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Tumor microbiome contributes to an aggressive phenotype in the basal-like subtype of pancreatic cancer

Communications biology, 2021-08, Vol.4 (1), p.1019-13, Article 1019

2021

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Alternative promoters influence alternative splicing at the genomic level

PloS one, 2008-06, Vol.3 (6), p.e2377-e2377

2008

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Knockdown of SLC39A7 inhibits cell growth and induces apoptosis in human colorectal cancer cells

Acta biochimica et biophysica Sinica, 2017-10, Vol.49 (10), p.926-934

2017

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Rare Germline GLMN Variants Identified from Blue Rubber Bleb Nevus Syndrome Might Impact mTOR Signaling

Combinatorial chemistry & high throughput screening, 2019-01, Vol.22 (10), p.675-682

2019

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Revisiting Non-BRCA1/2 Familial Whole Exome Sequencing Datasets Implicates NCK1 as a Cancer Gene

Frontiers in genetics, 2019-06, Vol.10, p.527-527

2019

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Escaping but not the inactive X-linked protein complex coding genes may achieve X-chromosome dosage compensation and underlie X chromosome inactivation-related diseases

Heliyon, 2023-07, Vol.9 (7), p.e17721-e17721, Article e17721

2023

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Natural Selection on Exonic SNPs Shapes Allelic Expression Imbalance (AEI) Adaptability in Lung Cancer Progression

Frontiers in genetics, 2020-06, Vol.11, p.665-665

2020

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Noisy splicing, more than expression regulation, explains why some exons are subject to nonsense-mediated mRNA decay

BMC biology, 2009-05, Vol.7 (23), p.23-23, Article 23

2009

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Genome-wide interaction-based association analysis identified multiple new susceptibility Loci for common diseases

PLoS genetics, 2011-03, Vol.7 (3), p.e1001338-e1001338

2011

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Evidence for OTUD-6B participation in B lymphocytes cell cycle after cytokine stimulation

PloS one, 2011-01, Vol.6 (1), p.e14514-e14514

2011

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Single-cell RNA sequencing reveals the suppressive effect of PPP1R15A inhibitor Sephin1 in antitumor immunity

iScience, 2023-02, Vol.26 (2), p.105954-105954, Article 105954

2023

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Assessing the activity of nonsense-mediated mRNA decay in lung cancer

BMC medical genomics, 2017-09, Vol.10 (1), p.55-55, Article 55

2017

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Characterization of the Blood and Cerebrospinal Fluid Microbiome in Children with Bacterial Meningitis and Its Potential Correlation with Inflammation

mSystems, 2021-06, Vol.6 (3), p.e0004921-e0004921

2021

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Abstract 2122: RNA editing reveals new regulatory functions in tumorigenesis

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.2122-2122

Hu, Landian

2015

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Protocol for PPP1R15A-inhibited mouse model establishment with subcutaneous B16F1 tumor and single-cell analysis

STAR protocols, 2023-12, Vol.4 (4), p.102616-102616, Article 102616

2023

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Intact regulation of G1/S transition renders esophageal squamous cell carcinoma sensitive to PI3Kα inhibitors

Signal transduction and targeted therapy, 2023-04, Vol.8 (1), p.153-153, Article 153

2023

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Gain-of-Function Mutation of KIT Ligand on Melanin Synthesis Causes Familial Progressive Hyperpigmentation

American journal of human genetics, 2009-05, Vol.84 (5), p.672-677

2009

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The impact of nucleosome positioning on the organization of replication origins in eukaryotes

Biochemical and biophysical research communications, 2009-07, Vol.385 (3), p.363-368

2009

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Uncovering the rare variants of DLC1 isoform 1 and their functional effects in a Chinese sporadic congenital heart disease cohort

PloS one, 2014-02, Vol.9 (2), p.e90215-e90215

2014

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Impact of personalized peptide neoantigen vaccines on immunologic responses in patients with pancreatic cancer

Journal of clinical oncology, 2024-06, Vol.42 (16_suppl), p.e16351-e16351

2024

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Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract

Nature genetics, 2002-07, Vol.31 (3), p.276-278

2002

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Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

Nature genetics, 2001-02, Vol.27 (2), p.201-204

2001

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MicroRNA or NMD： Why Have Two RNA Silencing Systems

Journal of genetics and genomics, 2013-10, Vol.40 (10), p.497-513

2013

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Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study

Scientific reports, 2013-07, Vol.3 (1), p.2147-2147, Article 2147

2013

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Novel association strategy with copy number variation for identifying new risk Loci of human diseases

PloS one, 2010-08, Vol.5 (8), p.e12185-e12185

2010

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Tumor microbiome contributes to an aggressive phenotype in the basal-like subtype of pancreatic cancer

Alternative promoters influence alternative splicing at the genomic level

Knockdown of SLC39A7 inhibits cell growth and induces apoptosis in human colorectal cancer cells

Rare Germline GLMN Variants Identified from Blue Rubber Bleb Nevus Syndrome Might Impact mTOR Signaling

Revisiting Non-BRCA1/2 Familial Whole Exome Sequencing Datasets Implicates NCK1 as a Cancer Gene

Escaping but not the inactive X-linked protein complex coding genes may achieve X-chromosome dosage compensation and underlie X chromosome inactivation-related diseases

Natural Selection on Exonic SNPs Shapes Allelic Expression Imbalance (AEI) Adaptability in Lung Cancer Progression

Noisy splicing, more than expression regulation, explains why some exons are subject to nonsense-mediated mRNA decay

Genome-wide interaction-based association analysis identified multiple new susceptibility Loci for common diseases

Evidence for OTUD-6B participation in B lymphocytes cell cycle after cytokine stimulation

Single-cell RNA sequencing reveals the suppressive effect of PPP1R15A inhibitor Sephin1 in antitumor immunity

Assessing the activity of nonsense-mediated mRNA decay in lung cancer

Characterization of the Blood and Cerebrospinal Fluid Microbiome in Children with Bacterial Meningitis and Its Potential Correlation with Inflammation

Abstract 2122: RNA editing reveals new regulatory functions in tumorigenesis

Protocol for PPP1R15A-inhibited mouse model establishment with subcutaneous B16F1 tumor and single-cell analysis

Intact regulation of G1/S transition renders esophageal squamous cell carcinoma sensitive to PI3Kα inhibitors

Gain-of-Function Mutation of KIT Ligand on Melanin Synthesis Causes Familial Progressive Hyperpigmentation

The impact of nucleosome positioning on the organization of replication origins in eukaryotes

Uncovering the rare variants of DLC1 isoform 1 and their functional effects in a Chinese sporadic congenital heart disease cohort

Impact of personalized peptide neoantigen vaccines on immunologic responses in patients with pancreatic cancer

Mutant DNA-binding domain of HSF4 is associated with autosomal dominant lamellar and Marner cataract

Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

MicroRNA or NMD： Why Have Two RNA Silencing Systems

Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study

Novel association strategy with copy number variation for identifying new risk Loci of human diseases

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