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P Seeman

Showing results (271-280 of 325) with videos related to

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Journal of Psychiatry & Neuroscience : JPN|October 24, 1998
The human serotonin-7 receptor pseudogene: variation and chromosome locationD Nam, I H Qian, I Kusumi, et al.
European Journal of Neurology|April 16, 2008
A 71-nucleotide deletion in the periaxin gene in a Romani patient with early-onset slowly progressive demyelinating CMTL Baránková, D Sisková, K Hühne, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosisE Mikesová, K Hühne, B Rautenstrauss, et al.
European Journal of Pharmacology|October 1, 1992
The cloned dopamine D2 receptor reveals different densities for dopamine receptor antagonist ligands. Implications for human brain positron emission tomographyP Seeman, H C Guan, O Civelli, et al.
FEBS Letters|March 12, 1990
Cloning of two additional catecholamine receptors from rat brainB F O'Dowd, T Nguyen, A Tirpak, et al.
Endocrinology|October 10, 1997
Resistance of the dopamine D2L receptor to desensitization accompanies the up-regulation of receptors on to the surface of Sf9 cellsG Y Ng, G Varghese, H T Chung, et al.
Clinical Genetics|July 16, 2004
Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafnessP Seeman, M Malíková, D Rasková, et al.
European Journal of Neurology|September 21, 2007
Charcot-Marie-Tooth neuropathy type 1A combined with Duchenne muscular dystrophyP Vondracek, M Hermanova, J Sedlackova, et al.
Genes, Brain, and Behavior|July 13, 2010
Enhanced dopamine function in DISC1-L100P mutant mice: implications for schizophreniaT V Lipina, M Niwa, H Jaaro-Peled, et al.
Journal of Medical Genetics|July 22, 2005
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instabilityE Seemanová, K Sperling, H Neitzel, et al.
Pageof 33

Showing results (271-280 of 325) with videos related to

Sort By:
Pageof 33
Journal of Psychiatry & Neuroscience : JPN|October 24, 1998
The human serotonin-7 receptor pseudogene: variation and chromosome locationD Nam, I H Qian, I Kusumi, et al.
European Journal of Neurology|April 16, 2008
A 71-nucleotide deletion in the periaxin gene in a Romani patient with early-onset slowly progressive demyelinating CMTL Baránková, D Sisková, K Hühne, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosisE Mikesová, K Hühne, B Rautenstrauss, et al.
European Journal of Pharmacology|October 1, 1992
The cloned dopamine D2 receptor reveals different densities for dopamine receptor antagonist ligands. Implications for human brain positron emission tomographyP Seeman, H C Guan, O Civelli, et al.
FEBS Letters|March 12, 1990
Cloning of two additional catecholamine receptors from rat brainB F O'Dowd, T Nguyen, A Tirpak, et al.
Endocrinology|October 10, 1997
Resistance of the dopamine D2L receptor to desensitization accompanies the up-regulation of receptors on to the surface of Sf9 cellsG Y Ng, G Varghese, H T Chung, et al.
Clinical Genetics|July 16, 2004
Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafnessP Seeman, M Malíková, D Rasková, et al.
European Journal of Neurology|September 21, 2007
Charcot-Marie-Tooth neuropathy type 1A combined with Duchenne muscular dystrophyP Vondracek, M Hermanova, J Sedlackova, et al.
Genes, Brain, and Behavior|July 13, 2010
Enhanced dopamine function in DISC1-L100P mutant mice: implications for schizophreniaT V Lipina, M Niwa, H Jaaro-Peled, et al.
Journal of Medical Genetics|July 22, 2005
Nijmegen breakage syndrome (NBS) with neurological abnormalities and without chromosomal instabilityE Seemanová, K Sperling, H Neitzel, et al.
Pageof 33