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W C Mobley

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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 15, 1996

Endocytosis of activated TrkA: evidence that nerve growth factor induces formation of signaling endosomesM L Grimes, J Zhou, E C Beattie, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 16, 2001

Failed retrograde transport of NGF in a mouse model of Down's syndrome: reversal of cholinergic neurodegenerative phenotypes following NGF infusionJ D Cooper, A Salehi, J D Delcroix, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 12, 1996

Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndromeD M Holtzman, D Santucci, J Kilbridge, et al.

Neurobiology of Disease|October 21, 1999

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]H M Mitchison, D J Bernard, N D Greene, et al.

British Journal of Anaesthesia|March 27, 2018

Inhibition of RhoA reduces propofol-mediated growth cone collapse, axonal transport impairment, loss of synaptic connectivity, and behavioural deficitsM L Pearn, J M Schilling, M Jian, et al.

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Search research articles

Showing results (71-80 of 75) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 75 results.

The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 15, 1996

Endocytosis of activated TrkA: evidence that nerve growth factor induces formation of signaling endosomesM L Grimes, J Zhou, E C Beattie, et al.

Proceedings of the National Academy of Sciences of the United States of America|August 16, 2001

Failed retrograde transport of NGF in a mouse model of Down's syndrome: reversal of cholinergic neurodegenerative phenotypes following NGF infusionJ D Cooper, A Salehi, J D Delcroix, et al.

Proceedings of the National Academy of Sciences of the United States of America|November 12, 1996

Developmental abnormalities and age-related neurodegeneration in a mouse model of Down syndromeD M Holtzman, D Santucci, J Kilbridge, et al.

Neurobiology of Disease|October 21, 1999

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected]H M Mitchison, D J Bernard, N D Greene, et al.

British Journal of Anaesthesia|March 27, 2018

Inhibition of RhoA reduces propofol-mediated growth cone collapse, axonal transport impairment, loss of synaptic connectivity, and behavioural deficitsM L Pearn, J M Schilling, M Jian, et al.

Pageof 8