Characterization of the myotonic dystrophy region predicts multiple protein isoform-encoding mRNAs (Q34231532)

31 July 2017

title

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

1 reference

alternative mRNA splicing, via spliceosome

31 July 2017

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

repetitive DNA

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

genetic polymorphism

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

1

G. Jansen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

6

W. Hendriks

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

author name string

O'Hoy K

7

1 reference

31 July 2017

M. Mahadevan

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

C. Amemiya

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

N. Wormskamp

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

B. Segers

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

K. O'Hoy

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

S. Baird

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

L. Sabourin

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

G. Lennon

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:1302022

10 September 2022

language of work or name

English

0 references

publication date

1 July 1992

1 reference

31 July 2017

1 reference

31 July 2017

volume

1

1 reference

31 July 2017

issue

4

1 reference

31 July 2017

page(s)

261-266

1 reference

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

31 July 2017

cites work

1 reference

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

21 January 2018

1 reference

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

21 January 2018

1 reference

cAMP-dependent protein kinase: framework for a diverse family of regulatory enzymes

21 January 2018

1 reference

The P-loop--a common motif in ATP- and GTP-binding proteins

21 January 2018

1 reference

Functional domains of the Drosophila melanogaster muscle myosin heavy-chain gene are encoded by alternatively spliced exons

21 January 2018

1 reference

Excitation-contraction coupling in vertebrate skeletal muscle: a tale of two calcium channels

21 January 2018

1 reference

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

21 January 2018

1 reference

Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

1 reference

Hereditary unstable DNA: a new explanation for some old genetic questions?

21 January 2018

1 reference

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

21 January 2018

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

The syntenic relationship of proximal mouse chromosome 7 and the myotonic dystrophy gene region on human chromosome 19q

1 reference

7 January 2021

The protein kinase family: conserved features and deduced phylogeny of the catalytic domains

1 reference

7 January 2021

Whole body insulin resistance in myotonic dystrophy.

1 reference

7 January 2021

Muscle membrane protein kinase in myotonic muscular dystrophy

1 reference

7 January 2021

Activators of protein kinase C induce myotonia by lowering chloride conductance in muscle.

1 reference

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

7 January 2021

Anticipation in myotonic dystrophy: fact or fiction?

1 reference

7 January 2021

The problem of anticipation in pedigrees of dystrophia myotonica

1 reference

7 January 2021

Improved tools for biological sequence comparison

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG0792-261

1 reference

31 July 2017

1 reference