105,570 research outputs found
Dr. Lin Sun, CAU, March 2013
No full textThis video is a conversation with Dr. Lin Sun. Dr. Sun talks about an exhibit at the Woodruff Library titled "At The Boundary." Jordan Moore, AUC Woodruff Library, is the interviewer
An Analysis of <i>Judge Lin</i>
No full textBiography of Lin Wen Zhong Gong has another way to call, that is Judge Lin. The leading character is Lin Ze-Xu. This book is based on functionary experience of Lin Ze-Xu, with the captivating plots of court case, helping by highly skilled military attach\uc3\ua9s and chivalrous knights, and the history facts of Opium War. It makes Lin Ze-Xu\ue2s Confucian temperament and tragic mood more, also contrasts with author\ue2s sorrow and furiousness for the politics at the time. History, court case, martial arts\ue2\ua6\ue2\ua6etc. are essence of this book and it broadens the way of this writing style.
The topic of the thesis is \ue2An Analysis of Judge Lin\ue2. The following thesis will be divided into six different chapters. The introduction is Chapter one of the thesis, which is including researching motive and purpose, literature review of predecessors, researching version by existing information, raising questions, choosing research methods and arranging chapters. In chapter Two, I discuss the study of characters of Lin Ze-Xu, also makes a deep analysis of author\u27s purpose of writing him. In chapter Three, I analyze supporting actors and actress. Meanwhile, I illustrate author\u27s purpose of writing supporting actress because the author had different manner to describe supporting actress. Moving to the Chapter Four, I mainly focus on the plots of Judge Lin, and organize cases of Lin Ze-Xu and his subordinates to understand features of cases. In Chapter Five, I represent the causes of Opium War. China and England had difference of opinions of opium. Therefore, it is easier to comprehend what the author\u27s purpose is. In the last chapter I summarize the main points of the preceding chapters and confirm particularity of Judge Lin
Tz-Lin Hsu Piano Recital Program Notes
No full textThis is the Program Notes of Tz-Lin Hsu\ue2s piano recital held on May 20th, 2020. The recital program includes Johann Sebastian Bach\ue2s The Well-Tempered Clavier, Book 1, Prelude and Fugue No. 17 in A-flat Major, BWV 862; Ludwig van Beethoven\ue2s Sonata No. 7 in D Major, Op. 10, No. 3, Jakob Ludwig Felix Mendelssohn Bartholdy\ue2s Fantasy in F-sharp minor, Op. 28; and Ignacy Jan Paderewski\ue2s Th\uc3\ua8me vari\uc3\ua8 in A Major, Op. 16, No. 3. The program notes will briefly introduce these four composers\ue2 lives, their compositional backgrounds, and the structure of each work, including the tonal organization and thematic materials
[19] F. Lin and W. M. Wonham, 1990. Decentralized control and coordination of discrete event systems with partial observation.
No full textdiscrete event systems. Discrete Event Dynamic Systems: Theory and Applications, 4(3), pp. 221-236. [9] M. Heymann and F. Lin, 1996. Nonblocking supervisory control of nondeterministic systems, Technion CIS Report #9620, October 1996. [10] M. Heymann and F. Lin, 1995. On observability and nondeterminism in discrete event control, Proceedings of the 33rd Allerton Conference on Communication, Control, and Computing, pp. 136-145. [11] M. Heymann and F. Lin, 1996. Discrete event control of nondeterministic discrete event systems, Proceedings of the 35th IEEE Conference on Decision and Control, to appear. [12] J. E. Hopcroft and J. D. Ullman. Introduction to Automata Theory, Languages and Computation. Addison-Wesley, 1979. [13] K. Inan, 1994. Nondeterministic supervision under partial observation. in G. Cohen and J.-P. Quadrat, Eds., 11th International Conference on Analysis and Optimization o
LIN-2/CASK binds to both ACR-16 and UNC-29 through SH3 domain.
