Embodied views of language support that facial sensorimotor information can modulate language comprehension. The aim of this study is to test whether the syntactic processing of simple sentences, as measured with event-related brain potentials (ERP), could be affected by reader's facial expressions. Participants performed a correctness decision task using sentences that could be either correct (50%) or contain a morphosyntactic disagreement (either in gender or number), while making one of four facial expressions: participants either (a) posed no facial expression ("control" condition) (b) brought their eyebrows together, making the ends of two golf tees touch ("frown" condition), (c) held a pencil with their teeth ("smile" condition), or (d) held the pencil using their lips ("non-smile" condition). In all conditions the customary left anterior negativities did not appear. In contrast, an N400-like component emerged, which was larger for the "frown" condition and reduced in the "smile" and "non-smile" conditions. These results can be interpreted as the consequence of either an unconscious emotion induction or an interplay between the motor and the language systems subsequent to the effort needed to hold the facial expression.
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http://dx.doi.org/10.1016/j.brainres.2020.146745 | DOI Listing |
Craniofacial development gives rise to the complex structures of the face and involves the interplay of diverse cell types. Despite its importance, our understanding of human-specific craniofacial developmental mechanisms and their genetic underpinnings remains limited. Here, we present a comprehensive single-nucleus RNA sequencing (snRNA-seq) atlas of human craniofacial development from craniofacial tissues of 24 embryos that span six key time points during the embryonic period (4-8 post-conception weeks).
View Article and Find Full Text PDFJ Integr Neurosci
January 2025
Department of Psychology, The Affiliated Hospital of Jiangnan University, 214151 Wuxi, Jiangsu, China.
Background: Deficits in emotion recognition have been shown to be closely related to social-cognitive functioning in schizophrenic. This study aimed to investigate the event-related potential (ERP) characteristics of social perception in schizophrenia patients and to explore the neural mechanisms underlying these abnormal cognitive processes related to social perception.
Methods: Participants included 33 schizophrenia patients and 35 healthy controls (HCs).
Int J Mol Sci
January 2025
Department of Developmental and Regenerative Biology, Medical Research Institute, Institute of Science Tokyo, Tokyo 113-8510, Japan.
The eye primordium of vertebrates initially forms exactly at the side of the head. Later, the eyeball architecture is tuned to see ahead with better visual acuity, but its molecular basis is unknown. The position of both eyes in the face alters in patients with holoprosencephaly due to () mutations that disturb the development of the ventral midline of the neural tube.
View Article and Find Full Text PDFNeurol Int
January 2025
Department of Medicine, Faculty of Medicine, Srinakharinwirot University, Nakhon Nayok 26120, Thailand.
Background: Central facial palsy (CFP), resulting from upper motor neuron lesions in the corticofacial pathway, is traditionally characterized by the sparing of the upper facial muscles. However, reports of upper facial weakness in CFP due to acute ischemic stroke have challenged this long-held assumption. This study aimed to determine the prevalence of upper facial weakness in CFP and identify its associated clinical factors.
View Article and Find Full Text PDFHum Mol Genet
January 2025
Department of Facial Plastic and Reconstructive Surgery, ENT Institute, Eye & ENT Hospital, Fudan University, No. 83 Fenyang Road, Xuhui District, Shanghai 200031, China.
Waardenburg syndrome type 2 (WS2) is an autosomal dominant disorder characterized by congenital sensorineural hearing loss, blue iris, and abnormal pigmentation of the hair and skin. WS2 is genetically heterogeneous, often resulting from pathogenic mutations in SOX10 gene. We identified a novel heterozygous frameshift mutation in SOX10 (NM_006941.
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