Hao Deng, Ph.D. - Publications

Affiliations: 
2009 Georgia Institute of Technology, Atlanta, GA 
Area:
Applied Mathematics

201 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Yang C, Mei L, Deng H, Xu Z, Chen B, Kan R. Wavelength modulation spectroscopy by employing the first harmonic phase angle method. Optics Express. 27: 12137-12146. PMID 31052758 DOI: 10.1364/OE.27.012137  0.44
2019 Shen QK, Deng H, Wang SB, Tian YS, Quan ZS. Synthesis, and evaluation of in vitro and in vivo anticancer activity of 14-substituted oridonin analogs: A novel and potent cell cycle arrest and apoptosis inducer through the p53-MDM2 pathway. European Journal of Medicinal Chemistry. 173: 15-31. PMID 30981113 DOI: 10.1016/j.ejmech.2019.04.005  0.44
2019 Mei L, Li FZ, Lan JH, Wang CZ, Xu C, Deng H, Wu QY, Hu KQ, Wang L, Chai ZF, Chen J, Gibson JK, Shi WQ. Anion-adaptive crystalline cationic material for TcO trapping. Nature Communications. 10: 1532. PMID 30948745 DOI: 10.1038/s41467-019-09504-3  0.44
2019 Guo Y, Wang P, Li X, Zhu S, Xu H, Li S, Deng H, Yuan L. Identifying a c.5722_5723del mutation in a Han-Chinese family with breast cancer. Bioscience Reports. PMID 30940775 DOI: 10.1042/BSR20182471  0.52
2019 Xiang Q, Yuan L, Cao Y, Xu H, Li Y, Deng H. Identification of a Heterozygous Mutation in the Gene in a Hui-Chinese Family with Corneal Dystrophy. Journal of Ophthalmology. 2019: 2824179. PMID 30915236 DOI: 10.1155/2019/2824179  0.52
2019 Shaydenfish D, Scheffenbichler FT, Kelly BJ, Lihn AL, Deng H, Nourmahnad A, Xu X, Houle TT, Eikermann M, Forman SA. Effects of Anticholinesterase Reversal Under General Anesthesia on Postoperative Cardiovascular Complications: A Retrospective Cohort Study. Anesthesia and Analgesia. PMID 30896593 DOI: 10.1213/ANE.0000000000004099  0.32
2019 Wang P, Yuan L, Chen H, Xu H, Yang Z, Deng S, Deng H. Hemizygous F8 p.G201E mutation identified in a Chinese family with haemophilia A. Journal of the Chinese Medical Association : Jcma. 82: 25-29. PMID 30839399 DOI: 10.1097/JCMA.0000000000000002  0.52
2019 Wang M, Guo Y, Rong P, Xu H, Gong L, Deng H, Yuan L. COL1A2 p.Gly1066Val variant identified in a Han Chinese family with osteogenesis imperfecta type I. Molecular Genetics & Genomic Medicine. e619. PMID 30829463 DOI: 10.1002/mgg3.619  0.52
2019 Xia H, Huang X, Xu H, Zhou YA, Gong L, Yang Z, Lv J, Deng H. GJB2 c.235delC variant associated with autosomal recessive nonsyndromic hearing loss and auditory neuropathy spectrum disorder. Genetics and Molecular Biology. PMID 30816908 DOI: 10.1590/1678-4685-gmb-2017-0318  0.68
2019 Yu Z, Xia M, Li H, Zhong T, Zhao F, Deng H, Li Z, Li D, Wang D, Lai P. Implementation of digital optical phase conjugation with embedded calibration and phase rectification. Scientific Reports. 9: 1537. PMID 30733574 DOI: 10.1038/s41598-018-38326-4  0.4
2019 Xiao H, Huang X, Xu H, Chen X, Xiong W, Yang Z, Deng X, He Z, Deng H. A novel splice-site mutation in the ATP2C1 gene of a Chinese family with Hailey-Hailey disease. Journal of Cellular Biochemistry. 120: 3630-3636. PMID 30654607 DOI: 10.1002/jcb.27640  0.68
2019 Wu S, Deng S, Song Z, Xu H, Yang Z, Liu X, Qi L, Deng H, Yuan L. A Disease-Causing FRMD7 Variant in a Chinese Family with Infantile Nystagmus. Journal of Molecular Neuroscience : Mn. PMID 30618027 DOI: 10.1007/s12031-018-1245-5  0.52
2018 Luan T, Cao LH, Deng H, Shen QK, Tian YS, Quan ZS. Design and Synthesis of C-19 Isosteviol Derivatives as Potent and Highly Selective Antiproliferative Agents. Molecules (Basel, Switzerland). 24. PMID 30598028 DOI: 10.3390/molecules24010121  0.44
2018 Wang Q, Wang B, Deng H, Shangguan Y, Lin Y, Zhang Y, Zhang Z, Xiao Y, Guo H, Zhang C. Silver-Catalyzed Three-Component Difunctionalization of Alkenes via Radical Pathways: Access to CF3-Functionalized Alkyl-Substituted 1,4-Naphthoquinone Derivatives. The Journal of Organic Chemistry. PMID 30592606 DOI: 10.1021/acs.joc.8b02997  0.44
2018 Xiang Q, Cao Y, Xu H, Guo Y, Yang Z, Xu L, Yuan L, Deng H. Identification of Novel Pathogenic Variants in a Han Chinese Family with Stargardt Disease. Bioscience Reports. PMID 30563929 DOI: 10.1042/BSR20180872  0.52
2018 Liu D, Cheng D, Houle TT, Chen L, Zhang W, Deng H. Machine learning methods for automatic pain assessment using facial expression information: Protocol for a systematic review and meta-analysis. Medicine. 97: e13421. PMID 30544420 DOI: 10.1097/MD.0000000000013421  0.32
2018 Fan K, Zhu H, Xu H, Mao P, Yuan L, Deng H. The identification of a transthyretin variant p.D38G in a Chinese family with early-onset leptomeningeal amyloidosis. Journal of Neurology. PMID 30470998 DOI: 10.1007/s00415-018-9125-z  0.52
2018 Hu P, Yuan L, Deng H. Molecular genetics of the POMT1-related muscular dystrophy-dystroglycanopathies. Mutation Research. 778: 45-50. PMID 30454682 DOI: 10.1016/j.mrrev.2018.09.002  0.36
2018 Xiang Q, Guo Y, Cao Y, Xiong W, Deng X, Xu H, Li Y, Du D, Deng H. Identification of a CNGB1 Frameshift Mutation in a Han Chinese Family with Retinitis Pigmentosa. Optometry and Vision Science : Official Publication of the American Academy of Optometry. PMID 30451805 DOI: 10.1097/OPX.0000000000001305  0.52
2018 Li W, Liu J, Xiao C, Deng H, Xie Q, Han H. A Novel 3D Connection Algorithm of Mitochondria From ATUM-SEM Stacks Based on Segmentation Information in Context. Conference Proceedings : ... Annual International Conference of the Ieee Engineering in Medicine and Biology Society. Ieee Engineering in Medicine and Biology Society. Annual Conference. 2018: 5105-5108. PMID 30441489 DOI: 10.1109/EMBC.2018.8513488  0.52
2018 Li W, Liu J, Xiao C, Deng H, Xie Q, Han H. A fast forward 3D connection algorithm for mitochondria and synapse segmentations from serial EM images. Biodata Mining. 11: 24. PMID 30410581 DOI: 10.1186/s13040-018-0183-7  0.52
2018 Xiao H, Deng S, Deng X, Gu S, Yang Z, Yin H, Deng H. Mutation Analysis of the ATP7B Gene in Seven Chinese Families with Wilson's Disease. Digestion. 1-8. PMID 30384382 DOI: 10.1159/000493314  0.52
2018 Kong Y, Yan T, Gong S, Deng H, Zhang G, Wang J. Opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) and postoperative nausea and vomiting. American Journal of Translational Research. 10: 2764-2780. PMID 30323865  0.4
2018 Zhang T, Han Y, Wang J, Hou D, Deng H, Deng YL, Song Z. Comparative Epidemiological Investigation of Alzheimer's Disease and Colorectal Cancer: The Possible Role of Gastrointestinal Conditions in the Pathogenesis of AD. Frontiers in Aging Neuroscience. 10: 176. PMID 30323761 DOI: 10.3389/fnagi.2018.00176  0.4
