Year |
Citation |
Score |
2020 |
Greco R, Qu H, Qu H, Theilhaber J, Shapiro G, Gregory R, Winter C, Malkova N, Sun F, Jaworski J, Best A, Pao L, Hebert A, Levit M, Protopopov A, ... ... Wiederschain D, et al. Pan-TGFβ inhibition by SAR439459 relieves immunosuppression and improves antitumor efficacy of PD-1 blockade. Oncoimmunology. 9: 1811605. PMID 33224628 DOI: 10.1080/2162402X.2020.1811605 |
0.305 |
|
2020 |
Zhu C, Song Z, Wang A, Srinivasan S, Yang G, Greco R, Theilhaber J, Shehu E, Wu L, Yang ZY, Passe-Coutrin W, Fournier A, Tai YT, Anderson KC, Wiederschain D, et al. Isatuximab Acts Through Fc-Dependent, Independent, and Direct Pathways to Kill Multiple Myeloma Cells. Frontiers in Immunology. 11: 1771. PMID 32922390 DOI: 10.3389/Fimmu.2020.01771 |
0.309 |
|
2020 |
Theilhaber J, Pollard J, Pomponio R, Sanicola-Nadel M, Caron A, Naimi S, Wiederschain D, Lin TT, Wang R. Abstract 4321: Integrating multiplex immunohistochemistry (IHC) and transcriptomics for characterization of association between spatial heterogeneity of lymphocytic infiltration and TGFβ pathway activity in solid tumors Endocrinology. 80: 4321-4321. DOI: 10.1158/1538-7445.Am2020-4321 |
0.319 |
|
2018 |
Wagenaar TR, Hotz C, Gieseke F, Cao H, Diekmann J, Diken M, Grunwitz C, Hebert A, Hsu K, Jordan M, Kariko K, Kreiter S, Kuhn AN, Levit M, Malkova N, ... ... Wiederschain D, et al. Abstract LB-130: Combinatorial treatment with intratumoral cytokine mRNAs results in high frequency of tumor rejection and development of anti-tumor immunity across a range of preclinical cancer models Cancer Research. 78. DOI: 10.1158/1538-7445.Am2018-Lb-130 |
0.302 |
|
2018 |
Theilhaber J, Cavallo J, Madden SL, Manning C, Cao S, Mankoo P, Pomponio R, Qu H, Malkova N, Shapiro G, Winter C, Wiederschain D, Sanicola-Nadel M, Sun F, Lin TT, et al. Abstract 5550: Translational biomarkers for SAR439459, an anti-TGFβ antibody for cancer immunotherapy Cancer Research. 78: 5550-5550. DOI: 10.1158/1538-7445.Am2018-5550 |
0.314 |
|
2018 |
Henry C, Lampa M, He T, Ospina B, Zhang B, Deng G, Barberis C, Hoffmann D, Pollard J, Francisco A, Arlt H, Reeves J, Murtie J, Winter C, Richon V, ... ... Wiederschain D, et al. Abstract 5472: Basal-like breast cancer subtype is characterized by deregulated glutamine metabolism and is sensitive to GLS inhibition Cancer Research. 78: 5472-5472. DOI: 10.1158/1538-7445.Am2018-5472 |
0.314 |
|
2017 |
Lampa M, Arlt H, He T, Ospina B, Reeves J, Zhang B, Murtie J, Deng G, Barberis C, Hoffmann D, Cheng H, Pollard J, Winter C, Richon V, Garcia-Escheverria C, ... ... Wiederschain D, et al. Glutaminase is essential for the growth of triple-negative breast cancer cells with a deregulated glutamine metabolism pathway and its suppression synergizes with mTOR inhibition. Plos One. 12: e0185092. PMID 28950000 DOI: 10.1371/Journal.Pone.0185092 |
0.349 |
|
2015 |
Tateishi K, Wakimoto H, Iafrate AJ, Tanaka S, Loebel F, Lelic N, Wiederschain D, Bedel O, Deng G, Zhang B, He T, Shi X, Gerszten RE, Zhang Y, Yeh JR, et al. Extreme Vulnerability of IDH1 Mutant Cancers to NAD+ Depletion. Cancer Cell. 28: 773-84. PMID 26678339 DOI: 10.1016/J.Ccell.2015.11.006 |
