Neural mechanisms of active vision in the fovea
中央凹主动视觉的神经机制
基本信息
- 批准号:10641157
- 负责人:
- 金额:$ 24.9万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-08-01 至 2025-07-31
- 项目状态:未结题
- 来源:
- 关键词:AddressAge related macular degenerationAmericanBehaviorBehavioralBlindnessBrainCallithrixCodeCognitiveComputer ModelsCustomDataData SetDevelopmentDevelopment PlansDiseaseEnsureEsthesiaEyeEye MovementsFoundationsFrequenciesFundingGoalsGrantHumanImageLaboratoriesMachine LearningMeasurementMeasuresMentorsModelingModernizationMonkeysMotionNeuronsOutcomePeripheralPhasePhysiologyPopulationPositioning AttributePrimatesProcessRecoveryResearchResolutionRetinaRetinal DiseasesRoleSaccadesSamplingSeriesSignal TransductionStatistical ModelsStreamSystemTechniquesTestingTrainingUniversitiesV1 neuronV4 neuronVisionVisualVisual AcuityVisual CortexVisual FieldsVisual PathwaysVisual attentionWorkactive visionarea striataawakebasecareercareer developmentcentral visual fieldcomputerized toolsdata-driven modeldesignextrastriateextrastriate visual cortexflexibilityfovea centralisinterestlensneural modelneuromechanismneurophysiologynew technologynovelprofessorreceptive fieldrelating to nervous systemrepairedresponseretinal imagingsample fixationsensorskillsspatial visionspatiotemporalstatisticstoolvisual informationvisual neurosciencevisual processvisual processingvisual tracking
项目摘要
Neural mechanisms of active vision in the fovea
In many ways human vision is like a camera, with a lens that forms an image on a spatially
arranged sensor (the retina). However, it is unlike a camera because the sensor has uneven
sampling and is constantly moving with the eyes. Recent behavioral and theoretical work suggest
these eye movements serve a faciliatory role in high acuity vision – where the eye movements
are part of the computations and enhance spatial resolution. However, the neurophysiological
mechanisms to support this facilitation remain unknown. More broadly, little is known about the
neural mechanisms that integrate across the retinal motion generated by eye movements,
especially in the central visual field (the fovea). This is particularly important because over 8
million Americans suffer from central vision loss due to retinal disorders. Even if the retinal signals
could be repaired, it is imperative to understand how the brain reads out foveal signals to ensure
recovery of high-acuity visual processing, and fixational eye movements are a part of that process.
The proposed career development plan aims to address these questions by measuring visual
processing in the foveal representation of primary visual cortex (V1) during natural visual
behavior. This proposal uses custom high-resolution eye-tracking, a novel visual foraging
paradigm, largescale neurophysiology, and state-of-the-art machine learning to make these
measurements possible. The proposed research will not only generate fundamental
understanding of how eye-movements facilitate visual processing, but also will integrate the
experimental and theoretical tools required to support neurophysiological studies of active visual
processing without a loss of rigor or detail. The candidate has extensive expertise in awake-
behaving neurophysiology and computational modeling and the training plan is designed to
support his further training in statistical modeling, high-resolution eye-tracking, and modern
machine-learning techniques for analyzing neural population data. The primary mentor, Dr. Daniel
Butts, is a world expert in statistical models of neural activity during active vision; Co-mentor, Dr.
Michele Rucci, is a world leader in high-resolution eye tracking and theoretical approaches to
active vision; and Co-mentor, Dr. Jude Mitchell, is a pioneer in establishing the marmoset model
of visual neuroscience and an expert in neurophysiology of visual attention. Together, they will
provide the guidance to establish the candidate’s transition to a successful independent research
career.
