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Generation of an iPSC line from a patient with early-onset epileptic encephalopathy carrying CARS2 (p.G476R) mutation

Stem cell research, 2022-03, Vol.59, p.102633-102633, Article 102633

2022

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Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency

Journal of inherited metabolic disease, 2022-03, Vol.45 (2), p.264-277

2022

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Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome

Frontiers in pharmacology, 2021-03, Vol.12, p.605803-605803

2021

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Identification of a Novel Variant in MT-CO3 Causing MELAS

Frontiers in genetics, 2021-05, Vol.12, p.638749-638749

2021

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"A fly appeared": sable, a classic Drosophila mutation, maps to Yippee, a gene affecting body color, wings, and bristles

G3 : genes - genomes - genetics, 2022-05, Vol.12 (5)

2022

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Clinical Assessments and EEG Analyses of Encephalopathies Associated With Dynamin-1 Mutation

Frontiers in pharmacology, 2019-12, Vol.10, p.1454-1454

2019

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Biallelic COA7-Variants Leading to Developmental Regression With Progressive Spasticity and Brain Atrophy in a Chinese Patient

Frontiers in genetics, 2021-07, Vol.12, p.685035-685035

2021

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Corrigendum: Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome

Frontiers in pharmacology, 2021-06, Vol.12, p.686933-686933

2021

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Clinical Attributes and Electroencephalogram Analysis of Patients With Varying Alpers’ Syndrome Genotypes

Frontiers in pharmacology, 2021-10, Vol.12, p.669516-669516

2021

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Identification of a novel m.3955G > A variant in MT-ND1 associated with Leigh syndrome

Mitochondrion, 2022-01, Vol.62, p.13-23

2022

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Genotype and Phenotype Characteristics of 58 Cases of Mitochondrial Epilepsy with Nuclear DNA Mutations in Children

Neurological sciences, 2024-06

2024

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A full multigrid method for nonlinear eigenvalue problems

Science China. Mathematics, 2016-10, Vol.59 (10), p.2037-2048

2016

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Demonstration of in vivo engineered tandem duplications of varying sizes using CRISPR and recombinases in Drosophila melanogaster

G3 : genes - genomes - genetics, 2023-10, Vol.13 (10)

2023

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Whole genome and exome sequencing identify NDUFV2 mutations as a new cause of progressive cavitating leukoencephalopathy

Journal of medical genetics, 2022-04, Vol.59 (4), p.351-357

2022

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Profiling the Users of High Influence on Social Media in the Context of Public Events

Journal of database management, 2021-04, Vol.32 (2), p.36-49

2021

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Progress in respiratory function assessment and management for Duchenne muscular dystrophy

Zhonghua er ke za zhi, 2014-11, Vol.52 (11), p.831

2014

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Arsenic and Human Health: New Molecular Mechanisms For Arsenic-Induced Cancers

Current pollution reports, 2023-12, Vol.9 (4), p.784-797

2023

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Rare combination of dystrophinopathy and Klinefelter's syndrome in one patient

Zhonghua er ke za zhi, 2014-07, Vol.52 (7), p.548

2014

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From Classroom to Marketplace: Empowering Business English Students with Cross-Border Product Digital Storytelling

Journal of Research in Vocational Education, 2024-08, Vol.6 (8), p.73-79

2024

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A novel multilevel finite element method for a generalized nonlinear Schrödinger equation

Journal of computational and applied mathematics, 2025-03, Vol.457, p.116280, Article 116280

2025

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Multilevel local defect-correction method for the non-selfadjoint Steklov eigenvalue problems

BIT, 2024-06, Vol.64 (2), Article 21

2024

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Local and parallel multigrid method for semilinear Neumann problem with nonlinear boundary condition

Numerical algorithms, 2024-05, Vol.96 (1), p.185-210

2024

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IL-7 and CCL19-secreting CAR-T cell therapy for tumors with positive glypican-3 or mesothelin

Journal of hematology and oncology, 2021-07, Vol.14 (1), p.1-118, Article 118

2021

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An efficient adaptive multigrid method for the elasticity eigenvalue problem

BIT, 2022-12, Vol.62 (4), p.2005-2033

2022

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Generation of an iPSC line from a patient with early-onset epileptic encephalopathy carrying CARS2 (p.G476R) mutation

Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency

Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome

Identification of a Novel Variant in MT-CO3 Causing MELAS

"A fly appeared": sable, a classic Drosophila mutation, maps to Yippee, a gene affecting body color, wings, and bristles

Clinical Assessments and EEG Analyses of Encephalopathies Associated With Dynamin-1 Mutation

Biallelic COA7-Variants Leading to Developmental Regression With Progressive Spasticity and Brain Atrophy in a Chinese Patient

Corrigendum: Cinical, Metabolic, and Genetic Analysis and Follow-Up of Eight Patients With HIBCH Mutations Presenting With Leigh/Leigh-Like Syndrome

Clinical Attributes and Electroencephalogram Analysis of Patients With Varying Alpers’ Syndrome Genotypes

Identification of a novel m.3955G > A variant in MT-ND1 associated with Leigh syndrome

Genotype and Phenotype Characteristics of 58 Cases of Mitochondrial Epilepsy with Nuclear DNA Mutations in Children

A full multigrid method for nonlinear eigenvalue problems

Demonstration of in vivo engineered tandem duplications of varying sizes using CRISPR and recombinases in Drosophila melanogaster

Whole genome and exome sequencing identify NDUFV2 mutations as a new cause of progressive cavitating leukoencephalopathy

Profiling the Users of High Influence on Social Media in the Context of Public Events

Progress in respiratory function assessment and management for Duchenne muscular dystrophy

Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal Neuropathy

Arsenic and Human Health: New Molecular Mechanisms For Arsenic-Induced Cancers

Rare combination of dystrophinopathy and Klinefelter's syndrome in one patient

From Classroom to Marketplace: Empowering Business English Students with Cross-Border Product Digital Storytelling

A novel multilevel finite element method for a generalized nonlinear Schrödinger equation

Multilevel local defect-correction method for the non-selfadjoint Steklov eigenvalue problems

Local and parallel multigrid method for semilinear Neumann problem with nonlinear boundary condition

IL-7 and CCL19-secreting CAR-T cell therapy for tumors with positive glypican-3 or mesothelin

An efficient adaptive multigrid method for the elasticity eigenvalue problem

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