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Induction of a viable but non-culturable state in Salmonella Typhimurium by thermosonication and factors affecting resuscitation

FEMS microbiology letters, 2018-02, Vol.365 (2), p.1

2018

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Cys-functionalized AuNP substrates for improved sensing of the marine toxin STX by dynamic surface-enhanced Raman spectroscopy

Analytical and bioanalytical chemistry, 2020-07, Vol.412 (19), p.4609-4617

2020

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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy in Children: A Retrospective Analysis of 35 Cases

Frontiers in immunology, 2021-11, Vol.12, p.761354-761354

2021

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Clinical and genetic analysis of six Chinese children with Poirier-Bienvenu neurodevelopmental syndrome caused by CSNK2B mutation

Neurogenetics, 2021-10, Vol.22 (4), p.323-332

2021

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Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study

Frontiers in immunology, 2023-04, Vol.14, p.1140872-1140872

2023

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Video-electroencephalographic findings and clinical characteristics of bathing seizures in children

Frontiers in neurology, 2024-02, Vol.15, p.1366206-1366206

2024

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A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report

BMC pediatrics, 2021-06, Vol.21 (1), p.1-256, Article 256

2021

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Development of active packaging films utilized natural colorants derived from plants and their diverse applications in protein-rich food products

Food innovation and advances, 2023-07, Vol.2 (3), p.203-216

2023

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Host-Induced Gene Silencing of a Multifunction Gene Sscnd1 Enhances Plant Resistance Against Sclerotinia sclerotiorum

Frontiers in microbiology, 2021-10, Vol.12, p.693334-693334

2021

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Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children

Frontiers in neuroscience, 2023-05, Vol.17, p.1106214-1106214

2023

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Application of Thermosonication in Red Pitaya Juice Processing: Impacts on Native Microbiota and Quality Properties during Storage

Foods, 2021-05, Vol.10 (5), p.1041

2021

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ARHGEF9 gene variant leads to developmental and epileptic encephalopathy: Genotypic phenotype analysis and treatment exploration

Molecular genetics & genomic medicine, 2022-07, Vol.10 (7), p.e1967-n/a

2022

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Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort Study

Frontiers in pediatrics, 2022-07, Vol.10, p.880693-880693

2022

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Inactivation of microorganisms naturally present in raw bovine milk by high-pressure carbon dioxide

International journal of food science & technology, 2014-03, Vol.49 (3), p.696-702

2014

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Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report

BMC pediatrics, 2020-06, Vol.20 (1), p.315-315, Article 315

2020

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Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patients

Frontiers in neurology, 2023-12, Vol.14, p.1310419-1310419

2023

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Clinical Characteristics and Prognostic Factors of Children With Anti-N-Methyl-D-Aspartate Receptor Encephalitis

Frontiers in pediatrics, 2021-04, Vol.9, p.605042-605042

2021

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Effects of high-pressure carbon dioxide on proteins and DNA in Escherichia coli

Microbiology (Society for General Microbiology), 2011-03, Vol.157 (Pt 3), p.709-720

2011

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Mixed and Continuous Strategy Monitor-Forward Game Based Selective Forwarding Solution in WSN

International journal of distributed sensor networks, 2015-01, Vol.2015 (11), p.359780

2015

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Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study

Italian journal of pediatrics, 2023-07, Vol.49 (1), p.83-83, Article 83

2023

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Mutant BCL11B in a Patient With a Neurodevelopmental Disorder and T-Cell Abnormalities

Frontiers in pediatrics, 2020-10, Vol.8

2020

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Distribution characteristics of ABO and RhD blood groups among the voluntary blood donors in Chongqing: A retrospective study

Medicine (Baltimore), 2020-10, Vol.99 (42), p.e22689-e22689

2020

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SsdchA is a novel secretory cellobiohydrolase driving pathogenicity in Sclerotinia sclerotiorum

The Crop journal, 2024-04, Vol.12 (2), p.493-502

2024

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Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation

Frontiers in pediatrics, 2021-12, Vol.9, p.801719

2021

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Case Report: ISPD Gene Mutation Leads to Dystroglycanopathies: Genotypic Phenotype Analysis and Treatment Exploration

Frontiers in pediatrics, 2021-08, Vol.9

2021

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Induction of a viable but non-culturable state in Salmonella Typhimurium by thermosonication and factors affecting resuscitation

Cys-functionalized AuNP substrates for improved sensing of the marine toxin STX by dynamic surface-enhanced Raman spectroscopy

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy in Children: A Retrospective Analysis of 35 Cases

Clinical and genetic analysis of six Chinese children with Poirier-Bienvenu neurodevelopmental syndrome caused by CSNK2B mutation

Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study

Video-electroencephalographic findings and clinical characteristics of bathing seizures in children

A Chinese patient with developmental and epileptic encephalopathies (DEE) carrying a TRPM3 gene mutation: a paediatric case report

Development of active packaging films utilized natural colorants derived from plants and their diverse applications in protein-rich food products

Host-Induced Gene Silencing of a Multifunction Gene Sscnd1 Enhances Plant Resistance Against Sclerotinia sclerotiorum

Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children

Application of Thermosonication in Red Pitaya Juice Processing: Impacts on Native Microbiota and Quality Properties during Storage

ARHGEF9 gene variant leads to developmental and epileptic encephalopathy: Genotypic phenotype analysis and treatment exploration

Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort Study

Inactivation of microorganisms naturally present in raw bovine milk by high-pressure carbon dioxide

Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report

Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patients

Clinical Characteristics and Prognostic Factors of Children With Anti-N-Methyl-D-Aspartate Receptor Encephalitis

Effects of high-pressure carbon dioxide on proteins and DNA in Escherichia coli

Mixed and Continuous Strategy Monitor-Forward Game Based Selective Forwarding Solution in WSN

Association between blood eosinophil count and Duchenne muscular dystrophy severity and prognosis: a retrospective cohort study

Mutant BCL11B in a Patient With a Neurodevelopmental Disorder and T-Cell Abnormalities

Distribution characteristics of ABO and RhD blood groups among the voluntary blood donors in Chongqing: A retrospective study

SsdchA is a novel secretory cellobiohydrolase driving pathogenicity in Sclerotinia sclerotiorum

Case Report: Compound Heterozygous Variants of SLC13A3 Identified in a Chinese Patient With Acute Reversible Leukoencephalopathy and α-Ketoglutarate Accumulation

Case Report: ISPD Gene Mutation Leads to Dystroglycanopathies: Genotypic Phenotype Analysis and Treatment Exploration

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