(Q24539118)

6 July 2017

title

Reversal of the cellular phenotype in the premature aging disease Hutchinson-Gilford progeria syndrome (English)

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6 July 2017

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2

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Tom Misteli

series ordinal

2

object named as

Tom Misteli

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6 July 2017

Paola Scaffidi

1

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6 July 2017

language of work or name

English

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publication date

6 March 2005

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6 July 2017

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6 July 2017

volume

11

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6 July 2017

issue

4

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6 July 2017

page(s)

440-445

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Accumulation of mutant lamin A causes progressive changes in nuclear architecture in Hutchinson-Gilford progeria syndrome

6 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Translating the Histone Code

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Domain-specific interactions of human HP1-type chromodomain proteins and inner nuclear membrane protein LBR

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Genome-scale expression profiling of Hutchinson-Gilford progeria syndrome reveals widespread transcriptional misregulation leading to mesodermal/mesenchymal defects and accelerated atherosclerosis

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

A-type lamins regulate retinoblastoma protein function by promoting subnuclear localization and preventing proteasomal degradation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Therapeutic potential of antisense oligonucleotides as modulators of alternative splicing

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Lamin a truncation in Hutchinson-Gilford progeria.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Both emerin and lamin C depend on lamin A for localization at the nuclear envelope

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Morpholino antisense oligomers: the case for an RNase H-independent structural type

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Mitotic misregulation and human aging

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

The Hutchinson-Gilford progeria syndrome. Report of 4 cases and review of the literature

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Cellular uptake of antisense morpholino oligomers conjugated to arginine-rich peptides.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Alternative splicing in disease and therapy

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Novel lamin A/C gene (LMNA) mutations in atypical progeroid syndromes

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Morpholino antisense oligonucleotide induced dystrophin exon 23 skipping in mdx mouse muscle.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

A progeroid syndrome in mice is caused by defects in A-type lamins

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1351119

Morpholino and phosphorothioate antisense oligomers compared in cell-free and in-cell systems

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15750600

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Antisense morpholino oligonucleotide analog induces missplicing of C-myc mRNA

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15750600

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Searching for clues to premature aging

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15750600

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NM1204

1 reference

Dimensions Publication ID

6 July 2017

1045731227

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Fatcat ID

release_hsolhu7ir5gznkoxlvzxgguzsq

0 references

OpenCitations bibliographic resource ID

2901442

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

6 July 2017

1 reference