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S M Cashman

Showing results (1-10 of 7) with videos related to

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Gene Therapy|May 7, 2005
Towards mutation-independent silencing of genes involved in retinal degeneration by RNA interferenceS M Cashman, E A Binkley, R Kumar-Singh
Gene Therapy|July 20, 2012
Mutation-independent rescue of a novel mouse model of Retinitis PigmentosaD L Greenwald, S M Cashman, R Kumar-Singh
Gene Therapy|February 11, 2011
Adenovirus-mediated delivery of CD46 attenuates the alternative complement pathway on RPE: implications for age-related macular degenerationJ H Sweigard, S M Cashman, R Kumar-Singh
Journal of Medical Genetics|December 1, 1995
The Irish cystic fibrosis databaseS M Cashman, A Patino, M G Delgado, et al.
Clinical Genetics|November 1, 1992
Deletion delta F508 and clinical expression of cystic fibrosis-related liver diseaseM De Arce, S O'Brien, J Hegarty, et al.
Human Heredity|January 1, 1995
Identical intragenic microsatellite haplotype found in cystic fibrosis chromosomes bearing mutation G551D in Irish, English, Scottish, Breton and Czech patientsS M Cashman, A Patino, A Martinez, et al.
Nature Genetics|November 1, 1993
A mutation in CFTR produces different phenotypes depending on chromosomal backgroundS Kiesewetter, M Macek, C Davis, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Gene Therapy|May 7, 2005
Towards mutation-independent silencing of genes involved in retinal degeneration by RNA interferenceS M Cashman, E A Binkley, R Kumar-Singh
Gene Therapy|July 20, 2012
Mutation-independent rescue of a novel mouse model of Retinitis PigmentosaD L Greenwald, S M Cashman, R Kumar-Singh
Gene Therapy|February 11, 2011
Adenovirus-mediated delivery of CD46 attenuates the alternative complement pathway on RPE: implications for age-related macular degenerationJ H Sweigard, S M Cashman, R Kumar-Singh
Journal of Medical Genetics|December 1, 1995
The Irish cystic fibrosis databaseS M Cashman, A Patino, M G Delgado, et al.
Clinical Genetics|November 1, 1992
Deletion delta F508 and clinical expression of cystic fibrosis-related liver diseaseM De Arce, S O'Brien, J Hegarty, et al.
Human Heredity|January 1, 1995
Identical intragenic microsatellite haplotype found in cystic fibrosis chromosomes bearing mutation G551D in Irish, English, Scottish, Breton and Czech patientsS M Cashman, A Patino, A Martinez, et al.
Nature Genetics|November 1, 1993
A mutation in CFTR produces different phenotypes depending on chromosomal backgroundS Kiesewetter, M Macek, C Davis, et al.
Pageof 1