Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenon (Q47290612)

13 January 2018

title

Impaired cerebral glucose metabolism in myotonic dystrophy: a triplet-size dependent phenomenon (English)

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13 January 2018

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author name string

Annane D

1

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Fiorelli M

2

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Pappata S

4

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Eymard B

5

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Radvanyi H

6

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Junien C

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Fardeau M

8

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Merlet P

9

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Gajdos P

10

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Syrota A

11

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Sansom Y

12

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Duboc D

13

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publication date

1 February 1998

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13 January 2018

published in

Neuromuscular Disorders

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volume

8

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page(s)

39-45

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issue

1

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13 January 2018

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

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7 January 2021

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

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Phosphorylation reactions of recombinant human myotonic dystrophy protein kinase and their inhibition

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7 January 2021

Myotonic dystrophy kinase is a component of neuromuscular junctions

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7 January 2021

Characterization of myotonic dystrophy kinase (DMK) protein in human and rodent muscle and central nervous tissue.

1 reference

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7 January 2021

Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure

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7 January 2021

Effect of Myotonic Dystrophy Trinucleotide Repeat Expansion on DMPK Transcription and Processing

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7 January 2021

Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements

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7 January 2021

A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat

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7 January 2021

Whole body insulin resistance in myotonic dystrophy.

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7 January 2021

Correlation between decreased myocardial glucose phosphorylation and the DNA mutation size in myotonic dystrophy.

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7 January 2021

Decreased cerebral glucose utilization in myotonic dystrophy

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7 January 2021

Criteria for establishing the validity of genetic recombination in myotonic dystrophy

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7 January 2021

The [14C]deoxyglucose method for the measurement of local cerebral glucose utilization: theory, procedure, and normal values in the conscious and anesthetized albino rat.

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7 January 2021

A new look at the statistical model identification

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7 January 2021

Tomographic measurement of local cerebral glucose metabolic rate in humans with (F-18)2-fluoro-2-deoxy-D-glucose: Validation of method

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7 January 2021

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

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7 January 2021

Transport of glucose from blood to brain

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7 January 2021

Glucose transport and phosphorylation: which is rate limiting for brain glucose utilization?

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0960-8966%2897%2900144-2

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7 January 2021

Insulin stimulates macromolecular synthesis in cultured glial cells from rat brain.

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7 January 2021

The cellular and physiological actions of insulin in the central nervous system

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7 January 2021

Decreased insulin sensitivity of forearm muscle in myotonic dystrophy

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7 January 2021

Evaluation of insulin receptor in myotonic dystrophy

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7 January 2021

Studies on Insulin Resistance and Insulin Receptor Binding in Myotonia Dystrophica*

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7 January 2021

Glucose transport and oxidation in adipose tissue of patients with myotonic dystrophy

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7 January 2021

Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes.

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7 January 2021

10.1016/S0960-8966(97)00144-2

Identifiers

DOI

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13 January 2018

PubMed ID

9565989

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13 January 2018