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Francesca Pasutto

Showing results (11-20 of 56) with videos related to

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International Journal of Molecular Medicine|August 22, 2019
Impact of single nucleotide polymorphisms in the VEGFR2 gene on endothelial cell activation under non‑uniform shear stressNora M Schacher, Dorette Raaz-Schrauder, Francesca Pasutto, et al.
The American Journal of Pathology|November 1, 2008
Genotype-correlated expression of lysyl oxidase-like 1 in ocular tissues of patients with pseudoexfoliation syndrome/glaucoma and normal patientsUrsula Schlötzer-Schrehardt, Francesca Pasutto, Pascal Sommer, et al.
Investigative Ophthalmology & Visual Science|September 25, 2025
Establishment of an Advanced In Vitro Model for Pseudoexfoliation Syndrome and GlaucomaSai Pulasani, Matthias Zenkel, Robert Lämmer, et al.
Ophthalmology|May 29, 2012
LOXL1 deficiency in the lamina cribrosa as candidate susceptibility factor for a pseudoexfoliation-specific risk of glaucomaUrsula Schlötzer-Schrehardt, Christian M Hammer, Anita W Krysta, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucomaFrancesca Pasutto, Mandy Krumbiegel, Christian Y Mardin, et al.
Investigative Ophthalmology & Visual Science|January 4, 2008
Profiling of WDR36 missense variants in German patients with glaucomaFrancesca Pasutto, Christian Y Mardin, Karin Michels-Rautenstrauss, et al.
Journal of Glaucoma|June 15, 2010
Apolipoprotein E genotypes in pseudoexfoliation syndrome and pseudoexfoliation glaucomaMandy Krumbiegel, Francesca Pasutto, Christian Y Mardin, et al.
Investigative Ophthalmology & Visual Science|November 23, 2017
Posttranscriptional Regulation of LOXL1 Expression Via Alternative Splicing and Nonsense-Mediated mRNA Decay as an Adaptive Stress ResponseDaniel Berner, Matthias Zenkel, Francesca Pasutto, et al.
Investigative Ophthalmology & Visual Science|August 1, 2009
Heterozygous loss-of-function variants in CYP1B1 predispose to primary open-angle glaucomaFrancesca Pasutto, Gabriela Chavarria-Soley, Christian Y Mardin, et al.
Orphanet Journal of Rare Diseases|August 4, 2016
Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucomaLucia Mauri, Steffen Uebe, Heinrich Sticht, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
International Journal of Molecular Medicine|August 22, 2019
Impact of single nucleotide polymorphisms in the VEGFR2 gene on endothelial cell activation under non‑uniform shear stressNora M Schacher, Dorette Raaz-Schrauder, Francesca Pasutto, et al.
The American Journal of Pathology|November 1, 2008
Genotype-correlated expression of lysyl oxidase-like 1 in ocular tissues of patients with pseudoexfoliation syndrome/glaucoma and normal patientsUrsula Schlötzer-Schrehardt, Francesca Pasutto, Pascal Sommer, et al.
Investigative Ophthalmology & Visual Science|September 25, 2025
Establishment of an Advanced In Vitro Model for Pseudoexfoliation Syndrome and GlaucomaSai Pulasani, Matthias Zenkel, Robert Lämmer, et al.
Ophthalmology|May 29, 2012
LOXL1 deficiency in the lamina cribrosa as candidate susceptibility factor for a pseudoexfoliation-specific risk of glaucomaUrsula Schlötzer-Schrehardt, Christian M Hammer, Anita W Krysta, et al.
Investigative Ophthalmology & Visual Science|April 4, 2008
Association of LOXL1 common sequence variants in German and Italian patients with pseudoexfoliation syndrome and pseudoexfoliation glaucomaFrancesca Pasutto, Mandy Krumbiegel, Christian Y Mardin, et al.
Investigative Ophthalmology & Visual Science|January 4, 2008
Profiling of WDR36 missense variants in German patients with glaucomaFrancesca Pasutto, Christian Y Mardin, Karin Michels-Rautenstrauss, et al.
Journal of Glaucoma|June 15, 2010
Apolipoprotein E genotypes in pseudoexfoliation syndrome and pseudoexfoliation glaucomaMandy Krumbiegel, Francesca Pasutto, Christian Y Mardin, et al.
Investigative Ophthalmology & Visual Science|November 23, 2017
Posttranscriptional Regulation of LOXL1 Expression Via Alternative Splicing and Nonsense-Mediated mRNA Decay as an Adaptive Stress ResponseDaniel Berner, Matthias Zenkel, Francesca Pasutto, et al.
Investigative Ophthalmology & Visual Science|August 1, 2009
Heterozygous loss-of-function variants in CYP1B1 predispose to primary open-angle glaucomaFrancesca Pasutto, Gabriela Chavarria-Soley, Christian Y Mardin, et al.
Orphanet Journal of Rare Diseases|August 4, 2016
Expanding the clinical spectrum of COL1A1 mutations in different forms of glaucomaLucia Mauri, Steffen Uebe, Heinrich Sticht, et al.
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