4,275 results on '"Ge, S."'
Search Results
202. Transfusion of plasma from a blood donor induced hepatitis E in Rhesus monkey
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Xia, N.-S., Zhang, J., Zheng, Y.-J., Ge, S.-X., Ye, X.-Z., and Ou, S.-H.
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- 2004
203. Caveolae are involved in the response of astrocytes to MCP-1
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Pachter, J. S., Ge, S., Song, L., and Stomatovic, S.
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- 2003
204. Performance of the rapidly extracted auditory evoked potentials index to detect the recovery and loss of wakefulness in anesthetized and paralyzed patients
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GE, S. J., ZHUANG, X. L., WANG, Y. T., WANG, Z. D., CHEN, S. L., and LI, H. T.
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- 2003
205. Mössbauer study of Nd2Fe14B and Nd2(Fe1−xCox)14B compounds
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Ge, S. H., Zhang, Y. D., Li, F. S., and Zhou, R. J.
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- 1990
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206. Dynamic Motion Planning for Mobile Robots Using Potential Field Method
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Ge, S. S. and Cui, Y. J.
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- 2002
207. Changes in the rapidly extracted auditory evoked potentials index and the bispectral index during sedation induced by propofol or midazolam under epidural block
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Ge, S. J., Zhuang, X. L., Wang, Y. T., Wang, Z. D., and Li, H. T.
- Published
- 2002
208. The role of regional groundwater flow
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Garven, G., Person, M.A., Sverjensky, D.A., and Ge, S.
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North America -- Natural history ,Ore deposits -- Research ,Hydrothermal deposits -- Research ,Earth sciences - Abstract
Flow models have been created to analyze the influence of groundwater migration on the deposition of carbonate-hosted lead-zinc ores in the midcontinental basins of the US. Examples include discharge areas of the Arkoma Basin, Ozark Dome, southern Illinois, southern Wisconsin, Tennessee, Denver Basin, Forest City Basin, Mississippi Valley Graben and Missouri's Old Lead Belt.
- Published
- 1993
209. Mapping of the luteinizing hormone/choriogonadotropin receptor gene (LHCGR) to chicken chromosome 3
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Ge, S. F., Romanov, M. N., Sharp, P. J., Burt, D. W., Paton, I. R., and Dunn, I. C.
- Published
- 2001
210. Use of functionalized WS 2 nanotubes to produce new polystyrene/polymethylmethacrylate nanocomposites
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Zhang, W., Ge, S., Wang, Y., Rafailovich, M.H., Dhez, O., Winesett, D.A., Ade, H., Shafi, Kurikka V.P.M., Ulman, A., Popovitz-Biro, R., Tenne, R., and Sokolov, J.
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- 2003
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211. Adaptive region reaching control of fully actuated ocean surface vessels.
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Sun, X. M., Ge, S. S., Xu, Q., Zhou, Y., and Zheng, X. W.
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SHIPS ,POTENTIAL energy ,FORCE & energy ,ADAPTIVE control systems ,LYAPUNOV stability - Abstract
In this paper, region reaching controller is designed for fully actuated ocean surface vessels to reach a desired target region instead of a point. There are not the requirements for both the pre-specified trajectory outside the desired region and the desired pinpoint position inside the desired region. The controller design is based on the potential energy function, backstepping recursive design methodology, and the Lyapnov stability analysis theory. If the target region is specified arbitrarily small, the target region reduces to a point, and hence the region reaching control can be a generalisation of the setpoint control. Simulation results are presented to illustrate the performance of the proposed controller. [ABSTRACT FROM AUTHOR]
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- 2021
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212. P4648Retrograde flow in aortic isthmus in fetuses with congenital heart defects and computer flow dynamic modeling
- Author
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Chen, Z, primary, Lin, S H, additional, Amy, T, additional, Han, J C, additional, Yang, X, additional, Ge, S H P, additional, and He, Y H, additional
- Published
- 2019
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213. PT04.5: Reduced Postprandial Serum Triglyceride After a Meal Prepared Using Hot Air Frying: A Randomized Crossover Trial
- Author
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Ge, S., primary, Feng, X., additional, Li, M., additional, Liu, H., additional, Higgins, P.B., additional, Tang, Y., additional, Cao, Y., additional, Shen, J., additional, and Jin, S., additional
- Published
- 2019
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214. A Modified Particle Swarm Optimization for Parameters Identification of Photovoltaic Models
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Yu, K. J., primary, Ge, S. L., additional, Qu, B. Y., additional, and Liang, J. J., additional
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- 2019
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215. Effect of Feed Restriction and Photoperiod on Reproduction and LEPR, MELR mRNA Expression of Layers
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HAO, E, primary, Chen, H, additional, Ge, S, additional, and Huang, R, additional
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- 2019
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216. Experimental Tests for Improving Regenerator Efficiency of a V-M Cryocooler
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Li, Shimo, primary, Pan, Huaiyu, additional, Ge, S., additional, Zhao, B., additional, Lin, J., additional, Shao, H., additional, and Long, Yi, additional
- Published
- 1992
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217. Evaluation of IRI95 ionosphere model for radar altimeter applications
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Zhao, C., Bilitza, D., Shum, C., Schaer, S., Beutler, G., and Ge, S.
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- 2002
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218. EXPERIMENTAL STUDY ON PREVENTING THE OXIDATIVE INJURY INDUCED BY HEMODIALYSIS WITH TEA POLYPHENOLS
- Author
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Nai-Jie, Cui, Jia-Tai, Wang, Yi, Zhang, Qiang, Fu, and Ge, S. Z.
- Published
- 1997
219. A Preisach analysis of remanence isotherms for nanoparticles of Fe in alumina
- Author
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Roshko, R.M., Viddal, C.A., Ge, S., and Gao, M.
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Atmospheric temperature -- Research ,Electromagnetism -- Research ,Nanotechnology ,Business ,Electronics ,Electronics and electrical industries - Abstract
Measurements of the field and temperature dependence of the field cooled moment, the zero field cooled moment, the isothermal remanent moment (IRM), and the thermoremanent moment (TRM), are presented for a thin film of nanodimensional particles of Fe embedded in alumina ([Al.sub.2][O.sub.3]). At each measurement temperature, the TRM approaches saturation much more rapidly than the corresponding IRM, and warming accelerates the approach to saturation for both TRM and IRM isotherms. Comparisons of numerical simulations of the IRM and TRM, based on the Preisach formalism, which decomposes the metastable state excitation spectrum into an ensemble of double wells with dissipation fields Ha and bias fields [H.sub.s], with the measured isotherms, yields the distribution of characteristic fields p([H.sub.d], [H.sub.s]) and its variation with temperature. Index Terms--Hysteresis, nanoparticles, Preisach models.
