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| 1 | Fate and Transport of Antibiotic Residues and Antibiotic Resistance Genes following Land Application of Manure Waste显示文摘 | Chee-Sanford Joanne C Mackie Roderick I Koike Satoshi Krapac Ivan G Lin Yu-Feng Yannarell Anthony C Maxwell Scott Aminov Rustam I | 2009 | Journal of Environmental Quality2009，，3： | 3 |
| 2 | Business angel early stage decision making显示文摘 | Andrew L. Maxwell Scott A. Jeffrey Moren Lévesque | 2009 | Journal of Business Venturing2009，，2： | 1 |
| 3 | SAHA attenuates Takotsubo-like myocardial injury by targeting an epigenetic Ac/Dc axis显示文摘Dear Editor,Takotsubo syndrome(TS)is a stress-induced non-ischaemic cardiomyopathy that is more common in women,but is associated with higher morbidity and mortality in males.Also known as broken-heart syndrome,TS is characterised by transient left ventricular(LV)dysfunction independent of obstructive coronary artery disease.TS is a polygenic condition and nowhere is this more evident than the use of positive inotropes,such as isoprenaline(ISO)in pre-clinical models.1 There is no standard therapy for broken-heart syndrome because the mechanisms underlying the condition remain unknown.Furthermore,there is no consensus on predisposition for Takotsubo2 and our goal was to better understand the regulatory mechanism as a first step towards improved treatment plans.Suberanilohydroxamic acid or SAHA,a drug approved for cancer treatment by the US Food and Drug Administration has previously been shown to improve cardiopulmonary function.3 We tested the hypothesis that the cardioprotective benefit of SAHA in a pre-clinical model of Takotsubo is conferred by an epigenetic acetylation/deacetylation(Ac/Dc)axis. | Ishant Khurana Scott Maxwell Simon Royce Prabhu Mathiyalagan Tom Karagiannis Nadia Mazarakis Jitraporn Vongsvivut Harikrishnan K.N. Jun Okabe Keith Al-Hasani Chrishan Samuel Assam El-Osta | 2021 | Signal Transduction and Targeted Therapy2021，6，5： | 1 |
| 4 | Linux Core Kernel Commentary显示文摘 | Scott Maxwell | 2000 | The Coriolis Group2000，，： | 1 |
| 5 | Inhibitors of hepatitis C virus NS3·4A protease. Part 3: P 2 proline variants显示文摘 | Robert B Perni Luc J Farmer Kevin M Cottrell John J Court Lawrence F Courtney David D Deininger Cynthia A Gates Scott L Harbeson Joseph L Kim Chao Lin Kai Lin Yu-Ping Luong John P Maxwell Mark A Murcko Janos Pitlik B.Govinda Rao Wayne C Schairer Roger D T | 2004 | Bioorganic & Medicinal Chemistry Letters2004，，8： | 1 |
| 6 | Ty-4, a tomato yellow leaf curl virus resistance gene on chromosome 3 of tomato 显示文摘 | Ji Y Scott J W Maxwell D P | 2008 | Tomato Genet Coop Rep2008，58，： | 1 |
| 7 | Ty-4, a tomato yellow leaf curl virus resistance gene on chromosome 3 of tomato显示文摘 | Ji Y Scott JW Maxwell DP | 2008 | Rep Tomato Genet Coop2008，58，： | 1 |
| 8 | Outcomes of Low Anterior Resection Anastomotic Leak after Preoperative Chemoradiation Therapy for Rectal Cancer显示文摘 | Harris Lisa J Phillips Benjamin R Maxwell Pinckney J Isenberg Gerald A Goldstein Scott D | 2010 | The American Surgeon2010，，7： | 1 |
| 9 | Fate and Transport of Antibiotic Residues and Antibiotic Resistance Genes following Land Application of Manure Waste显示文摘 | Chee-Sanford Joanne C Mackie Roderick I Koike Satoshi Krapac Ivan G Lin Yu-Feng Yannarell Anthony C Maxwell Scott Aminov Rustam I | 2009 | Journal of Environmental Quality2009，，3： | 1 |
| 10 | An electrically assisted, Hybrid Vehicle显示文摘 | Scott Aylor Micheal Parten Tim Maxwell Jesse Jones | 1998 | IEEE1998，，： | 1 |
| 11 | Ty-4,a tomato yellow leaf cur l virus resistance gene on chromosome 3 of tomato显示文摘 | Ji Y F Scott J W Maxwell D P | 2008 | Tomato Genet Coop Rep2008，58，： | 1 |
