255,245 research outputs found
Lin D. Cartwright correspondence with Mrs. Willard Steele, 1933 September 28
No full textLetter from Lin D. Cartwright to Mrs. Willard Steele, expressing appreciation of Steele's efforts to preserve the cemetery at Brainerd Mission
Lin D. Cartwright correspondence with Mrs. Willard Steele, 1933 September 28
No full textLetter from Lin D. Cartwright to Mrs. Willard Steele, expressing appreciation of Steele's efforts to preserve the cemetery at Brainerd Mission
A single E-box in the <i>Cel-lin-3</i> CRM is not sufficient for <i>lin-3</i> expression in the anchor cell of <i>C</i>. <i>elegans</i>.
No full text(A) New cis-regulatory lin-3 alleles with deleted E-boxL and NHR or NHR and E-boxR. (B) Quantification of vulval induction in these new mutants. Note the complete absence of any induction in the recovered lin-3 alleles (n>30). Scorings of lin-3(1417) animals are the same as those reported in Fig 5 and are used here to indicate that this mutation leads to vulval hypo-induction rather than no induction at all. (C-D) smFISH in lin-3(mf72) (C) and N2 (D) animals. Green spots correspond to lin-3 transcripts and red spots to lag-2 that is used as an anchor cell marker. Blue is DAPI staining of nuclei. Note the absence of lin-3 expression in the anchor cell in the lin-3(mf72) mutant animal. Absence of lin-3 signal in the anchor cell was also confirmed for the other lin-3 alleles.</p
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
LIN-1 sumoylation is required for ventral toroid contraction.
No full text(A) Wild-type and K10A, K169A mutant LIN-1::GFP expression in L3 larvae at the Pn.px stage after VPC-specific degradation of AID::SMO-1 from the L2 stage onward. The 1° and 2° VPC descendants are underlined in white. The left panels show the corresponding DIC images overlaid with the LIN-1::GFP signal in green. (B) Quantification of LIN-1::GFP expression levels in 1° and 2° VPC descendants at the Pn.px stage in LIN-1::GFP wild-type and K10A, K169A double mutants under the indicated conditions. See S3 Fig for the corresponding measurements at the Pn.pxx stage. (C) Toroid morphogenesis defects in LIN-1 K10A and K169A single and double mutants at the L4 stage. Left panels show lateral views of z-projections. vulA and vulB1 toroids are outlined by the white rectangle in the top left panel and shown in top (xz) views in the right panels. (D) Quantification of vulA contraction, calculated as the ratio of the vulA and vulB1 toroid diameter. The box plots show the median values with the 25th and 75th percentiles and the whiskers indicate the maximum and minimum values. Where indicated, untreated controls are labelled with–IAA (blue) and animals treated with 1 mM auxin with +IAA (red). In each graph, the numbers of animals scored are indicated by the numbers in brackets. Statistical significance in (B) and (D) was calculated with unpaired two-tailed t-tests. p-values are indicated as * p ≤ 0.05; ** p ≤ 0.01; *** p ≤ 0.001. The scale bars are 10 μm.</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
Spatially coherent high-order harmonics generated at optimal high gas pressure with high-intensity one- or two-color laser pulses
No full textCitation: Jin, C., & Lin, C. D. (2016). Spatially coherent high-order harmonics generated at optimal high gas pressure with high-intensity one- or two-color laser pulses. Physical Review A, 94(4), 6. doi:10.1103/PhysRevA.94.043804We investigate the gas-pressure dependence of macroscopic harmonic spectra generated in a high-ionization medium using intense 800-nm laser pulses. The harmonics obtained at the optimal pressure show good spatial coherence with small divergence (less than 2 mrad) in the far field. By analyzing the evolution of the laser's electric field as it propagates, we find that dynamic phase matching conditions are fulfilled in the second half of the gas cell and that harmonic yields do not depend on the position of the gas cell with respect to the focusing position. We also demonstrate that harmonic yields at the optimal pressure can be further enhanced by increasing input laser energy or by adding a few percent of second or third harmonic to the fundamental
Spatial Chow-Lin Methods for Data Completion in Econometric Flow Models
No full textFlow data across regions can be modeled by spatial econometric models, see LeSage and Pace (2009). Recently, regional studies became interested in the aggregation and disaggregation of flow models, because trade data cannot be obtained at a disaggregated level but data are published on an aggregate level. Furthermore, missing data in disaggregated flow models occur quite often since detailed measurements are often not possible at all observation points in time and space. In this paper we develop classical and Bayesian methods to complete flow data. The Chow and Lin (1971) method was developed for completing disaggregated incomplete time series data. We will extend this method in a general framework to spatially correlated flow data using the cross-sectional Chow-Lin method of Polasek et al. (2009). The missing disaggregated data can be obtained either by feasible GLS prediction or by a Bayesian (posterior) predictive density.Missing values in spatial econometrics, MCMC, non-spatial Chow-Lin (CL) and spatial Chow-Lin (SCL) methods, spatial internal flow (SIF) models, origin and destination (OD) data
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