Antisense oligonucleotide induction of progerin in human myogenic cells - Test2 - elhamkhani - TriplyDB

Antisense oligonucleotide induction of progerin in human myogenic cells

Antisense oligonucleotide induction of progerin in human myogenic cells

http://www.wikidata.org/entity/Q35180565

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Metformin decreases progerin expression and alleviates pathological defects of Hutchinson-Gilford progeria syndrome cells.Enhanced SRSF5 Protein Expression Reinforces Lamin A mRNA Production in HeLa Cells and Fibroblasts of Progeria Patients.

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P2860

Antisense oligonucleotide induction of progerin in human myogenic cells

http://www.wikidata.org/entity/Q35180565

description

2014 nî lūn-bûn

@nan

2014 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի հունիսին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Antisense oligonucleotide induction of progerin in human myogenic cells

@ast

Antisense oligonucleotide induction of progerin in human myogenic cells

@en

type

label

Antisense oligonucleotide induction of progerin in human myogenic cells

@ast

Antisense oligonucleotide induction of progerin in human myogenic cells

@en

prefLabel

Antisense oligonucleotide induction of progerin in human myogenic cells

@ast

Antisense oligonucleotide induction of progerin in human myogenic cells

@en

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JOURNAL.PONE.0098306

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Antisense oligonucleotide induction of progerin in human myogenic cells

@en

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Abbie M Adams

http://www.w3.org/2001/XMLSchema#string

Frank L Mastaglia

http://www.w3.org/2001/XMLSchema#string

Russell D Johnsen

http://www.w3.org/2001/XMLSchema#string

Steve D Wilton

http://www.w3.org/2001/XMLSchema#string

Yue-Bei Luo

http://www.w3.org/2001/XMLSchema#string

P2860

The mutant form of lamin A that causes Hutchinson-Gilford progeria is a biomarker of cellular aging in human skin

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

Nesprin-2 is a multi-isomeric protein that binds lamin and emerin at the nuclear envelope and forms a subcellular network in skeletal muscle

Prelamin A acts to accelerate smooth muscle cell senescence and is a novel biomarker of human vascular aging

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

Restoration of correct splicing in thalassemic pre-mRNA by antisense oligonucleotides

Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study

Homozygous defects in LMNA, encoding lamin A/C nuclear-envelope proteins, cause autosomal recessive axonal neuropathy in human (Charcot-Marie-Tooth disorder type 2) and mouse

Lamin A-dependent misregulation of adult stem cells associated with accelerated ageing

Lamin A-dependent nuclear defects in human aging

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scholarly article

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10.1371/JOURNAL.PONE.0098306

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2014-06-03T00:00:00Z

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