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Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders

Nature neuroscience, 2016-04, Vol.19 (4), p.557-559

2016

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Convergence of mammalian RQC and C-end rule proteolytic pathways via alanine tailing

Molecular cell, 2021-05, Vol.81 (10), p.2112-2122.e7

2021

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NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

Nature communications, 2020-09, Vol.11 (1), p.4625-4625, Article 4625

2020

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A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin

Scientific reports, 2021-09, Vol.11 (1), p.18168-18168, Article 18168

2021

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A Direct HDAC4-MAP Kinase Crosstalk Activates Muscle Atrophy Program

Molecular cell, 2012-07, Vol.47 (1), p.122-132

2012

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Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease

PloS one, 2022-09, Vol.17 (9), p.e0274615-e0274615

2022

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MARF1 Regulates Essential Oogenic Processes in Mice

Science (American Association for the Advancement of Science), 2012-03, Vol.335 (6075), p.1496-1499

2012

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A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis

American journal of human genetics, 2011-06, Vol.88 (6), p.845-851

2011

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An Active Dominant Mutation of Glycyl-tRNA Synthetase Causes Neuropathy in a Charcot-Marie-Tooth 2D Mouse Model

Neuron (Cambridge, Mass.), 2006-09, Vol.51 (6), p.715-726

2006

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Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism

eLife, 2018-07, Vol.7

2018

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Author Correction: A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin

Scientific reports, 2021-09, Vol.11 (1), p.19743-19743, Article 19743

2021

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The Histone Deacetylase HDAC4 Connects Neural Activity to Muscle Transcriptional Reprogramming

The Journal of biological chemistry, 2007-11, Vol.282 (46), p.33752-33759

2007

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Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease

PloS one, 2015-03, Vol.10 (3), p.e0117848-e0117848

2015

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Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy

Human molecular genetics, 2011-10, Vol.20 (19), p.3841-3851

2011

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Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes

Cell reports (Cambridge), 2017-03, Vol.18 (13), p.3178-3191

2017

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Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

Nature communications, 2020-10, Vol.11 (1), p.5022-5022, Article 5022

2020

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Ankyrin Repeat Domain Protein 2 and Inhibitor of DNA Binding 3 Cooperatively Inhibit Myoblast Differentiation by Physical Interaction

The Journal of biological chemistry, 2013-08, Vol.288 (34), p.24560-24568

2013

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Dysferlin Deficiency and the Development of Cardiomyopathy in a Mouse Model of Limb-Girdle Muscular Dystrophy 2B

The American journal of pathology, 2009-12, Vol.175 (6), p.2299-2308

2009

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Alterations in Osteopontin Modify Muscle Size in Females in Both Humans and Mice

Medicine and science in sports and exercise, 2013-06, Vol.45 (6), p.1060-1068

2013

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Biochemical and genetic evidence for a role of IGHMBP2 in the translational machinery

Human molecular genetics, 2009-06, Vol.18 (12), p.2115-2126

2009

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Gait analysis detects early changes in transgenic SOD1(G93A) mice

Muscle & nerve, 2005-07, Vol.32 (1), p.43-50

2005

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Rhabdomyosarcomas in aging A/J mice

PloS one, 2011-08, Vol.6 (8), p.e23498-e23498

2011

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Development-on-chip: in vitro neural tube patterning with a microfluidic device

Development (Cambridge), 2016-06, Vol.143 (11), p.1884-1892

2016

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Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking

Human molecular genetics, 2006-01, Vol.15 (2), p.233-250

2006

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Understanding the muscular dystrophy caused by deletion of choline kinase beta in mice

Biochimica et biophysica acta, 2009-05, Vol.1791 (5), p.347-356

2009

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Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders

Convergence of mammalian RQC and C-end rule proteolytic pathways via alanine tailing

NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin

A Direct HDAC4-MAP Kinase Crosstalk Activates Muscle Atrophy Program

Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease

MARF1 Regulates Essential Oogenic Processes in Mice

A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis

An Active Dominant Mutation of Glycyl-tRNA Synthetase Causes Neuropathy in a Charcot-Marie-Tooth 2D Mouse Model

Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism

Author Correction: A microfluidic approach to rescue ALS motor neuron degeneration using rapamycin

The Histone Deacetylase HDAC4 Connects Neural Activity to Muscle Transcriptional Reprogramming

Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease

Muscle choline kinase beta defect causes mitochondrial dysfunction and increased mitophagy

Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes

Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

Ankyrin Repeat Domain Protein 2 and Inhibitor of DNA Binding 3 Cooperatively Inhibit Myoblast Differentiation by Physical Interaction

Dysferlin Deficiency and the Development of Cardiomyopathy in a Mouse Model of Limb-Girdle Muscular Dystrophy 2B

Alterations in Osteopontin Modify Muscle Size in Females in Both Humans and Mice

Biochemical and genetic evidence for a role of IGHMBP2 in the translational machinery

Gait analysis detects early changes in transgenic SOD1(G93A) mice

Rhabdomyosarcomas in aging A/J mice

Development-on-chip: in vitro neural tube patterning with a microfluidic device

Mice deficient in the Rab5 guanine nucleotide exchange factor ALS2/alsin exhibit age-dependent neurological deficits and altered endosome trafficking

Understanding the muscular dystrophy caused by deletion of choline kinase beta in mice

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