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Miles D Thompson

Showing results (11-20 of 38) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|August 25, 2014
G protein-coupled receptor accessory proteins and signaling: pharmacogenomic insightsMiles D Thompson, David E C Cole, Pedro A Jose, et al.
Pharmaceuticals (Basel, Switzerland)|October 10, 2017
Orexin Receptor Multimerization versus Functional Interactions: Neuropharmacological Implications for Opioid and Cannabinoid Signalling and PharmacogeneticsMiles D Thompson, Takeshi Sakurai, Innocenzo Rainero, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 29, 2008
G protein-coupled receptors disrupted in human genetic diseaseMiles D Thompson, Maire E Percy, W McIntyre Burnham, et al.
Epilepsia|July 12, 2021
Antiseizure effects of the cannabinoids in the amygdala-kindling modelMerrick S Fallah, Lukasz Dlugosz, Brian W Scott, et al.
Critical Reviews in Clinical Laboratory Sciences|January 1, 2025
Genetic variants of accessory proteins and G proteins in human genetic diseaseMiles D Thompson, Peter Chidiac, Pedro A Jose, et al.
Medicinal Research Reviews|August 9, 2006
Cysteinyl-leukotrienes and their receptors in asthma and other inflammatory diseases: critical update and emerging trendsValérie Capra, Miles D Thompson, Angelo Sala, et al.
Neuroreport|November 24, 2011
Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locusMiles D Thompson, Sandra Noble-Topham, Maire E Percy, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 25, 2014
G protein-coupled receptor mutations and human genetic diseaseMiles D Thompson, Geoffrey N Hendy, Maire E Percy, et al.
Pediatric Neurology|April 28, 2006
Hyperphosphatasia with neurologic deficit: a pyridoxine-responsive seizure disorder?Miles D Thompson, Annie Killoran, Maire E Percy, et al.
Genes|February 25, 2023
Excluding Digenic Inheritance of <i>PGAP2</i> and <i>PGAP3</i> Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with <i>PGAP2</i> Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)Miles D Thompson, Xueying Li, Michele Spencer-Manzon, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Methods in Molecular Biology (Clifton, N.J.)|August 25, 2014
G protein-coupled receptor accessory proteins and signaling: pharmacogenomic insightsMiles D Thompson, David E C Cole, Pedro A Jose, et al.
Pharmaceuticals (Basel, Switzerland)|October 10, 2017
Orexin Receptor Multimerization versus Functional Interactions: Neuropharmacological Implications for Opioid and Cannabinoid Signalling and PharmacogeneticsMiles D Thompson, Takeshi Sakurai, Innocenzo Rainero, et al.
Methods in Molecular Biology (Clifton, N.J.)|March 29, 2008
G protein-coupled receptors disrupted in human genetic diseaseMiles D Thompson, Maire E Percy, W McIntyre Burnham, et al.
Epilepsia|July 12, 2021
Antiseizure effects of the cannabinoids in the amygdala-kindling modelMerrick S Fallah, Lukasz Dlugosz, Brian W Scott, et al.
Critical Reviews in Clinical Laboratory Sciences|January 1, 2025
Genetic variants of accessory proteins and G proteins in human genetic diseaseMiles D Thompson, Peter Chidiac, Pedro A Jose, et al.
Medicinal Research Reviews|August 9, 2006
Cysteinyl-leukotrienes and their receptors in asthma and other inflammatory diseases: critical update and emerging trendsValérie Capra, Miles D Thompson, Angelo Sala, et al.
Neuroreport|November 24, 2011
Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locusMiles D Thompson, Sandra Noble-Topham, Maire E Percy, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 25, 2014
G protein-coupled receptor mutations and human genetic diseaseMiles D Thompson, Geoffrey N Hendy, Maire E Percy, et al.
Pediatric Neurology|April 28, 2006
Hyperphosphatasia with neurologic deficit: a pyridoxine-responsive seizure disorder?Miles D Thompson, Annie Killoran, Maire E Percy, et al.
Genes|February 25, 2023
Excluding Digenic Inheritance of <i>PGAP2</i> and <i>PGAP3</i> Variants in Mabry Syndrome (OMIM 239300) Patient: Phenotypic Spectrum Associated with <i>PGAP2</i> Gene Variants in Hyperphosphatasia with Mental Retardation Syndrome-3 (HPMRS3)Miles D Thompson, Xueying Li, Michele Spencer-Manzon, et al.
Pageof 4