2018 Yuan L, Deng X, Song Z, Deng S, Zheng W, Mao P, Deng H. Systematic analysis of genetic variants in patients with essential tremor. Brain and Behavior. e01100. PMID 30252209 DOI: 10.1002/brb3.1100  0.4
2018 Zhang Z, Yu T, Xie L, Li Y, Ke X, Liu Y, Huang S, Deng H, Bai Y. Biomechanical bearing-based typing method for osteonecrosis of the femoral head: ABC typing. Experimental and Therapeutic Medicine. 16: 2682-2688. PMID 30186501 DOI: 10.3892/etm.2018.6488  0.48
2018 Deng H, Fan K, Jankovic J. The Role of TMEM230 Gene in Parkinson's Disease. Journal of Parkinson's Disease. PMID 30175983 DOI: 10.3233/JPD-181421  0.36
2018 Wu Y, Yuan L, Guo Y, Lu A, Zheng W, Xu H, Yang Y, Hu P, Gu S, Wang B, Deng H. Identification of a GNE homozygous mutation in a Han-Chinese family with GNE myopathy. Journal of Cellular and Molecular Medicine. PMID 30160005 DOI: 10.1111/jcmm.13827  0.52
2018 Xia H, Huang X, Xu H, Guo Y, Hu P, Deng X, Yang Z, Liu A, Deng H. An Frameshift Variant Associated with Auditory Neuropathy Spectrum Disorder. Current Genomics. 19: 370-374. PMID 30065612 DOI: 10.2174/1389202919666171113152951  0.68
2018 Yan P, Tang H, Chen X, Ji S, Jin W, Zhang J, Shen J, Deng H, Zhao X, Shen Q, Huang H. Tamoxifen attenuates dialysate-induced peritoneal fibrosis by inhibiting GSK3β/β-catenin axis activation. Bioscience Reports. PMID 30061174 DOI: 10.1042/BSR20180240  0.32
2018 Xiao H, Yuan L, Xu H, Yang Z, Huang F, Song Z, Yang Y, Zeng C, Deng H. Novel and Recurring Disease-Causing NF1 Variants in Two Chinese Families with Neurofibromatosis Type 1. Journal of Molecular Neuroscience : Mn. PMID 30046999 DOI: 10.1007/s12031-018-1128-9  0.52
2018 Rudolph MI, Ng PY, Deng H, Scheffenbichler FT, Grabitz SD, Wanderer JP, Houle TT, Eikermann M. Comparison of a novel clinical score to estimate the risk of REsidual neuromuscular block Prediction Score and the last train-of-four count documented in the electronic anaesthesia record: A retrospective cohort study of electronic data on file. European Journal of Anaesthesiology. PMID 30020144 DOI: 10.1097/EJA.0000000000000861  0.32
2018 Xiao C, Li W, Deng H, Chen X, Yang Y, Xie Q, Han H. Effective automated pipeline for 3D reconstruction of synapses based on deep learning. Bmc Bioinformatics. 19: 263. PMID 30005590 DOI: 10.1186/s12859-018-2232-0  0.52
2018 Li W, Chen H, Deng H, Kuang Z, Long M, Chen D, Liao X, Li M, Rock DL, Luo S, Hao W. Orf Virus Encoded Protein ORFV119 Induces Cell Apoptosis Through the Extrinsic and Intrinsic Pathways. Frontiers in Microbiology. 9: 1056. PMID 29896166 DOI: 10.3389/fmicb.2018.01056  0.52
2018 Chen H, Yuan L, Song Z, Deng X, Yang Z, Gong L, Zi X, Deng H. Genetic Analysis of LRRK1 and LRRK2 Variants in Essential Tremor Patients. Genetic Testing and Molecular Biomarkers. PMID 29812962 DOI: 10.1089/gtmb.2017.0277  0.52
2018 Deng H, Sun C, Sun Y, Li H, Yang L, Wu D, Gao Q, Jiang X. Lipid, Protein, and MicroRNA Composition Within Mesenchymal Stem Cell-Derived Exosomes. Cellular Reprogramming. PMID 29782191 DOI: 10.1089/cell.2017.0047  0.4
2018 Xiao H, Guo Y, Yi J, Xia H, Xu H, Yuan L, Hu P, Yang Z, He Z, Lu H, Deng H. Identification of a Novel Keratin 9 Missense Mutation in a Chinese Family with Epidermolytic Palmoplantar Keratoderma. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 46: 1919-1929. PMID 29719290 DOI: 10.1159/000489381  0.52
2018 Tang L, Wei F, Wu Y, He Y, Shi L, Xiong F, Gong Z, Guo C, Li X, Deng H, Cao K, Zhou M, Xiang B, Li X, Li Y, et al. Role of metabolism in cancer cell radioresistance and radiosensitization methods. Journal of Experimental & Clinical Cancer Research : Cr. 37: 87. PMID 29688867 DOI: 10.1186/s13046-018-0758-7  0.4
2018 Shelton KT, Qu J, Bilotta F, Brown EN, Cudemus G, D'Alessandro DA, Deng H, DiBiasio A, Gitlin JA, Hahm EY, Hobbs LE, Houle TT, Ibala R, Loggia M, Pavone KJ, et al. Minimizing ICU Neurological Dysfunction with Dexmedetomidine-induced Sleep (MINDDS): protocol for a randomised, double-blind, parallel-arm, placebo-controlled trial. Bmj Open. 8: e020316. PMID 29678977 DOI: 10.1136/bmjopen-2017-020316  0.32
2018 Deng H, Zheng W, Song Z. The genetics and molecular biology of fever-associated seizures or epilepsy. Expert Reviews in Molecular Medicine. 20: e3. PMID 29661262 DOI: 10.1017/erm.2018.2  0.36
2018 Wang P, Guo Y, Song C, Liu Y, Deng H. PINK1 p.K520RfsX3 Mutation Identified in a Chinese Family with Early-onset Parkinson's disease. Neuroscience Letters. PMID 29655942 DOI: 10.1016/j.neulet.2018.04.020  0.48
2018 Wu Y, Xia H, Yuan J, Xu H, Deng X, Liu J, Zhang H, Deng H. Identification of a Missense Mutation in the α-galactosidase A Gene in a Chinese Family with Fabry Disease. Current Genomics. 19: 70-75. PMID 29491734 DOI: 10.2174/1389202918666170915155033  0.52
2018 Huang X, Yuan L, Xu H, Zheng W, Cao Y, Yi J, Guo Y, Yang Z, Li Y, Deng H. Identification of a Novel Mutation in the ABCA4 Gene in a Chinese Family with Retinitis Pigmentosa Using Exome Sequencing. Bioscience Reports. PMID 29437900 DOI: 10.1042/BSR20171300  0.68
2018 Zhao J, Li H, Deng H, Zhu L, Zhou B, Yang M, Liu Q, Luo G, Yang Y, Ma W. LncRNA gadd7, increased in varicocele patients, suppresses cell proliferation and promotes cell apoptosis. Oncotarget. 9: 5105-5110. PMID 29435165 DOI: 10.18632/oncotarget.23696  0.4
2018 Albrecht D, Ahmed S, Kettner N, Borra R, Cohen-Adad J, Deng H, Houle T, Opalacz A, Roth S, Melo MV, Chen L, Mao J, Hooker J, Loggia ML, Zhang Y. Neuroinflammation of the spinal cord and nerve roots in chronic radicular pain patients. Pain. PMID 29419657 DOI: 10.1097/j.pain.0000000000001171  0.44
2018 Jo I, Deng H, Liu Y, Pfeiffer LN, West KW, Baldwin KW, Shayegan M. Cyclotron Orbits of Composite Fermions in the Fractional Quantum Hall Regime. Physical Review Letters. 120: 016802. PMID 29350938 DOI: 10.1103/PhysRevLett.120.016802  0.48
2017 Deng H, Wang P, Jankovic J. The genetics of Parkinson disease. Ageing Research Reviews. PMID 29288112 DOI: 10.1016/j.arr.2017.12.007  0.48
2017 Xie Q, Chen X, Deng H, Liu D, Sun Y, Zhou X, Yang Y, Han H. An automated pipeline for bouton, spine, and synapse detection of in vivo two-photon images. Biodata Mining. 10: 40. PMID 29270230 DOI: 10.1186/s13040-017-0161-5  0.52
2017 Yuan L, Zheng W, Yang Z, Deng X, Song Z, Deng H. Association of the AADAC gene and Tourette syndrome in a Han Chinese cohort. Neuroscience Letters. PMID 29253601 DOI: 10.1016/j.neulet.2017.12.034  0.52
