Characterization of cardiac conduction system abnormalities in mice with targeted disruption of Six5 gene. (Q52547985)

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scientific article published in October 2002

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English	Characterization of cardiac conduction system abnormalities in mice with targeted disruption of Six5 gene.	scientific article published in October 2002

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Europe PubMed Central

PubMed publication ID

12397222

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3 May 2018

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http://europepmc.org/abstract/MED/12397222

title

Characterization of cardiac conduction system abnormalities in mice with targeted disruption of Six5 gene. (English)

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12397222

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3 May 2018

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http://europepmc.org/abstract/MED/12397222

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Hiroko Wakimoto

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1

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12397222

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Colin T Maguire

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2

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12397222

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Megan C Sherwood

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3

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12397222

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Marcel M Vargas

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4

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12397222

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Partha S Sarkar

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5

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12397222

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Jennifer Han

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6

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12397222

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Sita Reddy

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7

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12397222

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http://europepmc.org/abstract/MED/12397222

Charles I Berul

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8

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PubMed publication ID

12397222

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3 May 2018

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http://europepmc.org/abstract/MED/12397222

publication date

1 October 2002

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12397222

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3 May 2018

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http://europepmc.org/abstract/MED/12397222

published in

Journal of Interventional Cardiac Electrophysiology

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Europe PubMed Central

PubMed publication ID

12397222

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3 May 2018

reference URL

http://europepmc.org/abstract/MED/12397222

volume

7

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Europe PubMed Central

PubMed publication ID

12397222

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3 May 2018

reference URL

http://europepmc.org/abstract/MED/12397222

issue

2

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Europe PubMed Central

PubMed publication ID

12397222

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3 May 2018

reference URL

http://europepmc.org/abstract/MED/12397222

page(s)

127-135

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PubMed publication ID

12397222

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3 May 2018

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http://europepmc.org/abstract/MED/12397222

cites work

Foci of trinucleotide repeat transcripts in nuclei of myotonic dystrophy cells and tissues

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

In vivo cardiac electrophysiology studies in the mouse

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

Triplet repeat expansion in neuromuscular disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

Expansion of a CUG trinucleotide repeat in the 3' untranslated region of myotonic dystrophy protein kinase transcripts results in nuclear retention of transcripts

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

Cardiac involvement in a large kindred with myotonic dystrophy. Quantitative assessment and relation to size of CTG repeat expansion

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

Ion transport in human skeletal muscle cells: disturbances in myotonic dystrophy and Brody's disease

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

Is it possible to identify infrahissian cardiac conduction abnormalities in myotonic dystrophy by non-invasive methods?

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expansion of the myotonic dystrophy CTG repeat reduces expression of the flanking DMAHP gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

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inferred from PubMed ID database lookup

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

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stated in

PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DMPK dosage alterations result in atrioventricular conduction abnormalities in a mouse myotonic dystrophy model

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Phenotypic screening for heart rate variability in the mouse

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Progressive atrioventricular conduction block in a mouse myotonic dystrophy model.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruption of splicing regulated by a CUG-binding protein in myotonic dystrophy

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Left ventricular diastolic function in congenital myotonic dystrophy

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac involvement in myotonic dystrophy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

Measurement of heart rate and Q-T interval in the conscious mouse.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cardiac abnormalities and cytosine-thymineguanine trinucleotide repeats in myotonic dystrophy

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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Cooperation of six and eya in activation of their target genes through nuclear translocation of Eya

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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Induction of atrial tachycardia and fibrillation in the mouse heart

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

Mice lacking the myotonic dystrophy protein kinase develop a late onset progressive myopathy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

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inferred from PubMed ID database lookup

High Output Cardiac Failure

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/12397222

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the sites of conduction abnormalities in a mouse model of myotonic dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Natural history of cardiac involvement in myotonic dystrophy: Correlation with CTG repeats

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Trinucleotide repeat expansion at the myotonic dystrophy locus reduces expression of DMAHP

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiency of Na+/K(+)-ATPase and sarcoplasmic reticulum Ca(2+)-ATPase in skeletal muscle and cultured muscle cells of myotonic dystrophy patients

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterisation of expression of mDMAHP, a homeodomain-encoding gene at the murine DM locus.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/12397222

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Identifiers

DOI

10.1023/A:1020881520353

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12397222

retrieved

3 May 2018

reference URL

http://europepmc.org/abstract/MED/12397222

Dimensions Publication ID

1042010295

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PubMed publication ID

12397222

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12397222

retrieved

3 May 2018

reference URL

http://europepmc.org/abstract/MED/12397222

 

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