- Published
- 2004
220. Association of delayed time in the emergency department with the clinical outcomes for critically ill patients.
- Author
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Lin, S, Ge, S, He, W, and Zeng, M
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TREATMENT effectiveness , *CRITICALLY ill , *HOSPITAL emergency services , *MEDICAL personnel , *HOSPITAL mortality , *METABOLIC disorders - Abstract
Background Previous studies have shown the association of waiting time in the emergency department with the prognosis of critically ill patients, but these studies linking the waiting time to clinical outcomes have been inconsistent and limited by small sample size. Aim To determine the relationship between the waiting time in the emergency department and the clinical outcomes for critically ill patients in a large sample population. Design A retrospective cohort study of 13 634 patients. Methods We used the Medical Information Mart for Intensive Care III database. Multivariable logistic regression was used to determine the independent relationships of the in-hospital mortality rate with the delayed time and different groups. Interaction and stratified analysis were conducted to test whether the effect of delayed time differed across various subgroups. Results After adjustments, the in-hospital mortality in the ≥6 h group increased by 38.1% (OR 1.381, 95% CI 1.221–1.562). Moreover, each delayed hour was associated independently with a 1.0% increase in the risk of in-hospital mortality (OR 1.010, 95% CI 1.008–1.010). In the stratified analysis, intensive care unit (ICU) types, length of hospital stay, length of ICU stay, simplified acute physiology score II and diagnostic category were found to have interactions with ≥6 h group in in-hospital mortality. Conclusions In this large retrospective cohort study, every delayed hour was associated with an increase in mortality. Furthermore, clinicians should be cautious of patients diagnosed with sepsis, liver/renal/metabolic diseases, internal hemorrhage and cardiovascular disease, and if conditions permit, they should give priority to transferring to the corresponding ICUs. [ABSTRACT FROM AUTHOR]
- Published
- 2021
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221. Shear Modulation Force Microscopy Studies on Cross-linked Elastomer Thin Films
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Zhang, Y., Ge, S., Rafailovich, M. H., Sokolov, J. C., Peiffer, D. G., and Dias, A. J.
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- 2000
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222. P124 - A randomized, double-blind, placebo-controlled, phase 3 trial of infigratinib as adjuvant therapy in patients with invasive urothelial carcinoma harboring susceptible FGFR3 genetic alterations: PROOF 302
- Author
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Schnabel, M.J., Pal, S.K., Valderrama, B.P., Cole, S., Grivas, P., Fernandez, E.S., Diamond, E., Master, V., Masini, C., Eigl, B., Petros, F., Ge, S., Andresen, C., Roghmann, F., Rodriguez-Vida, A.M., Hoffman-Censits, J., and Daneshmand, S.
- Published
- 2021
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223. Novel characterization method of impedance cardiography signals using time-frequency distributions
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Universitat Politècnica de Catalunya. Departament d'Enginyeria de Sistemes, Automàtica i Informàtica Industrial, Universitat Politècnica de Catalunya. B2SLab - Bioinformatics and Biomedical Signals Laboratory, Escrivá Muñoz, Jesús, Pan, Y., Ge, S., Jensen, Erik Weber, Vallverdú Ferrer, Montserrat, Universitat Politècnica de Catalunya. Departament d'Enginyeria de Sistemes, Automàtica i Informàtica Industrial, Universitat Politècnica de Catalunya. B2SLab - Bioinformatics and Biomedical Signals Laboratory, Escrivá Muñoz, Jesús, Pan, Y., Ge, S., Jensen, Erik Weber, and Vallverdú Ferrer, Montserrat
- Abstract
The purpose of this document is to describe a methodology to select the most adequate time-frequency distribution (TFD) kernel for the characterization of impedance cardiography signals (ICG). The predominant ICG beat was extracted from a patient and was synthetized using time-frequency variant Fourier approximations. These synthetized signals were used to optimize several TFD kernels according to a performance maximization. The optimized kernels were tested for noise resistance on a clinical database. The resulting optimized TFD kernels are presented with their performance calculated using newly proposed methods. The procedure explained in this work showcases a new method to select an appropriate kernel for ICG signals and compares the performance of different time-frequency kernels found in the literature for the case of ICG signals. We conclude that, for ICG signals, the performance (P) of the spectrogram with either Hanning or Hamming windows (P¿=¿0.780) and the extended modified beta distribution (P¿=¿0.765) provided similar results, higher than the rest of analyzed kernels., Peer Reviewed, Postprint (published version)
- Published
- 2018
224. Interfacial properties of elastomer blends as studied by neutron reflectivity
- Author
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Zhang, Yimin, Li, W., Tang, B., Ge, S., Hu, X., Rafailovich, M.H., Sokolov, J.C., Gersappe, D., Peiffer, D.G., Li, Z., Dias, A.J., McElrath, K.O., Lin, M.Y., Satija, S.K., Urquhart, S.G., and Ade, H.
- Published
- 2001
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225. Efficacy and safety of biological agents in the treatment of patients with Takayasu arteritis: a systematic review and meta-analysis.
- Author
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SHUAI, Z.-Q., ZHANG, C.-X., SHUAI, Z.-W., and GE, S.-L.
