| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Monica Zilbovicius, Isabelle Meresse, Nadia Chabane, Francis Brunelle, Yves Samson, Nathalie Boddaer. Autism, the superior temporal sulcus and social perception. Trends in neurosciences. vol 29. issue 7. 2006-10-10. PMID:16806505. |
based on recent brain-imaging results, our hypothesis is that abnormalities in the superior temporal sulcus (sts) are highly implicated in asd. |
2006-10-10 |
2023-08-12 |
Not clear |
| Alejo Freire, Terri L Lewis, Daphne Maurer, Randolph Blak. The development of sensitivity to biological motion in noise. Perception. vol 35. issue 5. 2006-10-10. PMID:16836055. |
the comparison implies an immaturity at 6 years of age in the neural networks involved specifically in the processing of biological motion, networks that may include the superior temporal sulcus (sts). |
2006-10-10 |
2023-08-12 |
human |
| Alan Cowey, Linda Irving-Bel. Do parietal cortical lesions impair spatial attention or allocentric spatial perception? Cortex; a journal devoted to the study of the nervous system and behavior. vol 42. issue 5. 2006-09-20. PMID:16909636. |
monkeys with small posterior parietal (spp), large posterior parietal (lpp), superior temporal sulcus (sts), or frontal eye field (fef) lesions were tested on a landmark task in which the physical salience of the landmark and its location varied. |
2006-09-20 |
2023-08-12 |
monkey |
| Tomoko Akiyama, Motoichiro Kato, Taro Muramatsu, Fumie Saito, Satoshi Umeda, Haruo Kashim. Gaze but not arrows: a dissociative impairment after right superior temporal gyrus damage. Neuropsychologia. vol 44. issue 10. 2006-09-19. PMID:16616939. |
superior temporal sulcus (sts) activation has consistently been demonstrated in the normal brain when viewing eyes, and thus this area is implicated as a gaze processing region in humans. |
2006-09-19 |
2023-08-12 |
human |
| Jennifer T Crinion, Elizabeth A Warburton, Matthew A Lambon-Ralph, David Howard, Richard J S Wis. Listening to narrative speech after aphasic stroke: the role of the left anterior temporal lobe. Cerebral cortex (New York, N.Y. : 1991). vol 16. issue 8. 2006-09-05. PMID:16251507. |
the dorsal bank of the primate superior temporal sulcus (sts) is a polysensory area with rich connections to unimodal sensory association cortices. |
2006-09-05 |
2023-08-12 |
human |
| Tjeerd Jellema, David I Perret. Neural representations of perceived bodily actions using a categorical frame of reference. Neuropsychologia. vol 44. issue 9. 2006-08-28. PMID:16530792. |
some cells in the superior temporal sulcus (sts) of the macaque monkey have been reported to use such a categorical frame of reference to code for bodily postures and actions, but their small numbers prevented a detailed investigation. |
2006-08-28 |
2023-08-12 |
monkey |
| Teruo Hashimoto, Nobuo Usui, Masato Taira, Izuru Nose, Tomoki Haji, Shozo Kojim. The neural mechanism associated with the processing of onomatopoeic sounds. NeuroImage. vol 31. issue 4. 2006-08-09. PMID:16616863. |
by discriminating between the categories of target sounds (birds/nonbirds), the nouns resulted in activations in the left anterior superior temporal gyrus (stg), whereas the animal sounds resulted in activations in the bilateral superior temporal sulcus (sts) and the left inferior frontal gyrus (ifg). |
2006-08-09 |
2023-08-12 |
human |
| Justin Sauer, Dominic H ffytche, Clive Ballard, Richard G Brown, Robert Howar. Differences between Alzheimer's disease and dementia with Lewy bodies: an fMRI study of task-related brain activity. Brain : a journal of neurology. vol 129. issue Pt 7. 2006-08-03. PMID:16670180. |
comparing patterns of task-related activity across groups, dlb patients showed more activation than alzheimer patients within the superior temporal sulcus (sts) for the motion task (right sts: 44, 0, -20; p = 0.004 corrected; left sts: -40, -4, -26; p = 0.07 corrected). |
2006-08-03 |
2023-08-12 |
Not clear |
| Ghislaine Dehaene-Lambertz, Stanislas Dehaene, Jean-Luc Anton, Aurelie Campagne, Philippe Ciuciu, Guillaume P Dehaene, Isabelle Denghien, Antoinette Jobert, Denis Lebihan, Mariano Sigman, Christophe Pallier, Jean-Baptiste Polin. Functional segregation of cortical language areas by sentence repetition. Human brain mapping. vol 27. issue 5. 2006-07-19. PMID:16565949. |
repetition induced a decrease in amplitude and a speeding up of the bold response in the superior temporal sulcus (sts), while the most superior temporal regions were not affected. |
2006-07-19 |
2023-08-12 |
Not clear |
| Christian F Beckmann, Mark Jenkinson, Mark W Woolrich, Timothy E J Behrens, David E Flitney, Joseph T Devlin, Stephen M Smit. Applying FSL to the FIAC data: model-based and model-free analysis of voice and sentence repetition priming. Human brain mapping. vol 27. issue 5. 2006-07-19. PMID:16565953. |
the combination of hemodynamic response function (hrf) and mixture modeling, in particular, revealed that both sentence content and speaker voice priming effects occurred bilaterally along the length of the superior temporal sulcus (sts). |
2006-07-19 |
2023-08-12 |
Not clear |
| Koen Nelissen, Wim Vanduffel, Guy A Orba. Charting the lower superior temporal region, a new motion-sensitive region in monkey superior temporal sulcus. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 26. issue 22. 2006-06-23. PMID:16738235. |
