(Q28237642)

1

0 references

Niklas Darin

2

0 references

Elham Rekabdar

3

0 references

Mårten Kyllerman

4

0 references

Jan Wahlström

5

0 references

Anders Oldfors

European Journal of Human Genetics

7

0 references

language of work or name

English

0 references

publication date

May 2005

0 references

published in

0 references

volume

13

0 references

issue

5

0 references

page(s)

617-22

0 references

cites work

Mapping of a myosin-binding domain and a regulatory phosphorylation site in M-protein, a structural protein of the sarcomeric M band

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Molecular structure of the sarcomeric M band: mapping of titin and myosin binding domains in myomesin and the identification of a potential regulatory phosphorylation site in myomesin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Studies of the interaction between titin and myosin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Isolation and characterization of human myosin heavy chain genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

The mammalian myosin heavy chain gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Human cardiac myosin heavy chain genes and their linkage in the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Comparative sequence analysis of the complete human sarcomeric myosin heavy chain family: implications for functional diversity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Autosomal dominant myopathy: missense mutation (Glu-706 --> Lys) in the myosin heavy chain IIa gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Myosin storage myopathy associated with a heterozygous missense mutation in MYH7

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Low sequence variation in the gene encoding the human beta-myosin heavy chain.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Organization of human and mouse skeletal myosin heavy chain gene clusters is highly conserved

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

Human skeletal myosin heavy chain genes are tightly linked in the order embryonic-IIa-IId/x-ILb-perinatal-extraocular

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

7 January 2021

Type IIx myosin heavy chain transcripts are expressed in type IIb fibers of human skeletal muscle

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

7 January 2021

Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

7 January 2021

The in vitro motility activity of beta-cardiac myosin depends on the nature of the beta-myosin heavy chain gene mutation in hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201375

7 January 2021