Aberrant RNA splicing in sporadic amyotrophic lateral sclerosis (Q41737172)

8 October 2017

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title

Aberrant RNA splicing in sporadic amyotrophic lateral sclerosis (English)

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amyotrophic lateral sclerosis

8 October 2017

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author name string

Bai G

series ordinal

1

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PubMed ID

9539113

8 October 2017

Lipton SA

series ordinal

2

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PubMed ID

9539113

8 October 2017

language of work or name

English

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publication date

1 March 1998

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8 October 2017

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20

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3

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8 October 2017

363-366

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Exon recognition in vertebrate splicing

8 October 2017

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https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

The regulation of splice-site selection, and its role in human disease

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

The human gene mutation database

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter, in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

Construction of a novel database containing aberrant splicing mutations of mammalian genes

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

Initial splice-site recognition and pairing during pre-mRNA splicing

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https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

Mechanical devices of the spliceosome: motors, clocks, springs, and things

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

Specific transcription and RNA splicing defects in five cloned β-thalassaemia genes

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

Regulation of pre-mRNA splicing in metazoa

1 reference

https://api.crossref.org/works/10.1016%2FS0896-6273%2800%2980979-4

7 January 2021

10.1016/S0896-6273(00)80979-4

Identifiers

DOI

1 reference

8 October 2017

1 reference

PubMed ID

9539113