Gotowe bibliografie tematyczne / Jpcon

Gotowa bibliografia na temat „Jpcon”

Autor: Grafiati

Data publikacji: 25 lipca 2024

Data aktualizacji: 26 lipca 2024

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Artykuły w czasopismach na temat "Jpcon"

Maitinsky, Marcell, Maddy Walter, Amanda Cardoso, Md Jahurul Islam i Bryan Gick. "The effect of perceived human-likeness on voice-user interface–directed speech". Journal of the Acoustical Society of America 154, nr 4_supplement (1.10.2023): A160. http://dx.doi.org/10.1121/10.0023128.

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Many interact daily with voice–user interfaces (VUIs), but acoustic research on VUI-directed speech (VDS) is relatively new. Prior work indicates intensity and F0 correlate with VDS [Cohn et al., 2022, JPhon 90]. Multiple acoustic variables of VDS were analyzed to explore if VDS is a register distinct from human-directed speech (HDS) and whether perceived human-likeness of VUI voices affects VDS characteristics. 27 participants’ Zoom recordings of 13 pre-scripted prompts and pre-recorded responses from two Amazon AWS-Polly-generated VUI voices (rated for human-likeness independently and by participants) were acoustically analyzed for word-initial voiceless plosives voice onset time (VOT), pitch variation, and vowel quality and quantity. Results of linear mixed-effects models indicate evidence of VDS-specific acoustic characteristics, some of which are affected by participants’ perceived human-likeness of the voices. Differences in pre-exposure and VUI interactions occur for /p/ VOT in consonant clusters, vowel duration (except /ɪ/), and /ɑ/ F2. Statistical differences are found for /p/ VOT in consonant clusters and vowel quality (e.g., /ɑ/ F1 and F2, and /ɪ/ F2) based on perceived human-likeness by participants. This study contributes to the growing VDS work examining how humans speak with devices and what affects VDS, which may influence considerations of VUI voice development.

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Islam, Md Jahurul, Victor Wong, Dayeon Choi i Bryan Gick. "Location of constriction in velar sounds in French". Journal of the Acoustical Society of America 155, nr 3_Supplement (1.03.2024): A312. http://dx.doi.org/10.1121/10.0027621.

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This study examines the constriction location (CL) of the velar stop [k] in French. While previous studies have investigated how vocalic contexts influence the CL of velar stops [Liker & Gibbon (2008) Clin. Ling. & Phon. 22(2); Tabain (2000) JPhon 28(2)], few investigated high-level changes in CL. Building on our prior work [Islam & Gick (2023) JASA 154], which showed an unexpected palato-velar articulation of [k] followed by [a] compared with [w] followed by [a], we tested whether this [k]-palatalizing is universal or specific to [a]. Using a French MRI speech corpus [Isaieva et al., Scientific Data 8], we measured constriction in [k] before [i], [ɛ], [o], [u], and [a]. MRI video frames were manually traced to mark the upper surface of the tongue and the lower surface of the hard palate, resulting in two contours. Using Euclidean distance, the location of the constriction was identified as the narrowest point and distance, respectively, between the two contours. A Python script that measured Euclidean distance from traced MRI frames calculated these distances from the MRI frames. Results indicate a frontal shift in [k] across all contexts, indicating a general fronting articulation of [k] in French speech.

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Woodgate, R. "Part I: An introduction to conducting qualitative research in children with cancer". Journal of Pediatric Oncology Nursing 17, nr 4 (październik 2000): 192–206. http://dx.doi.org/10.1053/jpon.2000.16396.

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Woodgate, R. "Part II: A critical review of qualitative research related to children's experiences with cancer". Journal of Pediatric Oncology Nursing 17, nr 4 (październik 2000): 207–28. http://dx.doi.org/10.1053/jpon.2000.16397.

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Murray, J. "Development of two instruments measuring social support for siblings of children with cancer". Journal of Pediatric Oncology Nursing 17, nr 4 (październik 2000): 229–38. http://dx.doi.org/10.1053/jpon.2000.16398.

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Enskär, K. "Important aspects of care and assistance for children with cancer". Journal of Pediatric Oncology Nursing 17, nr 4 (październik 2000): 239–49. http://dx.doi.org/10.1053/jpon.2000.16399.

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O'Neil, J. "Are we acting as moral agents for our patients?" Journal of Pediatric Oncology Nursing 17, nr 4 (październik 2000): 250–52. http://dx.doi.org/10.1053/jpon.2000.16400.

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Gazzola, M. "What it's like". Journal of Pediatric Oncology Nursing 17, nr 4 (październik 2000): 253–54. http://dx.doi.org/10.1053/jpon.2000.16401.

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Kline, N. "Learning from our international colleagues". Journal of Pediatric Oncology Nursing 17, nr 4 (październik 2000): 191. http://dx.doi.org/10.1053/jpon.2000.20162.

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Kassner, Elizabeth. "Evaluation and Treatment of Chemotherapy Extravasation Injuries". Journal of Pediatric Oncology Nursing 17, nr 3 (lipiec 2000): 135–48. http://dx.doi.org/10.1053/jpon.2000.8063.

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Streszczenia konferencji na temat "Jpcon"

Asakura, S., N. Yoshida i M. Matsuda. "MONOCLONAL ANTIBODIES AGAINST THROHBIN-ANTITHROMBIN III COMPLEX: EPITOPE SPECIFICITY AND EFFECT ON THROMBIN-ANTITHROMBIN III INTERACTION". W XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643673.

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Among monoclonal antibodies (MCA´s) raised against human thrombin (T)-antithrombin m (AT) complex (TAT), two MCA´s designated as JITAT-16 and 17 with high affinity, Kd = 4.6nMand 4.1 nfi, respectively, were selected and characterized for specificity and functions. Their respective immunoglobulin subclasses are IgGi and IgG2a, and epitopes were found to be different from each Dther as shown by crisscross inhibition experiments. Immuno-alotting of normal plasma and serum electrophoresed on non-SDS aolyacrylamide gel showed that these antibodies reacted with normal serum but not with plasma. This was verified by an anzyme-linked differential antibody immunosorbent assay using aither one of the MCA´s as the first antibody and the other MCA labeled with peroxidase as the second one. By immunoblotting after SDS-PAGE, we found that both antibodies reacted with TAT, nut not with its respective nascent constituent, AT or T. However, they reacted with reactive site-cleaved AT (or thrombin-nodified AT, ATM) and also a complex of AT with activated factor K (Xa-AT). These results indicate that both of these antibodies recognize enzyme-treated forms of AT, including AT molecules :omplexed with enzymes reversibly or irreversibly as well as ATM. Jpon incubation of T with AT in the presence of JITAT-16, T activity remained nearly unchanged and formation of irreversible rAT did not proceed as expected. Moreover, AT was preferentially :onverted to ATM. When JITAT-16 was added after completion of FAT formation, however, neither recovery of T activity nor generation of ATM was observed. These findings were not obtained vhen JITAT-17 had been substituted for JITAT-16. These data suggest that JITAT-16 may have converted AT from an inhibitor to a substrate for T after having recognized a possible intermediate reversible complex of AT with T. Undoubtedly, in the presence of a polyclonal antibody against AT, neither TAT formation nor ATM neneration was observed at all. The mechanism of the unique Function of JITAT-16 has not been fully clarified as yet, but this antibody seems to give us new information on the kinetic study of TAT formation and ATM generation when AT was allowed to react with enzymes.

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