Year |
Citation |
Score |
2022 |
Yang L, Liu B, Dong X, Wu J, Sun C, Xi L, Cheng R, Wu B, Wang H, Tong S, Wang D, Luo F. Clinical severity prediction in children with osteogenesis imperfecta caused by COL1A1/2 defects. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. PMID 35044492 DOI: 10.1007/s00198-021-06263-0 |
0.01 |
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2022 |
Xiao T, Ni Q, Chen H, Wang H, Yang L, Wu B, Cao Y, Cheng G, Wang L, Hu L, Mei H, Lu Y, Gong M, Dong X, Zhou W. High-risk phenotypes of genetic disease in a Neonatal Intensive Care Unit population. Chinese Medical Journal. PMID 35026772 DOI: 10.1097/CM9.0000000000001959 |
0.01 |
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2021 |
Li W, Cheng T, Dong X, Chen H, Yang L, Qiu Z, Zhou W. KIF5C deficiency causes abnormal cortical neuronal migration, dendritic branching, and spine morphology in mice. Pediatric Research. PMID 34966180 DOI: 10.1038/s41390-021-01922-8 |
0.01 |
|
2021 |
Mei H, Dong X, Wu B, Wang H, Lu Y, Hu L, Wang J, Cao Y, Zhang R, Cheng G, Wang L, Li Z, Yang L, Zhou W. Clinical and genetic etiologies of neonatal unconjugated hyperbilirubinemia in the China Neonatal Genomes Project. The Journal of Pediatrics. PMID 34953813 DOI: 10.1016/j.jpeds.2021.12.038 |
0.01 |
|
2021 |
Xia M, Chen H, Chen T, Xue P, Dong X, Lin Y, Ma D, Zhou W, Shi W, Li H. Transcriptional Networks Identify BRPF1 as a Potential Drug Target Based on Inflammatory Signature in Primary Lower-Grade Gliomas. Frontiers in Oncology. 11: 766656. PMID 34926268 DOI: 10.3389/fonc.2021.766656 |
0.01 |
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2021 |
Mei H, Yang L, Xiao T, Wang S, Wu B, Wang H, Lu Y, Dong X, Yang H, Zhou W. Genetic Spectrum Identified by Exome Sequencing in a Chinese Pediatric Cerebral Palsy Cohort. The Journal of Pediatrics. PMID 34788679 DOI: 10.1016/j.jpeds.2021.11.019 |
0.01 |
|
2021 |
Ma H, Tang Z, Xiao F, Li L, Li Y, Tang W, Chen L, Kang W, Lu Y, Dong X, Cheng G, Wang L, Lu W, Yang L, Ni Q, et al. Neonatal Metabolic Acidosis in the Neonatal Intensive Care Unit: What Are the Genetic Causes? Frontiers in Pediatrics. 9: 727301. PMID 34733806 DOI: 10.3389/fped.2021.727301 |
0.01 |
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2021 |
Yang L, Wei Z, Chen X, Hu L, Peng X, Wang J, Lu C, Kong Y, Dong X, Ni Q, Lu Y, Wu B, Wang H, Meirelles K, Tian X, et al. Use of medical exome sequencing for identification of underlying genetic defects in NICU: experience in a cohort of 2,303 neonates in China. Clinical Genetics. PMID 34671977 DOI: 10.1111/cge.14075 |
0.01 |
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2021 |
Dong X, Kong Y, Xu Y, Zhou Y, Wang X, Xiao T, Chen B, Lu Y, Cheng G, Zhou W. Development and validation of Auto-Neo-electroencephalography (EEG) to estimate brain age and predict report conclusion for electroencephalography monitoring data in neonatal intensive care units. Annals of Translational Medicine. 9: 1290. PMID 34532427 DOI: 10.21037/atm-21-1564 |
0.01 |
|
2021 |