2017 Kong X, Deng H, Alston T, Kong Y, Wang J. Association of opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with nicotine dependence. Oncotarget. 8: 84329-84337. PMID 29137427 DOI: 10.18632/oncotarget.20939  0.4
2017 Lu Q, Guo Y, Yi J, Deng X, Yang Z, Yuan X, Deng H. Identification of an ND4 Mutation in Leber Hereditary Optic Neuropathy. Optometry and Vision Science : Official Publication of the American Academy of Optometry. PMID 29116953 DOI: 10.1097/OPX.0000000000001147  0.52
2017 Deng J, Yao D, Lu C, Wen Z, Yan Y, He Z, Wu H, Deng H. Oral Chinese herbal medicine for psoriasis vulgaris: protocol for a randomised, double-blind, double-dummy, multicentre clinical trial. Bmj Open. 7: e014475. PMID 29101128 DOI: 10.1136/bmjopen-2016-014475  0.32
2017 Kong X, Deng H, Gong S, Alston T, Kong Y, Wang J. Lack of associations of the opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with alcohol dependence: review and meta-analysis of retrospective controlled studies. Bmc Medical Genetics. 18: 120. PMID 29070014 DOI: 10.1186/s12881-017-0478-4  0.4
2017 Chen Q, Yuan L, Deng X, Yang Z, Zhang S, Deng S, Lu H, Deng H. A Missense Variant p.Ala117Ser in the Transthyretin Gene of a Han Chinese Family with Familial Amyloid Polyneuropathy. Molecular Neurobiology. PMID 28762097 DOI: 10.1007/s12035-017-0694-0  0.52
2017 Xia H, Hu P, Yuan L, Xiong W, Xu H, Yi J, Yang Z, Deng X, Guo Y, Deng H. A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder. Molecular Medicine Reports. PMID 28731162 DOI: 10.3892/mmr.2017.7053  0.52
2017 Burns SM, Turner DP, Sexton KE, Deng H, Houle TT. Using Search Engines to Investigate Shared Migraine Experiences. Headache. PMID 28660638 DOI: 10.1111/head.13130  0.32
2017 Lee JM, Akeju O, Terzakis K, Pavone KJ, Deng H, Houle TT, Firth PG, Shank ES, Brown EN, Purdon PL. A Prospective Study of Age-dependent Changes in Propofol-induced Electroencephalogram Oscillations in Children. Anesthesiology. PMID 28657957 DOI: 10.1097/ALN.0000000000001717  0.32
2017 Li W, Deng H, Rao Q, Xie Q, Chen X, Han H. An automated pipeline for mitochondrial segmentation on ATUM-SEM stacks. Journal of Bioinformatics and Computational Biology. 1750015. PMID 28610459 DOI: 10.1142/S0219720017500159  0.52
2017 He D, Hu P, Deng X, Song Z, Yuan L, Yuan X, Deng H. Genetic analysis of the RIC3 gene in Han Chinese patients with Parkinson's disease. Neuroscience Letters. PMID 28606768 DOI: 10.1016/j.neulet.2017.06.007  0.4
2017 Liu N, Deng H, He T, Liu Y, Zhang L, Li J. Measurements of new absorption lines of acetylene at 1.53μm using a tunable diode laser absorption spectrometer. Spectrochimica Acta. Part a, Molecular and Biomolecular Spectroscopy. 186: 1-7. PMID 28600991 DOI: 10.1016/j.saa.2017.05.062  0.48
2017 Deng H, Xiao H. The role of the ATP2C1 gene in Hailey-Hailey disease. Cellular and Molecular Life Sciences : Cmls. PMID 28551824 DOI: 10.1007/s00018-017-2544-7  0.36
2017 Deng H, Tan T, He Q, Lin Q, Yang Z, Zhu A, Guan L, Xiao J, Song Z, Guo Y. Identification of a missense HOXD13 mutation in a Chinese family with syndactyly type I-c using exome sequencing. Molecular Medicine Reports. PMID 28498426 DOI: 10.3892/mmr.2017.6576  0.52
2017 Yu J, Liu Y, Guo C, Zhang S, Gong Z, Tang Y, Yang L, He Y, Lian Y, Li X, Deng H, Liao Q, Li X, Li Y, Li G, et al. Upregulated long non-coding RNA LINC00152 expression is associated with progression and poor prognosis of tongue squamous cell carcinoma. Journal of Cancer. 8: 523-530. PMID 28367232 DOI: 10.7150/jca.17510  0.48
2017 Yuan L, Song Z, Deng X, Yang Z, Yang Y, Guo Y, Lu H, Deng H. Genetic Analysis of FBXO2, FBXO6, FBXO12, and FBXO41 Variants in Han Chinese Patients with Sporadic Parkinson's Disease. Neuroscience Bulletin. PMID 28341977 DOI: 10.1007/s12264-017-0122-5  0.52
2017 Ji S, Deng H, Jin W, Yan P, Wang R, Pang L, Zhou J, Zhang J, Chen X, Zhao X, Shen J. Beta-catenin participates in dialysate-induced peritoneal fibrosis via enhanced peritoneal cell epithelial-to-mesenchymal transition. Febs Open Bio. 7: 265-273. PMID 28174691 DOI: 10.1002/2211-5463.12182  0.32
2017 Hu P, Wu S, Yuan L, Lin Q, Zheng W, Xia H, Xu H, Guan L, Deng H. Compound heterozygous POMT1 mutations in a Chinese family with autosomal recessive muscular dystrophy-dystroglycanopathy C1. Journal of Cellular and Molecular Medicine. PMID 28157257 DOI: 10.1111/jcmm.13068  0.52
2017 Lu Q, Yuan L, Xu H, Huang X, Yang Z, Yi J, Ni B, Chen Y, Deng H. Identification of a missense mutation in the tyrosinase gene in a Chinese family with oculocutaneous albinism type 1. Molecular Medicine Reports. PMID 28112372 DOI: 10.3892/mmr.2017.6137  0.68
2016 Sun J, Deng H, Liu N, Wang H, Yu B, Li J. Mid-infrared gas absorption sensor based on a broadband external cavity quantum cascade laser. The Review of Scientific Instruments. 87: 123101. PMID 28040920 DOI: 10.1063/1.4968041  0.48
2016 Foo JN, Tan LC, Irwan ID, Au WL, Low HQ, Prakash KM, Ahmad-Annuar A, Bei J, Chan AY, Chen CM, Chen YC, Chung SJ, Deng H, Lim SY, Mok V, et al. Genome-wide association study of Parkinson's disease in East Asians. Human Molecular Genetics. PMID 28011712 DOI: 10.1093/hmg/ddw379  0.52
2016 Deng S, Xu H, Yuan J, Xiao J, Yuan L, Deng X, Guan L, Zhu A, Rong P, Zhang J, Deng H. Identification of a novel collagen type IV alpha-4 (COL4A4) mutation in a Chinese family with autosomal dominant Alport syndrome using exome sequencing. The Indian Journal of Medical Research. 144: 200-205. PMID 27934798 DOI: 10.4103/0971-5916.195026  0.52
2016 Deng H, Li Y, Wu L, Ma X. The novel composite mechanism of ammonium molybdophosphate loaded on silica matrix and its ion exchange breakthrough curves for cesium. Journal of Hazardous Materials. PMID 27823822 DOI: 10.1016/j.jhazmat.2016.10.068  0.4
2016 Yuan L, Song Z, Deng X, Zheng W, Guo Y, Yang Z, Deng H. Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease. Scientific Reports. 6: 33850. PMID 27653456 DOI: 10.1038/srep33850  0.52
2016 Zhang X, Wang Y, Yan Y, Wang C, Zhang G, Cheng Z, Ren F, Deng H, Zhang J. Origin of high thermoelectric performance of FeNb1-xZr/HfxSb1-ySny alloys: A first-principles study. Scientific Reports. 6: 33120. PMID 27604826 DOI: 10.1038/srep33120  0.32
2016 Liang F, Li Q, Li X, Li Z, Gong Z, Deng H, Xiang B, Zhou M, Li X, Li G, Zeng Z, Xiong W. TSC22D2 interacts with PKM2 and inhibits cell growth in colorectal cancer. International Journal of Oncology. PMID 27573352 DOI: 10.3892/ijo.2016.3599  0.4
