(Q45294431)

English

Etiology of (CAG)n triplet repeat neurodegenerative diseases such as Huntington's disease is connected to stimulation of glutamate receptors

scientific article published in May 1997

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

Etiology of (CAG)n triplet repeat neurodegenerative diseases such as Huntington's disease is connected to stimulation of glutamate receptors (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

Huntington's disease

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neurodegeneration

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based on heuristic

inferred from title

author name string

Fischer KM

1

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Europe PubMed Central

PubMed publication ID

11 December 2017

publication date

1 May 1997

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Europe PubMed Central

PubMed publication ID

11 December 2017

Medical Hypotheses

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Europe PubMed Central

PubMed publication ID

11 December 2017

48

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Europe PubMed Central

PubMed publication ID

11 December 2017

5

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Europe PubMed Central

PubMed publication ID

11 December 2017

393-398

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

Trinucleotide repeat expansions in neurological disease

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Molecular evidence that the myxozoan protists are metazoans.

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Trinucleotide repeat expansion in neurological disease

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A gene for familial hemiplegic migraine maps to chromosome 19

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Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11.

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Degenerative ataxias

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Treatment of hereditary ataxia with the levorotatory form of hydroxytryptophan

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Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.

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Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli.

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Regulation of V(D)J recombination activator protein RAG-2 by phosphorylation

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Genes for Prader Willi syndrome/Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression.

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

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

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Hints of a language in junk DNA.

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Evolution and consequences of transposable elements

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Group II self-splicing introns in bacteria.

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Adaptive mutation: who's really in the garden?

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Evolutionary biology. A boost for "adaptive" mutation.

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Chromosomal localization of long trinucleotide repeats in the human genome by fluorescence in situ hybridization

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Expanded CAG repeats in schizophrenia and bipolar disorder

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Anticipation of onset age in familial Parkinson's disease

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An international two–stage genome–wide search for schizophrenia susceptibility genes

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A manic depressive history.

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Trinucleotide repeats and genome variation

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Expression analysis of the ataxin-1 protein in tissues from normal and spinocerebellar ataxia type 1 individuals

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An intriguing new lead on Huntington's disease

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Huntingtin and DRPLA proteins selectively interact with the enzyme GAPDH.

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Identifiers

10.1016/S0306-9877(97)90034-7

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 December 2017

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