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J T Stout

Showing results (31-40 of 43) with videos related to

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Somatic Cell and Molecular Genetics|May 1, 1988
Spontaneous reversion of novel Lesch-Nyhan mutation by HPRT gene rearrangementT P Yang, J T Stout, D S Konecki, et al.
Neurology|December 31, 1997
Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS)J Jen, A H Cohen, Q Yue, et al.
Gene Therapy|March 1, 2000
Efficient and sustained transgene expression in human corneal cells mediated by a lentiviral vectorX Wang, B Appukuttan, S Ott, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 15, 2000
Clinical phenotype associated with the arg141 his mutation in the X-linked retinoschisis geneJ H Park, S H Ott, X Wang, et al.
Nature Genetics|May 10, 2000
Heterozygous loss of Six5 in mice is sufficient to cause ocular cataractsP S Sarkar, B Appukuttan, J Han, et al.
Nature|August 2, 1984
Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patientsT P Yang, P I Patel, A C Chinault, et al.
Physiological Genomics|December 18, 2003
Genetic architecture of fast- and slow-twitch skeletal muscle weight in 200-day-old mice of the C57BL/6J and DBA/2J lineageA Lionikas, D A Blizard, D J Vandenbergh, et al.
Physiological Genomics|February 3, 2005
Genetic determinants of weight of fast- and slow-twitch skeletal muscle in 500-day-old mice of the C57BL/6J and DBA/2J lineageA Lionikas, D A Blizard, G S Gerhard, et al.
Human Genetics|September 10, 1999
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locusI Zito, D L Thiselton, M B Gorin, et al.
Molecular Biology Reports|July 18, 2001
Isolation and characterization of the human homeobox gene HOX D1B Appukuttan, R Sood, S Ott, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Somatic Cell and Molecular Genetics|May 1, 1988
Spontaneous reversion of novel Lesch-Nyhan mutation by HPRT gene rearrangementT P Yang, J T Stout, D S Konecki, et al.
Neurology|December 31, 1997
Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS)J Jen, A H Cohen, Q Yue, et al.
Gene Therapy|March 1, 2000
Efficient and sustained transgene expression in human corneal cells mediated by a lentiviral vectorX Wang, B Appukuttan, S Ott, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 15, 2000
Clinical phenotype associated with the arg141 his mutation in the X-linked retinoschisis geneJ H Park, S H Ott, X Wang, et al.
Nature Genetics|May 10, 2000
Heterozygous loss of Six5 in mice is sufficient to cause ocular cataractsP S Sarkar, B Appukuttan, J Han, et al.
Nature|August 2, 1984
Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patientsT P Yang, P I Patel, A C Chinault, et al.
Physiological Genomics|December 18, 2003
Genetic architecture of fast- and slow-twitch skeletal muscle weight in 200-day-old mice of the C57BL/6J and DBA/2J lineageA Lionikas, D A Blizard, D J Vandenbergh, et al.
Physiological Genomics|February 3, 2005
Genetic determinants of weight of fast- and slow-twitch skeletal muscle in 500-day-old mice of the C57BL/6J and DBA/2J lineageA Lionikas, D A Blizard, G S Gerhard, et al.
Human Genetics|September 10, 1999
Identification of novel RPGR (retinitis pigmentosa GTPase regulator) mutations in a subset of X-linked retinitis pigmentosa families segregating with the RP3 locusI Zito, D L Thiselton, M B Gorin, et al.
Molecular Biology Reports|July 18, 2001
Isolation and characterization of the human homeobox gene HOX D1B Appukuttan, R Sood, S Ott, et al.
Pageof 5