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Elimination of huntingtin in the adult mouse leads to progressive behavioral deficits, bilateral thalamic calcification, and altered brain iron homeostasis

PLoS genetics, 2017-07, Vol.13 (7), p.e1006846-e1006846

2017

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Familial Dysautonomia: Mechanisms and Models

Genetics and molecular biology, 2016-10, Vol.39 (4), p.497-514

2016

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Striatum-specific mechanisms regulate neuronal cell cycle re-entry: the choice between life and death

Neural regeneration research, 2023-03, Vol.18 (3), p.523-524

2023

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Genetics and Neuropathology of Huntington's Disease

International Review of Neurobiology, 2011, Vol.98, p.325-372

2011

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Occludin deficiency promotes ethanol-induced disruption of colonic epithelial junctions, gut barrier dysfunction and liver damage in mice

Biochimica et biophysica acta, 2016-04, Vol.1860 (4), p.765-774

2016

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IKAP expression levels modulate disease severity in a mouse model of familial dysautonomia

Human molecular genetics, 2012-12, Vol.21 (23), p.5078-5090

2012

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Identification of cyclin D1 as a major modulator of 3-nitropropionic acid-induced striatal neurodegeneration

Neurobiology of disease, 2022-01, Vol.162, p.105581-105581, Article 105581

2022

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ELP1 Splicing Correction Reverses Proprioceptive Sensory Loss in Familial Dysautonomia

American journal of human genetics, 2019-04, Vol.104 (4), p.638-650

2019

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ATP-citrate lyase promotes axonal transport across species

Nature communications, 2021-10, Vol.12 (1), p.5878-5878, Article 5878

2021

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Sensory and autonomic deficits in a new humanized mouse model of familial dysautonomia

Human molecular genetics, 2016-03, Vol.25 (6), p.1116-1128

2016

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ALDH2 Deficiency Promotes Ethanol-Induced Gut Barrier Dysfunction and Fatty Liver in Mice

Alcoholism, clinical and experimental research, 2015-08, Vol.39 (8), p.1465-1475

2015

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Publisher Correction: ATP-citrate lyase promotes axonal transport across species

Nature communications, 2021-11, Vol.12 (1), p.6678-6678, Article 6678

2021

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Deletion of exon 20 of the Familial Dysautonomia gene Ikbkap in mice causes developmental delay, cardiovascular defects, and early embryonic lethality

PloS one, 2011-10, Vol.6 (10), p.e27015-e27015

2011

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ATAT1-enriched vesicles promote microtubule acetylation via axonal transport

Science advances, 2019-12, Vol.5 (12), p.eaax2705-eaax2705

2019

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IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation

PloS one, 2014-04, Vol.9 (4), p.e94612-e94612

2014

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Cysteine-rich domain isoforms of the neuregulin-1 gene are required for maintenance of peripheral synapses

Neuron (Cambridge, Mass.), 2000-01, Vol.25 (1), p.79-91

2000

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Huntingtin-associated protein 1 (Hap1) mutant mice bypassing the early postnatal lethality are neuroanatomically normal and fertile but display growth retardation

Human molecular genetics, 2004-12, Vol.13 (24), p.3115-3125

2004

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Neuronal deletion of Lepr elicits diabesity in mice without affecting cold tolerance or fertility

American journal of physiology: endocrinology and metabolism, 2005-09, Vol.289 (3), p.E403-E411

2005

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An allelic series for the leptin receptor gene generated by CRE and FLP recombinase

Mammalian genome, 2004-09, Vol.15 (9), p.677-685

2004

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Lactobacillus plantarum prevents and mitigates alcohol‐induced disruption of colonic epithelial tight junctions, endotoxemia, and liver damage by an EGF receptor‐dependent mechanism

The FASEB journal, 2018-11, Vol.32 (11), p.6274-6292

2018

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IKAP expression levels modulate disease severity in a mouse model of familial dysautonomia

Human molecular genetics, 2012-12, Vol.21 (23), p.5078-5090

2012

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Optimized regimen for expression of heat-inducible Cre in mice

BioTechniques, 2007-06, Vol.42 (6), p.710-714

2007

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Huntingtin Is Required for Mitotic Spindle Orientation and Mammalian Neurogenesis

Neuron (Cambridge, Mass.), 2010-08, Vol.67 (3), p.392-406

2010

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Expression of the Huntingtin-associated protein 1 gene in the developing and adult mouse

Neuroscience letters, 2000-03, Vol.282 (1), p.37-40

2000

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Selective retinal ganglion cell loss and optic neuropathy in a humanized mouse model of familial dysautonomia

Human molecular genetics, 2022-06, Vol.31 (11), p.1776-1787

2022

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Elimination of huntingtin in the adult mouse leads to progressive behavioral deficits, bilateral thalamic calcification, and altered brain iron homeostasis

Familial Dysautonomia: Mechanisms and Models

Striatum-specific mechanisms regulate neuronal cell cycle re-entry: the choice between life and death

Genetics and Neuropathology of Huntington's Disease

Occludin deficiency promotes ethanol-induced disruption of colonic epithelial junctions, gut barrier dysfunction and liver damage in mice

IKAP expression levels modulate disease severity in a mouse model of familial dysautonomia

Identification of cyclin D1 as a major modulator of 3-nitropropionic acid-induced striatal neurodegeneration

ELP1 Splicing Correction Reverses Proprioceptive Sensory Loss in Familial Dysautonomia

ATP-citrate lyase promotes axonal transport across species

Sensory and autonomic deficits in a new humanized mouse model of familial dysautonomia

ALDH2 Deficiency Promotes Ethanol-Induced Gut Barrier Dysfunction and Fatty Liver in Mice

Publisher Correction: ATP-citrate lyase promotes axonal transport across species

Deletion of exon 20 of the Familial Dysautonomia gene Ikbkap in mice causes developmental delay, cardiovascular defects, and early embryonic lethality

ATAT1-enriched vesicles promote microtubule acetylation via axonal transport

IKAP deficiency in an FD mouse model and in oligodendrocyte precursor cells results in downregulation of genes involved in oligodendrocyte differentiation and myelin formation

Cysteine-rich domain isoforms of the neuregulin-1 gene are required for maintenance of peripheral synapses

Huntingtin-associated protein 1 (Hap1) mutant mice bypassing the early postnatal lethality are neuroanatomically normal and fertile but display growth retardation

Neuronal deletion of Lepr elicits diabesity in mice without affecting cold tolerance or fertility

An allelic series for the leptin receptor gene generated by CRE and FLP recombinase

Lactobacillus plantarum prevents and mitigates alcohol‐induced disruption of colonic epithelial tight junctions, endotoxemia, and liver damage by an EGF receptor‐dependent mechanism

IKAP expression levels modulate disease severity in a mouse model of familial dysautonomia

Optimized regimen for expression of heat-inducible Cre in mice

Huntingtin Is Required for Mitotic Spindle Orientation and Mammalian Neurogenesis

Expression of the Huntingtin-associated protein 1 gene in the developing and adult mouse

Selective retinal ganglion cell loss and optic neuropathy in a humanized mouse model of familial dysautonomia

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