Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies. - Wikidata - wikimedia - TriplyDB

Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

http://www.wikidata.org/entity/Q37724771

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A calcium-relay mechanism in vertebrate phototransduction Structural insights for activation of retinal guanylate cyclase by GCAP1 Allosteric communication pathways routed by Ca(2+)/Mg(2+) exchange in GCAP1 selectively switch target regulation modes.Membrane guanylyl cyclase complexes shape the photoresponses of retinal rods and cones.A cyclic nucleotide-gated channel mutation associated with canine daylight blindness provides insight into a role for the S2 segment tri-Asp motif in channel biogenesis.Ca(2+)-sensors and ROS-GC: interlocked sensory transduction elements: a review.Antithetical modes of and the Ca(2+) sensors targeting in ANF-RGC and ROS-GC1 membrane guanylate cyclases.Understanding the physiological roles of the neuronal calcium sensor proteins.Dysfunction of outer segment guanylate cyclase caused by retinal disease related mutations.Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations.CaF2 nanoparticles as surface carriers of GCAP1, a calcium sensor protein involved in retinal dystrophies.The 2009 meeting of the study group 'Molecular Neurobiology' of the German Society for Biochemistry and Molecular Biology.Dysfunction of cGMP signalling in photoreceptors by a macular dystrophy-related mutation in the calcium sensor GCAP1.Retinal guanylyl cyclase activating protein 1 forms a functional dimer.

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Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

http://www.wikidata.org/entity/Q37724771

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

@tr

scientific article published on June 2010

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

@cs

name

Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

@en

Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

@nl

type

label

Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

@en

Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

@nl

prefLabel

Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

@en

Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

@nl

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Biological Chemistry

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Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies.

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Petra Behnen

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P2860

Functional consequences of a rod outer segment membrane guanylate cyclase (ROS-GC1) gene mutation linked with Leber's congenital amaurosis

GCAP1 (Y99C) mutant is constitutively active in autosomal dominant cone dystrophy

The Y99C mutation in guanylyl cyclase-activating protein 1 increases intracellular Ca2+ and causes photoreceptor degeneration in transgenic mice.

Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1.

The destabilization of human GCAP1 by a proline to leucine mutation might cause cone-rod dystrophy.

Apoptosis: final common pathway of photoreceptor death in rd, rds, and rhodopsin mutant mice.

Mechanisms of cell death in the inherited retinal degenerations

Molecular mechanisms of light-induced photoreceptor apoptosis and neuroprotection for retinal degeneration.

Positional preference of proline in alpha-helices.

Activation and inhibition of photoreceptor guanylyl cyclase by guanylyl cyclase activating protein 1 (GCAP-1): the functional role of Mg2+/Ca2+ exchange in EF-hand domains

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631-637

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scholarly article

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10.1515/BC.2010.063

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6

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391

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Karl-Wilhelm Koch

Daniele Dell'Orco

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2010-06-01T00:00:00Z

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20370318

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