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Travis Cossette

Research Profile

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Thomas J Conlon; Travis Cossette; Wen-Tao Deng; Kirsten Erger; Corinne R Abernathy; Fowzan S Alkuraya; Shannon E Boye; Sanford L Boye; Brian Cleaver; Nathalie Clément; Issam McDoom; Ji-Jing Pang; Marc C Peden; Renee Ryals; Mark B Sherwood; William W Hauswirth
Preclinical Potency and Safety Studies of an AAV2-Mediated Gene Therapy Vector for the Treatment of MERTK Associated Retinitis Pigmentosa.
Allison M Keeler; Christian Mueller; Scott A Shaffer; Qiushi Tang; Glenn Walter; Huadong Zeng; Thomas J Conlon; Travis Cossette; Fu Dungtao; Kirsten Erger; Terence R Flotte
Long-term correction of very long-chain acyl-coA dehydrogenase deficiency in mice using AAV9 gene therapy.
Sanford L Boye; Thomas J Conlon; Travis Cossette; Frank M Dyka; Kirsten Erger; William W Hauswirth; Andy Neeley; Jijing Pang; Renee Ryals; Shannon E Boye
Long-term preservation of cone photoreceptors and restoration of cone function by gene therapy in the guanylate cyclase-1 knockout (GC1KO) mouse.

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All Publications

2013: Thomas J Conlon; Travis Cossette; Wen-Tao Deng; Kirsten Erger; Corinne R Abernathy; Fowzan S Alkuraya; Shannon E Boye; Sanford L Boye; Brian Cleaver; Nathalie Clément; Issam McDoom; Ji-Jing Pang; Marc C Peden; Renee Ryals; Mark B Sherwood; William W Hauswirth
Preclinical Potency and Safety Studies of an AAV2-Mediated Gene Therapy Vector for the Treatment of MERTK Associated Retinitis Pigmentosa.
Human gene therapy. Clinical development 2013;24(1):23-8.
2012: Allison M Keeler; Christian Mueller; Scott A Shaffer; Qiushi Tang; Glenn Walter; Huadong Zeng; Thomas J Conlon; Travis Cossette; Fu Dungtao; Kirsten Erger; Terence R Flotte
Long-term correction of very long-chain acyl-coA dehydrogenase deficiency in mice using AAV9 gene therapy.
Molecular therapy : the journal of the American Society of Gene Therapy 2012;20(6):1131-8.
2011: Sanford L Boye; Thomas J Conlon; Travis Cossette; Frank M Dyka; Kirsten Erger; William W Hauswirth; Andy Neeley; Jijing Pang; Renee Ryals; Shannon E Boye
Long-term preservation of cone photoreceptors and restoration of cone function by gene therapy in the guanylate cyclase-1 knockout (GC1KO) mouse.
Investigative ophthalmology & visual science 2011;52(10):7098-108.
2011: Andrew Specht; Laurie Fiske; Kirsten Erger; Travis Cossette; John P Verstegen; Martha Campbell-Thompson; Maggie B Struck; Young Mok Lee; Janice Y Chou; Barry J Byrne; Catherine E Correia; Cathryn Mah; David A Weinstein; Thomas J Conlon
Glycogen storage disease type Ia in canines: a model for human metabolic and genetic liver disease.
Journal of biomedicine & biotechnology 2011;2011():646257.
2009: Rejean Liqun Wang; Thomas McLaughlin; Travis Cossette; Qiushi Tang; Kevin Foust; Martha Campbell-Thompson; Ashley Martino; Pedro Cruz; Scott A Loiler; Christian Mueller; Terence R Flotte
Recombinant AAV serotype and capsid mutant comparison for pulmonary gene transfer of alpha-1-antitrypsin using invasive and noninvasive delivery.
Molecular therapy : the journal of the American Society of Gene Therapy 2009;17(1):81-7.
2007: Pedro E Cruz; Christian Mueller; Travis Cossette; Alexandra Golant; Qiushi Tang; Stuart G Beattie; Mark L Brantly; Martha Campbell-Thompson; Keith Blomenkamp; Jeffrey H Teckman; Terence R Flotte
In vivo post-transcriptional gene silencing of alpha-1 antitrypsin by adeno-associated virus vectors expressing siRNA.
Laboratory investigation; a journal of technical methods and pathology 2007;87(9):893-902.
2006: Thomas J Conlon; Glenn Walter; Renius Owen; Travis Cossette; Kirsten Erger; Greg Gutierrez; Eric S Goetzman; Dietrich Matern; Jerry Vockley; Terence R Flotte
Systemic correction of a fatty acid oxidation defect by intramuscular injection of a recombinant adeno-associated virus vector.
Human gene therapy 2006;17(1):71-80.
2005: Thomas J Conlon; Travis Cossette; Kirsten Erger; Young-Kook Choi; Tracy Clarke; Marda Scott-Jorgensen; Sihong Song; Martha Campbell-Thompson; James Crawford; Terence R Flotte
Efficient hepatic delivery and expression from a recombinant adeno-associated virus 8 pseudotyped alpha1-antitrypsin vector.
Molecular therapy : the journal of the American Society of Gene Therapy 2005;12(5):867-75.