| Year |
Citation |
Score |
| Low-probability matches (unlikely to be authored by this person) |
| 2015 |
Sang Z, Qiang X, Li Y, Yuan W, Liu Q, Shi Y, Ang W, Luo Y, Tan Z, Deng Y. Design, synthesis and evaluation of scutellarein-O-alkylamines as multifunctional agents for the treatment of Alzheimer's disease. European Journal of Medicinal Chemistry. 94: 348-66. PMID 25778991 DOI: 10.1016/J.Ejmech.2015.02.063 |
0.29 |
|
| 2015 |
Liu Q, Qiang X, Li Y, Sang Z, Li Y, Tan Z, Deng Y. Design, synthesis and evaluation of chromone-2-carboxamido-alkylbenzylamines as multifunctional agents for the treatment of Alzheimer's disease. Bioorganic & Medicinal Chemistry. 23: 911-23. PMID 25678013 DOI: 10.1016/j.bmc.2015.01.042 |
0.288 |
|
| 2015 |
Sang Z, Li Y, Qiang X, Xiao G, Liu Q, Tan Z, Deng Y. Multifunctional scutellarin-rivastigmine hybrids with cholinergic, antioxidant, biometal chelating and neuroprotective properties for the treatment of Alzheimer's disease. Bioorganic & Medicinal Chemistry. 23: 668-80. PMID 25614117 DOI: 10.1016/j.bmc.2015.01.005 |
0.286 |
|
| 2016 |
Li Y, Qiang X, Li Y, Yang X, Luo L, Xiao G, Cao Z, Tan Z, Deng Y. Pterostilbene-O-acetamidoalkylbenzylamines derivatives as novel dual inhibitors of cholinesterase with anti-β-amyloid aggregation and antioxidant properties for the treatment of Alzheimer's disease. Bioorganic & Medicinal Chemistry Letters. PMID 26947607 DOI: 10.1016/j.bmcl.2016.02.079 |
0.285 |
|
| 2014 |
Qiang X, Sang Z, Yuan W, Li Y, Liu Q, Bai P, Shi Y, Ang W, Tan Z, Deng Y. Design, synthesis and evaluation of genistein-O-alkylbenzylamines as potential multifunctional agents for the treatment of Alzheimer's disease. European Journal of Medicinal Chemistry. 76: 314-31. PMID 24589487 DOI: 10.1016/J.Ejmech.2014.02.045 |
0.283 |
|
| 2016 |
Li Y, Qiang X, Luo L, Li Y, Xiao G, Tan Z, Deng Y. Synthesis and evaluation of 4-hydroxyl aurone derivatives as multifunctional agents for the treatment of Alzheimer's disease. Bioorganic & Medicinal Chemistry. PMID 27079124 DOI: 10.1016/j.bmc.2016.04.012 |
0.282 |
|
| 2014 |
Liu X, Xu Y, Chen S, Tan Z, Xiong K, Li Y, Ye Y, Luo ZP, He F, Gong Y. Rescue of proinflammatory cytokine-inhibited chondrogenesis by the antiarthritic effect of melatonin in synovium mesenchymal stem cells via suppression of reactive oxygen species and matrix metalloproteinases. Free Radical Biology & Medicine. 68: 234-46. PMID 24374373 DOI: 10.1016/j.freeradbiomed.2013.12.012 |
0.238 |
|
| 2015 |
Li Y, Li Y, Chen W, He F, Tan Z, Zheng J, Wang W, Zhao Q, Li J. NEAT expression is associated with tumor recurrence and unfavorable prognosis in colorectal cancer. Oncotarget. PMID 26314847 |
0.233 |
|
| 2014 |
Wang F, Sun G, Li C, Liu J, Hu S, Zheng H, Tan Z, Li Y. Finding the lost open-circuit voltage in polymer solar cells by UV-ozone treatment of the nickel acetate anode buffer layer. Acs Applied Materials & Interfaces. 6: 9458-65. PMID 24878826 DOI: 10.1021/Am5017705 |
0.228 |
|
| 2016 |
Wang Q, Tan R, Zhu X, Zhang Y, Tan Z, Su B, Li Y. Oncogenic K-ras confers SAHA resistance by up-regulating HDAC6 and c-myc expression. Oncotarget. PMID 26848526 DOI: 10.18632/Oncotarget.7134 |
0.222 |
|
| 2014 |
Xie J, Tan ZH, Tang X, Mo MS, Liu YP, Gan RL, Li Y, Zhang L, Li GQ. MiR-374b-5p suppresses RECK expression and promotes gastric cancer cell invasion and metastasis. World Journal of Gastroenterology : Wjg. 20: 17439-47. PMID 25516656 DOI: 10.3748/wjg.v20.i46.17439 |
0.216 |
|
| 2015 |
Wang X, Zhang J, Zhang F, Li J, Li Y, Tan Z, Hu J, Qi Y, Li Q, Yan B. The Clinical Status of Stem Cell Therapy for Ischemic Cardiomyopathy. Stem Cells International. 2015: 135023. PMID 26101528 DOI: 10.1155/2015/135023 |
0.215 |
|
| 2015 |
Li C, Wang F, Xu J, Yao J, Zhang B, Zhang C, Xiao M, Dai S, Li Y, Tan Z. Efficient perovskite/fullerene planar heterojunction solar cells with enhanced charge extraction and suppressed charge recombination. Nanoscale. 7: 9771-8. PMID 25962479 DOI: 10.1039/C4Nr06240J |