中心凹主动视觉的神经机制
在许多方面,人类视觉就像一台相机,它有一个透镜,在空间上形成图像。
视网膜(Retina)然而,它与相机不同,因为传感器具有不均匀的
采样并随着眼睛不断移动。最近的行为和理论研究表明
这些眼球运动在高敏锐度视觉中起促进作用,
是计算的一部分并增强空间分辨率。然而,神经生理学
支持这种便利的机制仍然未知。更广泛地说,人们对
整合了眼球运动产生的视网膜运动的神经机制,
尤其是在中央视野(中央凹)中。这一点尤为重要,因为超过8
数百万美国人因视网膜疾病而遭受中心视力丧失。即使视网膜发出信号
可以修复,必须了解大脑如何读取中央凹信号,以确保
高敏锐度视觉处理的恢复和注视性眼球运动是该过程的一部分。
拟议的职业发展计划旨在解决这些问题,
在自然视觉期间初级视皮层(V1)的中央凹代表中的处理
行为该提案使用定制的高分辨率眼动跟踪,一种新颖的视觉觅食
范式,大规模神经生理学和最先进的机器学习,使这些
测量可能。这项研究不仅将产生基本的
了解眼球运动如何促进视觉处理,但也将整合
支持主动视觉神经生理学研究的实验和理论工具
不损失严谨性或细节的处理。候选人在清醒方面有丰富的经验-
行为神经生理学和计算建模,训练计划旨在
支持他在统计建模,高分辨率眼动跟踪和现代
用于分析神经群体数据的机器学习技术。主要导师,丹尼尔博士
巴茨博士是主动视觉期间神经活动统计模型的世界专家;
Michele Rucci是高分辨率眼动追踪和理论方法的世界领导者,
主动视觉;共同导师Jude Mitchell博士是建立绒猴模型的先驱
他是视觉神经科学和视觉注意力神经生理学方面的专家。他们将共同
提供指导,以建立候选人的过渡到一个成功的独立研究
事业
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Jacob L Yates其他文献
Jacob L Yates的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Jacob L Yates', 18)}}的其他基金
相似海外基金
I(eye)-SCREEN: A real-world AI-based infrastructure for screening and prediction of progression in age-related macular degeneration (AMD) providing accessible shared care
I(eye)-SCREEN:基于人工智能的现实基础设施,用于筛查和预测年龄相关性黄斑变性 (AMD) 的进展,提供可及的共享护理
- 批准号:
10102692 - 财政年份:2024
- 资助金额:
$ 24.9万 - 项目类别:
EU-Funded
Inhibiting Neovascularization and Subretinal Fibrosis in Neovascular Age-Related Macular Degeneration
抑制新生血管性年龄相关性黄斑变性的新生血管形成和视网膜下纤维化
- 批准号:
10639785 - 财政年份:2023
- 资助金额:
$ 24.9万 - 项目类别:
Inhibition of melanogenesis in retinal pigment epithelium, a contributing factor in age-related macular degeneration
抑制视网膜色素上皮中的黑色素生成,这是年龄相关性黄斑变性的一个促成因素
- 批准号:
23K09052 - 财政年份:2023
- 资助金额:
$ 24.9万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Deciphering the role of osteopontin in the aging eye and age-related macular degeneration
破译骨桥蛋白在眼睛老化和年龄相关性黄斑变性中的作用
- 批准号:
10679287 - 财政年份:2023
- 资助金额:
$ 24.9万 - 项目类别:
Evaluation of New Anti-inflammatory Treatments for Age-Related Macular Degeneration
年龄相关性黄斑变性的新型抗炎治疗方法的评价
- 批准号:
10642988 - 财政年份:2023
- 资助金额:
$ 24.9万 - 项目类别:
Progression of Early Atrophic Lesions in Age-related Macular degeneration
年龄相关性黄斑变性早期萎缩性病变的进展
- 批准号:
10635325 - 财政年份:2023
- 资助金额:
$ 24.9万 - 项目类别:
Cellular and molecular mechanisms of AIM2 and NLRP3 inflammasome activation in age-related macular degeneration
年龄相关性黄斑变性中 AIM2 和 NLRP3 炎症小体激活的细胞和分子机制
- 批准号:
10584110 - 财政年份:2023
- 资助金额:
$ 24.9万 - 项目类别:
Elucidation of roles of mast cells and macrophages in the pathogenesis of age-related macular degeneration
阐明肥大细胞和巨噬细胞在年龄相关性黄斑变性发病机制中的作用
- 批准号:
22H03243 - 财政年份:2022
- 资助金额:
$ 24.9万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
AMD Mitochondria Modulate Expression of microRNA 135b-5p and 148a-3p in RPE Cybrids: Implications for Age-related Macular Degeneration
AMD 线粒体调节 RPE Cybrids 中 microRNA 135b-5p 和 148a-3p 的表达:对年龄相关性黄斑变性的影响
- 批准号:
10433610 - 财政年份:2022
- 资助金额:
$ 24.9万 - 项目类别:
Targeting the inflammatory response in age-related macular degeneration
针对年龄相关性黄斑变性的炎症反应
- 批准号:
10504138 - 财政年份:2022
- 资助金额:
$ 24.9万 - 项目类别:














{{item.name}}会员




