A mutation in serca underlies motility dysfunction in accordion zebrafish (Q45175395)

10 December 2017

A mutation in serca underlies motility dysfunction in accordion zebrafish (English)

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10 December 2017

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10 December 2017

Michelle R Gleason

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10 December 2017

Mark A Verdecia

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10 December 2017

Howard Sirotkin

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10 December 2017

Paul Brehm

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10 December 2017

Gail Mandel

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10 December 2017

language of work or name

English

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publication date

1 December 2004

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10 December 2017

Developmental Biology

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10 December 2017

276

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10 December 2017

441-451

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10 December 2017

2

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Ca2+ homeostasis in Brody's disease. A study in skeletal muscle and cultured muscle cells and the effects of dantrolene an verapamil

10 December 2017

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Synaptic drive to motoneurons during fictive swimming in the developing zebrafish

7 January 2021

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Acetylcholinesterase function is dispensable for sensory neurite growth but is critical for neuromuscular synapse stability

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Calcium binding activity of vesicular relaxing factor

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

A post-natal decrease in acetylcholine channel open time at rat end-plates

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

MOLSCRIPT: a program to produce both detailed and schematic plots of protein structures

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Contribution of cholinesterase to developmental decreases in the time course of synaptic potentials at an amphibian neuromuscular junction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Nonjunctional acetylcholine receptor channel open time decreases during development of Xenopus muscle

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Increased neuromuscular activity causes axonal defects and muscular degeneration

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Laser ablations reveal functional relationships of segmental hindbrain neurons in zebrafish

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Persistent electrical coupling and locomotory dysfunction in the zebrafish mutant shocked.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Ca2+ signalling and muscle disease

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

The mechanism of Ca2+ transport by sarco(endo)plasmic reticulum Ca2+-ATPases

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

NMR studies of the fifth transmembrane segment of sarcoplasmic reticulum Ca2+-ATPase reveals a hinge close to the Ca2+-ligating residues

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Mutations in the gene-encoding SERCA1, the fast-twitch skeletal muscle sarcoplasmic reticulum Ca2+ ATPase, are associated with Brody disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

The mutation of Pro789 to Leu reduces the activity of the fast-twitch skeletal muscle sarco(endo)plasmic reticulum Ca2+ ATPase (SERCA1) and is associated with Brody disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

The Zebrafish motility mutant twitch once reveals new roles for rapsyn in synaptic function

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Acetylcholine receptors direct rapsyn clusters to the neuromuscular synapse in zebrafish.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Targeted disruption of the ATP2A1 gene encoding the sarco(endo)plasmic reticulum Ca2+ ATPase isoform 1 (SERCA1) impairs diaphragm function and is lethal in neonatal mice.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Zebrafish genomics: from mutants to genes

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Scanning mutagenesis reveals a similar pattern of mutation sensitivity in transmembrane sequences M4, M5, and M6, but not in M8, of the Ca2+-ATPase of sarcoplasmic reticulum (SERCA1a)

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Structural changes in the calcium pump accompanying the dissociation of calcium

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Crystal structure of the calcium pump of sarcoplasmic reticulum at 2.6 A resolution

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Crystal structures of Ca2+-ATPase in various physiological states.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Pathfinding and synapse formation in a zebrafish mutant lacking functional acetylcholine receptors

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

Localization and quantification of endoplasmic reticulum Ca(2+)-ATPase isoform transcripts

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YDBIO.2004.09.008

10.1016/J.YDBIO.2004.09.008

7 January 2021

Identifiers

DOI

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10 December 2017

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