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| 1 | Al/Al_2O_3多层膜的表面和界面的分析研究显示文摘用热蒸发沉积和自然氧化及加热法制备纳米量级的Al/Al2 O3薄膜和多层膜。用X射线光电子谱仪 (XPS)和透射电镜 (TEM)对样品进行检测。XPS实验说明自然氧化的Al2 O3膜层厚在 2~ 5nm。Al/Al2 O3薄膜及多层膜的O与Al的原子浓度比为 1 4 3~ 1 85。Ar离子刻蚀的XPS实验结果 (刻蚀速率为 0 0 9nm/s)说明 :2个对层的Al/Al2 O3多层膜截面样品具有周期性结构。TEM观察到了 5个对层的Al/Al2 O3多层膜的层状态结构 ,其周期为 4nm。由此说明 ,热蒸发及自然氧化法是制备纳米量级的Al/Al2 | 薛钰芝 Martin A Green | 2002 | 真空科学与技术2002，22，1： | 13 |
| 2 | Dynamic chromatin states in human ES cells reveal potential regulatory sequences and genes involved in pluripotency显示文摘Pluripotency,一个细胞的能力区分并且产生所有胚胎的系,定义象胚胎的茎(ES ) 那样的哺乳动物的细胞类型的一个小数字细胞。当它通常被保持了时,那 pluripotency 是 transcriptional 的产品激活并且维持关键干细胞基因的表达式的规章的网络,积累的证据在建立并且保卫 ES 房间的 pluripotency 为 epigenetic 进程正在指向一个关键角色,象维持区分的房间类型的身份一样。以便更好在 pluripotency 理解 epigenetic 机制的角色,我们检验了在经历区别进一个 mesendodermal 系的人的 ES 房间(hESCs ) 染色体宽的染色质修正的动力学。我们发现在倡导者的染色质修正在区别期间仍然保持大部分不变,除了在在在 H3K27 的 acetylation 和 methylation 之间的一个动态开关标记在基因表示的激活和 silencing 之间的转变的倡导者的一个小数字,建议在在大多数差别上的房间命运承诺的一个层次表示了基因。我们也在 50 000 潜在的 enhancers 上印射,并且在染色质修正,特别 H3K4me1 和 H3K27ac 观察了大得多的动力学,它与他们的潜在的目标基因的表示相关。这些 enhancers 的进一步的分析揭示了 pluripotency 和可以在 hESCs 授与发展胜任的一个平衡状态的一口染色质签名陈述语气的潜在地关键的 transcriptional 管理者。我们的结果提供在定义 enhancers 和 pluripotency 支持染色质修正的角色的新证据。 | R David Hawkins Gary C Hon Chuhu Yang Jessica E Antosiewicz-Bourget Leonard K Lee Que-Minh Ngo Sarit Klugman Keith A Ching Lee E Edsall Zhen Ye Samantha Kuan Pengzhi Yu Hui Liu Xinmin Zhang Roland D Green Victor V Lobanenkov Ron Stewart James A Thomson Bing Ren | 2011 | Cell Research2011，21，10： | 6 |
| 3 | Al/Al_2O_3多层膜的表面分析与电性能的研究显示文摘用热蒸发沉积和自然氧化及加热法制备纳米量级的Al/Al2 O3 薄膜和多层膜。本文用X射线光电子能谱 (XPS)和紫外光电子能谱 (UPS)对样品进行价带能谱的检测与分析。获得的Al/Al2 O3 多层膜价带的XPS光电子能谱谱形基本相似 ;通过对Al/Al2 O3 三层膜在不同极角的UPS谱线的检测 ,得到其Ei (k∥i )关系曲线。此外 ,测定了低温下的I U特性 ,发现纳米量级的Al/Al2 O3 薄膜具有负阻特性。 | 薛钰芝 Martin A Green | 2002 | 真空科学与技术2002，22，6： | 6 |
| 4 | Apoptosis after intestinal ischemia-reperfusion injury显示文摘 | Shah K A Shndra S Green C J | 1997 | Transplantation1997，64，10： | 3 |
| 5 | Implementation of a polling protocol for predicting celiac disease in videocapsule analysis显示文摘AIM: To investigate the presence of small intestinal villous atrophy in celiac disease patients from quantitative analysis of videocapsule image sequences.METHODS: Nine celiac patient data with biopsy-proven villous atrophy and seven control patient data lacking villous atrophy were used for analysis. Celiacs had biopsy-proven disease with scores of Marsh Ⅱ-Ⅲ C except in the case of one hemophiliac patient. At four small intestinal levels (duodenal bulb, distal duodenum, jejunum, and ileum), video clips of length 200 frames (100 s) were analyzed. Twenty-four measurements were used for image characterization. These measurements were determined by quantitatively processing the videocapsule images via techniques for texture analysis, motility estimation, volumetric reconstruction using shape-from-shading principles, and image transformation. Each automated measurement method, or automaton, was