Li C, Zhu Z, Yuan H, Zhong P, Peng Q, Dong X, Huang M, Liu B, Ren Y, Kuang Y, Zeng X, Yu H, Yang X. Improved Retinal Microcirculation After Cardiac Surgery in Patients With Congenital Heart Disease. Frontiers in Cardiovascular Medicine. 8: 712308. PMID 34532349 DOI: 10.3389/fcvm.2021.712308 |
0.01 |
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2021 |
Dong X, Zeng L, Chu D, Sun X. Highly Sensitive Dual Parameter Sensor Based on a Hybrid Structure with Multimode Interferometer and Fiber Bragg Grating Fabricated by Femtosecond Laser. Sensors (Basel, Switzerland). 21. PMID 34502826 DOI: 10.3390/s21175938 |
0.01 |
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2021 |
Zhou J, Xiong Y, Dong X, Wang H, Qian Y, Ma D, Li X. Genome-wide methylation analysis reveals differentially methylated CpG sites and altered expression of heart development-associated genes in fetuses with cardiac defects. Experimental and Therapeutic Medicine. 22: 1032. PMID 34373718 DOI: 10.3892/etm.2021.10464 |
0.01 |
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2021 |
Dai D, Mei M, Hu L, Cao Y, Wang X, Wang L, Lu Y, Yang L, Dong X, Wang H, Wu B, Qian L. Prevalence of monogenic disease in paediatric patients with a predominant respiratory phenotype. Archives of Disease in Childhood. PMID 34134972 DOI: 10.1136/archdischild-2021-322058 |
0.01 |
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2021 |
Dai D, Mei M, Hu L, Cao Y, Wang X, Wang L, Lu Y, Yang L, Dong X, Wang H, Wu B, Qian L. Prevalence of monogenic disease in paediatric patients with a predominant respiratory phenotype. Archives of Disease in Childhood. PMID 34134972 DOI: 10.1136/archdischild-2021-322058 |
0.01 |
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2021 |
Luo Z, Dong X, Yu J, Xia Y, Berry KP, Rao R, Xu L, Xue P, Chen T, Lin Y, Yu J, Huang G, Li H, Zhou W, Lu QR. Genomic and Transcriptomic Analyses Reveals ZNF124 as a Critical Regulator in Highly Aggressive Medulloblastomas. Frontiers in Cell and Developmental Biology. 9: 634056. PMID 33681213 DOI: 10.3389/fcell.2021.634056 |
0.01 |
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2021 |
Dong X, Yang L, Liu K, Ji X, Tang C, Li W, Ma L, Mei Y, Peng T, Feng B, Wu Z, Tang Q, Gao Y, Yan K, Zhou W, et al. Transcriptional networks identify synaptotagmin-like 3 as a regulator of cortical neuronal migration during early neurodevelopment. Cell Reports. 34: 108802. PMID 33657377 DOI: 10.1016/j.celrep.2021.108802 |
0.01 |
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2021 |
Peng X, Lu Y, Wu B, Dong X, Li W, Wang H, Huang Y, Zhou W. A novel 333 bp deletion of IL10RA in Chinese patients with neonatal-onset inflammatory bowel disease. Journal of Clinical Immunology. PMID 33591424 DOI: 10.1007/s10875-021-00973-0 |
0.01 |
|
2021 |
Liu B, Zhang B, Hu Y, Cao D, Yang D, Wu Q, Hu Y, Yang J, Peng Q, Huang M, Zhong P, Dong X, Feng S, Li T, Lin H, et al. Automatic prediction of treatment outcomes in patients with diabetic macular edema using ensemble machine learning. Annals of Translational Medicine. 9: 43. PMID 33553336 DOI: 10.21037/atm-20-1431 |
0.01 |
|
2021 |
