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Silke Feil

Showing results (1-10 of 28) with videos related to

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Human Molecular Genetics|March 8, 2012
Norrin stimulates cell proliferation in the superficial retinal vascular plexus and is pivotal for the recruitment of mural cellsJurian Zuercher, Martin Fritzsche, Silke Feil, et al.
Investigative Ophthalmology & Visual Science|November 4, 2008
Differential gene expression in Ndph-knockout mice in retinal developmentNikolaus F Schäfer, Ulrich F O Luhmann, Silke Feil, et al.
International Journal of Molecular Sciences|December 9, 2023
Novel <i>CRYGC</i> Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital CataractFlora Delas, Samuel Koller, Silke Feil, et al.
Investigative Ophthalmology & Visual Science|September 26, 2003
NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface proteinChristina Zeitz, Harry Scherthan, Susanne Freier, et al.
Investigative Ophthalmology & Visual Science|August 31, 2002
Global gene expression analysis in a mouse model for Norrie disease: late involvement of photoreceptor cellsSteffen Lenzner, Sandra Prietz, Silke Feil, et al.
International Journal of Molecular Sciences|June 27, 2024
Limited Added Diagnostic Value of Whole Genome Sequencing in Genetic Testing of Inherited Retinal Diseases in a Swiss Patient CohortJordi Maggi, Samuel Koller, Silke Feil, et al.
International Journal of Molecular Sciences|February 15, 2022
Functional Characterization of an In-Frame Deletion in the Basic Domain of the Retinal Transcription Factor ATOH7David Atac, Lucas Mohn, Silke Feil, et al.
Molecular Vision|March 12, 2005
Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindnessChristina Zeitz, Roberta Minotti, Silke Feil, et al.
Human Mutation|April 4, 2007
Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein traffickingChristina Zeitz, Ursula Forster, John Neidhardt, et al.
Cells|July 12, 2024
Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal DevelopmentDavid Atac, Kevin Maggi, Silke Feil, et al.
Pageof 3

Showing results (1-10 of 28) with videos related to

Sort By:
Pageof 3
Human Molecular Genetics|March 8, 2012
Norrin stimulates cell proliferation in the superficial retinal vascular plexus and is pivotal for the recruitment of mural cellsJurian Zuercher, Martin Fritzsche, Silke Feil, et al.
Investigative Ophthalmology & Visual Science|November 4, 2008
Differential gene expression in Ndph-knockout mice in retinal developmentNikolaus F Schäfer, Ulrich F O Luhmann, Silke Feil, et al.
International Journal of Molecular Sciences|December 9, 2023
Novel <i>CRYGC</i> Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital CataractFlora Delas, Samuel Koller, Silke Feil, et al.
Investigative Ophthalmology & Visual Science|September 26, 2003
NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface proteinChristina Zeitz, Harry Scherthan, Susanne Freier, et al.
Investigative Ophthalmology & Visual Science|August 31, 2002
Global gene expression analysis in a mouse model for Norrie disease: late involvement of photoreceptor cellsSteffen Lenzner, Sandra Prietz, Silke Feil, et al.
International Journal of Molecular Sciences|June 27, 2024
Limited Added Diagnostic Value of Whole Genome Sequencing in Genetic Testing of Inherited Retinal Diseases in a Swiss Patient CohortJordi Maggi, Samuel Koller, Silke Feil, et al.
International Journal of Molecular Sciences|February 15, 2022
Functional Characterization of an In-Frame Deletion in the Basic Domain of the Retinal Transcription Factor ATOH7David Atac, Lucas Mohn, Silke Feil, et al.
Molecular Vision|March 12, 2005
Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindnessChristina Zeitz, Roberta Minotti, Silke Feil, et al.
Human Mutation|April 4, 2007
Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein traffickingChristina Zeitz, Ursula Forster, John Neidhardt, et al.
Cells|July 12, 2024
Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal DevelopmentDavid Atac, Kevin Maggi, Silke Feil, et al.
Pageof 3