Dr Tako Hensch

Takao Kurt Hensch, Ph.D.

Professor of Neurology, Boston Children's Hospital
Professor of Molecular and Cellular Biology, Faculty of Arts & Sciences
Tutor, Academic (Other Faculty), Faculty of Arts & Sciences
Harvard Title

Professor of Neurology
Professor of Molecular and Cellular Biology

Other Affiliations

Cellular Biology and Center for Brain Science

Address

Center for Brain Science (NW347.10)
Northwest Lab Building
52 Oxford Street  
Cambridge MA 02138

Publications View
Bidirectional plasticity in fast-spiking GABA circuits by visual experience.
Authors: Yazaki-Sugiyama Y, Kang S, Câteau H, Fukai T, Hensch TK.
Nature
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Common circuit defect of excitatory-inhibitory balance in mouse models of autism.
Authors: Gogolla N, Leblanc JJ, Quast KB, Südhof TC, Fagiolini M, Hensch TK.
J Neurodev Disord
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Development. Editorial overview.
Authors: Hensch TK, Brand AH.
Curr Opin Neurobiol
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From brain formation to plasticity: insights on Otx2 homeoprotein.
Authors: Sugiyama S, Prochiantz A, Hensch TK.
Dev Growth Differ
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Efhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility.
Authors: Suzuki T, Miyamoto H, Nakahari T, Inoue I, Suemoto T, Jiang B, Hirota Y, Itohara S, Saido TC, Tsumoto T, Sawamoto K, Hensch TK, Delgado-Escueta AV, Yamakawa K.
Hum Mol Genet
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A resource for transcriptomic analysis in the mouse brain.
Authors: Plessy C, Fagiolini M, Wagatsuma A, Harasawa N, Kuji T, Asaka-Oba A, Kanzaki Y, Fujishima S, Waki K, Nakahara H, Hensch TK, Carninci P.
PLoS One
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Experience-dependent transfer of Otx2 homeoprotein into the visual cortex activates postnatal plasticity.
Authors: Sugiyama S, Di Nardo AA, Aizawa S, Matsuo I, Volovitch M, Prochiantz A, Hensch TK.
Cell
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Critical period revisited: impact on vision.
Authors: Morishita H, Hensch TK.
Curr Opin Neurobiol
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Reliability of intensity dependence of auditory-evoked potentials.
Authors: Hensch T, Herold U, Diers K, Armbruster D, Brocke B.
Clin Neurophysiol
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Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.
Authors: Ogiwara I, Miyamoto H, Morita N, Atapour N, Mazaki E, Inoue I, Takeuchi T, Itohara S, Yanagawa Y, Obata K, Furuichi T, Hensch TK, Yamakawa K.
J Neurosci
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