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Literature DB >> 8348143

Trinucleotide repeat instability: when and where?

D L Nelson, S T Warren.

Abstract

Entities: Chemical

Mesh：

Year: 1993 PMID： 8348143 DOI： 10.1038/ng0693-107

Source DB: PubMed Journal: Nat Genet ISSN： 1061-4036 Impact factor: 38.330

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Cited

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10 in total

1. Genetic anticipation and musculoskeletal disease.

Authors: C M Deighton; G Thomson
Journal: Ann Rheum Dis Date: 1994-12 Impact factor: 19.103

2. Allele-specific quantification of Drosophila engrailed and invected transcripts.

Authors: A S Goldsborough; T B Kornberg
Journal: Proc Natl Acad Sci U S A Date: 1994-12-20 Impact factor: 11.205

Review 3. Organization of the human genome.

Authors: I W Craig
Journal: J Inherit Metab Dis Date: 1994 Impact factor: 4.982

4. Stability of intrastrand hairpin structures formed by the CAG/CTG class of DNA triplet repeats associated with neurological diseases.

Authors: J Petruska; N Arnheim; M F Goodman
Journal: Nucleic Acids Res Date: 1996-06-01 Impact factor: 16.971

5. Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene.

Authors: S D Pena; K T de Souza; M de Andrade; R Chakraborty
Journal: Proc Natl Acad Sci U S A Date: 1994-01-18 Impact factor: 11.205

6. A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

Authors: F Rousseau; D Heitz; J Tarleton; J MacPherson; H Malmgren; N Dahl; A Barnicoat; C Mathew; E Mornet; I Tejada
Journal: Am J Hum Genet Date: 1994-08 Impact factor: 11.025

Trinucleotide repeat instability: when and where?

1. Genetic anticipation and musculoskeletal disease.

2. Allele-specific quantification of Drosophila engrailed and invected transcripts.

Review 3. Organization of the human genome.

4. Stability of intrastrand hairpin structures formed by the CAG/CTG class of DNA triplet repeats associated with neurological diseases.

5. Allelic associations of two polymorphic microsatellites in intron 40 of the human von Willebrand factor gene.

6. A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases.

Review 7. Molecular basis of genetic neuropsychiatric disorders.

8. Hairpin properties of single-stranded DNA containing a GC-rich triplet repeat: (CTG)15.

Review 9. Autism: the point of view from fragile X studies.

10. Variable germline and embryonic instability of the human minisatellite MS32 (D1S8) in transgenic mice.