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Nele Schwarz

Showing results (11-20 of 16) with videos related to

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Human Molecular Genetics|December 5, 2013
Hsp90 inhibition protects against inherited retinal degenerationMònica Aguilà, Dalila Bevilacqua, Caroline McCulley, et al.
Human Molecular Genetics|October 9, 2014
Translational read-through of the RP2 Arg120stop mutation in patient iPSC-derived retinal pigment epithelium cellsNele Schwarz, Amanda-Jayne Carr, Amelia Lane, et al.
Human Molecular Genetics|May 24, 2012
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)Tom R Webb, David A Parfitt, Jessica C Gardner, et al.
Cell Stem Cell|May 7, 2016
Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic CupsDavid A Parfitt, Amelia Lane, Conor M Ramsden, et al.
Human Mutation|August 30, 2014
Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variantsJessica C Gardner, Gerald Liew, Ying-Hua Quan, et al.
American Journal of Human Genetics|July 16, 2013
Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosaAlice E Davidson, Nele Schwarz, Lina Zelinger, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Human Molecular Genetics|December 5, 2013
Hsp90 inhibition protects against inherited retinal degenerationMònica Aguilà, Dalila Bevilacqua, Caroline McCulley, et al.
Human Molecular Genetics|October 9, 2014
Translational read-through of the RP2 Arg120stop mutation in patient iPSC-derived retinal pigment epithelium cellsNele Schwarz, Amanda-Jayne Carr, Amelia Lane, et al.
Human Molecular Genetics|May 24, 2012
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)Tom R Webb, David A Parfitt, Jessica C Gardner, et al.
Cell Stem Cell|May 7, 2016
Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic CupsDavid A Parfitt, Amelia Lane, Conor M Ramsden, et al.
Human Mutation|August 30, 2014
Three different cone opsin gene array mutational mechanisms with genotype-phenotype correlation and functional investigation of cone opsin variantsJessica C Gardner, Gerald Liew, Ying-Hua Quan, et al.
American Journal of Human Genetics|July 16, 2013
Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosaAlice E Davidson, Nele Schwarz, Lina Zelinger, et al.
Pageof 2