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Clinical and genetic analysis of methylmalonic aciduria in 60 patients from Southern China: a single center retrospective study

Orphanet journal of rare diseases, 2024-05, Vol.19 (1), p.198-198, Article 198

2024

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Improved Performance of Sulfur-Driven Autotrophic Denitrification Process by Regulating Sulfur-Based Electron Donors

Water (Basel), 2024-03, Vol.16 (5), p.730

2024

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Review of antibiotics treatment by advance oxidation processes

Environmental advances, 2021-10, Vol.5, p.100111, Article 100111

2021

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Assessment of the diagnostic value of serum ceruloplasmin for Wilson's disease in children

BMC gastroenterology, 2022-03, Vol.22 (1), p.124-124, Article 124

2022

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Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature review

BMC pediatrics, 2019-11, Vol.19 (1), p.456-456, Article 456

2019

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Distinct severity of phenotype in Hajdu-Cheney syndrome: a case report and literature review

BMC musculoskeletal disorders, 2020-03, Vol.21 (1), p.154-154, Article 154

2020

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Phenotypic and Molecular Characteristics of Children with Progressive Familial Intrahepatic Cholestasis in South China

Pediatric Gastroenterology, 2020, Hepatology & Nutrition, 23(6), , pp.558-566

2020

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A two-stage degradation coupling photocatalysis to microalgae enhances the mineralization of enrofloxacin

Chemosphere (Oxford), 2022-04, Vol.293, p.133523-133523, Article 133523

2022

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Insight into integration of photocatalytic and microbial wastewater treatment technologies for recalcitrant organic pollutants: From sequential to simultaneous reactions

Chemosphere (Oxford), 2022-05, Vol.295, p.133952-133952, Article 133952

2022

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How Contagious Was the Panic of 1907? New Evidence from Trust Company Stocks

AEA papers and proceedings, 2021-05, Vol.111, p.514-519

2021

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Synthesis of ZnO@VC for enhancement of synergic photocatalytic degradation of SMX: Toxicity assessment, kinetics and transformation pathway determination

Chemical engineering and processing, 2023-11, Vol.193, p.109544, Article 109544

2023

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Accelerated Photocatalytic Degradation of Sulfamethoxazole and Cefixime: A Comprehensive Study of Biotoxicity, Degradation Kinetics and Pathway

Water, air, and soil pollution, 2024-06, Vol.235 (6), p.378, Article 378

2024

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The third case of Marbach-Rustad progeroid syndrome caused by a de novo LEMD2 variant

Clinical genetics, 2024-02, Vol.105 (2), p.209-213

2024

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Sooner or Later? Promising Delivery Speed in Online Retail

Manufacturing & service operations management, 2024-01, Vol.26 (1), p.233-251

2024

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The first Chinese case of Siddiqi syndrome caused by a homozygous FITM2 variant

Clinical genetics, 2022-09, Vol.102 (3), p.246-247

2022

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A novel homozygous splice‐site variant of NCAPD2 gene identified in two siblings with primary microcephaly: The second case report

Clinical genetics, 2019-07, Vol.96 (1), p.98-101

2019

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Clinical characteristics and prognosis of early diagnosed Wilson's disease: A large cohort study

Liver international, 2024-06

2024

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The EGFR‐P38 MAPK axis up‐regulates PD‐L1 through miR‐675‐5p and down‐regulates HLA‐ABC via hexokinase‐2 in hepatocellular carcinoma cells

Cancer communications (London, England), 2021-01, Vol.41 (1), p.62-78

2021

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Features of liver injury in 138 Chinese patients with NICCD

Journal of pediatric endocrinology & metabolism : JPEM, 2023-12, Vol.36 (12), p.1154

2023

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Two homozygous mutations in the exon 5 of BCKDHB gene that may cause the classic form of maple syrup urine disease

Metabolic brain disease, 2017-06, Vol.32 (3), p.765-772

2017

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Clinical features and mutational analysis in 114 young children with Wilson disease from South China

American journal of medical genetics. Part A, 2019-08, Vol.179 (8), p.1451-1458

2019

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Clinical features, BTD gene mutations, and their functional studies of eight symptomatic patients with biotinidase deficiency from Southern China

American journal of medical genetics. Part A, 2018-03, Vol.176 (3), p.589-596

2018

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Phenotypic and Molecular Characteristics of Children with Progressive Familial Intrahepatic Cholestasis in South China

Pediatric gastroenterology, hepatology & nutrition, 2020, Vol.23 (6), p.558-566

2020

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RCTE: Relation Candidate-guided few-shot relational Triple Extraction

Proceedings of the 2024 3rd International Conference on Cyber Security, Artificial Intelligence and Digital Economy, 2024, p.486-491

2024

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Learning Semantic Textual Similarity via Multi-Teacher Knowledge Distillation: A Multiple Data Augmentation method

2024 9th International Conference on Computer and Communication Systems (ICCCS), 2024, p.1197-1203

2024

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Clinical and genetic analysis of methylmalonic aciduria in 60 patients from Southern China: a single center retrospective study

Improved Performance of Sulfur-Driven Autotrophic Denitrification Process by Regulating Sulfur-Based Electron Donors

Review of antibiotics treatment by advance oxidation processes

Assessment of the diagnostic value of serum ceruloplasmin for Wilson's disease in children

Two novel mutations in the ALPL gene of unrelated Chinese children with Hypophosphatasia: case reports and literature review

Distinct severity of phenotype in Hajdu-Cheney syndrome: a case report and literature review

Phenotypic and Molecular Characteristics of Children with Progressive Familial Intrahepatic Cholestasis in South China

A two-stage degradation coupling photocatalysis to microalgae enhances the mineralization of enrofloxacin

Insight into integration of photocatalytic and microbial wastewater treatment technologies for recalcitrant organic pollutants: From sequential to simultaneous reactions

How Contagious Was the Panic of 1907? New Evidence from Trust Company Stocks

Synthesis of ZnO@VC for enhancement of synergic photocatalytic degradation of SMX: Toxicity assessment, kinetics and transformation pathway determination

Accelerated Photocatalytic Degradation of Sulfamethoxazole and Cefixime: A Comprehensive Study of Biotoxicity, Degradation Kinetics and Pathway

The third case of Marbach-Rustad progeroid syndrome caused by a de novo LEMD2 variant

Sooner or Later? Promising Delivery Speed in Online Retail

The first Chinese case of Siddiqi syndrome caused by a homozygous FITM2 variant

A novel homozygous splice‐site variant of NCAPD2 gene identified in two siblings with primary microcephaly: The second case report

Clinical characteristics and prognosis of early diagnosed Wilson's disease: A large cohort study

The EGFR‐P38 MAPK axis up‐regulates PD‐L1 through miR‐675‐5p and down‐regulates HLA‐ABC via hexokinase‐2 in hepatocellular carcinoma cells

Features of liver injury in 138 Chinese patients with NICCD

Two homozygous mutations in the exon 5 of BCKDHB gene that may cause the classic form of maple syrup urine disease

Clinical features and mutational analysis in 114 young children with Wilson disease from South China

Clinical features, BTD gene mutations, and their functional studies of eight symptomatic patients with biotinidase deficiency from Southern China

Phenotypic and Molecular Characteristics of Children with Progressive Familial Intrahepatic Cholestasis in South China

RCTE: Relation Candidate-guided few-shot relational Triple Extraction

Learning Semantic Textual Similarity via Multi-Teacher Knowledge Distillation: A Multiple Data Augmentation method

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