Calcium channel-dependent molecular maturation of photoreceptor synapses. - Wikidata - awgldk - TriplyDB

Calcium channel-dependent molecular maturation of photoreceptor synapses.

Calcium channel-dependent molecular maturation of photoreceptor synapses.

http://www.wikidata.org/entity/Q34723088

about

Neuronal remodeling in retinal circuit assembly, disassembly, and reassembly Voltage-Gated Cav1 Channels in Disorders of Vision and Hearing Cav1.4 IT mouse as model for vision impairment in human congenital stationary night blindness type 2.Dysregulation of Ca(v)1.4 channels disrupts the maturation of photoreceptor synaptic ribbons in congenital stationary night blindness type 2 Spectrum of Cav1.4 dysfunction in congenital stationary night blindness type 2 In vivo knockdown of Piccolino disrupts presynaptic ribbon morphology in mouse photoreceptor synapses.Characterization of Cav1.4 complexes (α11.4, β2, and α2δ4) in HEK293T cells and in the retina Cav1.4 L-Type Calcium Channels Contribute to Calpain Activation in Degenerating Photoreceptors of rd1 Mice.TULP1 mutations causing early-onset retinal degeneration: preserved but insensitive macular cones.TMEM16A is associated with voltage-gated calcium channels in mouse retina and its function is disrupted upon mutation of the auxiliary α2δ4 subunit.Gain-of-function nature of Cav1.4 L-type calcium channels alters firing properties of mouse retinal ganglion cells.How to make a synaptic ribbon: RIBEYE deletion abolishes ribbons in retinal synapses and disrupts neurotransmitter release.Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristics Mutation of wrb, a Component of the Guided Entry of Tail-Anchored Protein Pathway, Disrupts Photoreceptor Synapse Structure and Function.Photoreceptor degeneration in two mouse models for congenital stationary night blindness type 2 Presynaptic [Ca(2+)] and GCAPs: aspects on the structure and function of photoreceptor ribbon synapses.Functional architecture of the retina: development and disease.Illuminating the multifaceted roles of neurotransmission in shaping neuronal circuitry.Mechanism for Selective Synaptic Wiring of Rod Photoreceptors into the Retinal Circuitry and Its Role in Vision.Retinoschisin Facilitates the Function of L-Type Voltage-Gated Calcium Channels.Possible role of sialylation of retinal protein glycans in the regulation of electroretinogram response in mice.Cone dystrophy and ectopic synaptogenesis in a Cacna1f loss of function model of congenital stationary night blindness (CSNB2A).Development of cone photoreceptors and their synapses in the human and monkey fovea.Channeling Vision: CaV1.4-A Critical Link in Retinal Signal Transmission.

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Calcium channel-dependent molecular maturation of photoreceptor synapses.

http://www.wikidata.org/entity/Q34723088

description

2013 nî lūn-bûn

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2013 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2013 թվականի մայիսին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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name

Calcium channel-dependent molecular maturation of photoreceptor synapses.

@ast

Calcium channel-dependent molecular maturation of photoreceptor synapses.

@en

Calcium channel-dependent molecular maturation of photoreceptor synapses.

@nl

type

label

Calcium channel-dependent molecular maturation of photoreceptor synapses.

@ast

Calcium channel-dependent molecular maturation of photoreceptor synapses.

@en

Calcium channel-dependent molecular maturation of photoreceptor synapses.

@nl

prefLabel

Calcium channel-dependent molecular maturation of photoreceptor synapses.

@ast

Calcium channel-dependent molecular maturation of photoreceptor synapses.

@en

Calcium channel-dependent molecular maturation of photoreceptor synapses.

@nl

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Calcium channel-dependent molecular maturation of photoreceptor synapses.

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Nawal Zabouri

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Silke Haverkamp

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P2860

Essential role of Ca2+-binding protein 4, a Cav1.4 channel regulator, in photoreceptor synaptic function.

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness

Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness

Molecular dissection of the photoreceptor ribbon synapse: physical interaction of Bassoon and RIBEYE is essential for the assembly of the ribbon complex

The dynamic architecture of photoreceptor ribbon synapses: cytoskeletal, extracellular matrix, and intramembrane proteins

Identification and light-dependent translocation of a cone-specific antigen, cone arrestin, recognized by monoclonal antibody 7G6

Vesicular neurotransmitter transporter expression in developing postnatal rodent retina: GABA and glycine precede glutamate

The CACNA1F gene encodes an L-type calcium channel with unique biophysical properties and tissue distribution

Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina

Membrane-associated guanylate kinase proteins MPP4 and MPP5 associate with Veli3 at distinct intercellular junctions of the neurosensory retina

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