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Esther Glaus

Showing results (1-10 of 13) with videos related to

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General and Comparative Endocrinology|October 2, 2007
Glucocorticoid response to food availability in breeding barn swallows (Hirundo rustica)Susanne Jenni-Eiermann, Esther Glaus, Martin Grüebler, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 18, 2011
Gene therapeutic approach using mutation-adapted U1 snRNA to correct a RPGR splice defect in patient-derived cellsEsther Glaus, Fabian Schmid, Romain Da Costa, et al.
Human Mutation|April 4, 2007
Identification and characterization of a novel RPGR isoform in human retinaJohn Neidhardt, Esther Glaus, Daniel Barthelmes, et al.
Human Gene Therapy|October 19, 2012
A gene therapeutic approach to correct splice defects with modified U1 and U6 snRNPsFabian Schmid, Thomas Hiller, Germaine Korner, et al.
Investigative Ophthalmology & Visual Science|October 17, 2009
Mutation- and tissue-specific alterations of RPGR transcriptsFabian Schmid, Esther Glaus, Frans P M Cremers, et al.
Human Mutation|October 7, 2008
Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNAGaby Tanner, Esther Glaus, Daniel Barthelmes, et al.
Investigative Ophthalmology & Visual Science|March 26, 2010
ABCA4 and ROM1: implications for modification of the PRPH2-associated macular dystrophy phenotypeCharlotte M Poloschek, Michael Bach, Wolf A Lagrèze, et al.
Plos One|July 9, 2016
Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and LimitationsAmit Tiwari, Johannes Lemke, Janine Altmueller, et al.
The European Journal of Neuroscience|June 13, 2008
Vascular changes in the cerebellum of Norrin /Ndph knockout mice correlate with high expression of Norrin and Frizzled-4Ulrich F O Luhmann, John Neidhardt, Barbara Kloeckener-Gruissem, et al.
Human Mutation|April 27, 2011
U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutationFabian Schmid, Esther Glaus, Daniel Barthelmes, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
General and Comparative Endocrinology|October 2, 2007
Glucocorticoid response to food availability in breeding barn swallows (Hirundo rustica)Susanne Jenni-Eiermann, Esther Glaus, Martin Grüebler, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 18, 2011
Gene therapeutic approach using mutation-adapted U1 snRNA to correct a RPGR splice defect in patient-derived cellsEsther Glaus, Fabian Schmid, Romain Da Costa, et al.
Human Mutation|April 4, 2007
Identification and characterization of a novel RPGR isoform in human retinaJohn Neidhardt, Esther Glaus, Daniel Barthelmes, et al.
Human Gene Therapy|October 19, 2012
A gene therapeutic approach to correct splice defects with modified U1 and U6 snRNPsFabian Schmid, Thomas Hiller, Germaine Korner, et al.
Investigative Ophthalmology & Visual Science|October 17, 2009
Mutation- and tissue-specific alterations of RPGR transcriptsFabian Schmid, Esther Glaus, Frans P M Cremers, et al.
Human Mutation|October 7, 2008
Therapeutic strategy to rescue mutation-induced exon skipping in rhodopsin by adaptation of U1 snRNAGaby Tanner, Esther Glaus, Daniel Barthelmes, et al.
Investigative Ophthalmology & Visual Science|March 26, 2010
ABCA4 and ROM1: implications for modification of the PRPH2-associated macular dystrophy phenotypeCharlotte M Poloschek, Michael Bach, Wolf A Lagrèze, et al.
Plos One|July 9, 2016
Identification of Novel and Recurrent Disease-Causing Mutations in Retinal Dystrophies Using Whole Exome Sequencing (WES): Benefits and LimitationsAmit Tiwari, Johannes Lemke, Janine Altmueller, et al.
The European Journal of Neuroscience|June 13, 2008
Vascular changes in the cerebellum of Norrin /Ndph knockout mice correlate with high expression of Norrin and Frizzled-4Ulrich F O Luhmann, John Neidhardt, Barbara Kloeckener-Gruissem, et al.
Human Mutation|April 27, 2011
U1 snRNA-mediated gene therapeutic correction of splice defects caused by an exceptionally mild BBS mutationFabian Schmid, Esther Glaus, Daniel Barthelmes, et al.
Pageof 2