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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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Distinct alpha- and beta-tubulin isotypes are required for the positioning, differentiation and survival of neurons: new support for the 'multi-tubulin' hypothesis

Bioscience reports, 2010-10, Vol.30 (5), p.319

2010

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An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation

Human molecular genetics, 2012-12, Vol.21 (26), p.5484-5499

2012

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Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura

Developmental cell, 2017-09, Vol.42 (5), p.445-461.e5

2017

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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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Understanding the development, pathogenesis, and injury response of meningeal lymphatic networks through the use of animal models

Cellular and molecular life sciences : CMLS, 2023-11, Vol.80 (11), p.332-332, Article 332

2023

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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), p.1-17

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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Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

Cell, 2010-01, Vol.140 (1), p.74-87

2010

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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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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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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

Distinct alpha- and beta-tubulin isotypes are required for the positioning, differentiation and survival of neurons: new support for the 'multi-tubulin' hypothesis

An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation

Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura

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

Understanding the development, pathogenesis, and injury response of meningeal lymphatic networks through the use of animal models

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

Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

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

The people behind the papers – Matt Matrongolo and Max Tischfield

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

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