No full text(A) Summary of interactions by Yeast two-hybrid. Strong interaction (++); weak interaction (+), and no interactions (-) were indicated. (B) LIN-2A’s SH3 domain binds the ACR-16’s second intracellular loop (LoopII) in a Yeast two-hybrid assay. Y2HGold cells carrying indicated plasmids (Left) growing on selective media (-Trp/-Leu/-His/-Ade) is shown (Right). (C) LIN-2A’s SH3 domain binds the UNC-29’s second intracellular loop (LoopII) in the Yeast two-hybrid assay. (D-E) FRM-3 do not bind the ACR-16’s second intracellular loop (LoopII) (D) and UNC-29’s second intracellular loop (LoopII) (E) in the Yeast two-hybrid assay. (F-G) LIN-2A binds FRM-3 (F) and its FERM domain (G) requiring its PDZ domain, but not SH3 domain.</p
Singaporemma banxiaoensis Lin & Li 2014
No full textSingaporemma banxiaoensis Lin & Li, 2014 Figures 6B–b, 7C Singaporemma banxiaoensis Lin & Li, 2014: 42, figs 4–6, 16C–D, 20A Examined material. Holotype ♂, paratypes 1♂ and 1♀ (IZCAS), CHINA: Guangxi, Pingxiang, Xiashi Town, Xinming Village, Banxiaotun, Banxiao Cave, 22°5.542'N, 106°52.148'E, altitude 175 m, 26 July 2011, X. Wang leg. Diagnosis. Male of this species is similar to S. halongense (Fig. 6A) and S. lenachanae (Fig. 6D), but can be distinguished from the latter two by the narrower, pointed embolic tip (Fig. 6b vs. Fig. 6a, 6d), and by the vestigial white eyespots lacking black ocular base in the both sexes (see Lin & Li, 2014: fig. 4G–H vs. Lin et al., 2017: figs 16E–F, 21A). Female is close to S. takensis sp. n. in having a similar configuration of vulva, but differs from the latter by the inverted triangular inner vulval plate, the wider, shorter central process (Fig. 7C vs. Fig. 5C–D). Description. See Lin & Li, 2014: 42. Distribution. China (Guangxi) (Fig. 10).Published as part of Yan, Fanhu & Lin, Yucheng, 2018, A review of the spider genus Singaporemma (Araneae: Tetrablemmidae), with the description of a new species, pp. 329-346 in Zootaxa 4392 (2) on page 331, DOI: 10.11646/zootaxa.4392.2.6, http://zenodo.org/record/119544
Singaporemma bifurcata Lin & Li 2010
No full textSingaporemma bifurcata Lin & Li, 2010 Figures 1A–H, 2A–E, 6F–f, 8A Singaporemma bifurcata Lin & Li, 2010: 26, figs 29–37 Examined material. Topotypes 11♂ 25♀ (NHMSU), CHINA: Guizhou, Suiyang, Wenquan Town, Guihua Village, Hejiao Cave, 28°15´N, 107°17´E, altitude 695 m, 17 April 2015, Y. Lin and H. Yang leg. Diagnosis. With the exception of S. wulongensis, male of S. bifurcata can be distinguished from all other congeners by the embolus with an asymmetrically furcate end (Fig. 6f vs. Fig. 6a–d, 6g –h), and female of S. bifurcata differs by the stubby, sclerotized central process (Fig. 8A vs. Figs. 5C–D, 7A–C, 9A–B). S. bifurcata similar to S. wulongensis in the shape of palpal bulb and the configuration of vulva, but male of S. bifurcata can be distinguished from that of S. wulongensis by the starting position of embolus (Fig. 6F vs. Fig. 6E, the position indicated by the blue arrow) and the unequal length of branches of embolic tip (Fig. 6f vs. Fig. 6e); female of S. bifurcata separated by the smaller, “Ω”-shaped inner vulval plate, and the shorter central process (Fig. 8A vs. Fig. 8B). Description. See Figs 1A–H, 2A–E, 6F–f, 8A and Lin & Li, 2010: 26. Distribution. China (Guizhou) (Fig. 10).Published as part of Yan, Fanhu & Lin, Yucheng, 2018, A review of the spider genus Singaporemma (Araneae: Tetrablemmidae), with the description of a new species, pp. 329-346 in Zootaxa 4392 (2) on page 334, DOI: 10.11646/zootaxa.4392.2.6, http://zenodo.org/record/119544
LIN-39 promotes neuronal fate specification in the Q and V5 lineage.