Wang H, Xiao F, Dong X, Lu Y, Cheng G, Wang L, Lu W, Yang L, Chen L, Kang W, Li L, Pan X, Wei Q, Zhuang D, Chen D, et al. Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project (CNGP). Human Mutation. PMID 33502061 DOI: 10.1002/humu.24170 |
0.01 |
|
2020 |
Li J, Owusu IK, Geng Q, Folson AA, Zheng Z, Adu-Boakye Y, Dong X, Wu WC, Agyekum F, Fei H, Ayetey H, Deng M, Adomako-Boateng F, Jiang Z, Abubakari BB, et al. Cardiometabolic Risk Factors and Preclinical Target Organ Damage Among Adults in Ghana: Findings From a National Study. Journal of the American Heart Association. e017492. PMID 33283559 DOI: 10.1161/JAHA.120.017492 |
0.01 |
|
2020 |
Liu B, Wu B, Lu Y, Zhang P, Xiao F, Li G, Wang H, Dong X, Liu R, Li Y, Xie X, Zhou W, Wang J, Lu Y. A novel recurrent 3.6-kb deletion in the PYGL gene contributes to glycogen storage disease type VI. The Journal of Molecular Diagnostics : Jmd. PMID 32961316 DOI: 10.1016/j.jmoldx.2020.08.006 |
0.01 |
|
2020 |
Li C, Zhong P, Yuan H, Dong X, Peng Q, Huang M, Wu Q, Liu B, Xu M, Kuang Y, Zeng X, Xiao Y, Fang Y, Yu H, Yang X. Retinal microvasculature impairment in patients with congenital heart disease investigated by optical coherence tomography angiography. Clinical & Experimental Ophthalmology. PMID 32860305 DOI: 10.1111/ceo.13846 |
0.01 |
|
2020 |
Yang J, Dong X, Hu Y, Peng Q, Tao G, Ou Y, Cai H, Yang X. Fully Automatic Arteriovenous Segmentation in Retinal Images via Topology-Aware Generative Adversarial Networks. Interdisciplinary Sciences, Computational Life Sciences. PMID 32725575 DOI: 10.1007/S12539-020-00385-5 |
0.01 |
|
2020 |
Peng Q, Hu Y, Huang M, Wu Y, Zhong P, Dong X, Wu Q, Liu B, Li C, Xie J, Kuang Y, Yu D, Yu H, Yang X. Retinal Neurovascular Impairment in Patients with Essential Hypertension: An Optical Coherence Tomography Angiography Study. Investigative Ophthalmology & Visual Science. 61: 42. PMID 32725211 DOI: 10.1167/iovs.61.8.42 |
0.01 |
|
2020 |
Yang L, Chen X, Liu X, Dong X, Ye C, Deng D, Lu Y, Lin Y, Zhou W. Clinical features and underlying genetic causes in neonatal encephalopathy: a large cohort study. Clinical Genetics. PMID 32712949 DOI: 10.1111/cge.13818 |
0.01 |
|
2020 |
Wu J, Dong X, Li W, Zhao L, Zhou L, Sun S, Li H. Dibenzazepine promotes cochlear supporting cell proliferation and hair cell regeneration in neonatal mice. Cell Proliferation. e12872. PMID 32677724 DOI: 10.1111/cpr.12872 |
0.01 |
|
2020 |
Zou H, Zhao N, Li S, Sun S, Dong X, Yu C. Physicochemical and emulsifying properties of mussel water-soluble proteins as affected by lecithin concentration. International Journal of Biological Macromolecules. PMID 32599247 DOI: 10.1016/j.ijbiomac.2020.06.225 |
0.01 |
|
2020 |
Sun J, Yang L, Lu Y, Wang H, Peng X, Dong X, Cheng G, Cao Y, Wu B, Wang X, Zhou W. Screening for primary immunodeficiency diseases by next-generation sequencing in early life. Clinical & Translational Immunology. 9: e1138. PMID 32431812 DOI: 10.1002/cti2.1138 |
0.01 |
|
2020 |