0.302 |
|
2015 |
Deng G, Shen J, Yin M, McManus J, Mathieu M, Gee P, He T, Shi C, Bedel O, McLean LR, Le-Strat F, Zhang Y, Marquette JP, Gao Q, Zhang B, ... ... Wiederschain D, et al. Selective inhibition of mutant isocitrate dehydrogenase 1 (IDH1) via disruption of a metal binding network by an allosteric small molecule. The Journal of Biological Chemistry. 290: 762-74. PMID 25391653 DOI: 10.1074/Jbc.M114.608497 |
0.326 |
|
2014 |
Huang SM, Wang A, Greco R, Li Z, Barberis C, Tabart M, Patel V, Schio L, Hurley R, Chen B, Cheng H, Lengauer C, Pollard J, Watters J, Garcia-Echeverria C, ... Wiederschain D, et al. Combination of PIM and JAK2 inhibitors synergistically suppresses MPN cell proliferation and overcomes drug resistance. Oncotarget. 5: 3362-74. PMID 24830942 DOI: 10.18632/Oncotarget.1951 |
0.317 |
|
2014 |
Deng G, Licht S, Shen J, Yin M, McManus J, Gee P, He T, Gao G, Zhang B, Mathieu M, Rak A, Bedel O, Shi C, Gross S, Hoffmann D, ... ... Wiederschain D, et al. Abstract 4746: Selective inhibition of mutant IDH1 via small molecule binding to the dimer interface Cancer Research. 74: 4746-4746. DOI: 10.1158/1538-7445.Am2014-4746 |
0.323 |
|
2013 |
Gao Q, Mechin I, Kothari N, Guo Z, Deng G, Haas K, McManus J, Hoffmann D, Wang A, Wiederschain D, Rocnik J, Czechtizky W, Chen X, McLean L, Arlt H, et al. Evaluation of cancer dependence and druggability of PRP4 kinase using cellular, biochemical, and structural approaches. The Journal of Biological Chemistry. 288: 30125-38. PMID 24003220 DOI: 10.1074/Jbc.M113.473348 |
0.301 |
|
2013 |
Gao Q, Mechin I, Kothari N, Guo Z, Deng G, Wang A, Wiederschain D, Rocnik J, Czechtizky W, Liu F, Majid T, Patel V, Lengauer C, Garcia-Echeverria C, Zhang B, et al. Abstract 4376: Evaluation of PRP4 kinase as a potential drug target in cancer. Cancer Research. 73: 4376-4376. DOI: 10.1158/1538-7445.Am2013-4376 |
0.308 |
|
2007 |
Kawai H, Lopez-Pajares V, Kim MM, Wiederschain D, Yuan ZM. RING domain-mediated interaction is a requirement for MDM2's E3 ligase activity. Cancer Research. 67: 6026-30. PMID 17616658 DOI: 10.1158/0008-5472.Can-07-1313 |
0.663 |
|
2007 |
Kim MM, Wiederschain D, Kennedy D, Hansen E, Yuan ZM. Modulation of p53 and MDM2 activity by novel interaction with Ras-GAP binding proteins (G3BP). Oncogene. 26: 4209-15. PMID 17297477 DOI: 10.1038/Sj.Onc.1210212 |
0.757 |
|
2006 |
Wiederschain D, Yuan ZM. Functional inactivation of P53 as a potential mechanism of MLL leukemogenesis. Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences. 31: 617-20. PMID 17062917 |
0.665 |
|
2005 |
Wiederschain D, Kawai H, Shilatifard A, Yuan ZM. Multiple mixed lineage leukemia (MLL) fusion proteins suppress p53-mediated response to DNA damage. The Journal of Biological Chemistry. 280: 24315-21. PMID 15851483 DOI: 10.1074/Jbc.M412237200 |
0.686 |
|
2003 |
Kawai H, Wiederschain D, Kitao H, Stuart J, Tsai KK, Yuan ZM. DNA damage-induced MDMX degradation is mediated by MDM2. The Journal of Biological Chemistry. 278: 45946-53. PMID 12963717 DOI: 10.1074/Jbc.M308295200 |
