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Transient Opening of the Mitochondrial Permeability Transition Pore Induces Microdomain Calcium Transients in Astrocyte Processes

Neuron (Cambridge, Mass.), 2017-02, Vol.93 (3), p.587-605.e7

2017

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Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations

Current opinion in genetics & development, 2011-06, Vol.21 (3), p.286-294

2011

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Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon Regeneration

Cell reports (Cambridge), 2018-08, Vol.24 (7), p.1865-1879.e9

2018

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Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects

American journal of human genetics, 2016-06, Vol.98 (6), p.1220-1227

2016

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Recurrent Implication of Striatal Cholinergic Interneurons in a Range of Neurodevelopmental, Neurodegenerative, and Neuropsychiatric Disorders

Cells (Basel, Switzerland), 2021-04, Vol.10 (4), p.907

2021

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Planar cell polarity and the pathogenesis of Tourette Disorder: New hypotheses and perspectives

Developmental biology, 2022-09, Vol.489, p.14-20

2022

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The growth and expansion of meningeal lymphatic networks are affected in craniosynostosis

Development (Cambridge), 2022-01, Vol.149 (1)

2022

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The clinical spectrum of homozygous HOXA1 mutations

American journal of medical genetics. Part A, 2008-05, Vol.146A (10), p.1235-1240

2008

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Loss of Twist1 and balanced retinoic acid signaling from the meninges causes cortical folding in mice

Development (Cambridge), 2023-09, Vol.150 (18)

2023

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Cranium growth, patterning and homeostasis

Development (Cambridge), 2022-11, Vol.149 (22)

2022

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Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice

The Journal of clinical investigation, 2023-11, Vol.134 (4)

2023

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Mapping the neuroethological signatures of pain, analgesia, and recovery in mice

Neuron (Cambridge, Mass.), 2023-09, Vol.111 (18), p.2811-2830.e8

2023

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Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle

Investigative ophthalmology & visual science, 2017-04, Vol.58 (4), p.2388-2396

2017

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Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development

American journal of medical genetics. Part A, 2016-02, Vol.170A (2), p.297-305

2016

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Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

Nature genetics, 2005-10, Vol.37 (10), p.1035-1037

2005

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Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations

Investigative ophthalmology & visual science, 2010-09, Vol.51 (9), p.4600-4611

2010

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Piezol agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice

The Journal of clinical investigation, 2024-02, Vol.134 (4)

2024

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HOXA1 mutations are not a common cause of Duane anomaly

American journal of medical genetics. Part A, 2006-04, Vol.140A (8), p.900-902

2006

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Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice

Proceedings of the National Academy of Sciences - PNAS, 2024-05, Vol.121 (19), p.e2307156121

2024

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The people behind the papers – Matt Matrongolo and Max Tischfield

Development (Cambridge), 2023-09, Vol.150 (18)

2023

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Position and orientation of vaginal pessaries in situ on magnetic resonance imaging

International Urogynecology Journal, 2022-02, Vol.33 (2), p.369-376

2022

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Canonical WNT signaling components in vascular development and barrier formation

The Journal of clinical investigation, 2014-09, Vol.124 (9), p.3825-3846

2014

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TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse

Developmental biology, 2022-10, Vol.490, p.126-133

2022

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Transient Opening of the Mitochondrial Permeability Transition Pore Induces Microdomain Calcium Transients in Astrocyte Processes

Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations

Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon Regeneration

Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects

Recurrent Implication of Striatal Cholinergic Interneurons in a Range of Neurodevelopmental, Neurodegenerative, and Neuropsychiatric Disorders

Planar cell polarity and the pathogenesis of Tourette Disorder: New hypotheses and perspectives

The growth and expansion of meningeal lymphatic networks are affected in craniosynostosis

The clinical spectrum of homozygous HOXA1 mutations

Loss of Twist1 and balanced retinoic acid signaling from the meninges causes cortical folding in mice

Cranium growth, patterning and homeostasis

Piezo1 agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice

Mapping the neuroethological signatures of pain, analgesia, and recovery in mice

Ocular Motor Nerve Development in the Presence and Absence of Extraocular Muscle

Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

Evidence of an asymmetrical endophenotype in congenital fibrosis of extraocular muscles type 3 resulting from TUBB3 mutations

Piezol agonist restores meningeal lymphatic vessels, drainage, and brain-CSF perfusion in craniosynostosis and aged mice

HOXA1 mutations are not a common cause of Duane anomaly

Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice

The people behind the papers – Matt Matrongolo and Max Tischfield

Position and orientation of vaginal pessaries in situ on magnetic resonance imaging

Canonical WNT signaling components in vascular development and barrier formation

TWIST1, a gene associated with Saethre-Chotzen syndrome, regulates extraocular muscle organization in mouse

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