polled as to whether or not villous atrophy was present in the small intestine, indicating celiac disease. Each automaton's vote was determined based upon an optimized parameter threshold level, with the threshold levels being determined from prior data. A prediction of villous atrophy was made if it received the majority of votes (≥ 13), while no prediction was made for tie votes (12-12). Thus each set of images was classified as being from either a celiac disease patient or from a control patient. RESULTS: Separated by intestinal level, the overall sensitivity of automata polling for predicting villous atrophy and hence celiac disease was 83.9%, while the specificity was 92.9%, and the overall accuracy of automata-based polling was 88.1%. The method of image transformation yielded the highest sensitivity at 93.8%, while the method of texture analysis using subbands had the highest specificity at 76.0%. Similar results of prediction were observed at all four small intestinal locations, but there were more tie votes at location 4 (ileum). Incorrect prediction which reduced sensitivity occurred for two celiac patients with Marsh type Ⅱ pattern, which is characterized by crypt hyperplasia, but normal villous architecture. Pooled from all levels, there was a mean of 14.31 ± 3.28 automaton votes for celiac vs 9.67 ± 3.31 automaton votes for control when celiac patient data was analyzed (P<0.001). Pooled from all levels, there was a mean of 9.71 ± 2.8128 automaton votes for celiac vs 14.32 ± 2.7931 automaton votes for control when control patient data was analyzed (P<0.001). CONCLUSION: Automata-based polling may be useful to indicate presence of mucosal atrophy, indicative of celiac disease, across the entire small bowel, though this must be confirmed in a larger patient set. Since the method is quantitative and automated, it can potentially eliminate observer bias and enable the detectionof subtle abnormality in patients lacking a clear diagnosis. Our paradigm was found to be more efficacious at proximal small intestinal locations, which may suggest a greater presence and severity of villous atrophy at proximal as compared with distal locations. | Edward J Ciaccio Christina A Tennyson Govind Bhagat Suzanne K Lewis Peter H Green | 2013 | World Journal of Gastrointestinal Endoscopy2013，5，7： | 3 |
| 6 | Global prevalence of diabetes:estimates for the year 2000 and projections for 2030显示文摘 | Wild S Roglic G Green A | | 0，，05： | 3 |
| 7 | DNA damage induced by chronic inflammation contributes to colon carcinogenesis in mice显示文摘 | Meira Lisiane B Bugni James M Green Stephanie L Lee Chung-Wei Pang Bo Borenshtein Diana Rickman Barry H Rogers Arlin B Moroski-Erkul Catherine A McFaline Jose L Schauer David B Dedon Peter C Fox James G Samson Leona D | 2008 | Journal of Clinical Investigation2008，，7： | 2 |