0.214 |
|
| 2014 |
Tan Z, Li S, Wang F, Qian D, Lin J, Hou J, Li Y. High performance polymer solar cells with as-prepared zirconium acetylacetonate film as cathode buffer layer. Scientific Reports. 4: 4691. PMID 24732976 DOI: 10.1038/Srep04691 |
0.213 |
|
| 2016 |
Lian K, Guo X, Huang Q, Tan Z, Xia C, Wang R, Yi F, Li W, Liu J, Li Y, Guo S, Wang H, Ji Q, Tao L. Reduction Levels and the Effects of High-Molecular-Weight Adiponectin via AMPK/eNOS in Chinese Type 2 Diabetes. Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [and] German Diabetes Association. PMID 27437915 DOI: 10.1055/S-0042-109262 |
0.213 |
|
| 2016 |
Sun SJ, Lin Q, Sun Q, Li J, Zhang XY, Tan ZG, Song Y, Guo YT, Li Y. High HER-2 protein levels correlate with clinicopathological features in colorectal cancer. Journal of Cancer Research and Therapeutics. 12: 323-33. PMID 27072259 DOI: 10.4103/0973-1482.155977 |
0.212 |
|
| 2015 |
Zhu Z, Tan Z, Li Y, Luo H, Hu X, Tang M, Hescheler J, Mu Y, Zhang L. Docosahexaenoic acid alters Gsα localization in lipid raft and potentiates adenylate cyclase. Nutrition (Burbank, Los Angeles County, Calif.). 31: 1025-30. PMID 26059378 DOI: 10.1016/j.nut.2015.02.012 |
0.21 |
|
| 2015 |
Tan Z, Li Y, Zhu F, Zang D, Zhao C, Li C, Tong D, Zhang H, Chen Q. Children With Intracranial Arachnoid Cysts: Classification and Treatment. Medicine. 94: e1749. PMID 26554773 DOI: 10.1097/MD.0000000000001749 |
0.21 |
|
| 2015 |
Yu H, Ling T, Shi R, Shu Q, Li Y, Tan Z. [Expression of FBXW7 in esophageal squamous cell carcinoma and its clinical significance]. Zhonghua Zhong Liu Za Zhi [Chinese Journal of Oncology]. 37: 347-51. PMID 26463024 |
0.209 |
|
| 2013 |
Ma L, Xiang LH, Yu B, Yin R, Chen L, Wu Y, Tan ZJ, Liu YB, Tian HQ, Li HZ, Lin T, Wang XL, Li YH, Wang WZ, Yang HL, et al. Low-dose topical 5-aminolevulinic acid photodynamic therapy in the treatment of different severity of acne vulgaris. Photodiagnosis and Photodynamic Therapy. 10: 583-90. PMID 24284115 DOI: 10.1016/j.pdpdt.2013.06.007 |
0.207 |
|
| 2016 |
Tan Z, Li Y, Zang D, Zhang H, Zhao C, Jiang H, Chen Y, Cao D, Chen L, Liao J, Chen Q, Luan G. Altered regional homogeneity in epileptic patients with infantile spasm: A resting-state fMRI study. Journal of X-Ray Science and Technology. PMID 27002912 DOI: 10.3233/XST-160559 |
0.205 |
|
| 2016 |
Zhang M, Lv H, Tan Z, Li Y, Wang Y, Pang H, Li Z, Jiao Z, Jin Q. Improving the fermentation quality of wheat straw silage stored at low temperature by psychrotrophic lactic acid bacteria. Animal Science Journal = Nihon Chikusan Gakkaiho. PMID 27229440 DOI: 10.1111/asj.12632 |
0.203 |
|
| 2016 |
Guo D, Ye Y, Qi J, Xu L, Zhang L, Tan X, Tan Z, Yu X, Zhang Y, Ma Y, Li Y. MicroRNA-195a-5p inhibits mouse medullary thymic epithelial cells proliferation by directly targeting Smad7. Acta Biochimica Et Biophysica Sinica. PMID 26837421 DOI: 10.1093/abbs/gmv136 |
0.202 |
|
| 2016 |
Deng WW, Wu YL, Li YY, Tan Z, Wei CL. Molecular Cloning and Characterization of Hydroperoxide Lyase Gene in the Leaves of Tea Plant (Camellia sinensis). Journal of Agricultural and Food Chemistry. PMID 26886573 DOI: 10.1021/acs.jafc.5b05748 |
0.198 |
|
| 2015 |
Li Y, Zhao C, Tan Z, Wang Y, Zhang H, Wang J, Guo H, Zeng B, Huang W. Longitudinal Changes in the Brain Following Third Ventriculostomy in a Child With Hydrocephalus: A Case Report. Medicine. 94: e2095. PMID 26632724 DOI: 10.1097/MD.0000000000002095 |
0.192 |
|
| 2015 |
Li Y, Zhu ZR, Ou BC, Wang YQ, Tan ZB, Deng CM, Gao YY, Tang M, So JH, Mu YL, Zhang LQ. Dopamine D2/D3 but not dopamine D1 receptors are involved in the rapid antidepressant-like effects of ketamine in the forced swim test. Behavioural Brain Research. 279: 100-5. PMID 25449845 DOI: 10.1016/j.bbr.2014.11.016 |
0.191 |
|
| 2016 |
Fang Y, Zhu P, Li Q, Chen H, Li Y, Ren C, Hu Y, Tan Z, Gu J, Mao X. Multilocus sequence typing of 102 Burkholderia pseudomallei strains isolated from China. Epidemiology and Infection. 1-7. PMID 26744829 DOI: 10.1017/S0950268815003052 |