2016 Wu Y, Hu P, Xu H, Yuan J, Yuan L, Xiong W, Deng X, Deng H. A novel heterozygous COL4A4 missense mutation in a Chinese family with focal segmental glomerulosclerosis. Journal of Cellular and Molecular Medicine. PMID 27469977 DOI: 10.1111/jcmm.12924  0.52
2016 Lu Q, Song Z, Deng X, Xiong W, Xu H, Zhang Z, Lu H, Deng H. SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson's disease. Neuroscience Letters. PMID 27353511 DOI: 10.1016/j.neulet.2016.06.053  0.52
2016 Deng H, He D, Rong P, Xu H, Yuan L, Li L, Lu Q, Guo Y. Novel CLCN7 mutation identified in a Han Chinese family with autosomal dominant osteopetrosis-2. Molecular Pain. 12. PMID 27325559 DOI: 10.1177/1744806916652628  0.52
2016 Deng HX, Shi Y, Yang Y, Ahmeti KB, Miller N, Huang C, Cheng L, Zhai H, Deng S, Nuytemans K, Corbett NJ, Kim MJ, Deng H, Tang B, Yang Z, et al. Identification of TMEM230 mutations in familial Parkinson's disease. Nature Genetics. PMID 27270108 DOI: 10.1038/ng.3589  0.52
2016 Deng H, Zhang L, Mao X, Qu H. Interactive Urban Context-Aware Visualization via Multiple Disocclusion Operators. Ieee Transactions On Visualization and Computer Graphics. 22: 1862-1874. PMID 27244709 DOI: 10.1109/TVCG.2015.2469661  0.48
2016 Deng H, Huang X, Yuan L. Molecular genetics of the COL2A1-related disorders. Mutation Research. Reviews in Mutation Research. 768: 1-13. PMID 27234559 DOI: 10.1016/j.mrrev.2016.02.003  0.68
2016 Deng H, Deng S, Xu H, Deng HX, Chen Y, Yuan L, Deng X, Yang S, Guan L, Zhang J, Yuan H, Guo Y. Exome Sequencing of a Pedigree Reveals S339L Mutation in the TLN2 Gene as a Cause of Fifth Finger Camptodactyly. Plos One. 11: e0155180. PMID 27223613 DOI: 10.1371/journal.pone.0155180  0.68
2016 Deng H, Lu Q, Xu H, Deng X, Yuan L, Yang Z, Guo Y, Lin Q, Xiao J, Guan L, Song Z. Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing. Plos One. 11: e0155908. PMID 27196565 DOI: 10.1371/journal.pone.0155908  0.52
2016 Chen H, Huang X, Yuan L, Xia H, Xu H, Yang Y, Zheng W, Deng H. A homozygous parkin p.G284R mutation in a Chinese family with autosomal recessive juvenile parkinsonism. Neuroscience Letters. PMID 27177722 DOI: 10.1016/j.neulet.2016.05.011  0.68
2016 Lu Q, Deng X, Song Z, Guo Y, Yang Y, Deng H. Mutation analysis of the CHCHD2 gene in Chinese Han patients with Parkinson's disease. Parkinsonism & Related Disorders. PMID 27118487 DOI: 10.1016/j.parkreldis.2016.04.012  0.48
2016 Yuan L, Yi J, Lin Q, Xu H, Deng X, Xiong W, Xiao J, Jiang C, Yuan X, Chen Y, Deng H. Identification of a PRX variant in a Chinese family with congenital cataract by exome sequencing. Qjm : Monthly Journal of the Association of Physicians. PMID 27081207 DOI: 10.1093/qjmed/hcw058  0.68
2016 Zhou H, Deng H, Chen L, Yang Y, Jia C, Huang D. Exploiting syntactic and semantics information for chemical-disease relation extraction. Database : the Journal of Biological Databases and Curation. 2016. PMID 27081156 DOI: 10.1093/database/baw048  0.68
2016 Xia H, Xu H, Deng X, Yuan L, Xiong W, Yang Z, Deng H. Compound heterozygous GJB2 mutations associated to a consanguineous Han family with autosomal recessive non-syndromic hearing loss. Acta Oto-Laryngologica. 1-4. PMID 27045574 DOI: 10.3109/00016489.2016.1157727  0.52
2016 Yuan L, Song Z, Deng X, Zheng W, Yang Z, Yang Y, Deng H. Genetic analysis of FGF20 variants in Chinese Han patients with essential tremor. Neuroscience Letters. PMID 27040428 DOI: 10.1016/j.neulet.2016.03.055  0.52
2016 Jiang J, Deng H, Li X, Tong S, He P, Zhou H. Research on Effective Oxygen Window Influencing the Capacity of Li-O2 Batteries. Acs Applied Materials & Interfaces. PMID 27029322 DOI: 10.1021/acsami.6b02586  0.36
2016 Yuan L, Xu H, Yuan J, Deng X, Xiong W, Yang Z, Huang Y, Deng H. A novel FN1 variant associated with familial hematuria: TBMN? Clinical Biochemistry. PMID 26968105 DOI: 10.1016/j.clinbiochem.2016.01.026  0.52
2016 Wang Y, Pan X, Xue D, Li Y, Zhang X, Kuang B, Zheng J, Deng H, Li X, Xiong W, Zeng Z, Li G. [Application of next generation sequencing technology in mendelian movement disorders]. Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences. 41: 197-205. PMID 26932219 DOI: 10.11817/j.issn.1672-7347.2016.02.013  0.4
2016 Ma J, Yang Y, Dai X, Chen Y, Deng H, Zhou H, Guo S, Yan G. Effects of adding bulking agent, inorganic nutrient and microbial inocula on biopile treatment for oil-field drilling waste. Chemosphere. 150: 17-23. PMID 26891352 DOI: 10.1016/j.chemosphere.2016.01.123  0.68
2016 Yuan L, Song Z, Deng X, Xiong W, Yang Z, Deng H. Association of the MTHFR rs1801131 and rs1801133 variants in sporadic Parkinson's disease patients. Neuroscience Letters. PMID 26806866 DOI: 10.1016/j.neulet.2016.01.031  0.52
2015 Lu M, Zhao C, Wang Q, You G, Wang Y, Deng H, Chen G, Xia S, Zhao J, Wang B, Li X, Shao L, Wu Y, Zhao L, Zhou H. Preparation, characterization and in vivo investigation of blood-compatible hemoglobin-loaded nanoparticles as oxygen carriers. Colloids and Surfaces. B, Biointerfaces. 139: 171-179. PMID 26708138 DOI: 10.1016/j.colsurfb.2015.12.012  0.68
2015 Tan T, Song Z, Yuan L, Xiong W, Deng X, Ni B, Chen Y, Deng H. Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson's disease. Neuroscience Letters. PMID 26704436 DOI: 10.1016/j.neulet.2015.12.029  0.68
2015 Wang C, Lei S, Cao H, Qiu S, Liu J, Deng H, Yan C. Regioselective Copper-Catalyzed Dicarbonylation of Imidazo[1,2-a]pyridines with N,N-Disubstituted Acetamide or Acetone: An Approach to 1,2-Diketones using Molecular Oxygen. The Journal of Organic Chemistry. PMID 26595127 DOI: 10.1021/acs.joc.5b02417  0.52
2015 Deng H, Tan T, Yuan L. Advances in the molecular genetics of non-syndromic polydactyly. Expert Reviews in Molecular Medicine. 17: e18. PMID 26515020 DOI: 10.1017/erm.2015.18  0.36
2015 Zhou H, Li J, Yuan J, Chen T, Deng H, Zhang J, Zeng H, Shan Z, Chen W. The effects and mechanism of arsenic trioxide in combination with rmhTRAIL in multiple myeloma. Experimental Hematology. PMID 26505911 DOI: 10.1016/j.exphem.2015.10.004  0.68
2015 Hu Y, Deng H, Xu S, Zhang J. MicroRNAs Regulate Mitochondrial Function in Cerebral Ischemia-Reperfusion Injury. International Journal of Molecular Sciences. 16: 24895-917. PMID 26492239 DOI: 10.3390/ijms161024895  0.32
2015 Gong Z, Yang Q, Zeng Z, Zhang W, Li X, Zu X, Deng H, Chen P, Liao Q, Xiang B, Zhou M, Li X, Li Y, Xiong W, Li G. An integrative transcriptomic analysis reveals p53 regulated miRNA, mRNA, and lncRNA networks in nasopharyngeal carcinoma. Tumour Biology : the Journal of the International Society For Oncodevelopmental Biology and Medicine. PMID 26462838 DOI: 10.1007/s13277-015-4156-x  0.4
