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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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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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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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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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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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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 (Review)

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

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

2017

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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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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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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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Application of fusion PCR to the amplification of full-length ORF sequences of different splicing variants of from HeLa cells

Acta biochimica et biophysica Sinica, 2017-10, Vol.49 (10), p.962-965

2017

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Application of fusion PCR to the amplification of full-length ORF sequences of different splicing variants of NuMA1 from HeLa cells

Acta biochimica et biophysica Sinica, 2017-10, Vol.49 (10), p.962-965

2017

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Application of fusion PCR to the amplification of full-length ORF sequences of different splicing variants of NuMA 1 from HeLa cells

生物化学与生物物理学报：英文版, 2017, Vol.49 (10), p.962-965

2017

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Energy efficiency trade-offs drive nucleotide usage in transcribed regions

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

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

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

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

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 (Review)

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

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

MDM4 alternative splicing and implication in MDM4 targeted cancer therapies

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

Application of fusion PCR to the amplification of full-length ORF sequences of different splicing variants of from HeLa cells

Application of fusion PCR to the amplification of full-length ORF sequences of different splicing variants of NuMA1 from HeLa cells

Application of fusion PCR to the amplification of full-length ORF sequences of different splicing variants of NuMA 1 from HeLa cells

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