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Meeting Abstract (16)
Journal Articles (1)

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Investigative Ophthalmology & Visual Science (17)

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ARVO Annual Meeting Abstract (16)
Retinal Cell Biology (1)

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Biochemistry and Molecular Biology (1)
Eye Anatomy and Disorders (1)
Genetics (1)
Low Vision (1)
Retina (1)
Retinal Cell Biology (1)

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antibodies (1)
cos cells (1)
enzyme-linked immunosorbent assay (1)
genes (1)
in situ hybridization (1)
intracellular protein transport (1)
mice (1)
mutation (1)
night blindness, congenital stationary (1)
proteins (1)

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ARVO Annual Meeting Abstract June 2023

Efficacy and durability of EYS809 non-viral gene therapy in nAMD preclinical models

Karine Bigot; Pauline Gondouin; Romain Bénard; Marie Piazza; Elise Orhan; Francine F Behar-Cohen; Thierry Bordet

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):1300.

ARVO Annual Meeting Abstract June 2023

In vitro RPE cell models for iron toxicity studies

Emilie Picard; Jenny Youale Tembou; Thara Jaworski; Cécile Lebon; kimberley delaunay; Anais Francon; Elise Orhan; Karine Bigot; Thierry Bordet; Francine F Behar-Cohen

Invest. Ophthalmol. Vis. Sci.. 2023; 64(8):2602.

ARVO Annual Meeting Abstract June 2022

Transferrin protects RPE cells from oxidative damages

Jenny Youale; Thara Jaworski; Cecile Lebon; Anaïs Françon; kimberley delaunay; Elise Orhan; Karine Bigot; Thierry Bordet; Francine F Behar-Cohen; Emilie Picard

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):295 – F0098.

ARVO Annual Meeting Abstract June 2022

Transferrin confers neuroprotection in ex vivo and in vivo glaucoma rat models

Karine Bigot; Jenny Youale; Bindu Kodati; Thara Jaworski; Yan Fan; Nana Y Nsiah; Nathaniel Pappenhagen; Elise Orhan; Francine F Behar-Cohen; Thierry Bordet; Denise M Inman; Emilie Picard

Invest. Ophthalmol. Vis. Sci.. 2022; 63(7):1604 – A0427.

ARVO Annual Meeting Abstract June 2021

EYS809 Non-Viral Gene Therapy to Improve Convenience and Outcomes in Wet AMD

Elise Orhan; Karine Bigot; Pauline Gondouin; Romain Bénard; Marie Piazza; Ronald BUGGAGE; Francine F Behar-Cohen; Thierry Bordet

Invest. Ophthalmol. Vis. Sci.. 2021; 62(8):228.

ARVO Annual Meeting Abstract June 2020

GT005, a gene therapy for the treatment of dry age-related macular degeneration (AMD)

Scott Ellis; Anna Buchberger; Julie Holder; elise Orhan; Jane Hughes

Invest. Ophthalmol. Vis. Sci.. 2020; 61(7):2295.

ARVO Annual Meeting Abstract July 2019

A CCDC51 frameshift variant as a candidate gene defect for autosomal recessive rod-cone dystrophy

Christina Zeitz; Cécile Méjécase; Saddek Mohand-Saïd; Lisa Emmengger; Audrey Schalk; Marion Neuillé; Elise Orhan; Frédéric Blond; Camille Prévot; Sandra Sandra Chantot-Bastaraud; Thierry D Leveillard; Jose Alain Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2019; 60(9):415.

ARVO Annual Meeting Abstract September 2016

Gene Therapy for CSNB associated with GRM6 gene defects

Miguel Miranda de Sousa Dias; Thomas Pugliese; Marion Neuille; Elise Orhan; Christelle Michiels; Melissa Desrosiers; Jose Sahel; Deniz Dalkara; Isabelle S Audo; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):1182.

ARVO Annual Meeting Abstract June 2015

Genotypic and Phenotypic Characterization of the P23H Line 1 Rat Model

Elise Orhan; Deniz Dalkara; Christophe Lechauve; Serge A Picaud; Thierry D Leveillard; Jose Alain Sahel; Muna I Naash; Matthew M LaVail; Christina Zeitz; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):5391.

ARVO Annual Meeting Abstract June 2015

LRIT3 is essential to localize TRPM1 to the dendritic tips of ON-bipolar cells and may play a role in cone synapse formation

Marion Neuille; Catherine W Morgans; Elise Orhan; Christelle Michiels; Jose Alain Sahel; Isabelle S Audo; Robert M Duvoisin; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2015; 56(7 ):2612.

ARVO Annual Meeting Abstract April 2014

A novel mouse model for complete Congenital Stationary Night Blindness (cCSNB)

Marion Neuillé; Said El Shamieh; Elise Orhan; Christelle Michiels; Kinga Maria Bujakowska; Olivier Poch; Jose Alain Sahel; Isabelle Audo; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):1642.

ARVO Annual Meeting Abstract April 2014

Whole exome sequencing identifies a new ciliary gene in autosomal recessive rod-cone dystrophy

Isabelle Audo; Said El Shamieh; Marion Neuillé; Angélique Terray; Elise Orhan; Saddek Mohand-Saïd; Thierry D Leveillard; Olivier Goureau; Jose Alain Sahel; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2014; 55(13):405.

Retinal Cell Biology December 2013

Further Insights Into GPR179: Expression, Localization, and Associated Pathogenic Mechanisms Leading to Complete Congenital Stationary Night Blindness

PDF

Elise Orhan; Laurent Prézeau; Said El Shamieh; Kinga M. Bujakowska; Christelle Michiels; Yvrick Zagar; Claire Vol; Shomi S. Bhattacharya; José-Alain Sahel; Florian Sennlaub; Isabelle Audo; Christina Zeitz
TAGS: in situ hybridization, mice, mutation, night blindness, congenital stationary, proteins, retina, rna, antibodies, genes, enzyme-linked immunosorbent assay
Invest. Ophthalmol. Vis. Sci.. 2013; 54(13):8041-8050. https://doi.org/10.1167/iovs.13-12610

Includes: Supplemental Content

ARVO Annual Meeting Abstract June 2013

Whole exome sequencing identifies mutations in LRIT3 as a cause for autosomal recessive complete congenital stationary night blindness

Christina Zeitz; Samuel Jacobson; Christian Hamel; Kinga Bujakowska; Marion Neuillé; Elise Orhan; Xavier Zanlonghi; Jose Sahel; Shomi Bhattacharya; Isabelle Audo; CSNB study group

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):3350.

ARVO Annual Meeting Abstract June 2013

The familial dementia gene revisited: ITM2B missense mutation causes a new dominant retinal dystrophy

Isabelle Audo; Kinga Bujakowska; Elise Orhan; Florian Sennlaub; Xavier Guillonneau; Thierry Leveillard; Saddek Mohand-Said; Shomi Bhattacharya; Jose Sahel; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):3356.

ARVO Annual Meeting Abstract June 2013

Elucidation of physiopathological mechanisms of GPR179

Elise Orhan; Laurent Prezeau; Christelle Michiels; Claire Vol; Jose Sahel; Isabelle Audo; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2013; 54(15):5088.

ARVO Annual Meeting Abstract March 2012

Mutations In A Novel Gene, GPR179 Lead To Autosomal Recessive Complete Congenital Stationary Night Blindness

Christina Zeitz; Kinga Bujakowska; Elise Orhan; Jose-Alain Sahel; Shomi S. Bhattacharya; Isabelle Audo; CSNB study group

Invest. Ophthalmol. Vis. Sci.. 2012; 53(14):1729.

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