(Q37724771)

22 August 2017

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title

Involvement of the calcium sensor GCAP1 in hereditary cone dystrophies (English)

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22 August 2017

Daniele Dell'Orco

2

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Karl-Wilhelm Koch

object named as

Karl-Wilhelm Koch

series ordinal

3

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author name string

Petra Behnen

series ordinal

1

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22 August 2017

language of work or name

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1 June 2010

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22 August 2017

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22 August 2017

volume

391

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22 August 2017

issue

6

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22 August 2017

page(s)

631-637

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Spectrum of retGC1 mutations in Leber's congenital amaurosis

22 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

Positional preference of proline in alpha-helices

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

Mutation analysis identifies GUCY2D as the major gene responsible for autosomal dominant progressive cone degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

Mutations in the GUCA1A gene involved in hereditary cone dystrophies impair calcium-mediated regulation of guanylate cyclase

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

Mechanisms of cell death in the inherited retinal degenerations

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

Photoreceptor degeneration in vitamin A deprivation and retinitis pigmentosa: the equivalent light hypothesis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

Activation of multiple pathways during photoreceptor apoptosis in the rd mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

Ceramide is the key mediator of oxidative stress-induced apoptosis in retinal photoreceptor cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FBC.2010.063

21 January 2018

Identifiers

DOI

10.1515/BC.2010.063

1 reference

22 August 2017

1 reference