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Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia

Nature genetics, 2011-04, Vol.43 (4), p.309-315

2011

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DNMT3A Arg882 mutation drives chronic myelomonocytic leukemia through disturbing gene expression/DNA methylation in hematopoietic cells

Proceedings of the National Academy of Sciences - PNAS, 2014-02, Vol.111 (7), p.2620-2625

2014

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Multiregion sequencing reveals the intratumor heterogeneity of driver mutations in TP53‐driven non‐small cell lung cancer

International journal of cancer, 2017-01, Vol.140 (1), p.103-108

2017

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Natural history of persistent subretinal fluid following the successful repair of rhegmatogenous retinal detachment

International journal of ophthalmology, 2020-10, Vol.13 (10), p.1621-1628

Fu, Yan

2020

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Genomic landscape of CD34⁺ hematopoietic cells in myelodysplastic syndrome and gene mutation profiles as prognostic markers

Proceedings of the National Academy of Sciences - PNAS, 2014-06, Vol.111 (23), p.8589-8594

2014

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Protective effects of umbilical cord mesenchymal stem cell exosomes in a diabetic rat model through live retinal imaging

International journal of ophthalmology, 2021-12, Vol.14 (12), p.1828-1833

2021

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GSTT1 deletion is related to polycyclic aromatic hydrocarbons-induced DNA damage and lymphoma progression

PloS one, 2014-02, Vol.9 (2), p.e89302

2014

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Silencing USP22 by asymmetric structure of interfering RNA inhibits proliferation and induces cell cycle arrest in bladder cancer cells

Molecular and cellular biochemistry, 2011-01, Vol.346 (1-2), p.11-21

2011

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A refined study of FCRL genes from a genome-wide association study for Graves' disease

PloS one, 2013-03, Vol.8 (3), p.e57758-e57758

2013

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Exome sequencing identifies somatic mutations of DDX3X in natural killer/T-cell lymphoma

Nature genetics, 2015-09, Vol.47 (9), p.1061-1066

2015

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The effect of human umbilical cord mesenchymal stem cell-derived exosomes on diabetic retinal neurodegeneration in a rat model

Journal of chemical neuroanatomy, 2022-12, Vol.126, p.102181-102181, Article 102181

2022

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Dominant cystoid macular dystrophy associated with mutations in the RP1L1 gene

International journal of ophthalmology, 2019-12, Vol.12 (12), p.1982-1986

Fu, Yan

2019

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Gene mutation patterns and their prognostic impact in a cohort of 1185 patients with acute myeloid leukemia

Blood, 2011-11, Vol.118 (20), p.5593-5603

2011

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Mutations of Epigenetic Modifier Genes as a Poor Prognostic Factor in Acute Promyelocytic Leukemia Under Treatment With All-Trans Retinoic Acid and Arsenic Trioxide

EBioMedicine, 2015-06, Vol.2 (6), p.563-571

2015

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Recurrent retinal detachment after pars plana vitrectomy with silicone oil tamponade for rhegmatogenous retinal detachment

International ophthalmology, 2022-12, Vol.42 (12), p.3813-3820

2022

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Dense mapping of IL2RA shows no association with Graves' disease in Chinese Han population

Clinical endocrinology (Oxford), 2013-08, Vol.79 (2), p.267-274

2013

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The development of epiretinal membrane following rhegmatogenous retinal detachment repair: incidence, risk factors, and outcomes

Arquivos brasileiros de oftalmologia, 2021, Vol.85 (4), p.370-376

2021

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Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations

Human molecular genetics, 2014-10, Vol.23 (20), p.5505-5517

2014

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Characterization of Somatic Mutations in Air Pollution-Related Lung Cancer

EBioMedicine, 2015-06, Vol.2 (6), p.583-590

2015

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Identification of BACH2 as a susceptibility gene for Graves’ disease in the Chinese Han population based on a three-stage genome-wide association study

Human genetics, 2014-05, Vol.133 (5), p.661-671

2014

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Refined association of TSH receptor susceptibility locus to Graves' disease in the Chinese Han population

European journal of endocrinology, 2014-01, Vol.170 (1), p.109-119

2014

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Whole-exome sequencing to identify novel somatic mutations in squamous cell lung cancers

International journal of oncology, 2013-09, Vol.43 (3), p.755-764

2013

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Pharmacokinetic and Pharmacodynamic Efficacies of Continuous versus Intermittent Administration of Meropenem in Patients with Severe Sepsis and Septic Shock： A Prospective Randomized Pilot Study

Chinese medical journal, 2017-05, Vol.130 (10), p.1139-1145

2017

Volltextzugriff (PDF)

The development of epiretinal membrane following rhegmatogenous retinal detachment repair: incidence, risk factors, and outcomes

Arquivos brasileiros de oftalmologia, 2022-08, Vol.85 (4), p.370-376

2022

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Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis

Human molecular genetics, 2013-08, Vol.22 (16), p.3347-3362

2013

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Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia

DNMT3A Arg882 mutation drives chronic myelomonocytic leukemia through disturbing gene expression/DNA methylation in hematopoietic cells

Multiregion sequencing reveals the intratumor heterogeneity of driver mutations in TP53‐driven non‐small cell lung cancer

Natural history of persistent subretinal fluid following the successful repair of rhegmatogenous retinal detachment

Genomic landscape of CD34⁺ hematopoietic cells in myelodysplastic syndrome and gene mutation profiles as prognostic markers

Protective effects of umbilical cord mesenchymal stem cell exosomes in a diabetic rat model through live retinal imaging

GSTT1 deletion is related to polycyclic aromatic hydrocarbons-induced DNA damage and lymphoma progression

Silencing USP22 by asymmetric structure of interfering RNA inhibits proliferation and induces cell cycle arrest in bladder cancer cells

A refined study of FCRL genes from a genome-wide association study for Graves' disease

Exome sequencing identifies somatic mutations of DDX3X in natural killer/T-cell lymphoma

The effect of human umbilical cord mesenchymal stem cell-derived exosomes on diabetic retinal neurodegeneration in a rat model

Dominant cystoid macular dystrophy associated with mutations in the RP1L1 gene

Gene mutation patterns and their prognostic impact in a cohort of 1185 patients with acute myeloid leukemia

Mutations of Epigenetic Modifier Genes as a Poor Prognostic Factor in Acute Promyelocytic Leukemia Under Treatment With All-Trans Retinoic Acid and Arsenic Trioxide

Recurrent retinal detachment after pars plana vitrectomy with silicone oil tamponade for rhegmatogenous retinal detachment

Dense mapping of IL2RA shows no association with Graves' disease in Chinese Han population

The development of epiretinal membrane following rhegmatogenous retinal detachment repair: incidence, risk factors, and outcomes

Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations

Characterization of Somatic Mutations in Air Pollution-Related Lung Cancer

Identification of BACH2 as a susceptibility gene for Graves’ disease in the Chinese Han population based on a three-stage genome-wide association study

Refined association of TSH receptor susceptibility locus to Graves' disease in the Chinese Han population

Whole-exome sequencing to identify novel somatic mutations in squamous cell lung cancers

Pharmacokinetic and Pharmacodynamic Efficacies of Continuous versus Intermittent Administration of Meropenem in Patients with Severe Sepsis and Septic Shock： A Prospective Randomized Pilot Study

The development of epiretinal membrane following rhegmatogenous retinal detachment repair: incidence, risk factors, and outcomes

Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis

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