- Abstract
OBJECTIVE: We aimed to systematically review biological agents' efficacy and safety in patients with Takayasu arteritis (TAK). MATERIALS AND METHODS: A systematic literature search of 7 electronic databases, including MEDLINE (via PubMed), EMBASE, Elsevier ScienceDirect, EBSCO, Springer Link, Web of Science, and Cochrane Library on the efficacy of biological agents on patients with TAK was conducted. Only studies published in English and with a sample size >5 patients with TAK were included. Two reviewers independently selected studies, extracted data and assessed its methodological quality. Random effects meta-analyses of various effect measures were performed. RESULTS: According to the title and abstract, 961 studies were identified and screened. Subsequently, 31 studies from 29 observational studies and 2 randomized-controlled trials (RCTs), which included a total of 517 patients with TAK that met the inclusion and exclusion criteria, were selected. Observational studies showed a high risk of bias. Pooled remission rates of biological agents were 66% (95% CI: 58%-73%; I2=59%), and the remission rates of anti-tumor necrosis factor (TNF) agents and tocilizumab (TCZ) were similar: 65% (95% CI: 56%-73%; I2=49%) and 70% (95% CI: 55%-86%; I2=69%), respectively. Pooled relapse rates were 23% (95% CI: 15%-31%; I2=66%). The relapse rate was 28% (95% CI: 16%-40%; I2=68%) for anti-TNF agents and 17% (95% CI: 7%-26%; I2=49%) for TCZ. The remission rate of TCZ was slightly higher (p>0.05), but the relapse rate was statistically significantly lower than that of anti-TNF agents (p=0.017). Furthermore, biological agents significantly decreased the doses of glucocorticoid (GC) and levels of acute phase inflammation markers (ESR, CRP) while the proportion of patients with new angiographic lesions or progression of previously noted lesions were 11% (95% CI: 4%-18%; I2=59%). RCTs with a small sample size showed abatacept was ineffective, and TCZ was underpowered to detect a difference in time to relapse compared to placebo. The most common adverse event of biological agents was infection (6%, 95%CI: 2%-10%). No deaths were reported. CONCLUSIONS: A lthough the b eneficial e ffects of biological agents are encouraging in enhancing disease remission, reducing the levels of acute phase inflammation markers and decreasing the treatment doses of GC in patients with TAK, there is still a risk of relapse. More refined studies with larger cohorts are necessary before drawing a definitive opinion. [ABSTRACT FROM AUTHOR]
- Published
- 2021
226. Aire-deficient mice provide a model of corneal and lacrimal gland neuropathy in Sjögren’s syndrome
- Author
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Chen, FY, Lee, A, Ge, S, Nathan, S, Knox, SM, and McNamara, NA
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sense organs - Abstract
© 2017 Chen et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Sjögren’s syndrome (SS) is a chronic, autoimmune exocrinopathy that leads to severe dryness of the mouth and eyes. Exocrine function is highly regulated by neuronal mechanisms but little is known about the link between chronic inflammation, innervation and altered exocrine function in the diseased eyes and exocrine glands of SS patients. To gain a better understanding of neuronal regulation in the immunopathogenesis of autoimmune exocrinopathy, we profiled a mouse model of spontaneous, autoimmune exocrinopathy that possess key characteristics of peripheral neuropathy experienced by SS patients. Mice deficient in the autoimmune regulator (Aire) gene developed spontaneous, CD4+ T cell-mediated exocrinopathy and aqueous-deficient dry eye that were associated with loss of nerves innervating the cornea and lacrimal gland. Changes in innervation and tear secretion were accompanied by increased proliferation of corneal epithelial basal cells, limbal expansion of KRT19-positive progenitor cells, increased vascularization of the peripheral cornea and reduced nerve function in the lacrimal gland. In addition, we found extensive loss of MIST1+ secretory acinar cells in the Aire -/- lacrimal gland suggesting that acinar cells are a primary target of the disease, Finally, topical application of ophthalmic steroid effectively restored corneal innervation in Aire -/- mice thereby functionally linking nerve loss with local inflammation in the aqueous-deficient dry eye. These data provide important insight regarding the relationship between chronic inflammation and neuropathic changes in autoimmune-mediated dry eye. Peripheral neuropathies characteristic of SS appear to be tightly linked with the underlying immunopathological mechanism and Aire -/- mice provide an excellent tool to explore the interplay between SS-associated immunopathology and peripheral neuropathy.
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- 2017
227. Gaze-based hints during child-robot gameplay
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Mwangi, E., Barakova, Emilia I., Diaz, M.L.Z., Mallofre, A.C., Rauterberg, G.W.M., Kheddar, A., Yoshida, E., Sam Ge, S., Suzuki, K., Cabibihan, J.J., Eyssel, F., He, H., and Future Everyday
- Subjects
020203 distributed computing ,Matching (statistics) ,Computer science ,Robots for (special) education ,Joint attention design of human-robot interactions ,Matching game ,02 engineering and technology ,Gaze in HRI ,Gaze perception ,Gaze ,Human–computer interaction ,0202 electrical engineering, electronic engineering, information engineering ,Robot ,Games with social robots ,020201 artificial intelligence & image processing ,Session (computer science) ,Robots for (special) education, Joint attention design of human-robot interactions ,TUTOR ,computer ,computer.programming_language - Abstract
This paper presents a study that examines whether gaze hints provided by a robot tutor influences the behavior of children in a card matching game. In this regard, we conducted a within-subjects experiment, in which children played a card game “Memory” in the presence of a robot tutor in two sessions. In one session (Help), the robot tutor gives gaze hints to help children find matching cards and, in the other session (No_Help), the robot tutor does not provide help to the children. Gaze hints involved looking toward the correct matching cart. We analyzed the child-robot interaction regarding execution performance, gaze behavior, and level of engagement. Children performance was measured using the number of trials and overall time used to complete the game. We found that children used significantly fewer trials in the Help condition than in the No_Help condition. In addition, there were more instances of mutual gaze in the Help condition than in the No_Help condition. These findings suggest that designing a robot with dynamic gaze increases the effectiveness of the robot tutor as a helping agent.
