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Intrinsic BET inhibitor resistance in SPOP-mutated prostate cancer is mediated by BET protein stabilization and AKT–mTORC1 activation

Nature medicine, 2017-09, Vol.23 (9), p.1055-1062

2017

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Prime Editor 3 Mediated Beta-Thalassemia Mutations of the HBB Gene in Human Erythroid Progenitor Cells

International journal of molecular sciences, 2022-04, Vol.23 (9), p.5002

2022

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Structural insights into DNA cleavage activation of CRISPR-Cas9 system

Nature communications, 2017-11, Vol.8 (1), p.1375-9, Article 1375

2017

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Correction of Beta-Thalassemia IVS-II-654 Mutation in a Mouse Model Using Prime Editing

International journal of molecular sciences, 2022-05, Vol.23 (11), p.5948

2022

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The RNA-binding protein QKI suppresses cancer-associated aberrant splicing

PLoS genetics, 2014-04, Vol.10 (4), p.e1004289

2014

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pH-sensitive poly(glutamic acid) grafted mesoporous silica nanoparticles for drug delivery

International journal of pharmaceutics, 2013-06, Vol.450 (1-2), p.296-303

2013

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CRISPR/Cas9-mediated somatic and germline gene correction to restore hemostasis in hemophilia B mice

Human genetics, 2017-07, Vol.136 (7), p.875-883

2017

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The Loss-Function of KNL1 Causes Oligospermia and Asthenospermia in Mice by Affecting the Assembly and Separation of the Spindle through Flow Cytometry and Immunofluorescence

Sensors (Basel, Switzerland), 2023-02, Vol.23 (5), p.2571

2023

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Effect of polymorphisms in XPD on clinical outcomes of platinum-based chemotherapy for Chinese non-small cell lung cancer patients

PloS one, 2012-03, Vol.7 (3), p.e33200-e33200

2012

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Targeted next-generation sequencing and long-read HiFi sequencing provide novel insights into clinically significant KLF1 variants

BMC genomics, 2024-03, Vol.25 (1), p.230-230, Article 230

2024

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miR-1205/DNAJB1 reverses docetaxel chemoresistance in human triple negative breast carcinoma cells via regulation of mutp53/TAp63 signaling

Acta biochimica et biophysica Sinica, 2022-01, Vol.54 (1), p.37-46

2022

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TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice

Human molecular genetics, 2019-02, Vol.28 (4), p.539-547

2019

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Multi-Omics Analysis in β-Thalassemia Using an HBB Gene-Knockout Human Erythroid Progenitor Cell Model

International journal of molecular sciences, 2022-03, Vol.23 (5), p.2807

2022

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Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility

Journal of human genetics, 2022-02, Vol.67 (2), p.107-114

2022

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Promoter hypermethylation-mediated down-regulation of LATS1 and LATS2 in human astrocytoma

Neuroscience research, 2006-12, Vol.56 (4), p.450-458

2006

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Rationales, design and recruitment of the Taizhou Longitudinal Study

BMC public health, 2009-07, Vol.9 (1), p.223-223, Article 223

2009

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Berberine reduces methylation of the MTTP promoter and alleviates fatty liver induced by a high-fat diet in rats[S]

Journal of lipid research, 2010-09, Vol.51 (9), p.2504-2515

2010

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Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of SPTB

Frontiers in genetics, 2023-09, Vol.14, p.1221853-1221853

2023

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Searching across-cohort relatives in 54,092 GWAS samples via encrypted genotype regression

PLoS genetics, 2024-01, Vol.20 (1), p.e1011037-e1011037

2024

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Improved gene therapy for MFRP deficiency-mediated retinal degeneration by knocking down endogenous bicistronic Mfrp and Ctrp5 transcript

Molecular therapy. Nucleic acids, 2023-06, Vol.32, p.843-856

2023

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A meta-analysis of association between C677T polymorphism in the methylenetetrahydrofolate reductase gene and hypertension

European journal of human genetics : EJHG, 2007-12, Vol.15 (12), p.1239-1245

2007

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Iodoacetic Acid Activates Nrf2-Mediated Antioxidant Response in Vitro and in Vivo

Environmental science & technology, 2014-11, Vol.48 (22), p.13478-13488

2014

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Haplotype‐based non‐invasive prenatal diagnosis of recessive dystrophic epidermolysis bullosa via targeted capture sequencing of maternal plasma

Journal of dermatology, 2023-07, Vol.50 (7), p.946-950

2023

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Genetic Variants at 6p21.1 and 7p15.3 Are Associated with Risk of Multiple Cancers in Han Chinese

American journal of human genetics, 2012-11, Vol.91 (5), p.928-934

2012

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Intrinsic BET inhibitor resistance in SPOP-mutated prostate cancer is mediated by BET protein stabilization and AKT–mTORC1 activation

Prime Editor 3 Mediated Beta-Thalassemia Mutations of the HBB Gene in Human Erythroid Progenitor Cells

Structural insights into DNA cleavage activation of CRISPR-Cas9 system

Correction of Beta-Thalassemia IVS-II-654 Mutation in a Mouse Model Using Prime Editing

The RNA-binding protein QKI suppresses cancer-associated aberrant splicing

pH-sensitive poly(glutamic acid) grafted mesoporous silica nanoparticles for drug delivery

CRISPR/Cas9-mediated somatic and germline gene correction to restore hemostasis in hemophilia B mice

The Loss-Function of KNL1 Causes Oligospermia and Asthenospermia in Mice by Affecting the Assembly and Separation of the Spindle through Flow Cytometry and Immunofluorescence

Effect of polymorphisms in XPD on clinical outcomes of platinum-based chemotherapy for Chinese non-small cell lung cancer patients

Targeted next-generation sequencing and long-read HiFi sequencing provide novel insights into clinically significant KLF1 variants

A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese

miR-1205/DNAJB1 reverses docetaxel chemoresistance in human triple negative breast carcinoma cells via regulation of mutp53/TAp63 signaling

TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice

Multi-Omics Analysis in β-Thalassemia Using an HBB Gene-Knockout Human Erythroid Progenitor Cell Model

Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility

Promoter hypermethylation-mediated down-regulation of LATS1 and LATS2 in human astrocytoma

Rationales, design and recruitment of the Taizhou Longitudinal Study

Berberine reduces methylation of the MTTP promoter and alleviates fatty liver induced by a high-fat diet in rats[S]

Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of SPTB

Searching across-cohort relatives in 54,092 GWAS samples via encrypted genotype regression

Improved gene therapy for MFRP deficiency-mediated retinal degeneration by knocking down endogenous bicistronic Mfrp and Ctrp5 transcript

A meta-analysis of association between C677T polymorphism in the methylenetetrahydrofolate reductase gene and hypertension

Iodoacetic Acid Activates Nrf2-Mediated Antioxidant Response in Vitro and in Vivo

Haplotype‐based non‐invasive prenatal diagnosis of recessive dystrophic epidermolysis bullosa via targeted capture sequencing of maternal plasma

Genetic Variants at 6p21.1 and 7p15.3 Are Associated with Risk of Multiple Cancers in Han Chinese

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