(Q28306588)

1

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E Ohsaki

3

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T Shirayama

4

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K Tadokoro

5

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T Inoue

6

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M Yamada

https://scigraph.springernature.com/pub.10.1038/ng1094-177

7

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language of work or name

English

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publication date

October 1994

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published in

Nature Genetics

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volume

8

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page(s)

177-82

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issue

2

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exact match

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cites work

Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

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

21 April 2017

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Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 April 2017

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Sequence identification of 2,375 human brain genes

21 April 2017

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

21 April 2017

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Specific interactions between proteins implicated in splice site selection and regulated alternative splicing

21 April 2017

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A common RNA recognition motif identified within a defined U1 RNA binding domain of the 70K U1 snRNP protein

21 April 2017

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The human RD protein is closely related to nuclear RNA-binding proteins and has been highly conserved

21 April 2017

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Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias

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Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy

21 April 2017

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

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Anticipation in hereditary dentatorubral-pallidoluysian atrophy

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

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

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

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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

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

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

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A triplet repeat polymorphism in a gene expressed in human hypothalamus.

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7 January 2021

Expressed sequence tags and chromosomal localization of cDNA clones from a subtracted retinal pigment epithelium library

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7 January 2021

A method to identify distinctive charge configurations in protein sequences, with application to human herpesvirus polypeptides.

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7 January 2021

Identification of the human U7 snRNP as one of several factors involved in the 3' end maturation of histone premessenger RNA's

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Transcriptional activation modulated by homopolymeric glutamine and proline stretches

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Molecular cloning of androgen receptors from divergent species with a polymerase chain reaction technique: complete cDNA sequence of the mouse androgen receptor and isolation of androgen receptor cDNA probes from dog, guinea pig and clawed frog

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The rat androgen receptor: primary structure, autoregulation of its messenger ribonucleic acid, and immunocytochemical localization of the receptor protein

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SR proteins: a conserved family of pre-mRNA splicing factors

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Cloning and intracellular localization of the U2 small nuclear ribonucleoprotein auxiliary factor small subunit

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7 January 2021

Dual Bar homeo box genes of Drosophila required in two photoreceptor cells, R1 and R6, and primary pigment cells for normal eye development.

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7 January 2021

Identification and characterization of the gene causing type 1 spinocerebellar ataxia.

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