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A Transient Receptor Potential-Like Channel Mediates Synaptic Transmission in Rod Bipolar Cells

The Journal of neuroscience, 2009-05, Vol.29 (19), p.6088-6093

2009

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GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness

American journal of human genetics, 2012-02, Vol.90 (2), p.331-339

2012

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Presynaptic Expression of LRIT3 Transsynaptically Organizes the Postsynaptic Glutamate Signaling Complex Containing TRPM1

Cell reports (Cambridge), 2019-06, Vol.27 (11), p.3107-3116.e3

2019

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Gain control by sparse, ultra-slow glycinergic synapses

Cell reports (Cambridge), 2022-02, Vol.38 (8), p.110410-110410, Article 110410

2022

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Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness

Human molecular genetics, 2015-11, Vol.24 (21), p.6229-6239

2015

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GPR158/179 regulate G protein signaling by controlling localization and activity of the RGS7 complexes

The Journal of cell biology, 2012-06, Vol.197 (6), p.711-719

2012

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Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

American journal of human genetics, 2009-11, Vol.85 (5), p.730-736

2009

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GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells

The Journal of neuroscience, 2014-04, Vol.34 (18), p.6334-6343

2014

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LRIT3 expression in cone photoreceptors restores post-synaptic bipolar cell signalplex assembly and partial function in Lrit3−/− mice

iScience, 2023-04, Vol.26 (4), p.106499-106499, Article 106499

2023

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Intermolecular Interaction between Anchoring Subunits Specify Subcellular Targeting and Function of RGS Proteins in Retina ON-Bipolar Neurons

The Journal of neuroscience, 2016-03, Vol.36 (10), p.2915-2925

2016

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Neuromuscular synaptic patterning requires the function of skeletal muscle dihydropyridine receptors

Nature neuroscience, 2011-05, Vol.14 (5), p.570-577

2011

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Anesthetic requirement is increased in redheads

Anesthesiology (Philadelphia), 2004-08, Vol.101 (2), p.279-283

2004

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Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cells

The Journal of neuroscience, 2011-03, Vol.31 (11), p.3962-3967

2011

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rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA

Proceedings of the National Academy of Sciences - PNAS, 2011-01, Vol.108 (3), p.1099-1103

2011

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Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma

PLoS genetics, 2011-02, Vol.7 (2), p.e1001310-e1001310

2011

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Comparisons of structural and functional abnormalities in mouse b-wave mutants

The Journal of physiology, 2008-09, Vol.586 (18), p.4385-4392

2008

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Topological analysis of small leucine-rich repeat proteoglycan nyctalopin

PloS one, 2012-04, Vol.7 (4), p.e33137-e33137

2012

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Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylation

PloS one, 2010-10, Vol.5 (10), p.e13743-e13743

2010

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LRIT3 is Required for Nyctalopin Expression and Normal ON and OFF Pathway Signaling in the Retina

eNeuro, 2020-01, Vol.7 (1), p.ENEURO.0002-20.2020

2020

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The light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1)

The Journal of general physiology, 2006-05, Vol.127 (5), p.577-589

2006

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Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Journal of neurophysiology, 2012-11, Vol.108 (9), p.2442-2451

2012

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Nyctalopin Expression in Retinal Bipolar Cells Restores Visual Function in a Mouse Model of Complete X-Linked Congenital Stationary Night Blindness

Journal of neurophysiology, 2007-11, Vol.98 (5), p.3023-3033

2007

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Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD)

PloS one, 2009-12, Vol.4 (12), p.e8329-e8329

2009

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Cone Synaptic function is modulated by the leucine rich repeat (LRR) adhesion molecule LRFN2

eNeuro, 2024-03, Vol.11 (3), p.ENEURO.0120-23.2024

2024

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Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology

A Transient Receptor Potential-Like Channel Mediates Synaptic Transmission in Rod Bipolar Cells

GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness

Presynaptic Expression of LRIT3 Transsynaptically Organizes the Postsynaptic Glutamate Signaling Complex Containing TRPM1

Gain control by sparse, ultra-slow glycinergic synapses

Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindness

GPR158/179 regulate G protein signaling by controlling localization and activity of the RGS7 complexes

Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness

GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells

LRIT3 expression in cone photoreceptors restores post-synaptic bipolar cell signalplex assembly and partial function in Lrit3−/− mice

Intermolecular Interaction between Anchoring Subunits Specify Subcellular Targeting and Function of RGS Proteins in Retina ON-Bipolar Neurons

Neuromuscular synaptic patterning requires the function of skeletal muscle dihydropyridine receptors

Anesthetic requirement is increased in redheads

Autoantibodies in melanoma-associated retinopathy target TRPM1 cation channels of retinal ON bipolar cells

rnaset2 mutant zebrafish model familial cystic leukoencephalopathy and reveal a role for RNase T2 in degrading ribosomal RNA

Mutations in zebrafish lrp2 result in adult-onset ocular pathogenesis that models myopia and other risk factors for glaucoma

Comparisons of structural and functional abnormalities in mouse b-wave mutants

Topological analysis of small leucine-rich repeat proteoglycan nyctalopin

Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylation

LRIT3 is Required for Nyctalopin Expression and Normal ON and OFF Pathway Signaling in the Retina

The light peak of the electroretinogram is dependent on voltage-gated calcium channels and antagonized by bestrophin (best-1)

Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation

Nyctalopin Expression in Retinal Bipolar Cells Restores Visual Function in a Mouse Model of Complete X-Linked Congenital Stationary Night Blindness

Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD)

Cone Synaptic function is modulated by the leucine rich repeat (LRR) adhesion molecule LRFN2

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