T E Morton - JoVE Visualize

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International Journal of Radiation Applications and Instrumentation. Part A, Applied Radiation and Isotopes|March 1, 1992

Optimization of [11C]CO2 trapping efficiencies from nitrogen gas streamsR D Smith, R H Mach, T E Morton, et al.

Nuclear Medicine and Biology|April 1, 1993

Synthesis and in vivo evaluation of [18F]-N-(p-nitrobenzyl)spiperone ([18F]PNBS) in ratsR H Mach, P A Nowak, D A Moroney, et al.

Pharmacology, Biochemistry, and Behavior|July 1, 1997

Use of positron emission tomography to study the dynamics of psychostimulant-induced dopamine releaseR H Mach, M A Nader, R L Ehrenkaufer, et al.

Nuclear Medicine and Biology|April 1, 1999

(+)-p-([18F]fluorobenzyl)spirotrozamicol [(+)-[18F]spiro-FBT]: synthesis and biological evaluation of a high-affinity ligand for the vesicular acetylcholine transporter (VAChT)S M Efange, M A Nader, R L Ehrenkaufer, et al.

Nuclear Medicine and Biology|June 8, 2001

[[(18)F]N-(4'-fluorobenzyl)-4-(3-bromophenyl) acetamide for imaging the sigma receptor status of tumors: comparison with [(18)F]FDG, and [(125)I]IUDRR H Mach, Y Huang, N Buchheimer, et al.

Synapse (New York, N.Y.)|March 1, 1995

PET imaging studies of dopamine D2 receptors: comparison of [18F]N-methylspiperone and the benzamide analogues [18F]MABN and [18F]MBP in baboon brainR H Mach, R L Ehrenkaufer, J H Greenberg, et al.

Synapse (New York, N.Y.)|December 1, 1996

Comparison of two fluorine-18 labeled benzamide derivatives that bind reversibly to dopamine D2 receptors: in vitro binding studies and positron emission tomographyR H Mach, M A Nader, R L Ehrenkaufer, et al.

Nuclear Medicine and Biology|August 1, 1993

The use of [18F]4-fluorobenzyl iodide (FBI) in PET radiotracer synthesis: model alkylation studies and its application in the design of dopamine D1 and D2 receptor-based imaging agentsR H Mach, S T Elder, T E Morton, et al.

Synapse (New York, N.Y.)|April 1, 1997

Imaging of cholinergic terminals using the radiotracer [18F](+)-4-fluorobenzyltrozamicol: in vitro binding studies and positron emission tomography studies in nonhuman primatesR H Mach, M L Voytko, R L Ehrenkaufer, et al.

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International Journal of Radiation Applications and Instrumentation. Part A, Applied Radiation and Isotopes|March 1, 1992

Optimization of [11C]CO2 trapping efficiencies from nitrogen gas streamsR D Smith, R H Mach, T E Morton, et al.

Nuclear Medicine and Biology|April 1, 1993

Synthesis and in vivo evaluation of [18F]-N-(p-nitrobenzyl)spiperone ([18F]PNBS) in ratsR H Mach, P A Nowak, D A Moroney, et al.

Pharmacology, Biochemistry, and Behavior|July 1, 1997

Use of positron emission tomography to study the dynamics of psychostimulant-induced dopamine releaseR H Mach, M A Nader, R L Ehrenkaufer, et al.

Nuclear Medicine and Biology|April 1, 1999

(+)-p-([18F]fluorobenzyl)spirotrozamicol [(+)-[18F]spiro-FBT]: synthesis and biological evaluation of a high-affinity ligand for the vesicular acetylcholine transporter (VAChT)S M Efange, M A Nader, R L Ehrenkaufer, et al.

Nuclear Medicine and Biology|June 8, 2001

[[(18)F]N-(4'-fluorobenzyl)-4-(3-bromophenyl) acetamide for imaging the sigma receptor status of tumors: comparison with [(18)F]FDG, and [(125)I]IUDRR H Mach, Y Huang, N Buchheimer, et al.

Synapse (New York, N.Y.)|March 1, 1995

PET imaging studies of dopamine D2 receptors: comparison of [18F]N-methylspiperone and the benzamide analogues [18F]MABN and [18F]MBP in baboon brainR H Mach, R L Ehrenkaufer, J H Greenberg, et al.

Synapse (New York, N.Y.)|December 1, 1996

Comparison of two fluorine-18 labeled benzamide derivatives that bind reversibly to dopamine D2 receptors: in vitro binding studies and positron emission tomographyR H Mach, M A Nader, R L Ehrenkaufer, et al.

Nuclear Medicine and Biology|August 1, 1993

The use of [18F]4-fluorobenzyl iodide (FBI) in PET radiotracer synthesis: model alkylation studies and its application in the design of dopamine D1 and D2 receptor-based imaging agentsR H Mach, S T Elder, T E Morton, et al.

Synapse (New York, N.Y.)|April 1, 1997

Imaging of cholinergic terminals using the radiotracer [18F](+)-4-fluorobenzyltrozamicol: in vitro binding studies and positron emission tomography studies in nonhuman primatesR H Mach, M L Voytko, R L Ehrenkaufer, et al.

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