- Published
- 2017
228. TECHNOLOGY-BASED COGNITIVE INTERVENTIONS FOR INDIVIDUALS WITH MILD COGNITIVE IMPAIRMENT: A SYSTEMATIC REVIEW
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Ge, S, primary, Zhu, Z, additional, Wu, B, additional, and McConnell, E S, additional
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- 2018
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229. P01.03: Fetal echocardiographic features and whole-exome sequencing results of ventricular non-compaction cardiomyopathy
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Hao, X., primary, Gu, X., additional, Sun, H., additional, Zhang, Y., additional, Ge, S., additional, and He, Y., additional
- Published
- 2018
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230. OP22.01: Echocardiographic characteristics and clinical outcome in fetuses with complete closure of the ductus arteriosus
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Han, J., primary, Liu, X., additional, Gu, X., additional, Ge, S., additional, and He, Y., additional
- Published
- 2018
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231. Protein Classification of Diffuse-Type Gastric Cancer Using Formalin-Fixed Paraffin-Embedded Samples
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Huang, W., primary, Xia, X., additional, Gao, J., additional, Li, Z., additional, Ge, S., additional, Qin, J., additional, and Shen, L., additional
- Published
- 2018
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232. P13.07: Fetal aortic arch and its branches anomalies: prenatal ultrasound, vascular cast and gene detection
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Weng, Z., primary, Hao, X., additional, Gao, S., additional, Ge, S., additional, and He, Y., additional
- Published
- 2018
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233. OC26.03: Comparison of the prevalence of pathogenic copy number variation in tetralogy of Fallot and associated congenital heart defect diagnosed between fetuses and children
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Man, T., primary, Hao, X., additional, Ge, S., additional, and He, Y., additional
- Published
- 2018
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234. P01.02: Frequency of 22q11 microdeletion syndrome in fetuses with conotruncal heart disease
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Hao, X., primary, Gu, X., additional, Sun, H., additional, Ge, S., additional, and He, Y., additional
- Published
- 2018
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235. EP10.05: Prenatal diagnosis of common pulmonary vein atresia: evaluation by fetal echocardiography compared with cardiovascular cast model
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Gao, S., primary, Guo, Y., additional, Han, J., additional, Ge, S., additional, and He, Y., additional
- Published
- 2018
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236. OC11.07: Prenatal identification of atrioventricular septal defect and associated genomic abnormality by fetal echocardiography and whole-genome sequencing
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Gu, X., primary, Zhang, Y., additional, Sun, L., additional, Ge, S., additional, and He, Y., additional
- Published
- 2018
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237. P18.09: Differential diagnosis of fetal large ventricular septal defect and tetralogy of Fallot based on big data analysis
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Lv, J., primary, Gao, S., additional, Gu, X., additional, Ge, S., additional, and He, Y., additional
- Published
- 2018
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238. 4914Prenatal identification of atrioventricular septal defect and associated genomic abnormality by fetal echocardiography and whole genome sequencing
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Gu, X, primary, Hao, X Y, additional, Zhang, Y, additional, Sun, L I N, additional, Han, J C H, additional, Liu, X W, additional, and Ge, S H P, additional
- Published
- 2018
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239. Hydrodynamic Analysis Including Shielding Effects and Advanced DP Controls for Improved Uptime of a Floatel Connected to an FPSO by a Gangway
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Cong, P. -W., additional, Magee, A. R., additional, Jaiman, R., additional, Ge, S. -Z., additional, Zhang, Q., additional, Tu, F. -W., additional, Choudhary, A., additional, Merchant, A., additional, Hussain, A., additional, and Xu, W., additional
- Published
- 2018
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240. Evaluation of serum levels of C-reactive protein and lipid profiles in patients with chronic periodontitis and/or coronary heart disease in an ethnic Han population.
- Author
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Liu J, Wu Y, Ding Y, Meng S, Ge S, and Deng H
- Abstract
OBJECTIVE: To investigate the relationship of coronary heart disease (CHD)-associated factors-C-reactive protein (CRP) and lipid profiles-with periodontitis in an ethnic Han population. METHOD AND MATERIALS: Forty healthy individuals as control, 40 patients with chronic periodontitis (CP), 28 patients with CHD, and 47 patients with both CP and CHD were included in the study. Serum CRP levels, lipid profile concentrations, and three periodontal clinical parameters (probing depth, clinical attachment level, and bleeding on probing) were measured and analyzed. The chi-square test, Student-Newman-Keuls test, analysis of covariance, and a logistic regression analysis were used in this study. RESULTS: The mean CRP level of patients with CP alone was 2.4 +/- 1.5 mg/L. There were significant differences in mean serum CRP levels among groups after confounders were adjusted, with CP+CHD patients having the highest level (7.3 +/- 5.7 mg/L) and the controls the lowest (1.0 +/- 0.6 mg/L) (P < .001). Mean HDL cholesterol level of CP patients (1.1 +/- 0.7 mmol/L) was significantly lower than that of controls (1.4 +/- 0.6 mmol/L) (P < .05), although it was significantly higher than that of the other two groups with CHD (0.8 +/- 0.5 mmol/L and 0.7 +/- 0.4 mmol/L) (P < .001). Significant correlations of CRP and HDL cholesterol with the three clinical periodontal parameters were apparent (P < .05). CRP and HDL cholesterol were found to be significantly associated with an increased frequency of CHD in this regression model (OR = 3.7 and OR = 1.9, respectively, P < .05). CONCLUSIONS: In an ethnic Han population with a low normal range of serum CRP levels, chronic periodontitis is associated with increased CRP levels and decreased HDL cholesterol concentrations, which suggests that there may be some relationship between periodontal inflammation and CHD. [ABSTRACT FROM AUTHOR]
- Published
- 2010
241. VO2 films with strong semiconductor to metal phase transition prepared by the precursor oxidation process.
- Author
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Gurvitch, M., Luryi, S., Polyakov, A., Shabalov, A., Dudley, M., Wang, G., Ge, S., and Yakovlev, V.
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VANADIUM oxide ,THIN films ,PHASE transitions ,SCANNING electron microscopy ,ATOMIC force microscopy ,RAMAN spectroscopy - Abstract
We describe a relatively simple, reliable, and reproducible preparation technique, the precursor oxidation process, for making VO
2 films with strong semiconductor-to-metal phase transition. Sputter-deposited metal precursor V films were oxidized in situ in the deposition chamber for 2.5–7 h at 370–415 °C in 0.2 Torr O2 to form 22–220 nm VO2 . The strength [resistivity ratio, RR=ρS /ρM ] and sharpness (hysteresis width ΔTC ) of T-dependent semiconductor-to-metal hysteretic phase transition in VO2 were our most immediate and relevant quality indicators. In 200-nm-range films, the process was optimized to yield RR=(1–2)×103 , ΔTC ∼11 °C and absolute resistivity in a semiconducting phase ρS =0.4±0.2 Ω m, close to resistivity in bulk single crystals of VO2 . Films were characterized by scanning electron microscopy, atomic force microscopy, grazing-incidence x-ray diffraction, and Raman spectroscopy, and found to be polycrystalline single-phase VO2 . We also measured optical reflectivity RT (λ) from 200 to 1100 nm, and Rλ (T) from 20 to 100 °C. RT (λ) measured in thin-film interference structures allowed us to calculate the index of refraction in the two phases, which agrees well with the published data and, together with structural measurements, confirms that our films are essentially pure VO2 . The limited study of these films in terms of stability, aging, lithographic processing, and thermal cycling shows that they can be used in applications. [ABSTRACT FROM AUTHOR]- Published
- 2007
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242. Magnetic properties and the tunneling magnetoresistance effect in Co-MgF[sub 2] granular films.