0.191 |
|
| 2014 |
Tan Z, Wang H, Wei Y, Li Y, Zhong C, Jia S. [Effects of carbon and nitrogen sources on 5-keto-gluconic acid production]. Sheng Wu Gong Cheng Xue Bao = Chinese Journal of Biotechnology. 30: 76-82. PMID 24818481 |
0.187 |
|
| 2015 |
Xiong B, Li Y, Lv W, Tan Z, Jiang H, Zhang M. Ruthenium-Catalyzed Straightforward Synthesis of 1,2,3,4-Tetrahydronaphthyridines via Selective Transfer Hydrogenation of Pyridyl Ring with Alcohols. Organic Letters. 17: 4054-7. PMID 26250901 DOI: 10.1021/acs.orglett.5b01976 |
0.185 |
|
| 2016 |
Chen M, Chen Z, Wang Y, Tan Z, Zhu C, Li Y, Han Z, Chen L, Gao R, Liu L, Chen Q. Mitophagy receptor FUNDC1 regulates mitochondrial dynamics and mitophagy. Autophagy. 12: 689-702. PMID 27050458 DOI: 10.1080/15548627.2016.1151580 |
0.174 |
|
| 2021 |
Zhong AN, Yin Y, Tang BJ, Chen L, Shen HW, Tan ZP, Li WQ, He Q, Sun B, Zhu Y, Xiao J, Jiang ZP, Xu P. CircRNA Microarray Profiling Reveals hsa_circ_0058493 as a Novel Biomarker for Imatinib-Resistant CML. Frontiers in Pharmacology. 12: 728916. PMID 34588984 DOI: 10.3389/fphar.2021.728916 |
0.153 |
|
| 2023 |
Lin MJ, Tang XX, Yao GS, Tan ZP, Dai L, Wang YH, Zhu JQ, Xu QH, Mumin MA, Liang H, Wang Z, Deng Q, Luo JH, Wei JH, Cao JZ. A novel 7-chemokine-genes predictive signature for prognosis and therapeutic response in renal clear cell carcinoma. Frontiers in Pharmacology. 14: 1120562. PMID 37021054 DOI: 10.3389/fphar.2023.1120562 |
0.129 |
|
| 2021 |
Yuan ZZ, Xie XH, Gu H, Zhang WZ, Hu YQ, Yang YF, Tan ZP. Case Report: BAF-Opathies/SSRIDDs Due to a ACTL6A Variant, Previously Considered to Be Heart-Hand Syndrome. Frontiers in Cardiovascular Medicine. 8: 708033. PMID 34485408 DOI: 10.3389/fcvm.2021.708033 |
0.118 |
|
| 2012 |
Ren H, Tan ZP, Zhu X, Crosby K, Haack H, Ren JM, Beausoleil S, Moritz A, Innocenti G, Rush J, Zhang Y, Zhou XM, Gu TL, Yang YF, Comb MJ. Identification of anaplastic lymphoma kinase as a potential therapeutic target in ovarian cancer. Cancer Research. 72: 3312-23. PMID 22570254 DOI: 10.1158/0008-5472.Can-11-3931 |
0.118 |
|
| 2021 |
Gong K, Zhou H, Liu H, Xie T, Luo Y, Guo H, Chen J, Tan Z, Yang Y, Xie L. Identification and Integrate Analysis of Key Biomarkers for Diagnosis and Prognosis of Non-Small Cell Lung Cancer Based on Bioinformatics Analysis. Technology in Cancer Research & Treatment. 20: 15330338211060202. PMID 34825846 DOI: 10.1177/15330338211060202 |
0.117 |
|
| 2005 |
He LQ, Liu Y, Cai F, Tan ZP, Pan Q, Liang DS, Long ZG, Wu LQ, Huang LQ, Dai HP, Xia K, Xia JH, Zhang ZH. Intracellular distribution, assembly and effect of disease-associated connexin 31 mutants in HeLa cells. Acta Biochimica Et Biophysica Sinica. 37: 547-54. PMID 16077902 |
0.114 |
|
| 2017 |
Guo T, Yang K, Liu L, Tan ZP, Luo H. Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy. Molecular Medicine Reports. PMID 28339061 DOI: 10.3892/mmr.2017.6391 |
0.11 |
|
| 2017 |
Chao C, Li F, Tan Z, Zhang W, Yang Y, Luo C. miR-195 inhibited abnormal activation of osteoblast differentiation in MC3T3-E1 cells via targeting RAF-1. Experimental Cell Research. PMID 29197556 DOI: 10.1016/j.yexcr.2017.11.030 |
0.109 |
|
| 2008 |
Liao XB, Zhou XM, Li JM, Yang JF, Tan ZP, Hu ZW, Liu W, Lu Y, Yuan LQ. Taurine inhibits osteoblastic differentiation of vascular smooth muscle cells via the ERK pathway. Amino Acids. 34: 525-30. PMID 18060526 DOI: 10.1007/s00726-007-0003-8 |
0.109 |
|
| 2021 |
Xie XH, Tang JG, Liu ZH, Peng SJ, Yuan ZZ, Gu H, Hu YQ, Tan ZP. Case Report: Mutant Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to Pain. Frontiers in Neuroscience. 15: 697167. PMID 34335171 DOI: 10.3389/fnins.2021.697167 |
0.1 |
|
| 2014 |
Tan ZP, Xie L, Deng Y, Chen JL, Zhang WZ, Wang J, Yang JF, Yang YF. Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death. Scientific Reports. 4: 5616. PMID 25010007 DOI: 10.1038/srep05616 |
0.098 |
|
| 2023 |
