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Meeting Abstract (9)
Journal Articles (1)

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Investigative Ophthalmology & Visual Science (10)

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ARVO Annual Meeting Abstract (9)
Visual Neuroscience (1)

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Biochemistry and Molecular Biology (1)
Eye Anatomy and Disorders (1)
Retina (1)
Visual Neuroscience (1)

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biopharmaceutics classification system (1)
dendrites (1)
immunohistochemistry (1)
mice (1)
retina (1)
retinal bipolar cells (1)
retinal cone (1)
rod photoreceptors (1)
synapses (1)
synaptic transmission (1)

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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 July 2018

Development of two gene therapy approaches for Complete Congenital Stationary Night Blindness (cCSNB)

Juliette Varin; Miguel Miranda de Sousa Dias; Thomas Pugliese; Marion Neuillé; Nassima Bouzidi; Christelle Michiels; Melissa Desrosiers; José-Alain Sahel; Isabelle S Audo; Deniz Dalkara; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2018; 59(9):4526.

ARVO Annual Meeting Abstract June 2017

Identification of mutations in CACNA1F in patients with incomplete CSNB applying next generation sequencing approaches

Christina Zeitz; Christelle Michiels; Marion Neuille; Christoph Friedburg; Christel Condroyer; Fiona Boyard; Aline Antonio; Markus N Preising; Vincent Meyer; Anne Boland; Jean-François Deleuze; Lilia Mesrob; Bernhard Jurklies; Birgit Lorenz; Jose Alain Sahel; Isabelle S Audo

Invest. Ophthalmol. Vis. Sci.. 2017; 58(8):575.

Visual Neuroscience March 2017

LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells

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Marion Neuillé; Yan Cao; Romain Caplette; Debbie Guerrero-Given; Connon Thomas; Naomi Kamasawa; José-Alain Sahel; Christian P. Hamel; Isabelle Audo; Serge Picaud; Kirill A. Martemyanov; Christina Zeitz
TAGS: mice, retinal bipolar cells, retinal cone, synapses, synaptic transmission, rod photoreceptors, retina, dendrites, biopharmaceutics classification system, immunohistochemistry
Invest. Ophthalmol. Vis. Sci.. 2017; 58(3):1768-1778. https://doi.org/10.1167/iovs.16-20745

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ARVO Annual Meeting Abstract September 2016

Novel mutations in SLC24A1 leading to congenital stationary night blindness (CSNB)

Marion Neuille; Sivasankar Malaichamy; Maria Vadala; Ramya Sachidanandam; Tharigopala Arokiasamy; Jose Sahel; Parveen Sen; Isabelle S Audo; Nagasamy Soumittra; Christina Zeitz

Invest. Ophthalmol. Vis. Sci.. 2016; 57(12):658.

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

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.

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.

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Online ISSN: 1552-5783

Investigative Ophthalmology & Visual Science
Journal of Vision
Translational Vision Science & Technology

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