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D H Geschwind

Showing results (61-70 of 70) with videos related to

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Molecular Psychiatry|November 17, 2010
Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult miceD Ehninger, Y Sano, P J de Vries, et al.
Neurology|December 15, 2004
Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)J R M Oliveira, E Spiteri, M J Sobrido, et al.
Neurology|May 30, 2008
Biochemical markers in persons with preclinical familial Alzheimer diseaseJ M Ringman, S G Younkin, D Pratico, et al.
Science (New York, N.Y.)|December 4, 1998
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17M Hong, V Zhukareva, V Vogelsberg-Ragaglia, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2006
Analysis of oncogenic signaling networks in glioblastoma identifies ASPM as a molecular targetS Horvath, B Zhang, M Carlson, et al.
Molecular Psychiatry|September 10, 2014
Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneityJ Ellegood, E Anagnostou, B A Babineau, et al.
Molecular Psychiatry|February 5, 2015
3D visualization of the regional differencesJ Ellegood, E Anagnostou, B A Babineau, et al.
Neurology|December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN Finch, M M Carrasquillo, M Baker, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Molecular Psychiatry|November 17, 2010
Gestational immune activation and Tsc2 haploinsufficiency cooperate to disrupt fetal survival and may perturb social behavior in adult miceD Ehninger, Y Sano, P J de Vries, et al.
Neurology|December 15, 2004
Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)J R M Oliveira, E Spiteri, M J Sobrido, et al.
Neurology|May 30, 2008
Biochemical markers in persons with preclinical familial Alzheimer diseaseJ M Ringman, S G Younkin, D Pratico, et al.
Science (New York, N.Y.)|December 4, 1998
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17M Hong, V Zhukareva, V Vogelsberg-Ragaglia, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 28, 1998
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17L N Clark, P Poorkaj, Z Wszolek, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 9, 2006
Analysis of oncogenic signaling networks in glioblastoma identifies ASPM as a molecular targetS Horvath, B Zhang, M Carlson, et al.
Molecular Psychiatry|September 10, 2014
Clustering autism: using neuroanatomical differences in 26 mouse models to gain insight into the heterogeneityJ Ellegood, E Anagnostou, B A Babineau, et al.
Molecular Psychiatry|February 5, 2015
3D visualization of the regional differencesJ Ellegood, E Anagnostou, B A Babineau, et al.
Neurology|December 24, 2010
TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriersN Finch, M M Carrasquillo, M Baker, et al.
Molecular Psychiatry|August 2, 2007
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophreniaC Francks, S Maegawa, J Laurén, et al.
Pageof 7