Yang H, Gong K, Luo Y, Wang L, Tan Z, Yao Y, Xie L. Case report: A new mutation of the Troponin T2 gene in a Chinese patient with dilated cardiomyopathy. Frontiers in Cardiovascular Medicine. 10: 1288328. PMID 38054088 DOI: 10.3389/fcvm.2023.1288328 |
0.098 |
|
| 2021 |
Guo T, Tu CF, Yang DH, Ding SZ, Lei C, Wang RC, Liu L, Kang X, Shen XQ, Yang YF, Tan ZP, Tan YQ, Luo H. Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia. Human Genetics. PMID 33389130 DOI: 10.1007/s00439-020-02241-4 |
0.097 |
|
| 2016 |
Liu Z, Yin N, Gong L, Tan Z, Yin B, Yang Y, Luo C. Microduplication of 7q36.3 encompassing the SHH long‑range regulator (ZRS) in a patient with triphalangeal thumb‑polysyndactyly syndrome and congenital heart disease. Molecular Medicine Reports. PMID 28035386 DOI: 10.3892/mmr.2016.6092 |
0.096 |
|
| 2022 |
Guo X, Chen X, Chen J, Tan Z, Yang Y, Zhang H. Current Status and Evaluation of Randomized Clinical Trials of Traditional Chinese Medicine in the Treatment of Cardiovascular Diseases. Evidence-Based Complementary and Alternative Medicine : Ecam. 2022: 6181862. PMID 35069763 DOI: 10.1155/2022/6181862 |
0.096 |
|
| 2020 |
Yuan ZZ, Fan LL, Jiang ZC, Yang YF, Tan ZP. A Novel Nonsense Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient. Frontiers in Cardiovascular Medicine. 7: 582350. PMID 33240936 DOI: 10.3389/fcvm.2020.582350 |
0.095 |
|
| 2020 |
Lei C, Guo T, Ding S, Liao L, Peng H, Tan Z, Luo H. Whole-exome sequencing identified a novel homozygous ASPH frameshift variant causing Traboulsi syndrome in a Chinese family. Molecular Genetics & Genomic Medicine. e1553. PMID 33217155 DOI: 10.1002/mgg3.1553 |
0.094 |
|
| 2010 |
Wu Q, Tan Z, Liu H, Gao L, Wu S, Luo J, Zhang W, Zhao T, Yu J, Xu X. Chemical characterization of Auricularia auricula polysaccharides and its pharmacological effect on heart antioxidant enzyme activities and left ventricular function in aged mice. International Journal of Biological Macromolecules. 46: 284-8. PMID 20105437 DOI: 10.1016/j.ijbiomac.2010.01.016 |
0.094 |
|
| 2018 |
Zhang W, Li D, Wei S, Guo T, Wang J, Luo H, Yang Y, Tan Z. Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus. Journal of Human Genetics. PMID 30504913 DOI: 10.1038/s10038-018-0540-x |
0.093 |
|
| 2017 |
Zeng H, Tang JG, Yang YF, Tan ZP, Tan JQ. A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. Cytogenetic and Genome Research. PMID 28658676 DOI: 10.1159/000477428 |
0.093 |
|
| 2022 |
Gu H, Yuan ZZ, Xie XH, Yang YF, Tan ZP. A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient. Journal of Human Genetics. 67: 573-577. PMID 35691949 DOI: 10.1038/s10038-022-01053-w |
0.093 |
|
| 2012 |
Luo C, Yang YF, Yin BL, Chen JL, Huang C, Zhang WZ, Wang J, Zhang H, Yang JF, Tan ZP. Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome. American Journal of Medical Genetics. Part A. 158: 1918-23. PMID 22786616 DOI: 10.1002/ajmg.a.35471 |
0.092 |
|
| 2018 |
Fan LL, Chen YQ, Huang H, Jin JY, Li JJ, Tan ZP. Whole-exome sequencing reveals doubly novel heterozygous Myosin Binding Protein C and Titin mutations in a Chinese patient with severe dilated cardiomyopathy. Cardiology in the Young. 1-5. PMID 30109841 DOI: 10.1017/S1047951118001403 |
0.091 |
|
| 2007 |
Li TG, Liu XP, Zheng D, Sun JC, Li J, Tan ZP, Qin ZQ. [Familial and genetic study in a large Chinese kindred with hereditary nonpolyposis colorectal cancer]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 24: 227-9. PMID 17407090 |
0.09 |
|
| 2017 |
Huang H, Wang Y, Cao Y, Wu B, Li Y, Fan L, Tan Z, Jiang Y, Tang J, Hu J, Shi X. Interleukin-6, tumor necrosis factor-alpha and receptor activator of nuclear factor kappa ligand are elevated in hypertrophic gastric mucosa of pachydermoperiostosis. Scientific Reports. 7: 9686. PMID 28851954 DOI: 10.1038/s41598-017-09671-7 |
0.09 |
|
| 2019 |
Bu H, Liu L, Hu S, Tan Z, Zhao T. Targeted next‑generation sequencing for research and diagnostics in congenital heart disease, and cleft lip and/or palate. Molecular Medicine Reports. PMID 30896870 DOI: 10.3892/mmr.2019.10043 |
