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Xinying Hong

Showing results (1-10 of 43) with videos related to

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Molecular Genetics and Metabolism|August 22, 2018
One-step synthesis of carbon-13-labeled globotriaosylsphingosine (lyso-Gb3), an internal standard for biomarker analysis of Fabry diseaseXinying Hong, Michael H Gelb
Clinical Chemistry|April 3, 2023
Thymine Hyperexcretion in a Patient with Abnormal Newborn Screen for Glutaric Aciduria Type IParith Wongkittichote, Andrew Edmondson, Xinying Hong
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 21, 2020
A highly multiplexed biochemical assay for analytes in dried blood spots: application to newborn screening and diagnosis of lysosomal storage disorders and other inborn errors of metabolismXinying Hong, Martin Sadilek, Michael H Gelb
The Analyst|July 17, 2015
A simple approach to study the conformational switching of i-motif DNA by fluorescence anisotropyHongduan Huang, Xinying Hong, Feng Liu, et al.
Molecular Genetics and Metabolism Reports|November 17, 2022
Stratification of patients with lysosomal acid lipase deficiency by enzyme activity in dried blood spotsXinying Hong, Yicheng Chen, Marianne Barr, et al.
Clinical Chemistry|July 3, 2022
A 6-Month-Old Infant with Severe Failure to Thrive during COVID-19 PandemicXinying Hong, Hana Alharbi, Daniah Albokhari, et al.
The Journal of Applied Laboratory Medicine|February 27, 2026
Investigating Elevated Glutaric Acid in Early InfancyShubhnita Singh, Caitlin Menello, Xinying Hong, et al.
Molecular Genetics and Metabolism|April 23, 2018
Multiplex tandem mass spectrometry assay for newborn screening of X-linked adrenoleukodystrophy, biotinidase deficiency, and galactosemia with flexibility to assay other enzyme assays and biomarkersXinying Hong, Arun Babu Kumar, C Ronald Scott, et al.
JIMD Reports|March 6, 2024
Clinical, biochemical and molecular characterization of a new case with <i>FDX2</i>-related mitochondrial disorder: Potential biomarkers and treatment optionsParith Wongkittichote, Cassandra Pantano, Miao He, et al.
Molecular Genetics and Metabolism|October 11, 2023
Newborn screening for the full set of mucopolysaccharidoses in dried blood spots based on first-tier enzymatic assay followed by second-tier analysis of glycosaminoglycansZackary M Herbst, Xinying Hong, Martin Sadilek, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Molecular Genetics and Metabolism|August 22, 2018
One-step synthesis of carbon-13-labeled globotriaosylsphingosine (lyso-Gb3), an internal standard for biomarker analysis of Fabry diseaseXinying Hong, Michael H Gelb
Clinical Chemistry|April 3, 2023
Thymine Hyperexcretion in a Patient with Abnormal Newborn Screen for Glutaric Aciduria Type IParith Wongkittichote, Andrew Edmondson, Xinying Hong
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 21, 2020
A highly multiplexed biochemical assay for analytes in dried blood spots: application to newborn screening and diagnosis of lysosomal storage disorders and other inborn errors of metabolismXinying Hong, Martin Sadilek, Michael H Gelb
The Analyst|July 17, 2015
A simple approach to study the conformational switching of i-motif DNA by fluorescence anisotropyHongduan Huang, Xinying Hong, Feng Liu, et al.
Molecular Genetics and Metabolism Reports|November 17, 2022
Stratification of patients with lysosomal acid lipase deficiency by enzyme activity in dried blood spotsXinying Hong, Yicheng Chen, Marianne Barr, et al.
Clinical Chemistry|July 3, 2022
A 6-Month-Old Infant with Severe Failure to Thrive during COVID-19 PandemicXinying Hong, Hana Alharbi, Daniah Albokhari, et al.
The Journal of Applied Laboratory Medicine|February 27, 2026
Investigating Elevated Glutaric Acid in Early InfancyShubhnita Singh, Caitlin Menello, Xinying Hong, et al.
Molecular Genetics and Metabolism|April 23, 2018
Multiplex tandem mass spectrometry assay for newborn screening of X-linked adrenoleukodystrophy, biotinidase deficiency, and galactosemia with flexibility to assay other enzyme assays and biomarkersXinying Hong, Arun Babu Kumar, C Ronald Scott, et al.
JIMD Reports|March 6, 2024
Clinical, biochemical and molecular characterization of a new case with <i>FDX2</i>-related mitochondrial disorder: Potential biomarkers and treatment optionsParith Wongkittichote, Cassandra Pantano, Miao He, et al.
Molecular Genetics and Metabolism|October 11, 2023
Newborn screening for the full set of mucopolysaccharidoses in dried blood spots based on first-tier enzymatic assay followed by second-tier analysis of glycosaminoglycansZackary M Herbst, Xinying Hong, Martin Sadilek, et al.
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