(Q28238005)

English

Molecular analysis of RIM1 in autosomal recessive Retinitis pigmentosa

scientific article (publication date: 2005)

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Molecular analysis of RIM1 in autosomal recessive Retinitis pigmentosa (English)

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Isabel Barragan

1

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Irene Marcos

series ordinal

2

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Salud Borrego

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3

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Guillermo Antiñolo

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4

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language of work or name

English

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publication date

2005

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37

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issue

2

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page(s)

89-93

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cites work

Prime movers of synaptic vesicle exocytosis

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Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000084250

retrieved

21 January 2018

RIM1alpha forms a protein scaffold for regulating neurotransmitter release at the active zone

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Crossref

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https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

RIM1alpha is required for presynaptic long-term potentiation

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Crossref

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https://api.crossref.org/works/10.1159%2F000084250

retrieved

21 January 2018

Genomic organisation and alternative splicing of human RIM1, a gene implicated in autosomal dominant cone-rod dystrophy (CORD7)

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Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000084250

retrieved

21 January 2018

A major locus for autosomal recessive retinitis pigmentosa on 6q, determined by homozygosity mapping of chromosomal regions that contain gamma-aminobutyric acid-receptor clusters

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Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000084250

retrieved

21 January 2018

Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q

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reference URL

https://api.crossref.org/works/10.1159%2F000084250

retrieved

21 January 2018

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

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https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

A novel locus for Leber congenital amaurosis maps to chromosome 6q

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reference URL

https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR

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Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

Evaluation of the ELOVL4 gene in families with retinitis pigmentosa linked to the RP25 locus

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reference URL

https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

Rim is a putative Rab3 effector in regulating synaptic-vesicle fusion

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https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

RIM1: an edge for presynaptic plasticity

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https://api.crossref.org/works/10.1159%2F000084250

retrieved

21 January 2018

Direct interaction of the Rab3 effector RIM with Ca2+ channels, SNAP-25, and synaptotagmin

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reference URL

https://api.crossref.org/works/10.1159%2F000084250

retrieved

21 January 2018

SNARE function analyzed in synaptobrevin/VAMP knockout mice

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https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

A post-docking role for active zone protein Rim.

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https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

Functional interaction of the active zone proteins Munc13-1 and RIM1 in synaptic vesicle priming

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https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

The synaptic vesicle cycle: a cascade of protein-protein interactions

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https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

Excitatory amino acids as a final common pathway for neurologic disorders.

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https://api.crossref.org/works/10.1159%2F000084250

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21 January 2018

Vesicular restriction of synaptobrevin suggests a role for calcium in membrane fusion

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Crossref

reference URL

https://api.crossref.org/works/10.1159%2F000084250

retrieved

21 January 2018

Identifiers

DOI

10.1159/000084250

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PubMed publication ID

15746564

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(Q28238005)

Molecular analysis of RIM1 in autosomal recessive Retinitis pigmentosa

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