Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice. (Q50975967)

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31 October 2019

title

Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice (English)

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31 October 2019

1

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31 October 2019

François Radvanyi

2

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31 October 2019

author name string

Lia AS

3

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31 October 2019

Duros C

4

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31 October 2019

Blanche M

5

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31 October 2019

Abitbol M

6

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31 October 2019

Junien C

7

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31 October 2019

Hofmann-Radvanyi H

8

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31 October 2019

language of work or name

English

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publication date

1 February 1997

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31 October 2019

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31 October 2019

volume

15

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31 October 2019

issue

2

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31 October 2019

page(s)

190-192

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https://scigraph.springernature.com/pub.10.1038/ng0297-190

31 October 2019

exact match

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cites work

Somatic instability of CTG repeat in myotonic dystrophy

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Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses

21 January 2018

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Myotonic dystrophy: will the real gene please step forward!

21 January 2018

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7 January 2021

Different sex-dependent constraints in CTG length variation as explanation for congenital 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

Effects of the sex of myotonic dystrophy patients on the unstable triplet repeat in their affected offspring

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7 January 2021

Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy

1 reference

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7 January 2021

Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a casual involvement of methyl-directed DNA mismatch repair in triplet repeat stability

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7 January 2021

Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice

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7 January 2021

SCA1 transgenic mice: A model for neurodegeneration caused by an expanded CAG trinucleotide repeat

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7 January 2021

Absence of disease phenotype and intergenerational stability of the CAG repeat in transgenic mice expressing the human Huntington disease transcript

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7 January 2021

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

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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

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

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

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7 January 2021

Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

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7 January 2021

Origin of the expansion mutation in myotonic dystrophy

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7 January 2021

A tetranucleotide repeat mouse minisatellite displaying substantial somatic instability during early preimplantation development

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7 January 2021

Intergenerational stability of the myotonic dystrophy protomutation

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7 January 2021

Genealogical reconstruction of myotonic dystrophy in the Saguenay-Lac-Saint-Jean area (Quebec, Canada)

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7 January 2021

Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis

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7 January 2021

Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over

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7 January 2021

Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer

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7 January 2021

Analysis of a 70 kb segment of DNA containing the human zeta and alpha-globin genes linked to their regulatory element (HS-40) in transgenic mice

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7 January 2021

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