We employed a boundary paradigm to investigate how Chinese two-character compounds (i.e., compound words) are processed during reading. The first character of the compound was an ambiguous morpheme that had a dominant and subordinate meaning. In Experiment 1, there were three previews of the second character: identical to the target character; the preview provided subordinate biasing information (the subordinate condition); the preview provided dominant biasing information (the dominant condition). An invisible boundary was inserted between the two characters. We found that gaze durations and go-past times on the compounds were longer in the subordinate condition than those in the dominant or identical conditions. In Experiment 2, the semantic similarity between target and preview words in the dominant condition was manipulated to determine whether the differences in fixation durations in Experiment 1 resulted from the semantic similarity between the preview and target words. There were significant fixation duration differences on the target word between the dominant and subordinate conditions only when the preview and target words were semantically related. This finding indicated that the whole-word meaning plays an important role in processing Chinese compounds and that the whole-word access route is the principal processing route in reading two-character compounds in Chinese.
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http://dx.doi.org/10.1080/17470218.2016.1270975 | DOI Listing |
J Radiol Prot
January 2025
Department of Mechanical Engineering, University of Houston, Houston, 77204, UNITED STATES.
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Department of Urology, Peking University First Hospital, Beijing 100034, China.
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Molecular Synthesis Center, Key Laboratory of Marine Drugs of Ministry of Education, Shandong Key Laboratory of Glycoscience and Glycotherapeutics, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, China.
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January 2025
Beijing National Laboratory for Molecular Sciences, Key Laboratory of Analytical Chemistry for Living Biosystems, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China.
Ligand binding to membrane proteins initiates numerous therapeutic processes. Surface plasmon resonance (SPR), a popular method for analyzing molecular interactions, has emerged as a promising tool for in situ determination of membrane protein binding kinetics owing to its label-free detection, high surface sensitivity, and resistance to intracellular interference. However, the excitation of SPR relies on noble metal films, typically gold, which are biologically incompatible and can cause fluorescence quenching.
View Article and Find Full Text PDFBlood
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State Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College; Center for Stem Cell Medicine,, Tianjin, China.
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