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Xinying Hong

Showing results (21-30 of 43) with videos related to

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Clinical Chemistry|April 22, 2017
Multiplex Tandem Mass Spectrometry Enzymatic Activity Assay for Newborn Screening of the Mucopolysaccharidoses and Type 2 Neuronal Ceroid LipofuscinosisYang Liu, Fan Yi, Arun Babu Kumar, et al.
Plos Biology|July 5, 2022
Neuron-specific ablation of the Krabbe disease gene galactosylceramidase in mice results in neurodegenerationConlan Kreher, Jacob Favret, Nadav I Weinstock, et al.
Molecular Genetics and Metabolism|October 30, 2023
Clinical, radiological, biochemical and molecular characterization of a new case with multiple mitochondrial dysfunction syndrome due to IBA57: Lysine and tryptophan metabolites as potential biomarkersParith Wongkittichote, Cassandra Pantano, Emily Bogush, et al.
Molecular Therapy. Advances|June 15, 2026
<i>In vivo</i> adenine base editing rescues brain biochemistry and improves motor deficits in a common phenylketonuria variantMegan K Gautier, Kaitlyn King, Yongseok Han, et al.
The Journal of Pediatrics|November 17, 2019
Newborn Screening for Mucopolysaccharidoses: Results of a Pilot Study with 100 000 Dried Blood SpotsClifford Ronald Scott, Susan Elliott, Xinying Hong, et al.
Molecular Genetics and Metabolism|July 15, 2018
Detection of mucopolysaccharidosis III-A (Sanfilippo Syndrome-A) in dried blood spots (DBS) by tandem mass spectrometryFan Yi, Xinying Hong, Arun Babu Kumar, et al.
Molecular Genetics and Metabolism|July 5, 2023
Endogenous, non-reducing end glycosaminoglycan biomarkers are superior to internal disaccharide glycosaminoglycan biomarkers for newborn screening of mucopolysaccharidoses and GM1 gangliosidosisZackary M Herbst, Xinying Hong, Leslie Urdaneta, et al.
Molecular Therapy. Nucleic Acids|December 16, 2025
Base editing strategies for <i>in vivo</i> correction of two highly recurrent phenylketonuria variantsAidan Quigley, Ishaan Jindal, Thomas Campion, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2020
Toward newborn screening of cerebrotendinous xanthomatosis: results of a biomarker research study using 32,000 newborn dried blood spotsXinying Hong, Jessica Daiker, Martin Sadilek, et al.
Genome Biology|July 21, 2023
Predicting disease severity in metachromatic leukodystrophy using protein activity and a patient phenotype matrixMarena Trinidad, Xinying Hong, Steven Froelich, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Clinical Chemistry|April 22, 2017
Multiplex Tandem Mass Spectrometry Enzymatic Activity Assay for Newborn Screening of the Mucopolysaccharidoses and Type 2 Neuronal Ceroid LipofuscinosisYang Liu, Fan Yi, Arun Babu Kumar, et al.
Plos Biology|July 5, 2022
Neuron-specific ablation of the Krabbe disease gene galactosylceramidase in mice results in neurodegenerationConlan Kreher, Jacob Favret, Nadav I Weinstock, et al.
Molecular Genetics and Metabolism|October 30, 2023
Clinical, radiological, biochemical and molecular characterization of a new case with multiple mitochondrial dysfunction syndrome due to IBA57: Lysine and tryptophan metabolites as potential biomarkersParith Wongkittichote, Cassandra Pantano, Emily Bogush, et al.
Molecular Therapy. Advances|June 15, 2026
<i>In vivo</i> adenine base editing rescues brain biochemistry and improves motor deficits in a common phenylketonuria variantMegan K Gautier, Kaitlyn King, Yongseok Han, et al.
The Journal of Pediatrics|November 17, 2019
Newborn Screening for Mucopolysaccharidoses: Results of a Pilot Study with 100 000 Dried Blood SpotsClifford Ronald Scott, Susan Elliott, Xinying Hong, et al.
Molecular Genetics and Metabolism|July 15, 2018
Detection of mucopolysaccharidosis III-A (Sanfilippo Syndrome-A) in dried blood spots (DBS) by tandem mass spectrometryFan Yi, Xinying Hong, Arun Babu Kumar, et al.
Molecular Genetics and Metabolism|July 5, 2023
Endogenous, non-reducing end glycosaminoglycan biomarkers are superior to internal disaccharide glycosaminoglycan biomarkers for newborn screening of mucopolysaccharidoses and GM1 gangliosidosisZackary M Herbst, Xinying Hong, Leslie Urdaneta, et al.
Molecular Therapy. Nucleic Acids|December 16, 2025
Base editing strategies for <i>in vivo</i> correction of two highly recurrent phenylketonuria variantsAidan Quigley, Ishaan Jindal, Thomas Campion, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 12, 2020
Toward newborn screening of cerebrotendinous xanthomatosis: results of a biomarker research study using 32,000 newborn dried blood spotsXinying Hong, Jessica Daiker, Martin Sadilek, et al.
Genome Biology|July 21, 2023
Predicting disease severity in metachromatic leukodystrophy using protein activity and a patient phenotype matrixMarena Trinidad, Xinying Hong, Steven Froelich, et al.
Pageof 5