No full text(A) The expression of lin-39 in AVM, SDQL/R, PDEL/R, and PVDL/R, indicated by the overlapping with neurotransmitter identity markers and specific fate markers (uIs115[mec-17p::TagRFP] for AVM, otIs181[dat-1p::mCh] for PDE, uIs117[lad-2p::mCh] for SDQ). (B) The expression of mab-5 in SDQL. (C) Summary of lin-39 (green) and mab-5 (cyan) expression in the descendants of Q and V5 lineages. (D) The loss of gcy-37 expression in AQR and AVM neurons in lin-39(n1760) mutants and the mispositioning of PQR in mab-5(gk670) mutants; the loss of lad-2 expression in SDQR in lin-39(n1760) mutants, the displacement of SDQL in mab-5(gk670) mutants, and the loss of lad-2 expression in both SDQs in lin-39(n1760) mab-5(e1239) mutants. The right panels show the penetrance for the loss of marker expression and cell body mispositioning. Mean ± SD for the percentage of cells showing corresponding phenotypes from three biological replicates are shown. Double asterisks indicate statistically significant difference (p Chi-square test. (E) The loss of ser-2 expression in PVD and PDE neurons and the loss of F49H12.4 expression in PVD in lin-39(n1760) and ceh-20(u843) mutants. (F) Dopaminergic marker dat-1 is normally expressed in PDE neurons in lin-39 mutants, but PDE shows axonal growth defects. The arrows indicate the termini of PDE axons. The expression of glutamatergic identity marker eat-4 and the PVD terminal selector gene mec-3 in PVD neurons in lin-39 mutants.</p
Review of Mayer, R.; Knothe, F.; Shuo, H. (2022) Reflected beauty: Chinese reverse glass paintings from the Mei Lin Collection
No full textIn this well-documented, bilingual, and richly illustrated catalogue, published for the long-anticipated exhibition Reflected Beauty: Chinese Reverse Glass Paintings from the Mei Lin Collection at the University Museum and Art Gallery of the University of Hong Kong (September 2021-January 2022), the authors give us a profound insight into the phenomenon of reverse painting on glass and mirror paintings, with a particular focus on those from the Mei Lin Collection assembled by the Sinologist, author, and translator Rupprecht Mayer and his wife Haitang Mayer-Liem. Composed of over one hundred works acquired in East Asia between 1968 and 2012, this is one of the world's most important collections of Chinese reverse glass paintings from the late nineteenth and twentieth centuries.Modern and Contemporary Studie
LIN-2 and FRM-3 are required to maintain locomotory behaviour.
No full text(A) Genomic structure of lin-2 and frm-3 locus, mutant allele characterization, and protein architecture for LIN-2 and FRM-3. The whole promoter region of lin-2a and part of the kinase domain of LIN-2A is deleted in the e1309 mutants. The FERM domain in both frm-3a and frm-3b is deleted in the gk585 mutants. Syb1019 and syb1036 are stop codons in lin-2 and frm-3 that inactivate the expression of lin-2a and lin-2b, and frm-3a and frm-3b. (E, F) Locomotion speed is reduced by the loss of LIN-2 and FRM-3. Representative trajectories of locomotion in wild type (E) and mean locomotion speed in wild type, lin-2(e1309), frm-3(gk585), lin-2(syb1019), frm-3(syb1036), and lin-2(e1309);frm-3(gk585) mutants. To measure locomotion speed, young adult animals were washed with a drop of PBS and then transferred to fresh NGM plates with no bacterial lawn (30 worms per plate). Worm movement recordings (under room temperature 22°C) were started 10 min after the worms were transferred. A 2 min digital video of each plate was captured at 3.75 Hz frame rate by WormLab System (MBF Bioscience). Average speed and tracks were generated for each animal using WormLab software. To confirm the repeatability of the data, the locomotion speed was measured in two independent experiments in two days. For each mutant, around 10–40 animals were analyzed in one experiment. Significance was tested for each experiment. Data are mean ± SEM (**, p p < 0.001 when compared to wild type; n.s., non-significant; one-way ANOVA). The number of worms analyzed for each genotype is indicated in the bar.</p
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