| 8 | Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders显示文摘 | E Joanna Baxter Linda M Scott Peter J Campbell Clare East Nasios Fourouclas Soheila Swanton George S Vassiliou Anthony J Bench Elaine M Boyd Natasha Curtin Mike A Scott Wendy N Erber Anthony R Green | 2005 | The Lancet . 2005 (9464)2005，，： | 2 |
| 9 | Photovoltaic principles显示文摘 | Martin A Green | 2002 | Physica E: Low-dimensional Systems and Nanostructures2002，，1： | 2 |
| 10 | Survival and recurrence after concomitant chemotherapy and radiotherapy for cancer of the uterine cervix: a systematic review and meta-analysis显示文摘 | John A Green John M Kirwan Jayne F Tierney Paul Symonds Lydia Fresco Mandy Collingwood Christopher J Williams | 2001 | The Lancet . 2001 (9284)2001，，： | 2 |
| 11 | Anassessment of the relationship between chlorophyll fluorescence and CO2 gas exchange from field measurement on a moss and lichen 显示文摘 | GREEN T G A SCHROETER B KAPPEN L | 1998 | Planta1998，206，4： | 2 |
| 12 | Electronic transducers for industrial measurement of low value capacitance显示文摘 | S M Huang A L Stott R G Green | 1988 | Journal Physics Engineering Science Instrument1988，21，3： | 2 |
| 13 | 脊髓损伤后残存自主神经功能载录国际标准显示文摘近年来,脊髓损伤神经学分类园际标准(International Stand- ards for the Neurological Classification of Spinal Cord Injury, ISNCSCI)被用来记载脊髓损伤后运动和感觉功能的损害,目前该标准已是第六版。1992年第一份国际认可的标准出版时,曾进行了较大的修订,修订内容包括完全性损伤与不完全性损伤的定义, | MS Alexander AB Jackson W Donovan DE Graves SL Elliott A Krassioukov AW Sheel I Estoresl B Green A Gousse NL Braekett D Cardenas M Kennelly A-K Karlason F Biering-Sorensen K Krogh T Linsenmeyer R Marino J Ditunno CJ Mathias I Perkash G Creasey G Schilero J Wecht B Schurch V Dietz J Sonksen S Stiens D Bodner LA Wuermser J-J Wyndaele 周谋望 刘楠 S Charlifue | 2010 | 中华物理医学与康复杂志2010，32，4： | 2 |
| 14 | Global prevalence of diabetes:estimates for the year 2000 and projections for 2030 显示文摘 | Wild S Roglic G Green A | 2004 | Diabetes Care2004，27，5： | 1 |
| 15 | Mechanisms of Disease: the Myeloprolife Rative Disorders显示文摘 | Campbell P J Green A R | 2006 | N Engl J Med2006，355，： | 1 |
| 16 | Cyclin-dependent kinase 4 inhibitors as a treatment for cancer, part 1 : identification and optimisation of substituted 4,6-bis anilino pyrimidines 显示文摘 | Beattie J F Breault G A Green S | 2003 | Bioorg Med Chem Lett2003，13，18： | 1 |
| 17 | Comparative DNA sequence analysis of wheat and rice genomes显示文摘 | La Rota M Bermudez-Kandianis C E Greene R A Kantety R | 2003 | Genome Res2003，13，： | 1 |
| 18 | Forensic classification of ballpoint pen inks using high performance liquid chromatography and infrared spectroscopy with principal components analysis and linear discriminant analysis显示文摘 | KHER A MULHOLLAND M GREEN E REEDY B | 2006 | Vib Spectros2006，40，2： | 1 |
| 19 | Global prevalence of diabetes:estimates for the year 2000 and projections for 2030显示文摘 | Wild S Roglic G Green A | 2004 | Diabetes care2004，27，5： | 1 |
| 20 | Interactions of tea tannins and condensed tannins with proteins显示文摘 | Frazier R A Deaville E R Green R J | 2010 | Journal of Pharmaceutical and Biomedical Analysis2010，51，： | 1 |
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