2015 Guo Y, Tan T, Deng X, Song Z, Yang Z, Yang Y, Deng H. TCEANC2 rs10788972 and rs12046178 variants in the PARK10 region in Chinese Han patients with sporadic Parkinson's disease. Neurobiology of Aging. PMID 26432391 DOI: 10.1016/j.neurobiolaging.2015.09.002  0.52
2015 Hu Y, Liu N, Zhang P, Pan C, Zhang Y, Tang Y, Deng H, Aimaiti M, Zhang Y, Zhou H, Wu G, Tang Z. Preclinical Studies of Stem Cell Transplantation in Intracerebral Hemorrhage: a Systemic Review and Meta-Analysis. Molecular Neurobiology. PMID 26409481 DOI: 10.1007/s12035-015-9441-6  0.68
2015 Xu K, Xiong W, Zhou M, Wang H, Yang J, Li X, Chen P, Liao Q, Deng H, Li X, Li G, Zeng Z. Integrating ChIP-sequencing and digital gene expression profiling to identify BRD7 downstream genes and construct their regulating network. Molecular and Cellular Biochemistry. PMID 26407966 DOI: 10.1007/s11010-015-2568-y  0.4
2015 Zheng W, Chen H, Deng X, Yuan L, Yang Y, Song Z, Yang Z, Wu Y, Deng H. Identification of a Novel Mutation in the Titin Gene in a Chinese Family with Limb-Girdle Muscular Dystrophy 2J. Molecular Neurobiology. PMID 26392295 DOI: 10.1007/s12035-015-9439-0  0.52
2015 Zhou H, Zhang L, Wu L, Zou X, Luo X, Xia K, Wang Y, Xu X, Ge X, Sun C, Deng H, Fombonne E, Jiang YH, Yan W, Wang Y. Validity and reliability analysis of the Chinese parent version of the Autism Spectrum Rating Scale (6-18 years). Psychiatry Research. PMID 26384573 DOI: 10.1016/j.psychres.2015.09.003  0.68
2015 Deng S, Deng X, Song Z, Xiu X, Guo Y, Xiao J, Deng H. Systematic Genetic Analysis of the SMPD1 Gene in Chinese Patients with Parkinson's Disease. Molecular Neurobiology. PMID 26377108 DOI: 10.1007/s12035-015-9426-5  0.48
2015 Xia H, Huang X, Guo Y, Hu P, He G, Deng X, Xu H, Yang Z, Deng H. Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss. Plos One. 10: e0136306. PMID 26308726 DOI: 10.1371/journal.pone.0136306  0.68
2015 Deng H, Xia H, Deng S. Genetic basis of human left-right asymmetry disorders. Expert Reviews in Molecular Medicine. 16: e19. PMID 26258520 DOI: 10.1017/erm.2014.22  0.52
2015 Zeng Z, Bo H, Gong Z, Lian Y, Li X, Li X, Zhang W, Deng H, Zhou M, Peng S, Li G, Xiong W. AFAP1-AS1, a long noncoding RNA upregulated in lung cancer and promotes invasion and metastasis. Tumour Biology : the Journal of the International Society For Oncodevelopmental Biology and Medicine. PMID 26245991 DOI: 10.1007/s13277-015-3860-x  0.4
2015 Zhou H, Deng H, Huang D, Zhu M. Hedge Scope Detection in Biomedical Texts: An Effective Dependency-Based Method. Plos One. 10: e0133715. PMID 26218847 DOI: 10.1371/journal.pone.0133715  0.68
2015 Yuan L, Deng X, Song Z, Yang Z, Ni B, Chen Y, Deng H. Genetic analysis of the RAB39B gene in Chinese Han patients with Parkinson's disease. Neurobiology of Aging. 36: 2907.e11-2. PMID 26163985 DOI: 10.1016/j.neurobiolaging.2015.06.019  0.68
2015 Shen G, Zhou H, Jia Z, Deng H. Diagnostic performance of diffusion-weighted MRI for detection of pelvic metastatic lymph nodes in patients with cervical cancer: a systematic review and meta-analysis. The British Journal of Radiology. 88: 20150063. PMID 26111112 DOI: 10.1259/bjr.20150063  0.68
2015 Deng H, Riederer P, Deng HX, Le W, Xiong W, Guo Y. Human Genetic Diseases. Biomed Research International. 2015: 315216. PMID 26078946 DOI: 10.1155/2015/315216  0.48
2015 Huang X, Deng X, Xu H, Wu S, Yuan L, Yang Z, Yang Y, Deng H. Identification of a Novel Mutation in the COL2A1 Gene in a Chinese Family with Spondyloepiphyseal Dysplasia Congenita. Plos One. 10: e0127529. PMID 26030151 DOI: 10.1371/journal.pone.0127529  0.68
2015 Shen G, Zhou H, Jia Z, Deng H. Diagnostic performance of diffusion-weighted magnetic resonance imaging for detection of pelvic metastatic lymph nodes in patients with cervical cancer: A systematic review and meta-analysis. The British Journal of Radiology. 20150063. PMID 26023947 DOI: 10.1259/bjr.20150063  0.68
2015 Ding J, Huang X, Shao N, Zhou H, Lee DF, Faiola F, Fidalgo M, Guallar D, Saunders A, Shliaha PV, Wang H, Waghray A, Papatsenko D, Sánchez-Priego C, Li D, ... ... Deng H, et al. Tex10 Coordinates Epigenetic Control of Super-Enhancer Activity in Pluripotency and Reprogramming. Cell Stem Cell. 16: 653-68. PMID 25936917 DOI: 10.1016/j.stem.2015.04.001  0.68
2015 Zhang MF, Wang C, Huang H, Ding ZY, Liu Y, Deng H, Li SQ. [Prognostic determinants of adrenocortical carcinoma in adults]. Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition. 46: 248-52. PMID 25924439  0.48
2015 Wang H, Yang S, Zhou H, Sun M, Du L, Wei M, Luo M, Huang J, Deng H, Feng Y, Huang J, Zhou Y. Aloperine executes antitumor effects against multiple myeloma through dual apoptotic mechanisms. Journal of Hematology & Oncology. 8: 26. PMID 25886453 DOI: 10.1186/s13045-015-0120-x  0.68
2015 Yuan L, Guo Y, Yi J, Xiao J, Yuan J, Xiong W, Xu H, Yang Z, Zhang J, Deng H. Identification of a novel GJA3 mutation in congenital nuclear cataract. Optometry and Vision Science : Official Publication of the American Academy of Optometry. 92: 337-42. PMID 25635993 DOI: 10.1097/OPX.0000000000000518  0.52
2015 Guo Y, Li X, Lin C, Zhang Y, Hu G, Zhou J, Du J, Gao K, Gan Y, Deng H. MicroRNA‑133b inhibits connective tissue growth factor in colorectal cancer and correlates with the clinical stage of the disease. Molecular Medicine Reports. 11: 2805-12. PMID 25501363 DOI: 10.3892/mmr.2014.3075  0.48
2015 Yuan L, Wu S, Xu H, Xiao J, Yang Z, Xia H, Liu A, Hu P, Lu A, Chen Y, Xu F, Deng H. Identification of a novel PHEX mutation in a Chinese family with X-linked hypophosphatemic rickets using exome sequencing. Biological Chemistry. 396: 27-33. PMID 25060345 DOI: 10.1515/hsz-2014-0187  0.68
2015 Huan S, Deng H. Research on gravity compensation technology for extravehicular activity training facility Lecture Notes in Electrical Engineering. 356: 355-363. DOI: 10.1007/978-3-662-48224-7_43  0.32
2014 Wang L, Kusky TM, Polat A, Wang S, Jiang X, Zong K, Wang J, Deng H, Fu J. Partial melting of deeply subducted eclogite from the Sulu orogen in China. Nature Communications. 5: 5604. PMID 25517619 DOI: 10.1038/ncomms6604  0.4
2014 Zheng W, Zhang J, Deng X, Xiao J, Yuan L, Yang Y, Guan L, Song Z, Yang Z, Deng H. Identification of a Premature Termination Mutation in the Proline-Rich Transmembrane Protein 2 Gene in a Chinese Family with Febrile Seizures. Molecular Neurobiology. PMID 25502464 DOI: 10.1007/s12035-014-9047-4  0.52
