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An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

Nature genetics, 1999-04, Vol.21 (4), p.379-384

1999

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The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1)

Human molecular genetics, 2000-06, Vol.9 (10), p.1543-1551

2000

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Genetic mapping of a second myotonic dystrophy locus

Nature genetics, 1998-06, Vol.19 (2), p.196-198

1998

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The Kelch-like protein 1 modulates P/Q-type calcium current density

Neuroscience, 2007-03, Vol.145 (3), p.841-850

2007

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Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families

Neurology, 1998-12, Vol.51 (6), p.1666-1671

1998

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T-type current modulation by the actin-binding protein Kelch-like 1

American Journal of Physiology: Cell Physiology, 2010-06, Vol.298 (6), p.C1353-C1362

2010

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Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA

Nature genetics, 1998-01, Vol.18 (1), p.72-75

1998

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Kelch-like 1 protein upregulates T-type currents by an actin-F dependent increase in α(1H) channels via the recycling endosome

Channels (Austin, Tex.), 2009-11, Vol.3 (6), p.402-412

2009

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T-type current modulation by the actin-binding protein Kelch-like 1

American Journal of Physiology: Cell Physiology, 2010, Vol.67 (6)

2010

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Instability of CAG-trinucleotide Repeats in Chronic Lymphocytic Leukemia

Leukemia & lymphoma, 2002-10, Vol.43 (10), p.1987-1990

2002

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The Spinocerebellar Ataxia 8 Noncoding RNA Causes Neurodegeneration and Associates with Staufen in Drosophila

Current biology, 2004-02, Vol.14 (4), p.302-308

2004

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Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy ( DM2)

Neuromuscular disorders : NMD, 1999, Vol.9 (1), p.19-27

1999

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Comparison of expanded CAG repeat tracts in sperm and lymphocyte DNA from Machado Joseph disease and spinocerebellar ataxia type I patients

Human mutation, 1998, Vol.11 (S1), p.S74-S77

1998

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The KLHL1-antisense transcript ( KLHL1AS) is evolutionarily conserved

Mammalian genome, 2002-03, Vol.13 (3), p.134-141

2002

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Microbiological evaluation of wet and dry floor sanitization systems in hospital patient rooms

Applied and Environmental Microbiology, 1987-05, Vol.53 (5), p.1042-1045

1987

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Comparison of expanded CAG repeat tracts in sperm and lymphocyte DNA from Machado Joseph disease and spinocerebellar ataxia type I patients

Human mutation, 1998, Vol.Suppl 1, p.S74-S77

1998

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Human ACE2 Gene Replacement Mice Support SARS-CoV-2 Viral Replication and Nonlethal Disease Progression

ImmunoHorizons, 2024-09, Vol.8 (9), p.712

2024

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An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

The SCA8 transcript is an antisense RNA to a brain-specific transcript encoding a novel actin-binding protein (KLHL1)

Genetic mapping of a second myotonic dystrophy locus

The Kelch-like protein 1 modulates P/Q-type calcium current density

Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families

T-type current modulation by the actin-binding protein Kelch-like 1

Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA

Kelch-like 1 protein upregulates T-type currents by an actin-F dependent increase in α(1H) channels via the recycling endosome

T-type current modulation by the actin-binding protein Kelch-like 1

Instability of CAG-trinucleotide Repeats in Chronic Lymphocytic Leukemia

The Spinocerebellar Ataxia 8 Noncoding RNA Causes Neurodegeneration and Associates with Staufen in Drosophila

Clinical and genetic characteristics of a five-generation family with a novel form of myotonic dystrophy ( DM2)

Comparison of expanded CAG repeat tracts in sperm and lymphocyte DNA from Machado Joseph disease and spinocerebellar ataxia type I patients

The KLHL1-antisense transcript ( KLHL1AS) is evolutionarily conserved

Microbiological evaluation of wet and dry floor sanitization systems in hospital patient rooms

Comparison of expanded CAG repeat tracts in sperm and lymphocyte DNA from Machado Joseph disease and spinocerebellar ataxia type I patients

Human ACE2 Gene Replacement Mice Support SARS-CoV-2 Viral Replication and Nonlethal Disease Progression

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