0.089 |
|
| 2023 |
Tan Z, Chen Z, Yao G, Mumin MA, Wang Y, Zhu J, Xu Q, Chen W, Liang H, Wang Z, Deng Q, Luo J, Wei J, Cao J. Neoadjuvant and adjuvant chemotherapy share equivalent efficacy in improving overall survival and cancer-specific survival among muscle invasive bladder cancer patients who undergo radical cystectomy: a retrospective cohort study based on SEER database. Translational Andrology and Urology. 12: 330-346. PMID 36915890 DOI: 10.21037/tau-23-79 |
0.089 |
|
| 2021 |
Gong K, Xie T, Yang Y, Luo Y, Deng Y, Chen K, Tan Z, Guo H, Xie L. Establishment of a Dihydrofolate Reductase Gene Knock-In Zebrafish Strain to Aid Preliminary Analysis of Congenital Heart Disease Mechanisms. Frontiers in Cardiovascular Medicine. 8: 763851. PMID 34977180 DOI: 10.3389/fcvm.2021.763851 |
0.088 |
|
| 2014 |
Liu JJ, Fan LL, Chen JL, Tan ZP, Yang YF. A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect. Journal of Zhejiang University. Science. B. 15: 830-7. PMID 25183037 DOI: 10.1631/jzus.B1400062 |
0.087 |
|
| 2021 |
Yang B, Lei C, Yang D, Tan Z, Guo T, Luo H. Whole-Exome Sequencing Identified Variants in Two Consanguineous Families in China. Frontiers in Genetics. 12: 631221. PMID 34276759 DOI: 10.3389/fgene.2021.631221 |
0.087 |
|
| 2017 |
Guo T, Tan ZP, Chen HM, Zheng DY, Liu L, Huang XG, Chen P, Luo H, Yang YF. An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families. Scientific Reports. 7: 7905. PMID 28801648 DOI: 10.1038/s41598-017-08510-z |
0.086 |
|
| 2023 |
Wang R, Yang D, Tu C, Lei C, Ding S, Guo T, Wang L, Liu Y, Lu C, Yang B, Ouyang S, Gong K, Tan Z, Deng Y, Tan Y, et al. Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice. Frontiers of Medicine. PMID 37314648 DOI: 10.1007/s11684-023-0988-8 |
0.085 |
|
| 2011 |
Gu TL, Deng X, Huang F, Tucker M, Crosby K, Rimkunas V, Wang Y, Deng G, Zhu L, Tan Z, Hu Y, Wu C, Nardone J, MacNeill J, Ren J, et al. Survey of tyrosine kinase signaling reveals ROS kinase fusions in human cholangiocarcinoma. Plos One. 6: e15640. PMID 21253578 DOI: 10.1371/journal.pone.0015640 |
0.083 |
|
| 2013 |
Zhu X, Zhang Y, Wang J, Yang JF, Yang YF, Tan ZP. 576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy. Gene. 528: 352-5. PMID 23892090 DOI: 10.1016/j.gene.2013.07.024 |
0.083 |
|
| 2007 |
Rikova K, Guo A, Zeng Q, Possemato A, Yu J, Haack H, Nardone J, Lee K, Reeves C, Li Y, Hu Y, Tan Z, Stokes M, Sullivan L, Mitchell J, et al. Global survey of phosphotyrosine signaling identifies oncogenic kinases in lung cancer. Cell. 131: 1190-203. PMID 18083107 DOI: 10.1016/J.Cell.2007.11.025 |
0.083 |
|
| 2017 |
Luo JW, Yang H, Tan ZP, Tu M, Luo H, Yang YF, Xie L. A clinical and molecular analysis of a patient with Emanuel syndrome. Molecular Medicine Reports. PMID 28075445 DOI: 10.3892/mmr.2017.6107 |
0.082 |
|
| 2014 |
Li FF, Tan ZJ, Guo ZF. Enantioseparation of mandelic acid and α-Cyclohexylmandelic acid using an alcohol/salt-based aqueous two-Phase system Chemical Papers. 68: 1539-1545. DOI: 10.2478/s11696-014-0594-y |
0.081 |
|
| 2023 |
Gong K, Tan Z, Liu H, Liao X, Zhou X, Yin B, Zeng S, Yao Y, Yang Y, Xie L. A novel mutation of glycogen synthase kinase-3β leads to a reduced level of GSK3β protein in a patient with dilated cardiomyopathy. Genes & Diseases. 11: 84-86. PMID 37588225 DOI: 10.1016/j.gendis.2023.02.040 |
0.08 |
|
| 2018 |
Tan Z, Zeng H, Xu Z, Tian Q, Gao X, Zhou C, Zheng Y, Wang J, Ling G, Wang B, Yang Y, Ma L. Identification of ANKDD1B variants in an ankylosing spondylitis pedigree and a sporadic patient. Bmc Medical Genetics. 19: 111. PMID 29976160 DOI: 10.1186/s12881-018-0622-9 |
0.079 |
|
| 2012 |
Wu XM, Tang T, Yang JF, Tan ZP, Zhang W. [Experimental study of rat mesenchymal stem cells transfected with Sonic Hedgehog gene]. Zhonghua Yi Xue Za Zhi. 92: 705-8. PMID 22781301 |
0.079 |
|
| 2015 |
Deng Y, Wei S, Hu S, Chen J, Tan Z, Yang Y. Ehlers-Danlos syndrome type IV is associated with a novel G984R COL3A1 mutation. Molecular Medicine Reports. 12: 1119-24. PMID 25776230 DOI: 10.3892/mmr.2015.3488 |