2014 Liu J, Hu Z, Chen R, Yang H, Zheng W, Liu D, Zhang C, Deng H, Wang Q, Yin J, Song Z. Gene polymorphism of rs556621 but Not rs11984041 is associated with the risk of large artery atherosclerotic stroke in a Xinjiang Uyghur population. Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association. 23: 2641-5. PMID 25307434 DOI: 10.1016/j.jstrokecerebrovasdis.2014.06.015  0.52
2014 Wang X, Zou F, Deng H, Fu Z, Li Y, Wu L, Wang Z, Liu L. Characterization of sphere‑forming cells with stem‑like properties from the gastric cancer cell lines MKN45 and SGC7901. Molecular Medicine Reports. 10: 2937-41. PMID 25270642 DOI: 10.3892/mmr.2014.2601  0.68
2014 Deng H, Yin L, Zhang XT, Liu LJ, Wang ML, Wang ZY. ER-α variant ER-α36 mediates antiestrogen resistance in ER-positive breast cancer stem/progenitor cells. The Journal of Steroid Biochemistry and Molecular Biology. 144: 417-26. PMID 25158023 DOI: 10.1016/j.jsbmb.2014.08.017  0.68
2014 Deng S, Deng X, Yuan L, Song Z, Yang Z, Xiong W, Deng H. Genetic analysis of SNCA coding mutation in Chinese Han patients with Parkinson disease. Acta Neurologica Belgica. PMID 25092551 DOI: 10.1007/s13760-014-0347-2  0.52
2014 Zhang X, Deng H, Wang ZY. Estrogen activation of the mitogen-activated protein kinase is mediated by ER-α36 in ER-positive breast cancer cells. The Journal of Steroid Biochemistry and Molecular Biology. 143: 434-43. PMID 24973581 DOI: 10.1016/j.jsbmb.2014.06.009  0.32
2014 Xing R, Li S, Liu K, Yuan Y, Li Q, Deng H, Yang C, Huang J, Zhang Y, Fang J, Xiong C, Li Z. HIP-55 negatively regulates myocardial contractility at the single-cell level. Journal of Biomechanics. 47: 2715-20. PMID 24880669 DOI: 10.1016/j.jbiomech.2014.05.003  0.44
2014 Deng H, Yuan L. Genetic variants and animal models in SNCA and Parkinson disease. Ageing Research Reviews. 15: 161-76. PMID 24768741 DOI: 10.1016/j.arr.2014.04.002  0.36
2014 Deng H, Zhang XT, Wang ML, Zheng HY, Liu LJ, Wang ZY. ER-α36-mediated rapid estrogen signaling positively regulates ER-positive breast cancer stem/progenitor cells. Plos One. 9: e88034. PMID 24558373 DOI: 10.1371/journal.pone.0088034  0.68
2014 Guo Y, Yuan J, Liang H, Xiao J, Xu H, Yuan L, Gao K, Wu B, Tang Y, Li X, Deng H. Identification of a novel COL4A5 mutation in a Chinese family with X-linked Alport syndrome using exome sequencing. Molecular Biology Reports. 41: 3631-5. PMID 24522658 DOI: 10.1007/s11033-014-3227-1  0.52
2014 Guo Y, Song Z, Xu H, Yi J, Zheng W, Xiang H, Deng X, Lv H, Gao K, Qi Y, Deng H. Heterogeneous phenotype in a family with the FERM domain-containing 7 gene R335X mutation. Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie. 49: 50-3. PMID 24513357 DOI: 10.1016/j.jcjo.2013.09.001  0.52
2014 Gao K, Song Z, Liang H, Zheng W, Deng X, Yuan Y, Zhao Y, Deng H. Genetic analysis of the ATP1B4 gene in Chinese Han patients with Parkinson's disease. Molecular Biology Reports. 41: 2307-11. PMID 24420862 DOI: 10.1007/s11033-014-3084-y  0.4
2014 Fu Z, Zou F, Deng H, Zhou H, Liu L. Estrogen protects SGC7901 cells from endoplasmic reticulum stress-induced apoptosis by the Akt pathway. Oncology Letters. 7: 560-564. PMID 24396487 DOI: 10.3892/ol.2013.1701  0.68
2014 Deng H, Yuan L. Molecular genetics of congenital nuclear cataract. European Journal of Medical Genetics. 57: 113-22. PMID 24384146 DOI: 10.1016/j.ejmg.2013.12.006  0.36
2014 Deng H, Zheng W, Song Z. Genetics, molecular biology, and phenotypes of x-linked epilepsy. Molecular Neurobiology. 49: 1166-80. PMID 24258407 DOI: 10.1007/s12035-013-8589-1  0.36
2014 Tan J, You Y, Xu T, Yu P, Wu D, Deng H, Zhang Y, Bie P. Par-4 downregulation confers cisplatin resistance in pancreatic cancer cells via PI3K/Akt pathway-dependent EMT. Toxicology Letters. 224: 7-15. PMID 24144893 DOI: 10.1016/j.toxlet.2013.10.008  0.44
2014 Gao K, Zheng W, Deng X, Xiong W, Song Z, Yang Y, Deng H. Genetic analysis of the fused in sarcoma gene in Chinese Han patients with Parkinson's disease. Parkinsonism & Related Disorders. 20: 119-21. PMID 24080306 DOI: 10.1016/j.parkreldis.2013.09.010  0.4
2014 Deng H, Xiu X, Song Z. The molecular biology of genetic-based epilepsies. Molecular Neurobiology. 49: 352-67. PMID 23934645 DOI: 10.1007/s12035-013-8523-6  0.36
2014 Deng D, Deng H, Zhang L, Su Y. Determination of ephedrine and pseudoephedrine by field-amplified sample injection capillary electrophoresis. Journal of Chromatographic Science. 52: 357-62. PMID 23619557 DOI: 10.1093/chromsci/bmt039  0.48
2013 Guo Y, Yuan L, Yi J, Xiao J, Xu H, Lv H, Xiong W, Zheng W, Guan L, Zhang J, Xiang H, Qi Y, Deng H. Identification of a GJA3 mutation in a Chinese family with congenital nuclear cataract using exome sequencing. Indian Journal of Biochemistry & Biophysics. 50: 253-8. PMID 24772942  0.52
2013 Wang X, Deng H, Zou F, Fu Z, Chen Y, Wang Z, Liu L. ER-α36-mediated gastric cancer cell proliferation via the c-Src pathway. Oncology Letters. 6: 329-335. PMID 24137325 DOI: 10.3892/ol.2013.1416  0.68
2013 Guo Y, Yang H, Deng X, Song Z, Yang Z, Xiong W, Yuan L, Xu H, Deng S, Deng H. Genetic analysis of the S100B gene in Chinese patients with Parkinson disease. Neuroscience Letters. 555: 134-6. PMID 24076007 DOI: 10.1016/j.neulet.2013.09.037  0.52
2013 Liang H, Deng X, Deng H. Response to "A closer look at FBXO41 as a Parkinson's disease risk factor". Parkinsonism & Related Disorders. 19: 1177-8. PMID 24075933 DOI: 10.1016/j.parkreldis.2013.08.022  0.4
2013 Gao K, Deng X, Zheng W, Song Z, Zhu A, Xiu X, Deng H. Genetic analysis of the FBXO42 gene in Chinese Han patients with Parkinson's disease. Bmc Neurology. 13: 125. PMID 24063688 DOI: 10.1186/1471-2377-13-125  0.4
2013 Gu S, Yang H, Qi Y, Deng X, Zhang L, Guo Y, Huang Q, Li J, Shi X, Song Z, Deng H. Novel ATPase Cu(2+) transporting beta polypeptide mutations in Chinese families with Wilson's disease. Plos One. 8: e66526. PMID 23843956 DOI: 10.1371/journal.pone.0066526  0.48
2013 Fu Z, Deng H, Wang X, Yang X, Wang Z, Liu L. Involvement of ER-α36 in the malignant growth of gastric carcinoma cells is associated with GRP94 overexpression. Histopathology. 63: 325-33. PMID 23829397 DOI: 10.1111/his.12171  0.68
2013 Liang H, Song Z, Lei J, Tang J, Xu H, Deng X, Qi Y, Zheng W, Deng H. Genetic analysis of the F-box only protein 41 gene in Chinese Han patients with Parkinson's disease. Parkinsonism & Related Disorders. 19: 918-20. PMID 23777664 DOI: 10.1016/j.parkreldis.2013.05.018  0.52
2013 Guo M, Wang M, Deng H, Zhang X, Wang ZY. A novel anticancer agent Broussoflavonol B downregulates estrogen receptor (ER)-α36 expression and inhibits growth of ER-negative breast cancer MDA-MB-231 cells. European Journal of Pharmacology. 714: 56-64. PMID 23769740 DOI: 10.1016/j.ejphar.2013.05.047  0.32