| 12 | Ty-4, a tomato yellow leaf curl virus resistance gene on chromosome 3 of tomato 显示文摘 | Ji Y Scott JW Maxwell DP | 2008 | Tomato Genetic Cooperative Report2008，58，： | 1 |
| 13 | Inhibition of pancreatic EZH2 restores progenitor insulin in T1D donor显示文摘Type 1 diabetes(T1D)is an autoimmune disease that selectively destroys insulin-producingβ-cells in the pancreas.An unmet need in diabetes management,current therapy is focussed on transplantation.While the reprogramming of progenitor cells into functional insulin-producingβ-cells has also been proposed this remains controversial and poorly understood.The challenge is determining why default transcriptional suppression is refractory to exocrine reactivation.After the death of a 13-year-old girl with established insulin-dependent T1D,pancreatic cells were harvested in an effort to restore and understand exocrine competence.The pancreas showed classic silencing ofβ-cell progenitor genes with barely detectable insulin(Ins)transcript.GSK126,a highly selective inhibitor of EZH2 methyltransferase activity influenced H3K27me3 chromatin content and transcriptional control resulting in the expression of coreβ-cell markers and ductal progenitor genes.GSK126 also reinstated Ins gene expression despite absoluteβ-cell destruction.These studies show the refractory nature of chromatin characterises exocrine suppression influencingβ-cell plasticity.Additional regeneration studies are warranted to determine if the approach of this n-of-1 study generalises to a broader T1D population. | Keith Al-Hasani Ishant Khurana Lina Mariana Thomas Loudovaris Scott Maxwell K.N.Harikrishnan Jun Okabe Mark ECooper Assam El-Osta | 2022 | Signal Transduction and Targeted Therapy2022，7，8： | 0 |
| 14 | EZH2 inhibitors promote β-like cell regeneration in young and adult type 1 diabetes donors显示文摘β-cells are a type of endocrine cell found in pancreatic islets that synthesize,store and release insulin.In type 1 diabetes(T1D),T-cells of the immune system selectively destroy the insulin-producingβ-cells.Destruction of these cells leads to a lifelong dependence on exogenous insulin administration for survival.Consequently,there is an urgent need to identify novel therapies that stimulateβ-cell growth and induceβ-cell function.We and others have shown that pancreatic ductal progenitor cells are a promising source for regeneratingβ-cells for T1D owing to their inherent differentiation capacity.Default transcriptional suppression is refractory to exocrine reaction and tightly controls the regenerative potential by the EZH2 methyltransferase.In the present study,we show that transient stimulation of exocrine cells,derived from juvenile and adult T1D donors to the FDAapproved EZH2 inhibitors GSK126 and Tazemetostat(Taz)influence a phenotypic shift towards aβ-like cell identity.The transition from repressed to permissive chromatin states are dependent on bivalent H3K27me3 and H3K4me3 chromatin modification.Targeting EZH2 is fundamental toβ-cell regenerative potential.Reprogrammed pancreatic ductal cells exhibit insulin production and secretion in response to a physiological glucose challenge ex vivo.These pre-clinical studies underscore the potential of small molecule inhibitors as novel modulators of ductal progenitor differentiation and a promising new approach for the restoration ofβ-like cell function. | Keith Al-Hasani Safiya Naina Marikar Harikrishnan Kaipananickal Scott Maxwell Jun Okabe Ishant Khurana Thomas Karagiannis Julia J.Liang Lina Mariana Thomas Loudovaris Thomas Kay Assam El-Osta | 2024 | Signal Transduction and Targeted Therapy2024，9，2： | 0 |
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