- Author
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Chi, J. H., Ge, S. H., Liu, C. M., Kunkel, H. P., Zhou, X. Z., and Williams, G.
- Subjects
- *
GRANULAR materials , *THIN films , *MAGNETORESISTANCE , *FERROMAGNETISM - Abstract
Co - MgF[SUB2] granular films were deposited on glass substrates by rf co-sputtering at room temperature (RT). The influence of the Co volume fraction, f[SUBv], of these granular films on the tunneling magnetoresistance (TMR) and magnetic properties was studied systematically. In a magnetic field of 1.2 T, the TMR value at RT initially increases gradually with decreasing f[SUBv], reaches its maximum value of -8% for f[SUBv]=0.38, and then decreases. The corresponding magnetization curves indicate a change from ferromagnetism to superparamagnetism. A minimum in the coercivity, H[SUBc],(11 Oe) is obtained in the Co[SUB50]MgF[SUB2])[SUB50] granular film which also has a large zero field resistivity. This) magnetically soft granular film may consequently be a good candidate for high frequency applications. These variations of the TMR and magnetic properties can be ascribed to gradual changes in the film microstructure with decreasing f[SUBv], from interconnected metallic Co grains to nano-scaled Co particles dispersed in a crystallized insulating MgF[SUB2] matrix. The zero field cooled (ZFC) and field cooled (FC) curves for the samples were obtained in the temperature range 5-300 K in various magnetic fields. The peak in the ZFC curve shifts gradually towards lower temperature with increasing applied magnetic field and, with increasing f[SUBv], the peak temperature decreases more quickly with increasing field. The latter indicates that the magnetic interactions between grains become stronger, consistent with model predictions. [ABSTRACT FROM AUTHOR]
- Published
- 2003
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243. A brief review of different types of sweat-gland carcinomas in the eyelid and orbit
- Author
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Zhang L, Ge S, and Fan X
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lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens ,lcsh:RC254-282 ,eye diseases - Abstract
Leilei Zhang, Shengfang Ge, Xianqun Fan Department of Ophthalmology, Ninth People’s Hospital, Shanghai, People’s Republic of China Abstract: Sweat-gland carcinoma is a rare cutaneous appendage malignant tumor. Primary sweat-gland cancer can arise in the eyelid and orbit and is extremely rare. It has been classified into different types, and is usually locally recurrent after surgery. The tumors also appear in the orbit, which is characterized by metastasis. Therefore, great attention should be paid to the development of sweat-gland carcinomas. Specifically, our report briefly reviews the types of sweat-gland carcinomas that occur in the eyelid and orbit according to pathological classifications. Keywords: spiroma, syringomatous carcinoma, mucinous eccrine carcinoma, clear-cell eccrine gland carcinoma, eccrine porocarcinoma, orbit
- Published
- 2013
244. Microalgal cultivation with waste streams and metabolic constraints to triacylglycerides accumulation for biofuel production
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Ge, S, Champagne, P, Plaxton, W, Leite, G, Marazzi, F, MARAZZI, FRANCESCA ALICE, Ge, S, Champagne, P, Plaxton, W, Leite, G, Marazzi, F, and MARAZZI, FRANCESCA ALICE
- Abstract
Global increases in the generation of waste streams, including liquid, gaseous, and solid waste, have been posing serious challenges for waste management as a result of their potential impacts on receiving environments and climate change. The conversion of waste streams into useful bioenergy, biofuels, and bioproducts through recycling and/or recovery has been presented as a promising alternative. Coupling the bioremediation of waste streams with microalgae-based biofuel production, offers an alternative strategy to achieve waste-to-biofuel and bioenergy. A group of unicellular photosynthetic eukaryotes, microalgae require relatively simple nutrients and inorganic carbon sources to support their growth, while accumulating several biofuel precursors, such as starch or storage lipids. This review summarizes the current approaches to microalgal biomass production using waste streams, including waste-water; waste or CO2-enriched gas (flue gas and biogas); waste organics (i.e., crude glycerol); and waste heat, as well as the primary common operational challenges and corresponding mitigation strategies involved in cultivation approaches. Moreover, microalgal metabolic pathways supporting the biosynthesis of energy-rich molecules such as triacylglycerides (TAG) and starch are discussed. Metabolic constraints and potential approaches for the enhancement of microalgal TAG accumulation are systematically and critically analyzed. © 2016 Society of Chemical Industry and John Wiley & Sons, Ltd.
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- 2017
245. The Shenzhen Declaration on Plant Sciences-Uniting plant sciences and society to build a green, sustainable Earth
- Author
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Crane, PR, Ge, S, Hong, D-Y, Huang, H-W, Jiao, G-L, Knapp, S, Kress, WJ, Mooney, H, Raven, PH, Wen, J, Wu, W-H, Yang, H-M, Zhu, W-H, Zhu, Y-X, Crane, PR, Ge, S, Hong, D-Y, Huang, H-W, Jiao, G-L, Knapp, S, Kress, WJ, Mooney, H, Raven, PH, Wen, J, Wu, W-H, Yang, H-M, Zhu, W-H, and Zhu, Y-X
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- 2017
246. GSKB: A gene set database for pathway analysis in mouse
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Yuguang Ban, Bares, Arthur Liberzon, Wang W, Son Ew, Hennessey J, Jiang G, Xijin Ge S, Liming Lai, and Qi J
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Genetics ,0303 health sciences ,Database ,Genomics ,Context (language use) ,Biology ,computer.software_genre ,Biological pathway ,Bioconductor ,03 medical and health sciences ,0302 clinical medicine ,030220 oncology & carcinogenesis ,Gene expression ,KEGG ,Gene ,computer ,Functional genomics ,030304 developmental biology - Abstract
Interpretation of high-throughput genomics data based on biological pathways constitutes a constant challenge, partly because of the lack of supporting pathway database. In this study, we created a functional genomics knowledgebase in mouse, which includes 33,261 pathways and gene sets compiled from 40 sources such as Gene Ontology, KEGG, GeneSetDB, PANTHER, microRNA and transcription factor target genes, etc. In addition, we also manually collected and curated 8,747 lists of differentially expressed genes from 2,526 published gene expression studies to enable the detection of similarity to previously reported gene expression signatures. These two types of data constitute a Gene Set Knowledgebase (GSKB), which can be readily used by various pathway analysis software such as gene set enrichment analysis (GSEA). Using our knowledgebase, we were able to detect the correct microRNA (miR-29) pathway that was suppressed using antisense oligonucleotides and confirmed its role in inhibiting fibrogenesis, which might involve upregulation of transcription factor SMAD3. The knowledgebase can be queried as a source of published gene lists for further meta-analysis. Through meta-analysis of 56 published gene lists related to retina cells, we revealed two fundamentally different types of gene expression changes. One is related to stress and inflammatory response blamed for causing blindness in many diseases; the other associated with visual perception by normal retina cells. GSKB is available online at http://ge-lab.org/gs/, and also as a Bioconductor package (gskb, https://bioconductor.org/packages/gskb/). This database enables in-depth interpretation of mouse genomics data both in terms of known pathways and the context of thousands of published expression signatures.
