(Q28586388)

Spectrin repeat containing, nuclear envelope family member 3

GOA release 2020-03-11

1 reference

Experimental Cell Research

GOA release 2020-03-11

author name string

Kevin G. Young

series ordinal

1

1 reference

31 January 2017

Rashmi Kothary

series ordinal

2

1 reference

31 January 2017

language of work or name

English

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publication date

10 September 2008

1 reference

31 January 2017

1 reference

31 January 2017

314

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31 January 2017

15

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31 January 2017

2750–2761

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31 January 2017

Neurofilaments and neurological disease

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

The cytoskeleton in neurodegenerative diseases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Disruption of axo-glial junctions causes cytoskeletal disorganization and degeneration of Purkinje neuron axons

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Early axonopathy preceding neurofibrillary tangles in mutant tau transgenic mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Dystonin Is Essential for Maintaining Neuronal Cytoskeleton Organization.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Impaired fast axonal transport in neurons of the sciatic nerves from dystonia musculorum mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

The BPAG1 locus: Alternative splicing produces multiple isoforms with distinct cytoskeletal linker domains, including predominant isoforms in neurons and muscles

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Dystonin/Bpag1--a link to what?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Pathogenesis of two axonopathies does not require axonal neurofilaments.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Trafficking of macromolecules and organelles in cultured Dystonia musculorum sensory neurons is normal

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Molecular characterization of the genetic lesion in Dystonia musculorum (dt-Alb) mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Genetic alterations at the Bpag1 locus in dt mice and their impact on transcript expression

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Dissecting the sequence specific functions of alternative N-terminal isoforms of mouse bullous pemphigoid antigen 1

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

A Bpag1 isoform involved in cytoskeletal organization surrounding the nucleus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

A transgene containing lacZ inserted into the dystonia locus is expressed in neural tube.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Bpag1 localization to actin filaments and to the nucleus is regulated by its N-terminus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

An allele of the mouse mutant dystonia musculorum exhibits lesions in red nucleus and striatum

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Pathologic changes in the CNS of dystonia musculorum mutant mouse: an animal model for human spinocerebellar ataxia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

An intrinsic neuronal defect operates in dystonia musculorum: a study of dt/dt<==>+/+ chimeras

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Expression and localization of endothelin receptors: implications for the involvement of peripheral glia in nociception

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Activin induces tactile allodynia and increases calcitonin gene-related peptide after peripheral inflammation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Glial cell line-derived neurotrophic factor-responsive and neurotrophin-3-responsive neurons require the cytoskeletal linker protein dystonin for postnatal survival

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Dystonin expression in the developing nervous system predominates in the neurons that degenerate in dystonia musculorum mutant mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Expression of the mouse Macf2 gene during inner ear development.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Nesprin-3, a novel outer nuclear membrane protein, associates with the cytoskeletal linker protein plectin

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Genome-wide screen for modifiers of ataxin-3 neurodegeneration in Drosophila

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Endoplasmic reticulum stress response and neurodegeneration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Misfolded proteins, endoplasmic reticulum stress and neurodegeneration

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Prenatal onset of axonopathy in Dystonia musculorum mice.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

The intermediate filament protein peripherin is the specific interaction partner of mouse BPAG1-n (dystonin) in neurons

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Microtubule actin crosslinking factor 1b: a novel plakin that localizes to the Golgi complex

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Classification and genetics of dystonia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

TorsinA protein and neuropathology in early onset generalized dystonia with GAG deletion.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Mutant torsinA interferes with protein processing through the secretory pathway in DYT1 dystonia cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

BPAG1n4 is essential for retrograde axonal transport in sensory neurons

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

The 'spectraplakins': cytoskeletal giants with characteristics of both spectrin and plakin families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Mutations in the murine erythroid alpha-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

The Duchenne muscular dystrophy gene product is localized in sarcolemma of human skeletal muscle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021

Mutations in SYNE1 lead to a newly discovered form of autosomal recessive cerebellar ataxia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YEXCR.2008.06.021