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Max A Tischfield

Showing results (21-30 of 30) with videos related to

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Plos Pathogens|January 12, 2026
Inapparent maternal ZIKV infection impacts fetal brain development and postnatal behaviorTsui-Wen Chou, Micheal McCourt, Eduard Marmut, et al.
American Journal of Human Genetics|May 17, 2016
Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear DefectsJong G Park, Max A Tischfield, Alicia A Nugent, et al.
Human Molecular Genetics|September 25, 2012
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervationGustav Y Cederquist, Anna Luchniak, Max A Tischfield, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 2024
Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in miceCara Nasello, Lauren A Poppi, Junbing Wu, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in miceCara Nasello, Lauren A Poppi, Junbing Wu, et al.
Neuron|July 13, 2023
Mapping the neuroethological signatures of pain, analgesia, and recovery in miceManon Bohic, Luke A Pattison, Z Anissa Jhumka, et al.
International Journal of Molecular Sciences|November 13, 2025
A Celsr3 Mutation Linked to Tourette Disorder Disrupts Cortical Dendritic Patterning and Striatal Cholinergic Interneuron ExcitabilityCara Nasello, G Duygu Yilmaz, Lauren A Poppi, et al.
Cell Reports|August 16, 2018
Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon RegenerationAlban Latremoliere, Long Cheng, Michelle DeLisle, et al.
Cell|January 16, 2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disordersBelinda Wang, Matthew N Tran, Sheng Wang, et al.
Pageof 3

Showing results (21-30 of 30) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 30 results.
Plos Pathogens|January 12, 2026
Inapparent maternal ZIKV infection impacts fetal brain development and postnatal behaviorTsui-Wen Chou, Micheal McCourt, Eduard Marmut, et al.
American Journal of Human Genetics|May 17, 2016
Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear DefectsJong G Park, Max A Tischfield, Alicia A Nugent, et al.
Human Molecular Genetics|September 25, 2012
An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervationGustav Y Cederquist, Anna Luchniak, Max A Tischfield, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 2024
Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in miceCara Nasello, Lauren A Poppi, Junbing Wu, et al.
Biorxiv : the Preprint Server for Biology|December 11, 2023
Human mutations in high-confidence Tourette disorder genes affect sensorimotor behavior, reward learning, and striatal dopamine in miceCara Nasello, Lauren A Poppi, Junbing Wu, et al.
Neuron|July 13, 2023
Mapping the neuroethological signatures of pain, analgesia, and recovery in miceManon Bohic, Luke A Pattison, Z Anissa Jhumka, et al.
International Journal of Molecular Sciences|November 13, 2025
A Celsr3 Mutation Linked to Tourette Disorder Disrupts Cortical Dendritic Patterning and Striatal Cholinergic Interneuron ExcitabilityCara Nasello, G Duygu Yilmaz, Lauren A Poppi, et al.
Cell Reports|August 16, 2018
Neuronal-Specific TUBB3 Is Not Required for Normal Neuronal Function but Is Essential for Timely Axon RegenerationAlban Latremoliere, Long Cheng, Michelle DeLisle, et al.
Cell|January 16, 2010
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidanceMax A Tischfield, Hagit N Baris, Chen Wu, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Rare coding mutations identify 36 large-effect risk genes in obsessive-compulsive disorder and chronic tic disordersBelinda Wang, Matthew N Tran, Sheng Wang, et al.
Pageof 3