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- 2016
247. Letter of Intent: Jinping Neutrino Experiment
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Beacom, JF, Chen, S, Cheng, J, Doustimotlagh, SN, Gao, Y, Ge, S-F, Gong, G, Gong, H, Guo, L, Han, R, Huang, X, Li, J, Li, M, Li, X, Lin, G-L, Liu, Z, McDonough, W, Tang, J, Wan, L, Wang, Y, Wang, Z, Wei, H, Xi, Y, Xu, Y, Yang, Z, Yao, C, Yeh, M, Yue, Q, Zhang, L, Zhang, Y, Zhao, Z, Zheng, Y, Zhou, X, Zhu, X, and Zuber, K
- Subjects
High Energy Physics - Experiment (hep-ex) ,Physics - Instrumentation and Detectors ,hep-ex ,Physics::Instrumentation and Detectors ,Astrophysics::High Energy Astrophysical Phenomena ,FOS: Physical sciences ,High Energy Physics::Experiment ,Instrumentation and Detectors (physics.ins-det) ,physics.ins-det ,High Energy Physics - Experiment - Abstract
Jinping Neutrino Experiment (Jinping) is proposed to significantly improve measurements on solar neutrinos and geoneutrinos in China Jinping Laboratory - a lab with a number of unparalleled features, thickest overburden, lowest reactor neutrino background, etc., which identify it as the world-best low-energy neutrino laboratory. The proposed experiment will have target mass of 4 kilotons of liquid scintillator or water-based liquid scintillator, with a fiducial mass of 2 kilotons for neutrino-electron scattering events and 3 kilotons for inverse-beta interaction events. A number of initial sensitivities studies have been carried out, including on the transition phase for the solar neutrinos oscillation from the vacuum to the matter effect, the discovery of solar neutrinos from the carbon-nitrogen-oxygen (CNO) cycle, the resolution of the high and low metallicity hypotheses, and the unambiguous separation on U and Th cascade decays from the dominant crustal anti-electron neutrinos in China., Proposal for the Jinping Neutrino Experiment
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- 2016
248. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
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Klionsky, D.J. Abdelmohsen, K. Abe, A. Abedin, M.J. Abeliovich, H. Arozena, A.A. Adachi, H. Adams, C.M. Adams, P.D. Adeli, K. Adhihetty, P.J. Adler, S.G. Agam, G. Agarwal, R. Aghi, M.K. Agnello, M. Agostinis, P. Aguilar, P.V. Aguirre-Ghiso, J. Airoldi, E.M. Ait-Si-Ali, S. Akematsu, T. Akporiaye, E.T. Al-Rubeai, M. Albaiceta, G.M. Albanese, C. Albani, D. Albert, M.L. Aldudo, J. Algül, H. Alirezaei, M. Alloza, I. Almasan, A. Almonte-Beceril, M. Alnemri, E.S. Alonso, C. Altan-Bonnet, N. Altieri, D.C. Alvarez, S. Alvarez-Erviti, L. Alves, S. Amadoro, G. Amano, A. Amantini, C. Ambrosio, S. Amelio, I. Amer, A.O. Amessou, M. Amon, A. An, Z. Anania, F.A. Andersen, S.U. Andley, U.P. Andreadi, C.K. Andrieu-Abadie, N. Anel, A. Ann, D.K. Anoopkumar-Dukie, S. Antonioli, M. Aoki, H. Apostolova, N. Aquila, S. Aquilano, K. Araki, K. Arama, E. Aranda, A. Araya, J. Arcaro, A. Arias, E. Arimoto, H. Ariosa, A.R. Armstrong, J.L. Arnould, T. Arsov, I. Asanuma, K. Askanas, V. Asselin, E. Atarashi, R. Atherton, S.S. Atkin, J.D. Attardi, L.D. Auberger, P. Auburger, G. Aurelian, L. Autelli, R. Avagliano, L. Avantaggiati, M.L. Avrahami, L. Azad, N. Awale, S. Bachetti, T. Backer, J.M. Bae, D.-H. Bae, J.-S. Bae, O.-N. Bae, S.H. Baehrecke, E.H. Baek, S.-H. Baghdiguian, S. Bagniewska-Zadworna, A. Bai, H. Bai, J. Bai, X.-Y. Bailly, Y. Balaji, K.N. Balduini, W. Ballabio, A. Balzan, R. Banerjee, R. Bánhegyi, G. Bao, H. Barbeau, B. Barrachina, M.D. Barreiro, E. Bartel, B. Bartolomé, A. Bassham, D.C. Bassi, M.T. Bast, R.C., Jr. Basu, A. Batista, M.T. Batoko, H. Battino, M. Bauckman, K. Baumgarner, B.L. Bayer, K.U. Beale, R. Beaulieu, J.-F. Beck, G.R., Jr. Becker, C. Beckham, J.D. Bédard, P.