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Alleviating transcript insufficiency caused by Friedreich's ataxia triplet repeats

Nucleic acids research, 2000-12, Vol.28 (24), p.4930-4937

2000

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DNA repeat expansions and human disease

Cellular and molecular life sciences : CMLS, 2000-06, Vol.57 (6), p.914-931

2000

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A persistent RNA{middle dot}DNA hybrid formed by transcription of the Friedreich ataxia triplet repeat in live bacteria, and by T7 RNAP in vitro

Nucleic acids research, 2007-08, Vol.35 (16), p.5351-5359

2007

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Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model

Gene, 2007-06, Vol.395 (1), p.125-134

2007

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The GAATTC triplet repeat expanded in Friedreich's ataxia impedes transcription elongation by T7 RNA polymerase in a length and supercoil dependent manner

Nucleic acids research, 2000-07, Vol.28 (14), p.2815-2822

2000

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Generation of Microgram Quantities of Trinucleotide Repeat Tracts of Defined Length, Interspersion Pattern, and Orientation

Analytical biochemistry, 1999-02, Vol.267 (1), p.241-243

1999

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Dual regulation of GAP-43 gene expression by nerve growth factor and glucocorticoids

The Journal of biological chemistry, 1988-12, Vol.263 (36), p.19290-19295

1988

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A series of bidirectional tetracycline-inducible promoters provides coordinated protein expression

Analytical biochemistry, 2005-11, Vol.346 (2), p.210-216

2005

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Erratum to: DNA repeat expansions and human disease

Cellular and molecular life sciences : CMLS, 2000-10, Vol.57 (11), p.1667-1667

2000

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A Long Purine-Pyrimidine Homopolymer Acts as a Transcriptional Diode (∗)

The Journal of biological chemistry, 1995-01, Vol.270 (4), p.1791-1797

1995

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Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency

Brain research bulletin, 2001-10, Vol.56 (3-4), p.367-373

2001

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Long Uninterrupted CGG Repeats within the First Exon of the Human FMR1 Gene Are Not Intrinsically Unstable in Transgenic Mice

Genomics (San Diego, Calif.), 1998-06, Vol.50 (2), p.229-240

1998

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GAP-43 transgenic mice: dispersed genomic sequences confer a GAP-43- like expression pattern during development and regeneration

The Journal of neuroscience, 1994-02, Vol.14 (2), p.499-510

1994

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Cloning and Characterization of the Rat Gene Encoding GAP-43

The European journal of neuroscience, 1990-10, Vol.2 (10), p.822-827

1990

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GAP-43 gene expression during development: persistence in a distinctive set of neurons in the mature central nervous system

Brain research. Developmental brain research, 1989-04, Vol.46 (2), p.161-168

1989

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GAP-43 transgenic mice : dispersed genomic sequences confer a GAP-43-like expression pattern during development and regneration

The Journal of neuroscience, 1994, Vol.14 (2), p.499-510

1994

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GAP-43 gene expression during development: persistence in a distinctive set of neurons in the mature central nervous system

Brain research, 1989, Vol.46 (2), p.161-168

1989

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Somatic CAG expansion in Huntington's disease is dependent on the MLH3 endonuclease domain, which can be excluded via splice redirection

Nucleic acids research, 2021-04, Vol.49 (7), p.3907-3918

2021

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Alleviating transcript insufficiency caused by Friedreich's ataxia triplet repeats

DNA repeat expansions and human disease

A persistent RNA{middle dot}DNA hybrid formed by transcription of the Friedreich ataxia triplet repeat in live bacteria, and by T7 RNAP in vitro

Regional FMRP deficits and large repeat expansions into the full mutation range in a new Fragile X premutation mouse model

The GAATTC triplet repeat expanded in Friedreich's ataxia impedes transcription elongation by T7 RNA polymerase in a length and supercoil dependent manner

Generation of Microgram Quantities of Trinucleotide Repeat Tracts of Defined Length, Interspersion Pattern, and Orientation

Dual regulation of GAP-43 gene expression by nerve growth factor and glucocorticoids

A series of bidirectional tetracycline-inducible promoters provides coordinated protein expression

Erratum to: DNA repeat expansions and human disease

A Long Purine-Pyrimidine Homopolymer Acts as a Transcriptional Diode (∗)

Fragile X syndrome and Friedreich's ataxia: Two different paradigms for repeat induced transcript insufficiency

Long Uninterrupted CGG Repeats within the First Exon of the Human FMR1 Gene Are Not Intrinsically Unstable in Transgenic Mice

GAP-43 transgenic mice: dispersed genomic sequences confer a GAP-43- like expression pattern during development and regeneration

Cloning and Characterization of the Rat Gene Encoding GAP-43

GAP-43 gene expression during development: persistence in a distinctive set of neurons in the mature central nervous system

GAP-43 transgenic mice : dispersed genomic sequences confer a GAP-43-like expression pattern during development and regneration

GAP-43 gene expression during development: persistence in a distinctive set of neurons in the mature central nervous system

Somatic CAG expansion in Huntington's disease is dependent on the MLH3 endonuclease domain, which can be excluded via splice redirection

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