2013 Liang H, Song Z, Deng X, Xu H, Zhu A, Zheng W, Zhao Y, Deng H. Genetic analysis of the leucine-rich repeat and lg domain containing Nogo receptor-interacting protein 1 gene in essential tremor. Journal of Molecular Neuroscience : Mn. 51: 403-7. PMID 23754655 DOI: 10.1007/s12031-013-0029-1  0.52
2013 Li X, Lian FM, Guo D, Fan L, Tang J, Peng JB, Deng HW, Liu ZQ, Xiao XH, Wang YR, Qu KY, Deng S, Zhong Q, Sha YL, Zhu Y, et al. The rs1142345 in TPMT Affects the Therapeutic Effect of Traditional Hypoglycemic Herbs in Prediabetes. Evidence-Based Complementary and Alternative Medicine : Ecam. 2013: 327629. PMID 23737827 DOI: 10.1155/2013/327629  0.36
2013 Yang Y, Liao Q, Wei F, Li X, Zhang W, Fan S, Shi L, Li X, Gong Z, Ma J, Zhou M, Xiang J, Peng S, Xiang B, Deng H, et al. LPLUNC1 inhibits nasopharyngeal carcinoma cell growth via down-regulation of the MAP kinase and cyclin D1/E2F pathways. Plos One. 8: e62869. PMID 23650533 DOI: 10.1371/journal.pone.0062869  0.4
2013 Guo M, Wang M, Zhang X, Deng H, Wang ZY. Broussoflavonol B restricts growth of ER-negative breast cancer stem-like cells. Anticancer Research. 33: 1873-9. PMID 23645733  0.32
2013 Guo Y, Xu H, Ren Z, Yang Y, Xiong W, Gao K, Li X, Luo Z, Deng H. Genetic analysis of a Chinese Han family with multiple endocrine neoplasia type 2A. Indian Journal of Biochemistry & Biophysics. 50: 26-31. PMID 23617071  0.52
2013 Zhao MF, Qu XJ, Qu JL, Jiang YH, Zhang Y, Hou KZ, Deng H, Liu YP. The role of E3 ubiquitin ligase Cbl proteins in interleukin-2-induced Jurkat T-cell activation. Biomed Research International. 2013: 430861. PMID 23586039 DOI: 10.1155/2013/430861  0.44
2013 Zheng W, Deng X, Liang H, Song Z, Gao K, Yang Y, Deng H. Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor. Neurobiology of Aging. 34: 2078.e3-4. PMID 23582660 DOI: 10.1016/j.neurobiolaging.2013.03.001  0.4
2013 Yuan L, Song Z, Xu H, Gu S, Zhu A, Gong L, Zhao Y, Deng H. EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease. Neuroscience Letters. 543: 69-71. PMID 23562511 DOI: 10.1016/j.neulet.2013.02.056  0.52
2013 Xiu X, Song Z, Gao K, Deng X, Qi Y, Zhu A, Gong L, Deng H. Genetic analysis of the FBXO48 gene in Chinese Han patients with Parkinson disease. Neuroscience Letters. 541: 224-6. PMID 23485738 DOI: 10.1016/j.neulet.2013.02.031  0.52
2013 Gu S, Liu Y, Song Z, Zi X, Deng H. Acute myelitis in a patient with vogt-koyanagi-harada disease: case report and review of the literature. Journal of Clinical Neurology (Seoul, Korea). 9: 61-4. PMID 23346163 DOI: 10.3988/jcn.2013.9.1.61  0.48
2012 Guo Y, Liang H, Deng H. [Advances in the molecular genetics of brachydactyly]. Yi Chuan = Hereditas / Zhongguo Yi Chuan Xue Hui Bian Ji. 34: 1522-8. PMID 23262098  0.48
2012 Gong Z, Zhang S, Zhang W, Huang H, Li Q, Deng H, Ma J, Zhou M, Xiang J, Wu M, Li X, Xiong W, Li X, Li Y, Zeng Z, et al. Long non-coding RNAs in cancer. Science China. Life Sciences. 55: 1120-4. PMID 23233227 DOI: 10.1007/s11427-012-4413-9  0.4
2012 Liu X, Luo XP, Cao WT, Deng H. [Effects of transcatheter arterial chemoembolization with pingyangmycin-lipiodol emulsion on VX2 liver tumors in rabbits]. Zhonghua Gan Zang Bing Za Zhi = Zhonghua Ganzangbing Zazhi = Chinese Journal of Hepatology. 20: 611-6. PMID 23207156  0.36
2012 Lei J, Xu H, Liang H, Su L, Zhang J, Huang X, Song Z, Le W, Deng H. Gene expression changes in peripheral blood from Chinese Han patients with Tourette syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 977-80. PMID 23076970 DOI: 10.1002/ajmg.b.32103  0.68
2012 Guo Y, Deng X, Jankovic J, Su L, Zhang J, Le W, Xu H, Yang Z, Tang J, Kuang S, Deng H. Mutation screening of the HTR2B gene in patients with Tourette syndrome. Neuroscience Letters. 526: 150-3. PMID 22917605 DOI: 10.1016/j.neulet.2012.08.013  0.52
2012 Guo Y, Su L, Zhang J, Lei J, Deng X, Xu H, Yang Z, Kuang S, Tang J, Luo Z, Deng H. Analysis of the BTBD9 and HTR2C variants in Chinese Han patients with Tourette syndrome. Psychiatric Genetics. 22: 300-3. PMID 22914617 DOI: 10.1097/YPG.0b013e32835862b1  0.52
2012 Deng H, Zhen H, Fu Z, Huang X, Zhou H, Liu L. The antagonistic effect between STAT1 and Survivin and its clinical significance in gastric cancer. Oncology Letters. 3: 193-199. PMID 22740880 DOI: 10.3892/ol.2011.423  0.68
2012 Xu ZL, Deng H, Lei HT, Jiang YM, Campbell K, Shen YD, Yang JY, Wang H, Sun YM. Development of a broad-specificity monoclonal antibody-based immunoaffinity chromatography cleanup for organophosphorus pesticide determination in environmental samples. Journal of Agricultural and Food Chemistry. 60: 5847-52. PMID 22612520 DOI: 10.1021/jf300896z  0.4
2012 Guo Y, Deng X, Zhang J, Su L, Xu H, Luo Z, Deng H. Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD. Neuroscience Letters. 517: 18-20. PMID 22507240 DOI: 10.1016/j.neulet.2012.03.097  0.52
2012 Zhou H, Xiao B, Zhou F, Deng H, Zhang X, Lou Y, Gong Z, Du C, Guo J. MiR-421 is a functional marker of circulating tumor cells in gastric cancer patients. Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals. 17: 104-10. PMID 22263628 DOI: 10.3109/1354750X.2011.614961  0.68
2012 Song Z, Zheng W, Zhu H, Chen Y, Fan X, Hou D, Deng H. Prediction of coma and anisocoria based on computerized tomography findings in patients with supratentorial intracerebral hemorrhage. Clinical Neurology and Neurosurgery. 114: 634-8. PMID 22257515 DOI: 10.1016/j.clineuro.2011.12.029  0.68
2012 Liang H, Zheng W, Xu H, Lei J, Song Z, Jiang X, Zeng Z, Deng H. No evidence of association between the LINGO4 gene and essential tremor in Chinese Han patients. Parkinsonism & Related Disorders. 18: 303-5. PMID 22104011 DOI: 10.1016/j.parkreldis.2011.10.017  0.52
2012 Lei J, Deng X, Zhang J, Su L, Xu H, Liang H, Huang X, Song Z, Deng H. Mutation screening of the HDC gene in Chinese Han patients with Tourette syndrome. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 72-6. PMID 22095709 DOI: 10.1002/ajmg.b.32003  0.68
2012 Cheng J, Deng H, Xiao B, Zhou H, Zhou F, Shen Z, Guo J. piR-823, a novel non-coding small RNA, demonstrates in vitro and in vivo tumor suppressive activity in human gastric cancer cells. Cancer Letters. 315: 12-7. PMID 22047710 DOI: 10.1016/j.canlet.2011.10.004  0.68
2011 Guo Y, Lin H, Gao K, Xu H, Deng X, Zhang Q, Luo Z, Sun S, Deng H. Genetic analysis of IREB2, FAM13A and XRCC5 variants in Chinese Han patients with chronic obstructive pulmonary disease. Biochemical and Biophysical Research Communications. 415: 284-7. PMID 22027142 DOI: 10.1016/j.bbrc.2011.10.042  0.52
