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B17Characterisation Of A Huntington's Disease Cellular Model For The Transcriptome-based Expression Analysis Of Deubiquitinating Enzymes

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A14-A15

2014

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B19Lactate metabolism in the Huntington's disease mouse model R6/2

Journal of neurology, neurosurgery and psychiatry, 2012-09, Vol.83 (Suppl 1), p.A11-ai-A11

2012

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G05Cognitive Impairment And Psychiatric Symptoms In A Danish Cohort Of Huntington's Disease Gene-expansion Carriers

Journal of neurology, neurosurgery and psychiatry, 2014-09, Vol.85 (Suppl 1), p.A51-A51

2014

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Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genes

Clinical genetics, 2016-03, Vol.89 (3), p.320-327

2016

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Huntington's Disease Does Not Appear to Increase the Risk of Diabetes Mellitus

Journal of neuroendocrinology, 2009-09, Vol.21 (9), p.770-776

2009

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4p16.3 haplotype modifying age at onset of Huntington disease

Clinical genetics, 2009-03, Vol.75 (3), p.244-250

2009

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A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment

European journal of neurology, 2008-10, Vol.15 (10), p.1135-1139

2008

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The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa

American journal of human genetics, 1992-10, Vol.51 (4), p.755-762

1992

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Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease

Human molecular genetics, 1993-06, Vol.2 (6), p.637-637

1993

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Cells exposed to a huntingtin fragment containing an expanded polyglutamine tract show no sign of ion channel formation: Results arguing against the ion channel hypothesis

Journal of neuroscience research, 2003-01, Vol.71 (1), p.132-137

2003

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Antisense downregulation of mutant huntingtin in a cell model

The journal of gene medicine, 2003-06, Vol.5 (6), p.528-538

2003

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Trinucleotide repeat elongation in the Huntingtin gene in Huntington Disease patients from 71 Danish families

Human molecular genetics, 1993-09, Vol.2 (9), p.1475-1476

1993

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Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease

Clinical genetics, 1995-03, Vol.47 (3), p.113-117

1995

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Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease

Human molecular genetics, 1993-09, Vol.2 (9), p.1523-1523

1993

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Exclusion of DNA changes in the β-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's disease

Nature genetics, 1992-05, Vol.1 (2), p.104-108

1992

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Improved PCR conditions for the stretch of (CAG) sub(n) repeats causing Huntington's disease

Human molecular genetics, 1993-01, Vol.2 (6), p.637-638

1993

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Nucleotide sequence and PCR-amplification of a polymorphic MboI site in human DNA marker D4S95 linked to the Huntington disease locus

Clinical genetics, 1992-10, Vol.42 (4), p.210-211

1992

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A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease

Nature neuroscience, 2015-06, Vol.18 (6), p.807-816

2015

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Inhibition of endoplasmic reticulum stress counteracts neuronal cell death and protein aggregation caused by N-terminal mutant huntingtin proteins

Experimental cell research, 2008-03, Vol.314 (5), p.950-960

2008

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The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease in 2 Danish families

Molecular genetics and metabolism, 2018-02, Vol.123 (2), p.S44-S44

2018

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Reduced gluconeogenesis and lactate clearance in Huntington's disease

Neurobiology of disease, 2010-12, Vol.40 (3), p.656-662

2010

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Sequence variants in SPAST , SPG3A and HSPD1 in hereditary spastic paraplegia

Journal of the neurological sciences, 2009-09, Vol.284 (1), p.90-95

2009

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The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders

Parkinsonism & related disorders, 2011-06, Vol.17 (5), p.398-399

2011

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B17Characterisation Of A Huntington's Disease Cellular Model For The Transcriptome-based Expression Analysis Of Deubiquitinating Enzymes

B19Lactate metabolism in the Huntington's disease mouse model R6/2

G05Cognitive Impairment And Psychiatric Symptoms In A Danish Cohort Of Huntington's Disease Gene-expansion Carriers

Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genes

Huntington's Disease Does Not Appear to Increase the Risk of Diabetes Mellitus

4p16.3 haplotype modifying age at onset of Huntington disease

A novel presenilin 2 mutation (V393M) in early-onset dementia with profound language impairment

The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa

Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease

Cells exposed to a huntingtin fragment containing an expanded polyglutamine tract show no sign of ion channel formation: Results arguing against the ion channel hypothesis

Antisense downregulation of mutant huntingtin in a cell model

Trinucleotide repeat elongation in the Huntingtin gene in Huntington Disease patients from 71 Danish families

Correlation between magnitude of CAG repeat length alterations and length of the paternal repeat in paternally inherited Huntington's disease

Improved PCR conditions for the stretch of (CAG)n repeats causing Huntington's disease

Exclusion of DNA changes in the β-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's disease

Improved PCR conditions for the stretch of (CAG) sub(n) repeats causing Huntington's disease

Nucleotide sequence and PCR-amplification of a polymorphic MboI site in human DNA marker D4S95 linked to the Huntington disease locus

A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease

Inhibition of endoplasmic reticulum stress counteracts neuronal cell death and protein aggregation caused by N-terminal mutant huntingtin proteins

The D313Y variant in the GLA gene - no evidence of a pathogenic role in Fabry disease in 2 Danish families

Reduced gluconeogenesis and lactate clearance in Huntington's disease

Sequence variants in SPAST , SPG3A and HSPD1 in hereditary spastic paraplegia

The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders

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