Zhang Y, Xu J, Jia R, Yi C, Gu W, Liu P, Dong X, Zhou H, Shang B, Cheng S, Sun X, Ye J, Li X, Zhang J, Ling Z, et al. Protective humoral immunity in SARS-CoV-2 infected pediatric patients. Cellular & Molecular Immunology. PMID 32382126 DOI: 10.1038/s41423-020-0438-3 |
0.01 |
|
2020 |
Liu B, Lu Y, Wu B, Yang L, Liu R, Wang H, Dong X, Li G, Qin Q, Zhou W. SMN gene copy number analysis by exome-seq: assisting SMA diagnosis and carrier screening. The Journal of Molecular Diagnostics : Jmd. PMID 32092542 DOI: 10.1016/j.jmoldx.2020.01.015 |
0.01 |
|
2020 |
Dong X, Liu B, Yang L, Wang H, Wu B, Liu R, Chen H, Chen X, Yu S, Chen B, Wang S, Xu X, Zhou W, Lu Y. Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort. Journal of Medical Genetics. PMID 32005694 DOI: 10.1136/jmedgenet-2019-106377 |
0.01 |
|
2020 |
Wang H, Lu Y, Dong X, Lu G, Cheng G, Qian Y, Ni Q, Zhang P, Yang L, Wu B, Zhou W. Optimized trio genome sequencing (OTGS) as a first-tier genetic test in critically ill infants: practice in China. Human Genetics. PMID 31965297 DOI: 10.1007/s00439-019-02103-8 |
0.01 |
|
2019 |
Yu S, Wu B, Qian Y, Zhang P, Lu Y, Dong X, Wang Q, Zhao X, Liu R, Zhou W, Wang H. Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein-Taybi Syndrome kids with high frequency of polydactyly. Molecular Genetics & Genomic Medicine. e1009. PMID 31637876 DOI: 10.1002/mgg3.1009 |
0.01 |
|
2019 |
Hu Y, Wu Q, Liu B, Cao D, Dong X, Zhang L, Li T, Yang X, Yu H. Comparison of clinical outcomes of different components of diabetic macular edema on optical coherence tomography. Graefe's Archive For Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie. PMID 31529324 DOI: 10.1007/s00417-019-04471-3 |
0.01 |
|
2019 |
Liu X, Mei M, Chen X, Lu Y, Dong X, Hu L, Hu X, Cheng G, Cao Y, Yang L, Zhou W. Identification of genetic factors underlying persistent pulmonary hypertension of newborns in a cohort of Chinese neonates. Respiratory Research. 20: 174. PMID 31382961 DOI: 10.1186/s12931-019-1148-1 |
0.01 |
|
2019 |
Yang D, Cao D, Huang Z, Xie J, Meng Q, Dong X, Hu Y, Zeng Y, Zhang L. Macular Capillary Perfusion in Chinese Patients With Diabetic Retinopathy Obtained With Optical Coherence Tomography Angiography. Ophthalmic Surgery, Lasers & Imaging Retina. 50: e88-e95. PMID 30998251 DOI: 10.3928/23258160-20190401-12 |
0.01 |
|
2019 |
Weng Q, Wang J, Wang J, He D, Cheng Z, Zhang F, Verma R, Xu L, Dong X, Liao Y, He X, Potter A, Zhang L, Zhao C, Xin M, et al. Single-Cell Transcriptomics Uncovers Glial Progenitor Diversity and Cell Fate Determinants during Development and Gliomagenesis. Cell Stem Cell. PMID 30982771 DOI: 10.1016/J.Stem.2019.03.006 |
0.01 |
|
2019 |
Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W. Data on mutations and Clinical features in SCN1A or SCN2A gene. Data in Brief. 22: 492-501. PMID 30619928 DOI: 10.1016/j.dib.2018.08.122 |
0.01 |
|
2018 |
Qian Y, Wu B, Lu Y, Dong X, Qin Q, Zhou W, Wang H. Early-onset infant epileptic encephalopathy associated with a de novo PPP3CA gene mutation. Cold Spring Harbor Molecular Case Studies. PMID 30455226 DOI: 10.1101/mcs.a002949 |
0.01 |
|
2018 |
