| Year |
Citation |
Score |
| 2020 |
Yin H, Peng R, Chen Z, Wang H, Zhang T, Zheng Y. WDR34 mutation from anencephaly patients impaired both SHH and PCP signaling pathways. Journal of Human Genetics. PMID 32576942 DOI: 10.1038/S10038-020-0793-Z |
0.326 |
|
| 2020 |
Ye J, Tong Y, Lv J, Peng R, Chen S, Kuang L, Su K, Zheng Y, Zhang T, Zhang F, Jin L, Yang X, Wang H. Rare mutations in the autophagy-regulating gene AMBRA1 contribute to human neural tube defects. Human Mutation. PMID 32333458 DOI: 10.1002/Humu.24028 |
0.321 |
|
| 2020 |
Tang B, Li X, Maretzky T, Perez-Aguilar JM, McIlwain D, Xie Y, Zheng Y, Mak TW, Weinstein H, Blobel CP. Substrate-selective protein ectodomain shedding by ADAM17 and iRhom2 depends on their juxtamembrane and transmembrane domains. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 32103528 DOI: 10.1096/Fj.201902649R |
0.613 |
|
| 2019 |
Shi Z, Chen S, Han X, Peng R, Luo J, Yang L, Zheng Y, Wang H. The rare mutation in the endosome-associated recycling protein gene is associated with human neural tube defects. Molecular Cytogenetics. 12: 8. PMID 30828385 DOI: 10.1186/S13039-019-0421-9 |
0.334 |
|
| 2019 |
Zhu MJ, Ma XY, Ding PC, Tang HF, Peng R, Lu L, Li PQ, Qiao B, Yang XY, Zheng YF, Wang HY, Gao YQ, Chen FS. Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort. Journal of Human Genetics. PMID 30760879 DOI: 10.1038/S10038-019-0572-X |
0.305 |
|
| 2019 |
Lei Y, Kim SE, Chen Z, Cao X, Zhu H, Yang W, Shaw GM, Zheng Y, Zhang T, Wang HY, Finnell RH. Variants identified in PTK7 associated with neural tube defects. Molecular Genetics & Genomic Medicine. e584. PMID 30689296 DOI: 10.1002/Mgg3.584 |
0.312 |
|
| 2019 |
Xie Y, Ma A, Wang B, Peng R, Jing Y, Wang D, Finnell RH, Qiao B, Wang Y, Wang H, Zheng Y. Rare mutations of from TOFs induce hypertrophy in human embryonic stem cell-derived cardiomyocytes via HB-EGF signaling. Clinical Science (London, England : 1979). PMID 30610007 DOI: 10.1042/Cs20180842 |
0.328 |
|
| 2018 |
Li B, Yu L, Liu D, Yang X, Zheng Y, Gui Y, Wang H. MIB1 Mutations Reduce Notch Signaling Activation and Contribute to Congenital Heart Disease. Clinical Science (London, England : 1979). PMID 30322850 DOI: 10.1042/Cs20180732 |
0.331 |
|
| 2018 |
Wang B, Zhang Y, Dong H, Gong S, Wei B, Luo M, Wang H, Wu X, Liu W, Xu X, Zheng Y, Sun M. Loss of Tctn3 causes neuronal apoptosis and neural tube defects in mice. Cell Death & Disease. 9: 520. PMID 29725084 DOI: 10.1038/S41419-018-0563-4 |
0.312 |
|
| 2018 |
Chen M, Lyu G, Han M, Nie H, Shen T, Chen W, Niu Y, Song Y, Li X, Li H, Chen X, Wang Z, Xia Z, Li W, Tian XL, ... ... Zheng Y, et al. 3' UTR lengthening as a novel mechanism in regulating cellular senescence. Genome Research. PMID 29440281 DOI: 10.1101/Gr.224451.117 |
0.357 |
|
| 2017 |
Shi Z, Yang X, Li BB, Chen S, Yang L, Cheng L, Zhang T, Wang H, Zheng Y. Novel Mutation of LRP6 Identified in Chinese Han Population Links Canonical WNT Signaling to Neural Tube Defects. Birth Defects Research. PMID 28960852 DOI: 10.1002/Bdr2.1122 |
0.311 |
|
| 2016 |
Qiao X, Liu Y, Li P, Chen Z, Li H, Yang X, Finnell RH, Yang Z, Zhang T, Qiao B, Zheng Y, Wang H. Genetic analysis of rare coding mutations in CELSR1-3 in Chinese Congenital Heart and Neural Tube Defects. Clinical Science (London, England : 1979). PMID 27756857 DOI: 10.1042/Cs20160686 |
0.309 |
|
| 2016 |
Yu LW, Wang F, Yang XY, Sun SN, Zheng YF, Li BB, Gui YH, Wang HY. Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population. Scientific Reports. 6: 23662. PMID 27034249 DOI: 10.1038/Srep23662 |
0.301 |
|
| 2016 |
Liu B, Ma A, Zhang F, Wang Y, Li Z, Li Q, Xu Z, Zheng Y. MAZ mediates the cross-talk between CT-1 and NOTCH1 signaling during gliogenesis. Scientific Reports. 6: 21534. PMID 26867947 DOI: 10.1038/Srep21534 |
0.319 |
|
| 2014 |
