Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice. (Q47807997)

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17 January 2020

title

Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice (English)

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17 January 2020

main subject

spinal muscular atrophy

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5

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17 January 2020

Rocio Ruiz

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17 January 2020

Raquel Cano

4

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17 January 2020

author name string

Juan José Casañas

2

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17 January 2020

Laura Torres-Benito

3

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17 January 2020

language of work or name

English

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publication date

1 January 2010

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17 January 2020

published in

Journal of Neuroscience

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17 January 2020

volume

30

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17 January 2020

issue

3

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17 January 2020

page(s)

849-857

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Development of the vertebrate neuromuscular junction

17 January 2020

cites work

1 reference

12 December 2020

A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy

1 reference

12 December 2020

A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2.

1 reference

12 December 2020

The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy

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12 December 2020

Facilitation, augmentation and potentiation at central synapses

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12 December 2020

Calcium channels coupled to neurotransmitter release at dually innervated neuromuscular junctions in the newborn rat.

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12 December 2020

A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs

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12 December 2020

Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model

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12 December 2020

Diversification of synaptic strength: presynaptic elements

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12 December 2020

Essential role for the SMN complex in the specificity of snRNP assembly

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12 December 2020

Severe depletion of mitochondrial DNA in spinal muscular atrophy

1 reference

12 December 2020

Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding.

1 reference

12 December 2020

A further study of the statistical composition on the end-plate potential

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12 December 2020

Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons

1 reference

12 December 2020

SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN

1 reference

12 December 2020

Asynchronous GABA release generates long-lasting inhibition at a hippocampal interneuron-principal neuron synapse

1 reference

12 December 2020

Autonomous function of synaptotagmin 1 in triggering synchronous release independent of asynchronous release

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12 December 2020

Mitochondrial dysfunction and amyotrophic lateral sclerosis

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12 December 2020

The essential role of the mitochondria-dependent death-signaling cascade in chemotherapy-induced potentiation of Apo2L/TRAIL cytotoxicity in cultured thoracic cancer cells: amplified caspase 8 is indispensable for combination-mediated massive cell d

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12 December 2020

Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis.

1 reference

12 December 2020

A novel method for oral delivery of drug compounds to the neonatal SMNDelta7 mouse model of spinal muscular atrophy

1 reference

12 December 2020

Defective Ca2+ channel clustering in axon terminals disturbs excitability in motoneurons in spinal muscular atrophy

1 reference

12 December 2020

Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy

1 reference

12 December 2020

Selective targeting of different neural cell adhesion molecule isoforms during motoneuron myotube synapse formation in culture and the switch from an immature to mature form of synaptic vesicle cycling

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12 December 2020

Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy

1 reference

12 December 2020

Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy

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12 December 2020

Cysteine string protein-alpha is essential for the high calcium sensitivity of exocytosis in a vertebrate synapse

1 reference

12 December 2020

Mitochondrial abnormalities in spinal and bulbar muscular atrophy

1 reference

12 December 2020

The neuroprotective factor Wld(s) fails to mitigate distal axonal and neuromuscular junction (NMJ) defects in mouse models of spinal muscular atrophy

1 reference

12 December 2020

Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice

1 reference

12 December 2020

Mitochondrial dysfunction in a neural cell model of spinal muscular atrophy.

1 reference

12 December 2020

Release of acetylcholine from embryonic neurons upon contact with muscle cell

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12 December 2020

The kinetics of transmitter release at the frog neuromuscular junction

1 reference

12 December 2020

Neuromuscular transmission in new-born rats

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12 December 2020

Mitochondrial functions in chronic spinal muscular atrophy

1 reference

12 December 2020

Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients.

1 reference

12 December 2020

Identification and characterization of a spinal muscular atrophy-determining gene

1 reference

12 December 2020

An FCCP-sensitive Ca2+ store in bullfrog sympathetic neurons and its participation in stimulus-evoked changes in [Ca2+]i.

1 reference

12 December 2020

Alterations in synaptic strength preceding axon withdrawal

1 reference

12 December 2020

The neurobiology of childhood spinal muscular atrophy.

1 reference

12 December 2020

High resolution respirometry of permeabilized skeletal muscle fibers in the diagnosis of neuromuscular disorders.

1 reference

12 December 2020

The spinal muscular atrophy disease gene product, SMN, and its associated protein SIP1 are in a complex with spliceosomal snRNP proteins

1 reference

12 December 2020

The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis

1 reference

12 December 2020

10.1523/JNEUROSCI.4496-09.2010

Identifiers

DOI

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17 January 2020

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17 January 2020

PubMed publication ID

20089893

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