Yang S, Yin K, Dong X, He J, Duan JA. Laser Structuring of Underwater Bubble-Repellent Surface. Journal of Nanoscience and Nanotechnology. 18: 8381-8385. PMID 30189963 DOI: 10.1166/jnn.2018.16426 |
0.01 |
|
2018 |
Yin K, Yang S, Dong X, Chu D, Duan JA, He J. Ultrafast Achievement of a Superhydrophilic/Hydrophobic Janus Foam by Femtosecond Laser Ablation for Directional Water Transport and Efficient Fog Harvesting. Acs Applied Materials & Interfaces. PMID 30183242 DOI: 10.1021/acsami.8b11894 |
0.01 |
|
2018 |
Dong X, Du H, Sun X, Duan J. Simultaneous Strain and Temperature Sensor Based on a Fiber Mach-Zehnder Interferometer Coated with Pt by Iron Sputtering Technology. Materials (Basel, Switzerland). 11. PMID 30149670 DOI: 10.3390/ma11091535 |
0.01 |
|
2018 |
Chen H, Qian Y, Yu S, Xiao D, Guo X, Wang Q, Hao L, Lu Y, Dong X, Yan K, Zhou W, Wu B, Wang H. Early onset developmental delay and epilepsy in pediatric patients with WDR45 variants. European Journal of Medical Genetics. PMID 29981852 DOI: 10.1016/j.ejmg.2018.07.002 |
0.01 |
|
2018 |
Yang L, Kong Y, Dong X, Hu L, Lin Y, Chen X, Ni Q, Lu Y, Wu B, Wang H, Lu QR, Zhou W. Clinical and genetic spectrum of a large cohort of children with epilepsy in China. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29930392 DOI: 10.1038/s41436-018-0091-8 |
0.01 |
|
2018 |
Zhao C, Dong C, Frah M, Deng Y, Marie C, Zhang F, Xu L, Ma Z, Dong X, Lin Y, Koenig S, Nait-Oumesmar B, Martin DM, Wu LN, Xin M, et al. Dual Requirement of CHD8 for Chromatin Landscape Establishment and Histone Methyltransferase Recruitment to Promote CNS Myelination and Repair. Developmental Cell. 45: 753-768.e8. PMID 29920279 DOI: 10.1016/J.Devcel.2018.05.022 |
0.01 |
|
2018 |
Dong X, Du H, Sun X, Luo Z, Duan J. A Novel Strain Sensor with Large Measurement Range Based on All Fiber Mach-Zehnder Interferometer. Sensors (Basel, Switzerland). 18. PMID 29757975 DOI: 10.3390/s18051549 |
0.01 |
|
2018 |
Kong Y, Yan K, Hu L, Wang M, Dong X, Lu Y, Wu B, Wang H, Yang L, Zhou W. Association between SCN1A and SCN2A mutations and clinical/EEG features in Chinese patients from epilepsy or severe seizures. Clinica Chimica Acta; International Journal of Clinical Chemistry. PMID 29649454 DOI: 10.1016/j.cca.2018.03.027 |
0.01 |
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2018 |
Chen X, Gao Y, Yang L, Wu B, Dong X, Liu B, Lu Y, Zhou W, Wang H. Speech and language delay in a patient with WDR4 mutations. European Journal of Medical Genetics. PMID 29597095 DOI: 10.1016/j.ejmg.2018.03.007 |
0.01 |
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2018 |
He X, Zhang L, Queme LF, Liu X, Lu A, Waclaw RR, Dong X, Zhou W, Kidd G, Yoon SO, Buonanno A, Rubin JB, Xin M, Nave KA, Trapp BD, et al. A histone deacetylase 3-dependent pathway delimits peripheral myelin growth and functional regeneration. Nature Medicine. PMID 29431744 DOI: 10.1038/Nm.4483 |
0.01 |
|
2018 |
Li Y, Pang Z, Dong X, Liao X, Deng H, Liao C, Liao Y, Chen G, Huang L. MUC1 induces M2 type macrophage influx during postpartum mammary gland involution and triggers breast cancer. Oncotarget. 9: 3446-3458. PMID 29423058 DOI: 10.18632/oncotarget.23316 |
0.01 |
|
