(Q40712861)

English

Expression and biological activity of Baculovirus generated wild-type human slow alpha tropomyosin and the Met9Arg mutant responsible for a dominant form of nemaline myopathy

scientific article published on August 2002

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Expression and biological activity of Baculovirus generated wild-type human slow alpha tropomyosin and the Met9Arg mutant responsible for a dominant form of nemaline myopathy (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

object named as

Nigel Laing

5

1 reference

ORCID Public Data File 2021

author name string

P Anthony Akkari

1

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Yuhua Song

2

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Sarah Hitchcock-DeGregori

3

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

Lori Blechynden

4

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

publication date

1 August 2002

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

number of pages

5

1 reference

based on heuristic

inferred from page(s)

Biochemical and Biophysical Research Communications

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

296

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

300-304

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

The molecular basis for tropomyosin isoform diversity

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

High-level production of functional muscle alpha-tropomyosin in Pichia pastoris.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

NEMALINE MYOPATHY

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

A mutation in alpha-tropomyosin(slow) affects muscle strength, maturation and hypertrophy in a mouse model for nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

Nemaline myopathy mechanisms

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

Divergent abnormal muscle relaxation by hypertrophic cardiomyopathy and nemaline myopathy mutant tropomyosins

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

A novel nemaline myopathy in the Amish caused by a mutation in troponin T1

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

Renaturation of skeletal muscle tropomyosin: implications for in vivo assembly

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

NEMALINE MYOPATHY. A NEW CONGENITAL MYOPATHY

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900852-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0006-291X(02)00852-5

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 September 2017

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