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Energy efficiency trade-offs drive nucleotide usage in transcribed regions

Nature communications, 2016-04, Vol.7 (1), p.11334-11334, Article 11334

2016

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A Novel Etanercept-loaded Nano-emulsion for Targeted Treatment of Inflammatory Arthritis via Draining Lymph Node

Current drug delivery, 2024-01, Vol.21 (8), p.1106-1113

2024

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Comprehensive Analysis of the Structure and Function of Peptide:N-Glycanase 1 and Relationship with Congenital Disorder of Deglycosylation

Nutrients, 2022-04, Vol.14 (9), p.1690

2022

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Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism

Endocrine Journal, 2018, Vol.65(10), pp.1019-1028

2018

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Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin-Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing

BMC medical genomics, 2021-11, Vol.14 (1), p.270-270, Article 270

2021

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Visual and optical quality outcomes of SMILE and FS-LASIK for myopia in the very early phase after surgery

BMC ophthalmology, 2019-04, Vol.19 (1), p.88-88, Article 88

2019

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Identification of a de novo mutation of the FOXG1 gene and comprehensive analysis for molecular factors in Chinese FOXG1-related encephalopathies

Frontiers in molecular neuroscience, 2022-12, Vol.15, p.1039990-1039990

2022

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A c.726C>G (p.Tyr242Ter) nonsense mutation-associated with splicing alteration (NASA) of WDR45 gene underlies β-propeller protein-associated neurodegeneration (BPAN)

Heliyon, 2024-05, Vol.10 (9), p.e30438-e30438, Article e30438

2024

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Elevated D-dimer is associated with increased 28-day mortality in acute-on-chronic liver failure in China: a retrospective study

BMC gastroenterology, 2019-01, Vol.19 (1), p.20-20, Article 20

2019

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A de Novo ZMIZ1 Pathogenic Variant for Neurodevelopmental Disorder With Dysmorphic Facies and Distal Skeletal Anomalies

Frontiers in genetics, 2022-03, Vol.13, p.840577-840577

2022

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Hepatic Tumor Stiffness Measured by Shear Wave Elastography Is Prognostic for HCC Progression Following Treatment With Anti-PD-1 Antibodies Plus Lenvatinib: A Retrospective Analysis of Two Independent Cohorts

Frontiers in immunology, 2022-06, Vol.13, p.868809-868809

2022

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GAAD: A Gene and Autoimmiune Disease Association Database

Genomics, proteomics & bioinformatics, 2018-08, Vol.16 (4), p.252-261

2018

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A synonymous variant contributes to a rare Wiedemann-Rautenstrauch syndrome complicated with mild anemia via affecting pre-mRNA splicing

Frontiers in molecular neuroscience, 2022-10, Vol.15, p.1026530-1026530

2022

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Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism

ENDOCRINE JOURNAL, 2018, Vol.65 (10), p.1019-1028

2018

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Multiple functions of TBCK protein in neurodevelopment disorders and tumors

Oncology letters, 2021-01, Vol.21 (1), p.17-1

2021

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OGEE v2: an update of the online gene essentiality database with special focus on differentially essential genes in human cancer cell lines

Nucleic acids research, 2017-01, Vol.45 (D1), p.D940-D944

2017

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MDM4 alternative splicing and implication in MDM4 targeted cancer therapies

American journal of cancer research, 2021-01, Vol.11 (12), p.5864-5880

2021

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Minor role of hemostatic alternation in portal vein thrombosis pathogenesis revealed by global measurement

Journal of hepatology, 2022-01, Vol.76 (1), p.225-227

2022

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Suno: potential, prospects, and trends

Frontiers of information technology & electronic engineering, 2024-07, Vol.25 (7), p.1025-1030

2024

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Selection for energy efficiency drives strand-biased gene distribution in prokaryotes

Scientific reports, 2017-09, Vol.7 (1), p.10572-10572, Article 10572

2017

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Prognostic and therapeutic significance of microbial cell-free DNA in plasma of people with acute decompensation of cirrhosis

Journal of hepatology, 2023-02, Vol.78 (2), p.322-332

2023

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Tri‐typing of hepatitis B‐related acute‐on‐chronic liver failure defined by the World Gastroenterology Organization

Journal of gastroenterology and hepatology, 2021-01, Vol.36 (1), p.208-216

2021

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A de novo germline mutation of APC for inheritable colon cancer in a Chinese family using multigene next generation sequencing

Biochemical and biophysical research communications, 2014-05, Vol.447 (3), p.503-507

2014

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Abundant and broad expression of transcription-induced chimeras and protein products in mammalian genomes

Biochemical and biophysical research communications, 2016-02, Vol.470 (3), p.759-765

2016

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Association of IL12A Expression Quantitative Trait Loci (eQTL) With Primary Biliary Cirrhosis in a Chinese Han Population

Medicine (Baltimore), 2016-05, Vol.95 (19), p.e3665-e3665

2016

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Energy efficiency trade-offs drive nucleotide usage in transcribed regions

A Novel Etanercept-loaded Nano-emulsion for Targeted Treatment of Inflammatory Arthritis via Draining Lymph Node

Comprehensive Analysis of the Structure and Function of Peptide:N-Glycanase 1 and Relationship with Congenital Disorder of Deglycosylation

Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism

Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin-Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing

Visual and optical quality outcomes of SMILE and FS-LASIK for myopia in the very early phase after surgery

Identification of a de novo mutation of the FOXG1 gene and comprehensive analysis for molecular factors in Chinese FOXG1-related encephalopathies

A c.726C>G (p.Tyr242Ter) nonsense mutation-associated with splicing alteration (NASA) of WDR45 gene underlies β-propeller protein-associated neurodegeneration (BPAN)

Elevated D-dimer is associated with increased 28-day mortality in acute-on-chronic liver failure in China: a retrospective study

A de Novo ZMIZ1 Pathogenic Variant for Neurodevelopmental Disorder With Dysmorphic Facies and Distal Skeletal Anomalies

Hepatic Tumor Stiffness Measured by Shear Wave Elastography Is Prognostic for HCC Progression Following Treatment With Anti-PD-1 Antibodies Plus Lenvatinib: A Retrospective Analysis of Two Independent Cohorts

GAAD: A Gene and Autoimmiune Disease Association Database

A synonymous variant contributes to a rare Wiedemann-Rautenstrauch syndrome complicated with mild anemia via affecting pre-mRNA splicing

Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism

Multiple functions of TBCK protein in neurodevelopment disorders and tumors

OGEE v2: an update of the online gene essentiality database with special focus on differentially essential genes in human cancer cell lines

MDM4 alternative splicing and implication in MDM4 targeted cancer therapies

Minor role of hemostatic alternation in portal vein thrombosis pathogenesis revealed by global measurement

Suno: potential, prospects, and trends

Selection for energy efficiency drives strand-biased gene distribution in prokaryotes

Prognostic and therapeutic significance of microbial cell-free DNA in plasma of people with acute decompensation of cirrhosis

Tri‐typing of hepatitis B‐related acute‐on‐chronic liver failure defined by the World Gastroenterology Organization

A de novo germline mutation of APC for inheritable colon cancer in a Chinese family using multigene next generation sequencing

Abundant and broad expression of transcription-induced chimeras and protein products in mammalian genomes

Association of IL12A Expression Quantitative Trait Loci (eQTL) With Primary Biliary Cirrhosis in a Chinese Han Population

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