Max A. Tischfield

Johns Hopkins Medical School/HHMI, Baltimore, MD, United States 
Cell Biology and Neuroscience
"Max Tischfield"
Mean distance: 106866
Cross-listing: Cell Biology Tree

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Nasello C, Poppi LA, Wu J, et al. (2023) Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in mice. Biorxiv : the Preprint Server For Biology
Wu J, Poppi LA, Tischfield MA. (2022) Planar cell polarity and the pathogenesis of Tourette Disorder: New hypotheses and perspectives. Developmental Biology. 489: 14-20
Poppi LA, Ho-Nguyen KT, Shi A, et al. (2021) Recurrent Implication of Striatal Cholinergic Interneurons in a Range of Neurodevelopmental, Neurodegenerative, and Neuropsychiatric Disorders. Cells. 10
Latremoliere A, Cheng L, DeLisle M, et al. (2018) Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon Regeneration. Cell Reports. 24: 1865-1879.e9
Tischfield MA, Robson CD, Gilette NM, et al. (2017) Cerebral Vein Malformations Result from Loss of Twist1 Expression and BMP Signaling from Skull Progenitor Cells and Dura. Developmental Cell
Park JG, Tischfield MA, Nugent AA, et al. (2016) Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects. American Journal of Human Genetics
Whitman MC, Andrews C, Chan WM, et al. (2015) Two unique TUBB3 mutations cause both CFEOM3 and malformations of cortical development. American Journal of Medical Genetics. Part A
Zhou Y, Wang Y, Tischfield M, et al. (2014) Canonical WNT signaling components in vascular development and barrier formation. The Journal of Clinical Investigation. 124: 3825-46
Cederquist GY, Luchniak A, Tischfield MA, et al. (2012) An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation. Human Molecular Genetics. 21: 5484-99
Tischfield MA, Cederquist GY, Gupta ML, et al. (2011) Phenotypic spectrum of the tubulin-related disorders and functional implications of disease-causing mutations. Current Opinion in Genetics & Development. 21: 286-94
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