(Q28250966)

1

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K Sato

3

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T Shirayama

4

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E Ohsaki

5

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M Bundo

6

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T Takeda

7

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K Tadokoro

8

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I Kondo

9

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N Murayama

https://scigraph.springernature.com/pub.10.1038/ng0194-14

10

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language of work or name

English

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publication date

January 1994

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published in

Nature Genetics

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volume

6

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page(s)

14-8

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issue

1

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exact match

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cites work

Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms

1 reference

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

21 April 2017

1 reference

Sequence identification of 2,375 human brain genes

21 April 2017

1 reference

A transcriptional analysis of the gene encoding mouse U7 small nuclear RNA

21 April 2017

1 reference

Unusual form of cerebellar ataxia; combined dentato-rubral and pallido-Luysian degeneration

21 April 2017

1 reference

Combined degeneration of globus pallidus and dentate nucleus and their projections.

21 January 2018

1 reference

Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

21 January 2018

1 reference

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

21 January 2018

1 reference

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

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

21 January 2018

1 reference

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

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

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

21 January 2018

1 reference

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

21 January 2018

1 reference

Human genes containing polymorphic trinucleotide repeats

21 January 2018

1 reference

Trinucleotide repeat length instability and age of onset in Huntington's disease

21 January 2018

1 reference

Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease

21 January 2018

1 reference

Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family

21 January 2018

1 reference

7 January 2021

Exclusion mapping of the hereditary dentatorubropallidoluysian atrophy gene from the Huntington's disease locus

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

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

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Polymerase chain reaction (PCR) for detection of APal polymorphism at the insulin like growth factor II gene (IGF2)

1 reference

7 January 2021