Foust K - Search Results

1

Recombinant AAV serotype and capsid mutant comparison for pulmonary gene transfer of alpha-1-antitrypsin using invasive and noninvasive delivery.

Liqun Wang R, McLaughlin T, Cossette T, Tang Q, Foust K, Campbell-Thompson M, Martino A, Cruz P, Loiler S, Mueller C, Flotte TR. Liqun Wang R, et al. Among authors: foust k. Mol Ther. 2009 Jan;17(1):81-7. doi: 10.1038/mt.2008.217. Epub 2008 Oct 21. Mol Ther. 2009. PMID: 18941444 Free PMC article.

2

Enhancing rAAV vector expression in the lung.

Virella-Lowell I, Zusman B, Foust K, Loiler S, Conlon T, Song S, Chesnut KA, Ferkol T, Flotte TR. Virella-Lowell I, et al. Among authors: foust k. J Gene Med. 2005 Jul;7(7):842-50. doi: 10.1002/jgm.759. J Gene Med. 2005. PMID: 15838934

3

Recombinant adeno-associated viral vectors as therapeutic agents to treat neurological disorders.

Mandel RJ, Manfredsson FP, Foust KD, Rising A, Reimsnider S, Nash K, Burger C. Mandel RJ, et al. Among authors: foust kd. Mol Ther. 2006 Mar;13(3):463-83. doi: 10.1016/j.ymthe.2005.11.009. Epub 2006 Jan 18. Mol Ther. 2006. PMID: 16412695 Free article. Review.

4

Neonatal intraperitoneal or intravenous injections of recombinant adeno-associated virus type 8 transduce dorsal root ganglia and lower motor neurons.

Foust KD, Poirier A, Pacak CA, Mandel RJ, Flotte TR. Foust KD, et al. Hum Gene Ther. 2008 Jan;19(1):61-70. doi: 10.1089/hum.2007.093. Hum Gene Ther. 2008. PMID: 18052722

5

Recombinant adeno-associated virus-mediated global anterograde delivery of glial cell line-derived neurotrophic factor to the spinal cord: comparison of rubrospinal and corticospinal tracts in the rat.

Foust KD, Flotte TR, Reier PJ, Mandel RJ. Foust KD, et al. Hum Gene Ther. 2008 Jan;19(1):71-82. doi: 10.1089/hum.2007.104. Hum Gene Ther. 2008. PMID: 18072858

6

Nigrostriatal rAAV-mediated GDNF overexpression induces robust weight loss in a rat model of age-related obesity.

Manfredsson FP, Tumer N, Erdos B, Landa T, Broxson CS, Sullivan LF, Rising AC, Foust KD, Zhang Y, Muzyczka N, Gorbatyuk OS, Scarpace PJ, Mandel RJ. Manfredsson FP, et al. Mol Ther. 2009 Jun;17(6):980-91. doi: 10.1038/mt.2009.45. Epub 2009 Mar 10. Mol Ther. 2009. PMID: 19277011 Free PMC article.

7

AAV as a gene transfer vector for the treatment of neurological disorders: novel treatment thoughts for ALS.

Hester ME, Foust KD, Kaspar RW, Kaspar BK. Hester ME, et al. Among authors: foust kd. Curr Gene Ther. 2009 Oct;9(5):428-33. doi: 10.2174/156652309789753383. Curr Gene Ther. 2009. PMID: 19860657 Review.

8

Systemic gene delivery in large species for targeting spinal cord, brain, and peripheral tissues for pediatric disorders.

Bevan AK, Duque S, Foust KD, Morales PR, Braun L, Schmelzer L, Chan CM, McCrate M, Chicoine LG, Coley BD, Porensky PN, Kolb SJ, Mendell JR, Burghes AH, Kaspar BK. Bevan AK, et al. Among authors: foust kd. Mol Ther. 2011 Nov;19(11):1971-80. doi: 10.1038/mt.2011.157. Epub 2011 Aug 2. Mol Ther. 2011. PMID: 21811247 Free PMC article.

9

Improving single injection CSF delivery of AAV9-mediated gene therapy for SMA: a dose-response study in mice and nonhuman primates.

Meyer K, Ferraiuolo L, Schmelzer L, Braun L, McGovern V, Likhite S, Michels O, Govoni A, Fitzgerald J, Morales P, Foust KD, Mendell JR, Burghes AH, Kaspar BK. Meyer K, et al. Among authors: foust kd. Mol Ther. 2015 Mar;23(3):477-87. doi: 10.1038/mt.2014.210. Epub 2014 Oct 31. Mol Ther. 2015. PMID: 25358252 Free PMC article.

10

Intravenous AAV9 efficiently transduces myenteric neurons in neonate and juvenile mice.

Gombash SE, Cowley CJ, Fitzgerald JA, Hall JC, Mueller C, Christofi FL, Foust KD. Gombash SE, et al. Front Mol Neurosci. 2014 Oct 15;7:81. doi: 10.3389/fnmol.2014.00081. eCollection 2014. Front Mol Neurosci. 2014. PMID: 25360081 Free PMC article.

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