Wu X, Cao MP, Shen YY, Chu KP, Tao WB, Song WT, Liu LP, Wang XH, Zheng YF, Chen SD, Zeng QL, Xia RH. Weak power frequency magnetic field acting similarly to EGF stimulation, induces acute activations of the EGFR sensitive actin cytoskeleton motility in human amniotic cells. Plos One. 9: e87626. PMID 24505297 DOI: 10.1371/Journal.Pone.0087626 |
0.325 |
|
| 2014 |
Zhang X, Hong S, Kang Y, Zheng Y, Sun H, Xu C. Expression and purification of the extracellular domain of the human follicle-stimulating hormone receptor using Escherichia coli. The Journal of Obstetrics and Gynaecology Research. 40: 501-8. PMID 24147778 DOI: 10.1111/Jog.12203 |
0.34 |
|
| 2013 |
Li Q, Zhang Z, Li Z, Zhou M, Liu B, Pan L, Ma Z, Zheng Y. ADAM17 is critical for multipolar exit and radial migration of neuronal intermediate progenitor cells in mice cerebral cortex. Plos One. 8: e65703. PMID 23755270 DOI: 10.1371/Journal.Pone.0065703 |
0.31 |
|
| 2013 |
Wang E, Sun S, Qiao B, Duan W, Huang G, An Y, Xu S, Zheng Y, Su Z, Gu X, Jin L, Wang H. Identification of functional mutations in GATA4 in patients with congenital heart disease. Plos One. 8: e62138. PMID 23626780 DOI: 10.1371/Journal.Pone.0062138 |
0.31 |
|
| 2012 |
Peng C, Ye J, Yan S, Kong S, Shen Y, Li C, Li Q, Zheng Y, Deng K, Xu T, Tao W. Ablation of vacuole protein sorting 18 (Vps18) gene leads to neurodegeneration and impaired neuronal migration by disrupting multiple vesicle transport pathways to lysosomes. The Journal of Biological Chemistry. 287: 32861-73. PMID 22854957 DOI: 10.1074/Jbc.M112.384305 |
0.311 |
|
| 2012 |
Li J, Liu B, Gao X, Ma Z, CaoSong T, Mei YA, Zheng Y. Overexpression of sigma-1 receptor inhibits ADAM10 and ADAM17 mediated shedding in vitro. Protein & Cell. 3: 153-9. PMID 22322890 DOI: 10.1007/S13238-012-2006-9 |
0.342 |
|
| 2011 |
Zhou L, Zhang Z, Zheng Y, Zhu Y, Wei Z, Xu H, Tang Q, Kong X, Hu L. SKAP2, a novel target of HSF4b, associates with NCK2/F-actin at membrane ruffles and regulates actin reorganization in lens cell. Journal of Cellular and Molecular Medicine. 15: 783-95. PMID 20219016 DOI: 10.1111/J.1582-4934.2010.01048.X |
0.361 |
|
| 2009 |
Kang Y, Zhang XY, Jiang W, Wu CQ, Chen CM, Gu JR, Zheng YF, Xu CJ. The piggyBac transposon is an integrating non-viral gene transfer vector that enhances the efficiency of GDEPT. Cell Biology International. 33: 509-15. PMID 19353779 DOI: 10.1016/J.Cellbi.2009.01.017 |
0.31 |
|
| 2008 |
Ly A, Nikolaev A, Suresh G, Zheng Y, Tessier-Lavigne M, Stein E. DSCAM is a netrin receptor that collaborates with DCC in mediating turning responses to netrin-1. Cell. 133: 1241-54. PMID 18585357 DOI: 10.1016/J.Cell.2008.05.030 |
0.661 |
|
| 2006 |
Sahin U, Weskamp G, Zheng Y, Chesneau V, Horiuchi K, Blobel CP. A sensitive method to monitor ectodomain shedding of ligands of the epidermal growth factor receptor. Methods in Molecular Biology (Clifton, N.J.). 327: 99-113. PMID 16780215 DOI: 10.1385/1-59745-012-X:99 |
0.688 |
|
| 2004 |
Zheng Y, Saftig P, Hartmann D, Blobel C. Evaluation of the contribution of different ADAMs to tumor necrosis factor alpha (TNFalpha) shedding and of the function of the TNFalpha ectodomain in ensuring selective stimulated shedding by the TNFalpha convertase (TACE/ADAM17). The Journal of Biological Chemistry. 279: 42898-906. PMID 15292243 DOI: 10.1074/Jbc.M403193200 |
0.576 |
|
| 2003 |
Chesneau V, Becherer JD, Zheng Y, Erdjument-Bromage H, Tempst P, Blobel CP. Catalytic properties of ADAM19. The Journal of Biological Chemistry. 278: 22331-40. PMID 12682046 DOI: 10.1074/Jbc.M302781200 |
0.604 |
|
| 2002 |
Zheng Y, Schlondorff J, Blobel CP. Evidence for regulation of the tumor necrosis factor alpha-convertase (TACE) by protein-tyrosine phosphatase PTPH1. The Journal of Biological Chemistry. 277: 42463-70. PMID 12207026 DOI: 10.1074/Jbc.M207459200 |
0.697 |
|
| 2001 |
Howard L, Zheng Y, Horrocks M, Maciewicz RA, Blobel C. Catalytic activity of ADAM28. Febs Letters. 498: 82-6. PMID 11389903 DOI: 10.1016/S0014-5793(01)02506-6 |
0.576 |
|
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