New cardiac and skeletal protein aggregate myopathy associated with combined MuRF1 and MuRF3 mutations. (Q50449574)

14 March 2018

title

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

1 reference

14 March 2018

author

Montse Olive

1

1 reference

14 March 2018

author name string

Saba Abdul-Hussein

2

1 reference

14 March 2018

Anders Oldfors

3

1 reference

14 March 2018

José González-Costello

4

1 reference

14 March 2018

Peter F M van der Ven

5

1 reference

14 March 2018

Dieter O Fürst

6

1 reference

14 March 2018

Laura González

7

1 reference

14 March 2018

Dolores Moreno

8

1 reference

14 March 2018

Benjamín Torrejón-Escribano

9

1 reference

14 March 2018

Josefina Alió

10

1 reference

14 March 2018

Adolf Pou

11

1 reference

14 March 2018

Isidro Ferrer

12

1 reference

14 March 2018

Homa Tajsharghi

13

1 reference

14 March 2018

publication date

23 March 2015

1 reference

14 March 2018

published in

Human Molecular Genetics

1 reference

14 March 2018

volume

24

1 reference

14 March 2018

issue

13

1 reference

14 March 2018

page(s)

3638-3650

1 reference

14 March 2018

Protein aggregate myopathies. Introduction

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

21 January 2018

Myofibrillar myopathies

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Skeletal muscle α-actin diseases (actinopathies): pathology and mechanisms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Myosin storage myopathy associated with a heterozygous missense mutation in MYH7

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Differential proteomic analysis of abnormal intramyoplasmic aggregates in desminopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Myofibrillar myopathies: new developments.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Myosinopathies: pathology and mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

21 January 2018

RING for destruction?

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Recent advances in the biology and therapy of muscle wasting

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Regulation of microtubule dynamics and myogenic differentiation by MURF, a striated muscle RING-finger protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Identification of ubiquitin ligases required for skeletal muscle atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Cooperative control of striated muscle mass and metabolism by MuRF1 and MuRF2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

MURF-1 and MURF-2 target a specific subset of myofibrillar proteins redundantly: towards understanding MURF-dependent muscle ubiquitination

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Muscle ring finger 1 mediates cardiac atrophy in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Does p.Q247X in TRIM63 cause human hypertrophic cardiomyopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

The proteasome and the delicate balance between destruction and rescue

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Sarcomere formation occurs by the assembly of multiple latent protein complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Targeted disruption of mouse centromere protein C gene leads to mitotic disarray and early embryo death

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Glycogenin-1 deficiency and inactivated priming of glycogen synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic era.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

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

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDV108

21 January 2018

Identifiers

DOI

10.1093/HMG/DDV108

1 reference

14 March 2018

PubMed ID

25801283

1 reference

14 March 2018