0.657 |
|
2003 |
Kawai H, Wiederschain D, Yuan ZM. Critical contribution of the MDM2 acidic domain to p53 ubiquitination. Molecular and Cellular Biology. 23: 4939-47. PMID 12832479 DOI: 10.1128/Mcb.23.14.4939-4947.2003 |
0.703 |
|
2003 |
Wiederschain D, Kawai H, Gu J, Shilatifard A, Yuan ZM. Molecular basis of p53 functional inactivation by the leukemic protein MLL-ELL. Molecular and Cellular Biology. 23: 4230-46. PMID 12773566 DOI: 10.1128/Mcb.23.12.4230-4246.2003 |
0.7 |
|
2002 |
Gu J, Kawai H, Nie L, Kitao H, Wiederschain D, Jochemsen AG, Parant J, Lozano G, Yuan ZM. Mutual dependence of MDM2 and MDMX in their functional inactivation of p53. The Journal of Biological Chemistry. 277: 19251-4. PMID 11953423 DOI: 10.1074/Jbc.C200150200 |
0.716 |
|
2001 |
Gu J, Nie L, Wiederschain D, Yuan ZM. Identification of p53 sequence elements that are required for MDM2-mediated nuclear export. Molecular and Cellular Biology. 21: 8533-46. PMID 11713288 DOI: 10.1128/Mcb.21.24.8533-8546.2001 |
0.708 |
|
2001 |
Kawai H, Nie L, Wiederschain D, Yuan ZM. Dual role of p300 in the regulation of p53 stability. The Journal of Biological Chemistry. 276: 45928-32. PMID 11591713 DOI: 10.1074/Jbc.M107770200 |
0.693 |
|
2001 |
Wiederschain D, Gu J, Yuan ZM. Evidence for a distinct inhibitory factor in the regulation of p53 functional activity. The Journal of Biological Chemistry. 276: 27999-8005. PMID 11382762 DOI: 10.1074/Jbc.M102400200 |
0.723 |
|
2001 |
Gu J, Kawai H, Wiederschain D, Yuan ZM. Mechanism of functional inactivation of a Li-Fraumeni syndrome p53 that has a mutation outside of the DNA-binding domain. Cancer Research. 61: 1741-6. PMID 11245491 |
0.65 |
|
2000 |
LaMontagne KR, Moses MA, Wiederschain D, Mahajan S, Holden J, Ghazizadeh H, Frank DA, Arbiser JL. Inhibition of MAP kinase kinase causes morphological reversion and dissociation between soft agar growth and in vivo tumorigenesis in angiosarcoma cells. The American Journal of Pathology. 157: 1937-45. PMID 11106566 DOI: 10.1016/S0002-9440(10)64832-8 |
0.345 |
|
2000 |
Fang J, Shing Y, Wiederschain D, Yan L, Butterfield C, Jackson G, Harper J, Tamvakopoulos G, Moses MA. Matrix metalloproteinase-2 is required for the switch to the angiogenic phenotype in a tumor model. Proceedings of the National Academy of Sciences of the United States of America. 97: 3884-9. PMID 10760260 DOI: 10.1073/Pnas.97.8.3884 |
0.307 |
|
1999 |
O'Reilly MS, Wiederschain D, Stetler-Stevenson WG, Folkman J, Moses MA. Regulation of angiostatin production by matrix metalloproteinase-2 in a model of concomitant resistance. The Journal of Biological Chemistry. 274: 29568-71. PMID 10506224 DOI: 10.1074/Jbc.274.41.29568 |
0.316 |
|
1999 |
Moses MA, Wiederschain D, Wu I, Fernandez CA, Ghazizadeh V, Lane WS, Flynn E, Sytkowski A, Tao T, Langer R. Troponin I is present in human cartilage and inhibits angiogenesis. Proceedings of the National Academy of Sciences of the United States of America. 96: 2645-50. PMID 10077564 DOI: 10.1073/Pnas.96.6.2645 |
0.321 |
|
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