Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcripts. (Q52088534)

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scientific article published in September 2004

Language	Label	Description	Also known as
English	Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcripts.	scientific article published in September 2004

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcripts. (English)

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

1

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

Vilma-Lotta Lehtokari

object named as

Vilma-Lotta Lehtokari

3

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object named as

Katarina Pelin

5

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author name string

Maria Sandbacka

2

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

Carina Wallgren-Pettersson

4

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

publication date

1 September 2004

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

European Journal of Human Genetics

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Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

12

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

9

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

744-751

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

Correlation Between Conformational and Binding Properties of Nebulin Repeats

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201242

7 January 2021

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Myopalladin, a novel 145-kilodalton sarcomeric protein with multiple roles in Z-disc and I-band protein assemblies

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201242

7 January 2021

based on heuristic

inferred from DOI database lookup

The SH3 domain of nebulin binds selectively to type II peptides: theoretical prediction and experimental validation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201242

7 January 2021

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Molecular dissection of the interaction of desmin with the C-terminal region of nebulin

1 reference

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7 January 2021

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Characterization of nebulette and nebulin and emerging concepts of their roles for vertebrate Z-discs

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201242

7 January 2021

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The complete gene sequence of titin, expression of an unusual approximately 700-kDa titin isoform, and its interaction with obscurin identify a novel Z-line to I-band linking system

1 reference

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7 January 2021

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Muscle-specific alternative splicing of myotubularin-related 1 gene is impaired in DM1 muscle cells

1 reference

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7 January 2021

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The N-terminal end of nebulin interacts with tropomodulin at the pointed ends of the thin filaments.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201242

7 January 2021

based on heuristic

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Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Nebulin mutations in autosomal recessive nemaline myopathy: an update

1 reference

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7 January 2021

based on heuristic

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Mutations in the nebulin gene can cause severe congenital nemaline myopathy.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormalities in the expression of nebulin in chromosome-2 linked nemaline myopathy.

1 reference

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7 January 2021

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

1 reference

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7 January 2021

based on heuristic

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

1 reference

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Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy

1 reference

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7 January 2021

based on heuristic

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Mutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy

1 reference

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

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The complete mouse nebulin gene sequence and the identification of cardiac nebulin

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based on heuristic

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Basic local alignment search tool

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201242

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Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201242

7 January 2021

based on heuristic

inferred from DOI database lookup

BCM Search Launcher--an integrated interface to molecular biology data base search and analysis services available on the World Wide Web.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201242

7 January 2021

based on heuristic

inferred from DOI database lookup

Myogenesis in the mouse embryo: differential onset of expression of myogenic proteins and the involvement of titin in myofibril assembly

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201242

7 January 2021

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inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5201242

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

21 April 2018

http://europepmc.org/abstract/MED/15266303

ResearchGate publication ID

0 references

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