-A. Bednarski, P.J. Begley, T.J. Behl, C. Behrends, C. Behrens, G.M.N. Behrns, K.E. Bejarano, E. Belaid, A. Belleudi, F. Bénard, G. Berchem, G. Bergamaschi, D. Bergami, M. Berkhout, B. Berliocchi, L. Bernard, A. Bernard, M. Bernassola, F. Bertolotti, A. Bess, A.S. Besteiro, S. Bettuzzi, S. Bhalla, S. Bhattacharyya, S. Bhutia, S.K. Biagosch, C. Bianchi, M.W. Biard-Piechaczyk, M. Billes, V. Bincoletto, C. Bingol, B. Bird, S.W. Bitoun, M. Bjedov, I. Blackstone, C. Blanc, L. Blanco, G.A. Blomhoff, H.K. Boada-Romero, E. Böckler, S. Boes, M. Boesze-Battaglia, K. Boise, L.H. Bolino, A. Boman, A. Bonaldo, P. Bordi, M. Bosch, J. Botana, L.M. Botti, J. Bou, G. Bouché, M. Bouchecareilh, M. Boucher, M.-J. Boulton, M.E. Bouret, S.G. Boya, P. Boyer-Guittaut, M. Bozhkov, P.V. Brady, N. Braga, V.M.M. Brancolini, C. Braus, G.H. Bravo-San-Pedro, J.M. Brennan, L.A. Bresnick, E.H. Brest, P. Bridges, D. Bringer, M.-A. Brini, M. Brito, G.C. Brodin, B. Brookes, P.S. Brown, E.J. Brown, K. Broxmeyer, H.E. Bruhat, A. Brum, P.C. Brumell, J.H. Brunetti-Pierri, N. Bryson-Richardson, R.J. Buch, S. Buchan, A.M. Budak, H. Bulavin, D.V. Bultman, S.J. Bultynck, G. Bumbasirevic, V. Burelle, Y. Burke, R.E. Burmeister, M. Bütikofer, P. Caberlotto, L. Cadwell, K. Cahova, M. Cai, D. Cai, J. Cai, Q. Calatayud, S. Camougrand, N. Campanella, M. Campbell, G.R. Campbell, M. Campello, S. Candau, R. Caniggia, I. Cantoni, L. Cao, L. Caplan, A.B. Caraglia, M. Cardinali, C. Cardoso, S.M. Carew, J.S. Carleton, L.A. Carlin, C.R. Carloni, S. Carlsson, S.R. Carmona-Gutierrez, D. Carneiro, L.A.M. Carnevali, O. Carra, S. Carrier, A. Carroll, B. Casas, C. Casas, J. Cassinelli, G. Castets, P. Castro-Obregon, S. Cavallini, G. Ceccherini, I. Cecconi, F. Cederbaum, A.I. Ceña, V. Cenci, S. Cerella, C. Cervia, D. Cetrullo, S. Chaachouay, H. Chae, H.-J. Chagin, A.S. Chai, C.-Y. Chakrabarti, G. Chamilos, G. Chan, E.Y.W. Chan, M.T.V. Chandra, D. Chandra, P. Chang, C.-P. Chang, R.C.-C. Chang, T.Y. Chatham, J.C. Chatterjee, S. Chauhan, S. Che, Y. Cheetham, M.E. Cheluvappa, R. Chen, C.-J. Chen, G. Chen, G.-C. Chen, G. Chen, H. Chen, J.W. Chen, J.-K. Chen, M. Chen, M. Chen, P. Chen, Q. Chen, Q. Chen, S.-D. Chen, S. Chen, S.S.-L. Chen, W. Chen, W.-J. Chen, W.Q. Chen, W. Chen, X. Chen, Y.-H. Chen, Y.-G. Chen, Y. Chen, Y. Chen, Y. Chen, Y.-J. Chen, Y.-Q. Chen, Y. Chen, Z. Chen, Z. Cheng, A. Cheng, C.H.K. Cheng, H. Cheong, H. Cherry, S. Chesney, J. Cheung, C.H.A. Chevet, E. Chi, H.C. Chi, S.-G. Chiacchiera, F. Chiang, H.-L. Chiarelli, R. Chiariello, M. Chieppa, M. Chin, L.-S. Chiong, M. Chiu, G.N.C. Cho, D.-H. Cho, S.-G. Cho, W.C. Cho, Y.-Y. Cho, Y.-S. Choi, A.M.K. Choi, E.-J. Choi, E.-K. Choi, J. Choi, M.E. Choi, S.-I. Chou, T.-F. Chouaib, S. Choubey, D. Choubey, V. Chow, K.-C. Chowdhury, K. Chu, C.T. Chuang, T.-H. Chun, T. Chung, H. Chung, T. Chung, Y.-L. Chwae, Y.-J. Cianfanelli, V. Ciarcia, R. Ciechomska, I.A. Ciriolo, M.R. Cirone, M. Claerhout, S. Clague, M.J. Cl� ria, J. Clarke, P.G.H. Clarke, R. Clementi, E. Cleyrat, C. Cnop, M. Coccia, E.M. Cocco, T. Codogno, P. Coers, J. Cohen, E.E.W. Colecchia, D. Coletto, L. Coll, N.S. Colucci-Guyon, E. Comincini, S. Condello, M. Cook, K.L. Coombs, G.H. Cooper, C.D. Cooper, J.M. Coppens, I. Corasaniti, M.T. Corazzari, M. Corbalan, R. Corcelle-Termeau, E. Cordero, M.D. Corral-Ramos, C. Corti, O. Cossarizza, A. Costelli, P. Costes, S. Cotman, S.L. Coto-Montes, A. Cottet, S. Couve, E. Covey, L.R. Cowart, L.A. Cox, J.S. Coxon, F.P. Coyne, C.B. Cragg, M.S. Craven, R.J. Crepaldi, T. Crespo, J.L. Criollo, A. Crippa, V. Cruz, M.T. Cuervo, A.M. Cuezva, J.M. Cui, T. Cutillas, P.R. Czaja, M.J. Czyzyk-Krzeska, M.F. Dagda, R.K. Dahmen, U. Dai, C. Dai, W. Dai, Y. Dalby, K.N. Valle, L.D. Dalmasso, G. D'amelio, M. Damme, M. Darfeuille-Michaud, A. Dargemont, C. Darley-Usmar, V.M. Dasarathy, S. Dasgupta, B. Dash, S. Dass, C.R. Davey, H.M. Davids, L.M. Dávila, D. Davis, R.J. Dawson, T.M. Dawson, V.L. Daza, P. de Belleroche, J. de Figueiredo, P. de Figueiredo, R.C.B.Q. de la Fuente, J. De Martino, L. De Matteis, A. De Meyer, G.R.Y. De Milito, A. De Santi, M. de Souza, W. De Tata, V. De Zio, D. Debnath, J. Dechant, R. Decuypere, J.