2018 |
Dong X, Du H, Luo Z, Duan J. Highly Sensitive Strain Sensor Based on a Novel Mach-Zehnder Interferometer with TCF-PCF Structure. Sensors (Basel, Switzerland). 18. PMID 29346296 DOI: 10.3390/s18010278 |
0.01 |
|
2017 |
Dong X, Xie Z, Zhou C, Yin K, Luo Z, Duan J. Temperature sensitivity enhancement of platinum-nanoparticle-coated long period fiber gratings fabricated by femtosecond laser. Applied Optics. 56: 6549-6553. PMID 29047949 |
0.01 |
|
2017 |
Yin K, Du H, Dong X, Wang C, Duan JA, He J. A simple way to achieve bioinspired hybrid wettability surface with micro/nanopatterns for efficient fog collection. Nanoscale. PMID 28936519 DOI: 10.1039/c7nr05683d |
0.01 |
|
2017 |
Yin K, Chu D, Dong X, Wang C, Duan JA, He J. Femtosecond laser induced robust periodic nanoripple structured mesh for highly efficient oil-water separation. Nanoscale. PMID 28914319 DOI: 10.1039/c7nr04582d |
0.01 |
|
2017 |
Liang H, Yin C, Dong X, Acharya G, Li X. Clusters of week-specific maternal gestational weight gain pattern and their association with birthweight:an observational cohort study. Acta Obstetricia Et Gynecologica Scandinavica. PMID 28815546 DOI: 10.1111/aogs.13204 |
0.01 |
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2017 |
Zhao J, Liao Y, Chen J, Dong X, Gao Z, Zhang H, Wu X, Liu Z, Wu Y. Aberrant Buildup of All-Trans-Retinal Dimer, a Nonpyridinium Bisretinoid Lipofuscin Fluorophore, Contributes to the Degeneration of the Retinal Pigment Epithelium. Investigative Ophthalmology & Visual Science. 58: 1063-1075. PMID 28192797 DOI: 10.1167/iovs.16-20734 |
0.01 |
|
2016 |
Dong X, Wang X, Zhang F, Tian W. Genome-wide identification of regulatory sequences undergoing accelerated evolution in the human genome. Molecular Biology and Evolution. PMID 27401230 DOI: 10.1093/Molbev/Msw128 |
0.01 |
|
2016 |
Ma Y, Hu J, Zhang N, Dong X, Li Y, Yang B, Tian W, Wang X. Prediction of Candidate Drugs for Treating Pancreatic Cancer by Using a Combined Approach. Plos One. 11: e0149896. PMID 26910401 DOI: 10.1371/journal.pone.0149896 |
0.01 |
|
2016 |
Liu Q, Luo T, Dong X, Sun G, Liu Z, Gan M, Wu J, Shen X, Gao Q. Genetic features of Mycobacterium tuberculosis modern Beijing sublineage. Emerging Microbes & Infections. 5: e14. PMID 26905026 DOI: 10.1038/Emi.2016.14 |
0.01 |
|
2016 |
Dong X, Hao Y, Wang X, Tian W. LEGO: a novel method for gene set over-representation analysis by incorporating network-based gene weights. Scientific Reports. 6: 18871. PMID 26750448 DOI: 10.1038/srep18871 |
0.01 |
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2015 |
Zhang SS, Sun L, Dong X, Lu SJ, Tian W, Liu JX. Cellulose synthesis genes CESA6 and CSI1 are important for salt stress tolerance in Arabidopsis. Journal of Integrative Plant Biology. PMID 26503768 DOI: 10.1111/Jipb.12442 |
0.01 |
|
2014 |
Yu X, Lyu D, Dong X, He J, Yao K. Hypertension and risk of cataract: a meta-analysis. Plos One. 9: e114012. PMID 25474403 DOI: 10.1371/journal.pone.0114012 |
0.01 |
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2014 |
