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Correlation of clinical and molecular features in spinal bulbar muscular atrophy

Neurology, 2014-06, Vol.82 (23), p.2077-2084

2014

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Down syndrome—recent progress and future prospects

Human molecular genetics, 2009-04, Vol.18 (R1), p.R75-R83

2009

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DYNLRB1 is essential for dynein mediated transport and neuronal survival

Neurobiology of disease, 2020-07, Vol.140, p.104816-104816, Article 104816

2020

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Opinion: more mouse models and more translation needed for ALS

Molecular neurodegeneration, 2023-05, Vol.18 (1), p.30-30, Article 30

2023

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Is SOD1 loss of function involved in amyotrophic lateral sclerosis?

Brain (London, England : 1878), 2013-08, Vol.136 (Pt 8), p.2342-2358

2013

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Affordable optical clearing and immunolabelling in mouse brain slices

BMC research notes, 2023-09, Vol.16 (1), p.1-246, Article 246

2023

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Imaging the accumulation and suppression of tau pathology using multiparametric MRI

Neurobiology of aging, 2016-03, Vol.39, p.184-194

2016

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Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome

Human molecular genetics, 2009-04, Vol.18 (8), p.1449-1463

2009

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Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling Endosomes

Cell reports (Cambridge), 2020-03, Vol.30 (11), p.3655-3662.e2

2020

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Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion

Neurobiology of aging, 2015-01, Vol.36 (1), p.546.e1-546.e7

2015

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Aging rather than aneuploidy affects monoamine neurotransmitters in brain regions of Down syndrome mouse models

Neurobiology of disease, 2017-09, Vol.105, p.235-244

2017

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Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy

Neurobiology of aging, 2014-06, Vol.35 (6), p.1491-1498

2014

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mutation in dynein rescues axonal transport defects and extends the life span of ALS mice

The Journal of cell biology, 2005-05, Vol.169 (4), p.561-567

2005

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Tc1 mouse model of trisomy-21 dissociates properties of short- and long-term recognition memory

Neurobiology of learning and memory, 2016-04, Vol.130, p.118-128

2016

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Altered regulation of tau phosphorylation in a mouse model of down syndrome aging

Neurobiology of aging, 2012-04, Vol.33 (4), p.828.e31-828.e44

2012

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Genealogies of mouse inbred strains

Nature genetics, 2000-01, Vol.24 (1), p.23-25

2000

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A Motor-Driven Mechanism for Cell-Length Sensing

Cell reports (Cambridge), 2012-06, Vol.1 (6), p.608-616

2012

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A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome

Nature reviews. Neuroscience, 2015-09, Vol.16 (9), p.564-574

2015

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Altered Hippocampal-Prefrontal Neural Dynamics in Mouse Models of Down Syndrome

Cell reports (Cambridge), 2020-01, Vol.30 (4), p.1152-1163.e4

2020

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Cytoplasmic dynein nomenclature

The Journal of cell biology, 2005-11, Vol.171 (3), p.411-413

2005

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Cytoplasmic dynein heavy chain: the servant of many masters

Trends in neurosciences (Regular ed.), 2013-11, Vol.36 (11), p.641-651

2013

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Calyptogena magnifica Chemoautotrophic Symbiont Genome

Science (American Association for the Advancement of Science), 2007-02, Vol.315 (5814), p.998-1000

2007

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Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease

The Journal of cell biology, 2007-11, Vol.179 (3), p.485-500

2007

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Neurodegenerative Mutation in Cytoplasmic Dynein Alters Its Organization and Dynein-Dynactin and Dynein-Kinesin Interactions

The Journal of biological chemistry, 2010-12, Vol.285 (51), p.39922-39934

2010

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TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43

Neurobiology of disease, 2024-04, Vol.193, p.106437, Article 106437

2024

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Correlation of clinical and molecular features in spinal bulbar muscular atrophy

Down syndrome—recent progress and future prospects

DYNLRB1 is essential for dynein mediated transport and neuronal survival

Opinion: more mouse models and more translation needed for ALS

Is SOD1 loss of function involved in amyotrophic lateral sclerosis?

Affordable optical clearing and immunolabelling in mouse brain slices

Imaging the accumulation and suppression of tau pathology using multiparametric MRI

Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome

Mice Carrying ALS Mutant TDP-43, but Not Mutant FUS, Display In Vivo Defects in Axonal Transport of Signaling Endosomes

Screening a UK amyotrophic lateral sclerosis cohort provides evidence of multiple origins of the C9orf72 expansion

Aging rather than aneuploidy affects monoamine neurotransmitters in brain regions of Down syndrome mouse models

Widespread RNA metabolism impairment in sporadic inclusion body myositis TDP43-proteinopathy

mutation in dynein rescues axonal transport defects and extends the life span of ALS mice

Tc1 mouse model of trisomy-21 dissociates properties of short- and long-term recognition memory

Altered regulation of tau phosphorylation in a mouse model of down syndrome aging

Genealogies of mouse inbred strains

A Motor-Driven Mechanism for Cell-Length Sensing

A genetic cause of Alzheimer disease: mechanistic insights from Down syndrome

Altered Hippocampal-Prefrontal Neural Dynamics in Mouse Models of Down Syndrome

Cytoplasmic dynein nomenclature

Cytoplasmic dynein heavy chain: the servant of many masters

Calyptogena magnifica Chemoautotrophic Symbiont Genome

Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease

Neurodegenerative Mutation in Cytoplasmic Dynein Alters Its Organization and Dynein-Dynactin and Dynein-Kinesin Interactions

TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43

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