-P. Deegan, S. Dehay, B. Del Bello, B. Del Re, D.P. Delage-Mourroux, R. Delbridge, L.M.D. Deldicque, L. Delorme-Axford, E. Deng, Y. Dengjel, J. Denizot, M. Dent, P. Der, C.J. Deretic, V. Derrien, B. Deutsch, E. Devarenne, T.P. Devenish, R.J. Di Bartolomeo, S. Di Daniele, N. Di Domenico, F. Di Nardo, A. Di Paola, S. Di Pietro, A. Di Renzo, L. Di Antonio, A. Díaz-Araya, G. Díaz-Laviada, I. Diaz-Meco, M.T. Diaz-Nido, J. Dickey, C.A. Dickson, R.C. Diederich, M. Digard, P. Dikic, I. Dinesh-Kumar, S.P. Ding, C. Ding, W.-X. Ding, Z. Dini, L. Distler, J.H.W. Diwan, A. Djavaheri-Mergny, M. Dmytruk, K. Dobson, R.C.J. Doetsch, V. Dokladny, K. Dokudovskaya, S. Donadelli, M. Dong, X.C. Dong, X. Dong, Z. Donohue, T.M., Jr. Donohue-Jr, T.M. Doran, K.S. D'orazi, G. Dorn, G.W., II Dosenko, V. Dridi, S. Drucker, L. Du, J. Du, L.-L. Du, L. du Toit, A. Dua, P. Duan, L. Duann, P. Dubey, V.K. Duchen, M.R. Duchosal, M.A. Duez, H. Dugail, I. Dumit, V.I. Duncan, M.C. Dunlop, E.A. Dunn, W.A., Jr. Dupont, N. Dupuis, L. Durán, R.V. Durcan, T.M. Duvezin-Caubet, S. Duvvuri, U. Eapen, V. Ebrahimi-Fakhari, D. Echard, A. Eckhart, L. Edelstein, C.L. Edinger, A.L. Eichinger, L. Eisenberg, T. Eisenberg-Lerner, A. Eissa, N.T. El-Deiry, W.S. El-Khoury, V. Elazar, Z. Eldar-Finkelman, H. Elliott, C.J.H. Emanuele, E. Emmenegger, U. Engedal, N. Engelbrecht, A.-M. Engelender, S. Enserink, J.M. Erdmann, R. Erenpreisa, J. Eri, R. Eriksen, J.L. Erman, A. Escalante, R. Eskelinen, E.-L. Espert, L. Esteban-Martínez, L. Evans, T.J. Fabri, M. Fabrias, G. Fabrizi, C. Facchiano, A. Færgeman, N.J. Faggioni, A. Fairlie, W.D. Fan, C. Fan, D. Fan, J. Fang, S. Fanto, M. Fanzani, A. Farkas, T. Faure, M. Favier, F.B. Fearnhead, H. Federici, M. Fei, E. Felizardo, T.C. Feng, H. Feng, Y. Feng, Y. Ferguson, T.A. Fernández, Á.F. Fernandez-Barrena, M.G. Fernandez-Checa, J.C. Fernández-López, A. Fernandez-Zapico, M.E. Feron, O. Ferraro, E. Ferreira-Halder, C.V. Fesus, L. Feuer, R. Fiesel, F.C. Filippi-Chiela, E.C. Filomeni, G. Fimia, G.M. Fingert, J.H. Finkbeiner, S. Finkel, T. Fiorito, F. Fisher, P.B. Flajolet, M. Flamigni, F. Florey, O. Florio, S. Floto, R.A. Folini, M. Follo, C. Fon, E.A. Fornai, F. Fortunato, F. Fraldi, A. Franco, R. Francois, A. François, A. Frankel, L.B. Fraser, I.D.C. Frey, N. Freyssenet, D.G. Frezza, C. Friedman, S.L. Frigo, D.E. Fu, D. Fuentes, J.M. Fueyo, J. Fujitani, Y. Fujiwara, Y. Fujiya, M. Fukuda, M. Fulda, S. Fusco, C. Gabryel, B. Gaestel, M. Gailly, P. Gajewska, M. Galadari, S. Galili, G. Galindo, I. Galindo, M.F. Galliciotti, G. Galluzzi, L. Galluzzi, L. Galy, V. Gammoh, N. Gandy, S. Ganesan, A.K. Ganesan, S. Ganley, I.G. Gannagé, M. Gao, F.-B. Gao, F. Gao, J.-X. Nannig, L.G. Véscovi, E.G. Garcia-Macía, M. Garcia-Ruiz, C. Garg, A.D. Garg, P.K. Gargini, R. Gassen, N.C. Gatica, D. Gatti, E. Gavard, J. Gavathiotis, E. Ge, L. Ge, P. Ge, S. Gean, P.-W. Gelmetti, V. Genazzani, A.A. Geng, J. Genschik, P. Gerner, L. Gestwicki, J.E. Gewirtz, D.A. Ghavami, S. Ghigo, E. Ghosh, D. Giammarioli, A.M. Giampieri, F. Giampietri, C. Giatromanolaki, A. Gibbings, D.J. Gibellini, L. Gibson, S.B. Ginet, V. Giordano, A. Giorgini, F. Giovannetti, E. Girardin, S.E. Gispert, S. Giuliano, S. Gladson, C.L. Glavic, A. Gleave, M. Godefroy, N. Gogal, R.M., Jr. Gokulan, K. Goldman, G.H. Goletti, D. Goligorsky, M.S. Gomes, A.V. Gomes, L.C. Gomez, H. Gomez-Manzano, C. Gómez-Sánchez, R. Gonçalves, D.A.P. Goncu, E. Gong, Q. Gongora, C. Gonzalez, C.B. Gonzalez-Alegre, P. Gonzalez-Cabo, P. González-Polo, R.A. Goping, I.S. Gorbea, C. Gorbunov, N.V. Goring, D.R. Gorman, A.M. Gorski, S.M. Goruppi, S. Goto-Yamada, S. Gotor, C. Gottlieb, R.A. Gozes, I. Gozuacik, D. Graba, Y. Graef, M. Granato, G.E. Grant, G.D. Grant, S. Gravina, G.L. Green, D.R. Greenhough, A. Greenwood, M.T. Grimaldi, B. Gros, F. Grose, C. Groulx, J.-F. Gruber, F. Grumati, P. Grune, T. Guan, J.-L. Guan, K.-L. Guerra, B. Guillen, C. Gulshan, K. Gunst, J. Guo, C. Guo, L. Guo, M. Guo, W. Guo, X.-G. Gust, A.A. Gustafsson, Å.B. Gutierrez, E. Gutierrez, M.G. Gwak, H.-S. Haas, A. Haber, J.E. Hadano, S. Hagedorn, M. Hahn, D.R. Halayko, A.J. 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- Published
- 2016
250. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
- Author
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