Max A. Tischfield
Affiliations: | Johns Hopkins Medical School/HHMI, Baltimore, MD, United States |
Area:
Cell Biology and NeuroscienceGoogle:
"Max Tischfield"Mean distance: 106866
Cross-listing: Cell Biology Tree
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Publications
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| Nasello C, Poppi LA, Wu J, et al. (2024) 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 of the United States of America. 121: e2307156121 |
| 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 |