Large CTG repeats trigger p16-dependent premature senescence in myotonic dystrophy type 1 muscle precursor cells
about
A muscle stem cell for every muscle: variability of satellite cell biology among different muscle groupsMuscle wasting in myotonic dystrophies: a model of premature agingc-Flip overexpression affects satellite cell proliferation and promotes skeletal muscle agingMyotonic dystrophy protein kinase (DMPK) prevents ROS-induced cell death by assembling a hexokinase II-Src complex on the mitochondrial surfaceMMP-14 is necessary but not sufficient for invasion of three-dimensional collagen by human muscle satellite cells.Immortalized human myotonic dystrophy muscle cell lines to assess therapeutic compounds.Quiescence of human muscle stem cells is favored by culture on natural biopolymeric films.Premature senescence in primary muscle cultures of myotonic dystrophy type 2 is not associated with p16 induction.Establishment of clonal myogenic cell lines from severely affected dystrophic muscles - CDK4 maintains the myogenic population.Regenerative potential of human muscle stem cells in chronic inflammation.Molecular signatures of age-associated chronic degeneration of shoulder muscles.Age-dependent alteration in muscle regeneration: the critical role of tissue niche.Molecular mechanisms of muscle atrophy in myotonic dystrophies.Skeletal muscle characteristics are preserved in hTERT/cdk4 human myogenic cell lines.From cellular senescence to age-associated diseases: the miRNA connection.Molecular therapy in myotonic dystrophy: focus on RNA gain-of-function.PABPN1 gene therapy for oculopharyngeal muscular dystrophyActivation of the innate immune response and interferon signalling in myotonic dystrophy type 1 and type 2 cataracts.Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features: ultrastructural evidence.Myotonic Dystrophy Type 2: An Update on Clinical Aspects, Genetic and Pathomolecular Mechanism.Myotonic dystrophy type 2 and modifier genes: an update on clinical and pathomolecular aspects.Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders.FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy.Satellite cell dysfunction contributes to the progressive muscle atrophy in myotonic dystrophy type 1.Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy.Cells of Matter-In Vitro Models for Myotonic Dystrophy.RNA processing is altered in skeletal muscle nuclei of patients affected by myotonic dystrophyAbnormalities of satellite cells function in amyotrophic lateral sclerosis
P2860
Q26779289-621D58C7-A4D2-434A-AF9C-BE2881B6F192Q26798784-89BF79DA-9C55-4769-A7DA-68B520C79728Q28587861-8D6A9EE2-6901-45B1-9872-FFCAEB45C9D7Q30009539-71078346-9C21-4562-AF1F-D1B3E162CE82Q30583897-74F410EB-8D2B-42BA-A9AA-F1CCDB2217EAQ33588075-A94543F4-90CD-4848-B33C-73C551AFAF6FQ33630478-FD27E3D2-9825-42FF-AB90-183490136AEFQ34905434-C41EB061-E81D-47A3-BC24-E45CEE81AA6DQ35166244-07CE6CCE-2809-4806-A722-28D190258162Q35907825-F45674FB-16D7-4B26-9F2A-65ABF47DF0C6Q36962331-F0ED76AE-CC50-4495-A06B-A88043D2C2FDQ37034374-2C88496D-E99C-4E54-9C7C-B102F636A34CQ37138514-E6788BBD-88DD-4FDA-99E1-7A23CE420514Q37487702-AAB3B1A1-C926-4808-883E-AECE69FF8CB1Q37581213-1A6F785C-C3AF-42F1-A16A-EF43BAEF1A48Q37734660-A66496E6-018F-45D1-93F1-EAF719A105C8Q37737844-36BEC932-2B1F-4E4A-8915-0458013642C9Q38330480-F9B97E9E-35D0-40AB-A91C-E69BEDF8271EQ38852912-E419D196-AEF6-4870-A3DB-DAB19ED952F7Q39012035-A38457DF-364A-4E56-BF60-B86766D75DDDQ39081415-DCD1F09E-6FDE-4DB9-9EF1-2E22449F39A3Q39738924-35E55FEF-DDA4-4473-AE87-E2CE35298CEDQ51290025-17CC96B2-AFCD-4D49-94ED-E1ED6D99A009Q51829611-E5848C0C-20D0-440D-9DBF-4493720FCF82Q54982478-B6B448C5-7587-4700-A3CD-B809FCD5167AQ55100992-09C54AD2-2ED6-4E32-BF51-94A054C96183Q57085790-09146C5E-6E36-49A6-8F6E-398BADA22827Q57268487-28E3281C-1933-4C78-B37E-DDE751B0BAEB
P2860
Large CTG repeats trigger p16-dependent premature senescence in myotonic dystrophy type 1 muscle precursor cells
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 26 February 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Large CTG repeats trigger p16- ...... type 1 muscle precursor cells
@en
Large CTG repeats trigger p16- ...... type 1 muscle precursor cells.
@nl
type
label
Large CTG repeats trigger p16- ...... type 1 muscle precursor cells
@en
Large CTG repeats trigger p16- ...... type 1 muscle precursor cells.
@nl
prefLabel
Large CTG repeats trigger p16- ...... type 1 muscle precursor cells
@en
Large CTG repeats trigger p16- ...... type 1 muscle precursor cells.
@nl
P2860
P50
P1476
Large CTG repeats trigger p16- ...... type 1 muscle precursor cells
@en
P2093
Erwan Gasnier
Virginie Jacquemin
P2860
P304
P356
10.2353/AJPATH.2009.080560
P407
P577
2009-02-26T00:00:00Z