0.078 |
|
| 2017 |
Hu S, Yang Y, Liu L, Tan Z, Zhao T. High-resolution single nucleotide polymorphism arrays identified an atypical microdeletion of the Williams-Beuren syndrome interval in a patient presenting with a different phenotype. Molecular Medicine Reports. PMID 28259930 DOI: 10.3892/mmr.2017.6279 |
0.077 |
|
| 2018 |
Peng JX, Wang LZ, Diao JF, Tan ZJ, Zhong XS, Zhen ZP, Chen GH, He JM. Major hepatectomy for primary hepatolithiasis: a comparative study of laparoscopic versus open treatment. Surgical Endoscopy. PMID 29616339 DOI: 10.1007/s00464-018-6176-2 |
0.077 |
|
| 2019 |
Zhang W, Li D, Wei S, Guo T, Wang J, Luo H, Yang Y, Tan Z. Correction: Whole-exome sequencing identifies a novel CCDC151 mutation, c.325GT (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus. Journal of Human Genetics. PMID 31178588 DOI: 10.1038/s10038-019-0624-2 |
0.077 |
|
| 2015 |
Zhu X, Fu-Rong D, Wang J, Zhang Y, Tan ZP, Zhang Y. Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome. Gene. PMID 26196063 DOI: 10.1016/j.gene.2015.07.061 |
0.076 |
|
| 2014 |
Chen JL, Zhu X, Zhao TL, Wang J, Yang YF, Tan ZP. Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11. Molecular Cytogenetics. 7: 28. PMID 24739123 DOI: 10.1186/1755-8166-7-28 |
0.074 |
|
| 2021 |
Yang G, Yin Y, Tan Z, Liu J, Deng X, Yang Y. Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss. Bmc Medical Genomics. 14: 24. PMID 33478437 DOI: 10.1186/s12920-021-00871-9 |
0.074 |
|
| 2003 |
Huang LQ, Shi XL, Tan ZP, Fang HY, Zheng D, Xia JH, Xia K. [Translational frameshift may be occur in p11, an interaction protein of Cx31, in yeast]. Sheng Wu Hua Xue Yu Sheng Wu Wu Li Xue Bao Acta Biochimica Et Biophysica Sinica. 34: 219-24. PMID 12007000 |
0.073 |
|
| 2018 |
Zeng H, Xie L, Tang M, Yang Y, Tan Z. [A de novo GJA1 mutation identified by whole-exome sequencing in a patient with oculodentodigital dysplasia]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics. 35: 268-271. PMID 29653008 DOI: 10.3760/cma.j.issn.1003-9406.2018.02.028 |
0.072 |
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| 2023 |
Luo Y, Gong K, Xie T, Liu R, Wang L, Liu H, Tan Z, Yao Y, Xie L. A Novel Variant of CDH2 in Dilated Cardiomyopathy. Qjm : Monthly Journal of the Association of Physicians. PMID 36961336 DOI: 10.1093/qjmed/hcad047 |
0.071 |
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| 2020 |
Bu H, Yang Y, Wu Q, Tan Z, Gong X, Hu S, Zhao T. Identification of KIAA0196 as a novel susceptibility gene for myofibril structural disorganization in cardiac development. International Journal of Cardiology. PMID 32417190 DOI: 10.1016/j.ijcard.2020.05.029 |
0.071 |
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| 2017 |
Liu L, Bu H, Yang Y, Tan Z, Zhang F, Hu S, Zhao T. A Targeted, Next-Generation Genetic Sequencing Study on Tetralogy of Fallot, Combined With Cleft Lip and Palate. The Journal of Craniofacial Surgery. PMID 28230599 DOI: 10.1097/SCS.0000000000003598 |
0.07 |
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| 2015 |
Sun G, Tan Z, Fan L, Wang J, Yang Y, Zhang W. 1q21.1 microduplication in a patient with mental impairment and congenital heart defect. Molecular Medicine Reports. 12: 5655-8. PMID 26238956 DOI: 10.3892/mmr.2015.4166 |
0.068 |
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| 2015 |
Luo J, Xu Z, Tan Z, Zhang Z, Ma L. Neuropeptide receptors NPR-1 and NPR-2 regulate Caenorhabditis elegans avoidance response to the plant stress hormone methyl salicylate. Genetics. 199: 523-31. PMID 25527285 DOI: 10.1534/genetics.114.172239 |
0.068 |
|
| 2015 |
Tang M, Yang YF, Xie L, Chen JL, Zhang WZ, Wang J, Zhao TL, Yang JF, Tan ZP. Duplication of 10q22.3-q23.3 encompassing BMPR1A and NGR3 associated with congenital heart disease, microcephaly, and mild intellectual disability. American Journal of Medical Genetics. Part A. PMID 26383923 DOI: 10.1002/ajmg.a.37347 |
0.068 |
|
| 2010 |
