Correction of alternative splicing of tau in frontotemporal dementia and parkinsonism linked to chromosome 17. (Q38296901)

1 September 2017

Correction of alternative splicing of tau in frontotemporal dementia and parkinsonism linked to chromosome 17. (English)

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Frontotemporal dementia and parkinsonism linked to chromosome 17

1 September 2017

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frontotemporal dementia

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based on heuristic

inferred from title

alternative mRNA splicing, via spliceosome

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based on heuristic

inferred from title

parkinsonian syndrome

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Kalbfuss B

1

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1 September 2017

Mabon SA

series ordinal

2

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1 September 2017

Misteli T

series ordinal

3

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1 September 2017

language of work or name

English

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publication date

17 September 2001

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Journal of Biological Chemistry

1 September 2017

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1 September 2017

276

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1 September 2017

46

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1 September 2017

42986-42993

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Alternative splicing of human genes: more the rule than the exception?

1 September 2017

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https://api.crossref.org/works/10.1074%2FJBC.M105113200

RNA processing and human disease

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M105113200

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

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M105113200

Tau protein pathology in neurodegenerative diseases.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M105113200

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M105113200

The tangled biology of tau.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M105113200

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M105113200

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Structural and functional differences between 3-repeat and 4-repeat tau isoforms. Implications for normal tau function and the onset of neurodegenetative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Structure of tau protein and assembly into paired helical filaments

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

The microtubule binding domain of tau protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Tau mutations cause frontotemporal dementias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

5' splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Complex regulation of tau exon 10, whose missplicing causes frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Probing the structure and function of U2 snRNP with antisense oligonucleotides made of 2'-OMe RNA.

21 January 2018

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https://api.crossref.org/works/10.1074%2FJBC.M105113200

Identification of a bidirectional splicing enhancer: differential involvement of SR proteins in 5' or 3' splice site activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Tau isoform expression and phosphorylation state during differentiation of cultured neuronal cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Repair of thalassemic human beta-globin mRNA in mammalian cells by antisense oligonucleotides

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Restoration of hemoglobin A synthesis in erythroid cells from peripheral blood of thalassemic patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Correction of aberrant splicing of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by antisense oligonucleotides

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Induction of endogenous Bcl-xS through the control of Bcl-x pre-mRNA splicing by antisense oligonucleotides

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Identification of functional exonic splicing enhancer motifs recognized by individual SR proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Competition for microtubule-binding with dual expression of tau missense and splice isoforms

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Abnormal Tau proteins in progressive supranuclear palsy. Similarities and differences with the neurofibrillary degeneration of the Alzheimer type.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Genetic evidence for the involvement of tau in progressive supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

Tau protein isoforms, phosphorylation and role in neurodegenerative disorders11These authors contributed equally to this work

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M105113200

21 January 2018

Identifiers

DOI

10.1074/JBC.M105113200

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1 September 2017

1 reference