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Methods in Molecular Biology (Clifton, N.J.)
|
August 25, 2014
G protein-coupled receptor accessory proteins and signaling: pharmacogenomic insights
Miles 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 Pharmacogenetics
Miles 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 disease
Miles D Thompson, Maire E Percy, W McIntyre Burnham, et al.
Epilepsia
|
July 12, 2021
Antiseizure effects of the cannabinoids in the amygdala-kindling model
Merrick 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 disease
Miles 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 trends
Valérie Capra, Miles D Thompson, Angelo Sala, et al.
Neuroreport
|
November 24, 2011
Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locus
Miles 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 disease
Miles 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.
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of 4
Search research articles
Search
Showing results (11-20 of 38) with videos related to
Sort By:
Page
of 4
Methods in Molecular Biology (Clifton, N.J.)
|
August 25, 2014
G protein-coupled receptor accessory proteins and signaling: pharmacogenomic insights
Miles 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 Pharmacogenetics
Miles 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 disease
Miles D Thompson, Maire E Percy, W McIntyre Burnham, et al.
Epilepsia
|
July 12, 2021
Antiseizure effects of the cannabinoids in the amygdala-kindling model
Merrick 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 disease
Miles 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 trends
Valérie Capra, Miles D Thompson, Angelo Sala, et al.
Neuroreport
|
November 24, 2011
Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locus
Miles 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 disease
Miles 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.
Page
of 4