossley R, Sheard V, Howe SJ, Buckley SM, Coughlan L, Gilham DE, Hawkins RE, McKay TR. Waddington SN, et al. Mol Ther. 2010 Dec;18(12):2104-11. doi: 10.1038/mt.2010.174. Epub 2010 Aug 24. Mol Ther. 2010. PMID: 20736928 Free PMC article.

8

Development of S/MAR minicircles for enhanced and persistent transgene expression in the mouse liver.

Argyros O, Wong SP, Fedonidis C, Tolmachov O, Waddington SN, Howe SJ, Niceta M, Coutelle C, Harbottle RP. Argyros O, et al. J Mol Med (Berl). 2011 May;89(5):515-29. doi: 10.1007/s00109-010-0713-3. Epub 2011 Feb 8. J Mol Med (Berl). 2011. PMID: 21301798

9

Evidence for contribution of CD4+ CD25+ regulatory T cells in maintaining immune tolerance to human factor IX following perinatal adenovirus vector delivery.

Nivsarkar MS, Buckley SM, Parker AL, Perocheau D, McKay TR, Rahim AA, Howe SJ, Waddington SN. Nivsarkar MS, et al. Among authors: howe sj. J Immunol Res. 2015;2015:397879. doi: 10.1155/2015/397879. Epub 2015 Jan 31. J Immunol Res. 2015. PMID: 25759840 Free PMC article.

10

Systemic gene delivery following intravenous administration of AAV9 to fetal and neonatal mice and late-gestation nonhuman primates.

Mattar CN, Wong AM, Hoefer K, Alonso-Ferrero ME, Buckley SM, Howe SJ, Cooper JD, Waddington SN, Chan JK, Rahim AA. Mattar CN, et al. Among authors: howe sj. FASEB J. 2015 Sep;29(9):3876-88. doi: 10.1096/fj.14-269092. Epub 2015 Jun 10. FASEB J. 2015. PMID: 26062602 Free PMC article.

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