Loss of HCN1 enhances disease progression in mouse models of CNG channel-linked retinitis pigmentosa and achromatopsia

Biology and therapy of inherited retinal degenerative disease: insights from mouse models

(2015) Shobi Veleri et al.   Disease Models & Mechanisms

Retinitis pigmentosa: impact of differentPde6apoint mutations on the disease phenotype

(2015) Vithiyanjali Sothilingam et al.   HUMAN MOLECULAR GENETICS

Towards a Quantitative OCT Image Analysis

(2014) Marina Garcia Garrido et al.   PLoS One

Identification of a Common Non-Apoptotic Cell Death Mechanism in Hereditary Retinal Degeneration

(2014) Blanca Arango-Gonzalez et al.   PLoS One

Cellular responses following retinal injuries and therapeutic approaches for neurodegenerative diseases

(2014) Nicolás Cuenca et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Mouse rods signal through gap junctions with cones

(2014) Sabrina Asteriti et al.   eLife

Mosaic synaptopathy and functional defects in Cav1.4 heterozygous mice and human carriers of CSNB2

(2013) Stylianos Michalakis et al.   HUMAN MOLECULAR GENETICS

Long-Term In Vivo Imaging of Fibrillar Tau in the Retina of P301S Transgenic Mice

(2013) Christian Schön et al.   PLoS One

Gene therapy restores vision and delays degeneration in the CNGB1-/- mouse model of retinitis pigmentosa

(2012) S. Koch et al.   HUMAN MOLECULAR GENETICS

The photovoltage of rods and cones in the dark-adapted mouse retina

(2012) Lorenzo Cangiano et al.   JOURNAL OF PHYSIOLOGY-LONDON

Ivabradine: An Intelligent Drug for the Treatment of Ischemic Heart Disease

(2012) Graziano Riccioni   MOLECULES

Processing of Retinal Signals in Normal and HCN Deficient Mice

(2012) Luca Della Santina et al.   PLoS One

Genome-wide transcriptome analysis in murine neural retina using high-throughput RNA sequencing

(2011) Ece D. Gamsiz et al.   GENOMICS

Modulation of rod photoreceptor output by HCN1 channels is essential for regular mesopic cone vision

(2011) Mathias W. Seeliger et al.   Nature Communications

Complementary conductance changes by Ikxand Ihcontribute to membrane impedance stability during the rod light response

(2010) Andrew J. Barrow et al.   Channels

Differences in RDS trafficking, assembly and function in cones versus rods: insights from studies of C150S-RDS

(2010) Dibyendu Chakraborty et al.   HUMAN MOLECULAR GENETICS

Anisometropes adapt to different retinal image sizes via post-receptoral mechanisms, not by differences in photoreceptor density

(2010) K. Y. Li et al.   JOURNAL OF VISION

Restoration of Cone Vision in the CNGA3−/− Mouse Model of Congenital Complete Lack of Cone Photoreceptor Function

(2010) Stylianos Michalakis et al.   MOLECULAR THERAPY

Vision tests in the mouse: Functional phenotyping with electroretinography

(2009) Naoyuki Tanimoto   Frontiers in Bioscience-Landmark

Hyperpolarization-Activated Cation Channels: From Genes to Function

(2009) Martin Biel et al.   PHYSIOLOGICAL REVIEWS

Light responses in the mouse retina are prolonged upon targeted deletion of the HCN1 channel gene

(2008) Gabriel C. Knop et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

Photoreceptor Cell Death Mechanisms in Inherited Retinal Degeneration

(2008) Javier Sancho-Pelluz et al.   MOLECULAR NEUROBIOLOGY

How vision begins: An odyssey

(2008) D.-G. Luo et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Cellular mechanisms underlying the pharmacological induction of phosphenes

(2007) L Cervetto et al.   BRITISH JOURNAL OF PHARMACOLOGY