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Klinische Monatsblatter Fur Augenheilkunde
|
March 14, 2018
[Ciliopathies]
Christina Gerth-Kahlert, Samuel Koller
The Journal of Biological Chemistry
|
January 31, 2013
Inhibition of G-protein-coupled receptor kinase 2 (GRK2) triggers the growth-promoting mitogen-activated protein kinase (MAPK) pathway
Xuebin Fu, Samuel Koller, Joshua Abd Alla, et al.
Biochemical and Biophysical Research Communications
|
May 24, 2011
A cleavable signal peptide enhances cell surface delivery and heterodimerization of Cerulean-tagged angiotensin II AT1 and bradykinin B2 receptor
Ursula Quitterer, Armin Pohl, Andreas Langer, et al.
Genes
|
July 19, 2020
De Novo Assembly-Based Analysis of <i>RPGR</i> Exon ORF15 in an Indigenous African Cohort Overcomes Limitations of a Standard Next-Generation Sequencing (NGS) Data Analysis Pipeline
Jordi Maggi, Lisa Roberts, Samuel Koller, 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 Cataract
Flora Delas, Samuel Koller, 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 Cohort
Jordi 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 ATOH7
David Atac, Lucas Mohn, Silke Feil, et al.
Cells
|
July 12, 2024
Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development
David Atac, Kevin Maggi, Silke Feil, et al.
Genes
|
January 8, 2025
Retinal Dystrophy Associated with Homozygous Variants in <i>NRL</i>
Jordi Maggi, James V M Hanson, Lisa Kurmann, et al.
International Journal of Molecular Sciences
|
July 12, 2025
Novel Genetic Variants and Clinical Profiles in Peters Anomaly Spectrum Disorders
Flora Delas, Samuel Koller, Jordi Maggi, et al.
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of 3
Search research articles
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Showing results (1-10 of 30) with videos related to
Sort By:
Page
of 3
Klinische Monatsblatter Fur Augenheilkunde
|
March 14, 2018
[Ciliopathies]
Christina Gerth-Kahlert, Samuel Koller
The Journal of Biological Chemistry
|
January 31, 2013
Inhibition of G-protein-coupled receptor kinase 2 (GRK2) triggers the growth-promoting mitogen-activated protein kinase (MAPK) pathway
Xuebin Fu, Samuel Koller, Joshua Abd Alla, et al.
Biochemical and Biophysical Research Communications
|
May 24, 2011
A cleavable signal peptide enhances cell surface delivery and heterodimerization of Cerulean-tagged angiotensin II AT1 and bradykinin B2 receptor
Ursula Quitterer, Armin Pohl, Andreas Langer, et al.
Genes
|
July 19, 2020
De Novo Assembly-Based Analysis of <i>RPGR</i> Exon ORF15 in an Indigenous African Cohort Overcomes Limitations of a Standard Next-Generation Sequencing (NGS) Data Analysis Pipeline
Jordi Maggi, Lisa Roberts, Samuel Koller, 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 Cataract
Flora Delas, Samuel Koller, 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 Cohort
Jordi 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 ATOH7
David Atac, Lucas Mohn, Silke Feil, et al.
Cells
|
July 12, 2024
Identification and Characterization of ATOH7-Regulated Target Genes and Pathways in Human Neuroretinal Development
David Atac, Kevin Maggi, Silke Feil, et al.
Genes
|
January 8, 2025
Retinal Dystrophy Associated with Homozygous Variants in <i>NRL</i>
Jordi Maggi, James V M Hanson, Lisa Kurmann, et al.
International Journal of Molecular Sciences
|
July 12, 2025
Novel Genetic Variants and Clinical Profiles in Peters Anomaly Spectrum Disorders
Flora Delas, Samuel Koller, Jordi Maggi, et al.
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of 3