Chen J, Li B, Yang Y, Hu J, Zhao T, Gong Y, Tan Z. Mutations of the TGFBR2 gene in Chinese patients with Marfan-related syndrome. Clinical and Investigative Medicine. MéDecine Clinique Et Experimentale. 33: E14-21. PMID 20144264 |
0.067 |
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| 2021 |
Bu H, Sun G, Zhu Y, Yang Y, Tan Z, Zhao T, Hu S. The M310T mutation in the GATA4 gene is a novel pathogenic target of the familial atrial septal defect. Bmc Cardiovascular Disorders. 21: 12. PMID 33413087 DOI: 10.1186/s12872-020-01822-5 |
0.067 |
|
| 2009 |
Tang T, Yang J, Li F, Zhou W, Liu J, Tan Z, Zheng W, Yang Y, Zhou X, Hu J. Experimental study of the effects of marrow mesenchymal stem cells transfected with hypoxia-inducible factor-1 Gene Journal of Biomedicine and Biotechnology. 2009. PMID 19587827 DOI: 10.1155/2009/128627 |
0.067 |
|
| 2012 |
Chen JL, Yang YF, Huang C, Wang J, Yang JF, Tan ZP. Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies. American Journal of Medical Genetics. Part A. 158: 685-8. PMID 22307725 DOI: 10.1002/ajmg.a.34434 |
0.066 |
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| 2014 |
Xie L, Chen JL, Zhang WZ, Wang SZ, Zhao TL, Huang C, Wang J, Yang JF, Yang YF, Tan ZP. Rare de novo copy number variants in patients with congenital pulmonary atresia. Plos One. 9: e96471. PMID 24826987 DOI: 10.1371/journal.pone.0096471 |
0.066 |
|
| 2012 |
Tan ZJ, Li FF, Xu XL. Extraction and purification of anthraquinones derivatives from Aloe vera L. using alcohol/salt aqueous two-phase system. Bioprocess and Biosystems Engineering. 36: 1105-13. PMID 23207826 DOI: 10.1007/s00449-012-0864-4 |
0.065 |
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| 2022 |
Luo Y, Gong K, Xie T, Liu R, Guo H, Wang L, Tan Z, Hu SJ, Yang Y, Xie L. Case Report: A Young Man With Giant Pericardial Synovial Sarcoma. Frontiers in Cardiovascular Medicine. 9: 829328. PMID 35155638 DOI: 10.3389/fcvm.2022.829328 |
0.064 |
|
| 2011 |
Ma L, Tan Z, Teng Y, Hoersch S, Horvitz HR. In vivo effects on intron retention and exon skipping by the U2AF large subunit and SF1/BBP in the nematode Caenorhabditis elegans. Rna (New York, N.Y.). 17: 2201-11. PMID 22033331 DOI: 10.1261/rna.027458.111 |
0.064 |
|
| 2012 |
Huang C, Yang YF, Yin N, Chen JL, Wang J, Zhang H, Tan ZP. Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion. Gene. 498: 308-10. PMID 22366306 DOI: 10.1016/j.gene.2012.01.083 |
0.062 |
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| 2022 |
Hou C, Zhang X, Tang Y, Zhuang J, Tan Z, Huang H, Chen W, Wei S, He Y, Luo S. Detection and localization of citrus fruit based on improved You Only Look Once v5s and binocular vision in the orchard. Frontiers in Plant Science. 13: 972445. PMID 35968138 DOI: 10.3389/fpls.2022.972445 |
0.059 |
|
| 2016 |
Chen XJ, Zhang H, Tan ZP, Hu W, Yang YF. Novel mutation of EXT2 identified in a large family with multiple osteochondromas. Molecular Medicine Reports. PMID 27748933 DOI: 10.3892/mmr.2016.5814 |
0.058 |
|
| 2022 |
Xie T, Yang Y, Gong K, Luo Y, Guo H, Liu R, Wang L, Tan Z, Luo J, Xie L. Whole-Exome Sequencing Identifies a Novel Variant (c.1538T > C) of in Arrhythmogenic Right Ventricular Cardiomyopathy. Frontiers in Cardiovascular Medicine. 9: 843837. PMID 35274013 DOI: 10.3389/fcvm.2022.843837 |
0.058 |
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| 2013 |
Yang YF, Ai Q, Huang C, Chen JL, Wang J, Xie L, Zhang WZ, Yang JF, Tan ZP. A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region. Gene. 528: 51-4. PMID 23639964 DOI: 10.1016/j.gene.2013.03.145 |
0.057 |
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| 2022 |
Fan LL, Yuan ZZ, Jiao ZJ, Zeng H, Yang YF, Tan ZP. Haploinsufficiency of syncoilin leads to hypertrophic cardiomyopathy. Genes & Diseases. 9: 1412-1414. PMID 36157493 DOI: 10.1016/j.gendis.2022.02.011 |
0.056 |
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| 2022 |