2011 Guo Y, Deng X, Zheng W, Xu H, Song Z, Liang H, Lei J, Jiang X, Luo Z, Deng H. HLA rs3129882 variant in Chinese Han patients with late-onset sporadic Parkinson disease. Neuroscience Letters. 501: 185-7. PMID 21791235 DOI: 10.1016/j.neulet.2011.05.245  0.52
2011 Cui L, Lou Y, Zhang X, Zhou H, Deng H, Song H, Yu X, Xiao B, Wang W, Guo J. Detection of circulating tumor cells in peripheral blood from patients with gastric cancer using piRNAs as markers. Clinical Biochemistry. 44: 1050-7. PMID 21704610 DOI: 10.1016/j.clinbiochem.2011.06.004  0.68
2011 Guo Y, Le WD, Jankovic J, Yang HR, Xu HB, Xie WJ, Song Z, Deng H. Systematic genetic analysis of the PITX3 gene in patients with Parkinson disease. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 1729-32. PMID 21469209 DOI: 10.1002/mds.23693  0.48
2011 Guo Y, Jankovic J, Song Z, Yang H, Zheng W, Le W, Tang X, Deng X, Yang Y, Deng S, Luo Z, Deng H. LINGO1 rs9652490 variant in Parkinson disease patients. Neuroscience Letters. 487: 174-6. PMID 20951767 DOI: 10.1016/j.neulet.2010.10.016  0.48
2010 Lu CJ, Luo Y, Zhou H, Qin XL, Chen BJ, Tang XC, Deng H, Liang ZH, Ou AH. A preliminary study on the medical expenditure of Chinese medicine and integrative medicine treatment for influenza A (H1N1) in the fever clinics. Chinese Journal of Integrative Medicine. 16: 493-7. PMID 21110173 DOI: 10.1007/s11655-010-0563-4  0.68
2010 Yang HR, Qi Y, Song Z, Deng H. [Advances of genetic research on the SPG4 gene]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 27: 282-5. PMID 20533266 DOI: 10.3760/cma.j.issn.1003-9406.2010.0.010  0.36
2010 Deng H, Huang X, Fan J, Wang L, Xia Q, Yang X, Wang Z, Liu L. A variant of estrogen receptor-alpha, ER-alpha36 is expressed in human gastric cancer and is highly correlated with lymph node metastasis. Oncology Reports. 24: 171-6. PMID 20514458  0.68
2010 Wu C, Guo X, Wang W, Wang Y, Shan Y, Zhang B, Song W, Ma S, Ge J, Deng H, Zhu M. N-Acetylgalactosaminyltransferase-14 as a potential biomarker for breast cancer by immunohistochemistry. Bmc Cancer. 10: 123. PMID 20356418 DOI: 10.1186/1471-2407-10-123  0.32
2010 Chen XQ, Yu YC, Deng HH, Sun JZ, Dai Z, Wu YW, Yang M. Plasma IL-17A is increased in new-onset SLE patients and associated with disease activity. Journal of Clinical Immunology. 30: 221-5. PMID 20107878 DOI: 10.1007/s10875-009-9365-x  0.36
2010 Deng H, Yang H, Le W, Deng X, Xu H, Xiong W, Zhu S, Xie W, Song Z, Jankovic J. Examination of the MASH1 gene in patients with Parkinson's disease. Biochemical and Biophysical Research Communications. 392: 548-50. PMID 20097173 DOI: 10.1016/j.bbrc.2010.01.061  0.52
2010 Liu L, Deng H, Wu L, Zheng C, Hou X. UV-induced carbonyl generation with formic acid for sensitive determination of nickel by atomic fluorescence spectrometry. Talanta. 80: 1239-44. PMID 20006081 DOI: 10.1016/j.talanta.2009.09.016  0.68
2008 Zhou H, Yong J, Sun X, Wang C, Yang W, Zhang P, Zhu J, Shi C, Ding M, Deng H. A human endothelial cell feeder system that efficiently supports the undifferentiated growth of mouse embryonic stem cells. Differentiation; Research in Biological Diversity. 76: 923-30. PMID 18557766 DOI: 10.1111/j.1432-0436.2008.00280.x  0.68
2008 Li L, Li F, Qi H, Feng G, Yuan K, Deng H, Zhou H. Coexpression of Pdx1 and betacellulin in mesenchymal stem cells could promote the differentiation of nestin-positive epithelium-like progenitors and pancreatic islet-like spheroids. Stem Cells and Development. 17: 815-23. PMID 18439098 DOI: 10.1089/scd.2008.0060  0.68
2006 Yang YL, Ding ZY, Li Q, Zhou H, Deng HX, Tian L, Wei YQ. [Anti-tumor effects of recombinant adenovirus encoding survivin encapsulated in cationic liposome]. Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition. 37: 704-7. PMID 17037732  0.68
2006 Deng H, Wu RL, Zhou HY, Huang X, Chen Y, Liu LJ. Significance of Survivin and PTEN expression in full lymph node-examined gastric cancer. World Journal of Gastroenterology. 12: 1013-7. PMID 16534839  0.68
2005 Deng H, Li HX. Hybrid spectral/neural model based integrated control and supervision of a distributed thermal process in IC packaging Proceedings of the American Control Conference. 1: 256-261.  0.96
2004 Yang SJ, Dong XP, Zhao CF, Zhou HY, Deng HQ, Yang S, Xiong T. [Epidemiological study of influenza in a middle school students in Dongyang City, Hubei Province]. Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi. 25: 1095. PMID 15769382  0.68
2004 Xiong W, Zeng ZY, Xia JH, Xia K, Shen SR, Li XL, Hu DX, Tan C, Xiang JJ, Zhou J, Deng H, Fan SQ, Li WF, Wang R, Zhou M, et al. A susceptibility locus at chromosome 3p21 linked to familial nasopharyngeal carcinoma. Cancer Research. 64: 1972-4. PMID 15026332  0.4
2004 Deng H, Li HX. Functional observers for linear systems with unknown inputs Asian Journal of Control. 6: 462-468.  0.96
2003 Li YB, Deng HC, Zheng D, Li HL, Zhou HB. [Role of P38 mitogen-activated protein kinase in expression of P-selectin on human umbilical vein endothelial cells]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi = Chinese Journal of Cellular and Molecular Immunology. 19: 291-3. PMID 15155098  0.44
2003 Lu Y, Wei YQ, Tian L, Zhao X, Yang L, Hu B, Kan B, Wen YJ, Liu F, Deng HX, Li J, Mao YQ, Lei S, Huang MJ, Peng F, et al. Immunogene therapy of tumors with vaccine based on xenogeneic epidermal growth factor receptor. Journal of Immunology (Baltimore, Md. : 1950). 170: 3162-70. PMID 12626574  0.68
2003 Deng H, Li HX. Hybrid intelligence based modeling for nonlinear distributed parameter process with applications to the curing process Proceedings of the Ieee International Conference On Systems, Man and Cybernetics. 4: 3506-3511.  0.96
2000 Sun M, Zhou HY, Deng HZ. [Study of the risk factors of blood pressure in children]. Hunan Yi Ke Da Xue Xue Bao = Hunan Yike Daxue Xuebao = Bulletin of Hunan Medical University. 25: 238-40. PMID 12212152  0.68
1999 Deng H, Zhou H, Sun M. [Roles of sex hormones and oxygen free radical in coronary heart disease]. Hunan Yi Ke Da Xue Xue Bao = Hunan Yike Daxue Xuebao = Bulletin of Hunan Medical University. 24: 343-6. PMID 12080642  0.68
1990 Deng H, Yang X. Chemical composition of the penis and testes of deer before and after processing Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica. 15: 154-156, 190. PMID 2085401  0.32
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