(Q50449574)

14 March 2018

title

New cardiac and skeletal protein aggregate myopathy associated with combined MuRF1 and MuRF3 mutations. (English)

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14 March 2018

author

Montse Olive

1

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14 March 2018

author name string

Saba Abdul-Hussein

2

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14 March 2018

Anders Oldfors

3

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14 March 2018

José González-Costello

4

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14 March 2018

Peter F M van der Ven

5

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14 March 2018

Dieter O Fürst

6

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14 March 2018

Laura González

7

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14 March 2018

Dolores Moreno

8

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14 March 2018

Benjamín Torrejón-Escribano

9

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14 March 2018

Josefina Alió

10

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14 March 2018

Adolf Pou

11

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14 March 2018

Isidro Ferrer

12

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14 March 2018

Homa Tajsharghi

13

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14 March 2018

publication date

23 March 2015

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14 March 2018

published in

Human Molecular Genetics

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14 March 2018

volume

24

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14 March 2018

issue

13

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14 March 2018

page(s)

3638-3650

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14 March 2018

Protein aggregate myopathies. Introduction

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Myosin storage myopathy associated with a heterozygous missense mutation in MYH7

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A combined laser microdissection and mass spectrometry approach reveals new disease relevant proteins accumulating in aggregates of filaminopathy patients

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Myosin accumulation and striated muscle myopathy result from the loss of muscle RING finger 1 and 3

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RING for destruction?

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Muscle ring finger 1, but not muscle ring finger 2, regulates cardiac hypertrophy in vivo

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Loss of muscle-specific RING-finger 3 predisposes the heart to cardiac rupture after myocardial infarction

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21 January 2018

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An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1

21 January 2018

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Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy

21 January 2018

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Muscle ring finger 1 mediates cardiac atrophy in vivo

21 January 2018

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Cardiac muscle ring finger-1 increases susceptibility to heart failure in vivo

21 January 2018

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Human molecular genetic and functional studies identify TRIM63, encoding Muscle RING Finger Protein 1, as a novel gene for human hypertrophic cardiomyopathy.

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Rare variants in genes encoding MuRF1 and MuRF2 are modifiers of hypertrophic cardiomyopathy.

21 January 2018

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The proteasome and the delicate balance between destruction and rescue

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Atypical ubiquitin chains: new molecular signals. 'Protein Modifications: Beyond the Usual Suspects' review series

21 January 2018

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The E3 Ligase MuRF1 degrades myosin heavy chain protein in dexamethasone-treated skeletal muscle

21 January 2018

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Muscle-specific RING finger-1 interacts with titin to regulate sarcomeric M-line and thick filament structure and may have nuclear functions via its interaction with glucocorticoid modulatory element binding protein-1

21 January 2018

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Sarcomere formation occurs by the assembly of multiple latent protein complexes

21 January 2018

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Microtubule-dependent transport and organization of sarcomeric myosin during skeletal muscle differentiation

21 January 2018

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21 January 2018

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Defective chromosome segregation, microtubule bundling and nuclear bridging in inner centromere protein gene (Incenp)-disrupted mice

21 January 2018

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21 January 2018

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21 January 2018

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Acute quadriplegia and loss of muscle myosin in patients treated with nondepolarizing neuromuscular blocking agents and corticosteroids: Mechanisms at the cellular and molecular levels

21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/HMG/DDV108

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14 March 2018

PubMed ID

25801283

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14 March 2018