(Q28513178)

25 January 2017

title

Identification of a novel protein, DMAP, which interacts with the myotonic dystrophy protein kinase and shows strong homology to D1 snRNP (English)

1 reference

LSM2 homolog, U6 small nuclear RNA and mRNA degradation associated

25 January 2017

main subject

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Dystrophia myotonica-protein kinase

GOA release 2020-03-11

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GOA release 2020-03-11

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Y. H. Fu

1

1 reference

25 January 2017

language of work or name

English

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publication date

1 January 1996

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25 January 2017

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25 January 2017

volume

97

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25 January 2017

issue

1

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25 January 2017

page(s)

117–125

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Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs

25 January 2017

cites work

1 reference

12 December 2020

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

12 December 2020

A protein kinase substrate identified by the two-hybrid system

1 reference

12 December 2020

Myotonic dystrophy kinase is a component of neuromuscular junctions

1 reference

12 December 2020

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

12 December 2020

Expression of apamin receptor in muscles of patients with myotonic muscular dystrophy

1 reference

12 December 2020

The retinoblastoma protein associates with the protein phosphatase type 1 catalytic subunit

1 reference

12 December 2020

A comparative electron spin resonance study of the erythrocyte membrane in myotonic muscular dystrophy

1 reference

12 December 2020

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

1 reference

12 December 2020

Molecular cloning of a cDNA encoding the human Sm-D autoantigen

1 reference

12 December 2020

Triplet repeat mutations in human disease

1 reference

12 December 2020

Characterization of SAP-1, a protein recruited by serum response factor to the c-fos serum response element

1 reference

12 December 2020

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

12 December 2020

Decreased expression of myotonin-protein kinase messenger RNA and protein in adult form of myotonic dystrophy.

1 reference

12 December 2020

A novel genetic system to detect protein-protein interactions

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12 December 2020

Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase

1 reference

12 December 2020

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

1 reference

12 December 2020

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

12 December 2020

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

12 December 2020

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

1 reference

12 December 2020

Convergent transcripts of the yeast PRP38-SMD1 locus encode two essential splicing factors, including the D1 core polypeptide of small nuclear ribonucleoprotein particles

1 reference

12 December 2020

Unstable DNA sequence in myotonic dystrophy

1 reference

12 December 2020

Dimensions Publication ID

Identifiers

DOI

10.1007/BF00132588

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1034141319

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