ABSTRACT: We report new substrates for quantitative enzyme activity measurements of human palmitoyl protein thioesterase (PPT1) and tripeptidyl peptidase (TPP1) in dried blood spots from newborns using tandem mass spectrometry. Deficiencies in these enzyme activities due to inborn errors of metabolism cause neuronal ceroid lipofuscinoses. The assays use synthetic compounds that were designed to mimic the natural substrates. Incubation produces nanomole quantities of enzymatic products per a blood spot that are quantified by tandem mass spectrometry using synthetic internal standards and selected reaction monitor-ing. The assays utilize a minimum steps for sample workup and can be run in a duplex format for the detection of neuronal ceroid l...
OBJECTIVES: High-throughput mass spectrometry methods have been developed to screen newborns for lys...
Thesis (Ph.D.)--University of Washington, 2018Newborn screening has been an important public health ...
lysosomal enzymes that cause Fabry, Gaucher, Krabbe, Niemann–Pick A/B, and Pompe diseases is warrant...
We report new substrates for quantitative enzyme activity measurements of human palmitoyl protein th...
A new tandem mass spectrometry (MS/MS)-based approach for measurement of the enzymatic activity of p...
Neuronal ceroid lipofuscinoses (NCLs) are a group of neurodegenerative diseases predominantly in chi...
Palmitoyl-protein thioesterase (PPT) deficiency was recently shown to be the primary defec...
BACKGROUND: Treatments now available for mucopo-lysaccharidosis I require early detection for optimu...
washington.edu) Background: A treatment for mucopolysaccharidosis II (Hunter syndrome) has recently ...
ABSTRACT: Tandem mass spectrometry for the multiplex and quantitative analysis of enzyme activities ...
AbstractMutations in the gene encoding a recently described lysosomal enzyme, palmitoyl-protein thio...
Background: With ongoing efforts to develop improved treatments for Sanfilippo Syndrome Type A (MPS-...
Tandem mass spectrometry for the multiplex and quantitative analysis of enzyme activities in dried b...
In this data article we provide a detailed standard operating procedure for performing a tandem mass...
AbstractIn this data article we provide a detailed standard operating procedure for performing a tan...
OBJECTIVES: High-throughput mass spectrometry methods have been developed to screen newborns for lys...
Thesis (Ph.D.)--University of Washington, 2018Newborn screening has been an important public health ...
lysosomal enzymes that cause Fabry, Gaucher, Krabbe, Niemann–Pick A/B, and Pompe diseases is warrant...
We report new substrates for quantitative enzyme activity measurements of human palmitoyl protein th...
A new tandem mass spectrometry (MS/MS)-based approach for measurement of the enzymatic activity of p...
Neuronal ceroid lipofuscinoses (NCLs) are a group of neurodegenerative diseases predominantly in chi...
Palmitoyl-protein thioesterase (PPT) deficiency was recently shown to be the primary defec...
BACKGROUND: Treatments now available for mucopo-lysaccharidosis I require early detection for optimu...
washington.edu) Background: A treatment for mucopolysaccharidosis II (Hunter syndrome) has recently ...
ABSTRACT: Tandem mass spectrometry for the multiplex and quantitative analysis of enzyme activities ...
AbstractMutations in the gene encoding a recently described lysosomal enzyme, palmitoyl-protein thio...
Background: With ongoing efforts to develop improved treatments for Sanfilippo Syndrome Type A (MPS-...
Tandem mass spectrometry for the multiplex and quantitative analysis of enzyme activities in dried b...
In this data article we provide a detailed standard operating procedure for performing a tandem mass...
AbstractIn this data article we provide a detailed standard operating procedure for performing a tan...
OBJECTIVES: High-throughput mass spectrometry methods have been developed to screen newborns for lys...
Thesis (Ph.D.)--University of Washington, 2018Newborn screening has been an important public health ...
lysosomal enzymes that cause Fabry, Gaucher, Krabbe, Niemann–Pick A/B, and Pompe diseases is warrant...