Jin QX, Dong XR, Chen JM, Yao K, Wu YL. Effects of organic solvents on two retinal pigment epithelial lipofuscin fluorophores, A2E and all-trans-retinal dimer. Journal of Zhejiang University. Science. B. 15: 661-9. PMID 25001225 DOI: 10.1631/jzus.B1300194 |
0.01 |
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2014 |
Zhou J, Dong X, Zhou Q, Wang H, Qian Y, Tian W, Ma D, Li X. microRNA expression profiling of heart tissue during fetal development. International Journal of Molecular Medicine. 33: 1250-60. PMID 24604530 DOI: 10.3892/ijmm.2014.1691 |
0.01 |
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2014 |
Yang C, Liu J, Dong X, Cai Z, Tian W, Wang X. Short-term and continuing stresses differentially interplay with multiple hormones to regulate plant survival and growth. Molecular Plant. 7: 841-55. PMID 24499771 DOI: 10.1093/Mp/Ssu013 |
0.01 |
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2013 |
Li J, Yao K, Yu X, Dong X, Gan L, Luo C, Wu Y. Identification of a novel lipofuscin pigment (iisoA2E) in retina and its effects in the retinal pigment epithelial cells. The Journal of Biological Chemistry. 288: 35671-82. PMID 24169698 DOI: 10.1074/jbc.M113.511386 |
0.01 |
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2013 |
Wang S, Dong X, Zhu Y, Wang C, Sun G, Luo T, Tian W, Zheng H, Gao Q. Revealing of Mycobacterium marinum transcriptome by RNA-seq. Plos One. 8: e75828. PMID 24098731 DOI: 10.1371/journal.pone.0075828 |
0.01 |
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2013 |
Radivojac P, Clark WT, Oron TR, Schnoes AM, Wittkop T, Sokolov A, Graim K, Funk C, Verspoor K, Ben-Hur A, Pandey G, Yunes JM, Talwalkar AS, Repo S, Souza ML, ... Dong X, et al. A large-scale evaluation of computational protein function prediction. Nature Methods. 10: 221-7. PMID 23353650 DOI: 10.1038/Nmeth.2340 |
0.01 |
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2012 |
Ma H, Hao Y, Dong X, Gong Q, Chen J, Zhang J, Tian W. Molecular mechanisms and function prediction of long noncoding RNA. Thescientificworldjournal. 2012: 541786. PMID 23319885 DOI: 10.1100/2012/541786 |
0.01 |
|
2012 |
Sun G, Luo T, Yang C, Dong X, Li J, Zhu Y, Zheng H, Tian W, Wang S, Barry CE, Mei J, Gao Q. Dynamic population changes in Mycobacterium tuberculosis during acquisition and fixation of drug resistance in patients. The Journal of Infectious Diseases. 206: 1724-33. PMID 22984115 DOI: 10.1093/infdis/jis601 |
0.01 |
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2012 |
Kang Y, Dong X, Zhou Q, Zhang Y, Cheng Y, Hu R, Su C, Jin H, Liu X, Ma D, Tian W, Li X. Identification of novel candidate maternal serum protein markers for Down syndrome by integrated proteomic and bioinformatic analysis. Prenatal Diagnosis. 32: 284-92. PMID 22430729 DOI: 10.1002/pd.3829 |
0.01 |
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2012 |
Sun S, Dong X, Fu Y, Tian W. An iterative network partition algorithm for accurate identification of dense network modules. Nucleic Acids Research. 40: e18. PMID 22121225 DOI: 10.1093/nar/gkr1103 |
0.01 |
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