although the role of the middle temporal (mt/v5) area and its medial superior temporal (mst) satellites in motion processing has been well explored, relatively little is known about motion regions located more rostrally in the superior temporal sulcus (sts), such as the fundus of the superior temporal (fst) area, the superior temporal polysensory (stp) region, or beyond. |
2006-06-23 |
2023-08-12 |
monkey |
| Lars M Rimol, Karsten Specht, Kenneth Hugdah. Controlling for individual differences in fMRI brain activation to tones, syllables, and words. NeuroImage. vol 30. issue 2. 2006-05-23. PMID:16343948. |
previous neuroimaging studies have consistently reported bilateral activation to speech stimuli in the superior temporal gyrus (stg) and have identified an anteroventral stream of speech processing along the superior temporal sulcus (sts). |
2006-05-23 |
2023-08-12 |
human |
| Lisa A de la Mothe, Suzanne Blumell, Yoshinao Kajikawa, Troy A Hacket. Cortical connections of the auditory cortex in marmoset monkeys: core and medial belt regions. The Journal of comparative neurology. vol 496. issue 1. 2006-05-22. PMID:16528722. |
cm was densely connected with caudal auditory fields, the retroinsular (ri) area of the somatosensory cortex, the superior temporal sulcus (sts), and the posterior parietal and entorhinal cortex. |
2006-05-22 |
2023-08-12 |
monkey |
| Lisa Aziz-Zadeh, Lisa Koski, Eran Zaidel, John Mazziotta, Marco Iacobon. Lateralization of the human mirror neuron system. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 26. issue 11. 2006-04-21. PMID:16540574. |
reliably increased signal in the right superior temporal sulcus (sts) was observed for both left-sided and right-sided imitation tasks, although subthreshold activity was also observed in the left sts. |
2006-04-21 |
2023-08-12 |
human |
| Tomoko Akiyama, Motoichiro Kato, Taro Muramatsu, Fumie Saito, Ryoko Nakachi, Haruo Kashim. A deficit in discriminating gaze direction in a case with right superior temporal gyrus lesion. Neuropsychologia. vol 44. issue 2. 2006-04-13. PMID:16005033. |
the superior temporal sulcus (sts) region is well recognized as being heavily involved in detecting and discriminating gaze. |
2006-04-13 |
2023-08-12 |
human |
| Hideki Kondo, Kadharbatcha S Saleem, Joseph L Pric. Differential connections of the perirhinal and parahippocampal cortex with the orbital and medial prefrontal networks in macaque monkeys. The Journal of comparative neurology. vol 493. issue 4. 2006-03-07. PMID:16304624. |
outside the frontal cortex, the perirhinal cortex and the orbital prefrontal network are both interconnected with the ventral part of the temporal pole (tg), area te and the ventral bank and fundus of the superior temporal sulcus (sts), and the dysgranular insula. |
2006-03-07 |
2023-08-12 |
monkey |
| Hiroki C Tanabe, Manabu Honda, Norihiro Sadat. Functionally segregated neural substrates for arbitrary audiovisual paired-association learning. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 27. 2006-02-28. PMID:16000632. |
in both the audiovisual and visuo-visual tasks, the mri signal in the superior temporal sulcus (sts) in response to the second stimulus and feedback peaked during the early phase of learning and then decreased, indicating that the sts might be key to the creation of paired associations, regardless of stimulus type. |
2006-02-28 |
2023-08-12 |
human |
| James C Thompson, Michele Clarke, Tennille Stewart, Aina Puc. Configural processing of biological motion in human superior temporal sulcus. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 25. issue 39. 2006-02-21. PMID:16192397. |
here, we used functional magnetic resonance imaging to test the hypothesis that the superior temporal sulcus (sts) uses form cues to aid biological movement tracking. |
2006-02-21 |
2023-08-12 |
human |
| Céline Cappe, Pascal Baron. Heteromodal connections supporting multisensory integration at low levels of cortical processing in the monkey. The European journal of neuroscience. vol 22. issue 11. 2006-02-07. PMID:16324124. |
finally, a visuo-auditory projection arises from an area anterior to the superior temporal sulcus (sts) toward the auditory core. |
2006-02-07 |
2023-08-12 |
monkey |
| J E Aspell, T Tanskanen, A C Hurlber. Neuromagnetic correlates of visual motion coherence. The European journal of neuroscience. vol 22. issue 11. 2006-02-07. PMID:16324128. |
we show that: (i) visual-motion-evoked magnetic fields, measured with a whole-scalp neuromagnetometer, reveal two transient events, within which we identify two significant peaks--the 'on-m220' peak approximately 220 ms after the onset of incoherent motion and the 'tr-m230' peak, approximately 230 ms after the transition from incoherent to coherent motion; (ii) in lateral occipital channels, the tr-m230 peak amplitude varies with the percentage of motion coherence; (iii) two main sources are active in response to the transition from incoherent to coherent motion, the human medial temporal area complex/v3 accessory area (hmt+/v3a) and the superior temporal sulcus (sts), and (iv) these distinct areas show a similar, significant dependence of response strength and latency on motion coherence. |
2006-02-07 |
2023-08-12 |
human |