Wang J, Zhao T, Tan Z, Gong X, Ahemaiti Y, Wei L, Hu S. Deletion of 11q24.2-qter in a male child with cleft lip and palate: an atypical feature of Jacobsen syndrome. Journal of Genetics. 101. PMID 36156508 |
0.054 |
|
| 2016 |
Dong HY, Zeng H, Hu YQ, Xie L, Wang J, Wang XY, Yang YF, Tan ZP. 19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome. Molecular Cytogenetics. 9: 71. PMID 27688808 DOI: 10.1186/s13039-016-0282-4 |
0.053 |
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| 2021 |
Gong K, Xie T, Luo Y, Guo H, Chen J, Tan Z, Yang Y, Xie L. Comprehensive analysis of lncRNA biomarkers in kidney renal clear cell carcinoma by lncRNA-mediated ceRNA network. Plos One. 16: e0252452. PMID 34101736 DOI: 10.1371/journal.pone.0252452 |
0.052 |
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| 2015 |
Hu W, Fu S, Diao J, Wan D, Tan Z, Zhi Q, He J. The prognostic value of serum LDH levels in patients with hepatocellualr carcinoma after hepatic resection Anti-Cancer Agents in Medicinal Chemistry. 15: 1-1. DOI: 10.2174/1871520615666150716110942 |
0.052 |
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| 2012 |
Luo H, Xie L, Wang SZ, Chen JL, Huang C, Wang J, Yang JF, Zhang WZ, Yang YF, Tan ZP. Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly. European Journal of Medical Genetics. 55: 646-9. PMID 22902603 DOI: 10.1016/j.ejmg.2012.07.006 |
0.052 |
|
| 2012 |
Huang H, Jiang H, Kong X, Liu T, Tan Z, Chen P, Luo H. [Association of intercellular adhesion molecule-1 gene K469E polymorphism with chronic obstructive pulmonary disease]. Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences. 37: 78-83. PMID 22349390 DOI: 10.3969/j.issn.1672-7347.2012.01.014 |
0.051 |
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| 2003 |
Tan ZP, Huang LQ, Zheng D. [Expression and purification of p11 fusion protein in E. coli and preparation of antiserum against GST-p11]. Hunan Yi Ke Da Xue Xue Bao = Hunan Yike Daxue Xuebao = Bulletin of Hunan Medical University. 27: 189-91. PMID 12575286 |
0.048 |
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| 2022 |
Li D, Yi Z, Wu Q, Huang Y, Yao H, Tan Z, Yang Y, Zhang W. Denovo DCHS1 splicing mutation in a patient with mitral valve prolapse. Qjm : Monthly Journal of the Association of Physicians. PMID 36053189 DOI: 10.1093/qjmed/hcac214 |
0.047 |
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| 2023 |
Gong K, Yang K, Xie T, Luo Y, Guo H, Tan Z, Chen J, Wu Q, Gong Y, Wei L, Luo J, Yao Y, Yang Y, Xie L. Identification of circRNA-miRNA-mRNA regulatory network and its role in cardiac hypertrophy. Plos One. 18: e0279638. PMID 36952519 DOI: 10.1371/journal.pone.0279638 |
0.037 |
|
| 2015 |
Chen LL, Li FF, Tan ZJ. Chiral separation of α-cyclohexylmandelic acid enantiomers using ionic liquid/salt aqueous two-phase system Chemical Papers. 69: 1465-1472. DOI: 10.1515/chempap-2015-0162 |
0.037 |
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| 2020 |
Liu R, Tan Z, Li J, Yan Y, Ren W, Zhang M, Yang S, Zhao H. Improvements to the retractor and muscle flap design for minimally invasive cochlear implantation. Journal of Otology. 15: 41-44. PMID 32110240 DOI: 10.1016/j.joto.2019.09.003 |
0.035 |
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| 2020 |
Yang DH, Guo T, Yuan ZZ, Lei C, Ding SZ, Yang YF, Tan ZP, Luo H. Mutant CARD10 in a family with progressive immunodeficiency and autoimmunity. Cellular & Molecular Immunology. PMID 32238915 DOI: 10.1038/s41423-020-0423-x |
0.03 |
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| 2009 |
Chen J, Yang Y, Tan Z, Wang Y, Tang X, Gong Y. [Noonan syndrome: a case report and literature review]. Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences. 34: 1261-5. PMID 20045924 |
0.027 |
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| 2012 |
Tan Z, Li F. Cloud-point extraction and preconcentration of bisphenol A from water samples Journal of Central South University. 19: 2136-2141. DOI: 10.1007/S11771-012-1256-2 |
0.014 |
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