Cortical basis of binocular depth perception

双目深度知觉的皮质基础

基本信息

  • 批准号:
    10681944
  • 负责人:
  • 金额:
    $ 39.89万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2023
  • 资助国家:
    美国
  • 起止时间:
    2023-07-01 至 2028-06-30
  • 项目状态:
    未结题

项目摘要

Abstract The functional properties of the visual system are most sensitive to disruptions of normal vision during developmental ‘critical periods’. Interestingly, the critical periods for several functional properties, such as ocular dominance and acuity, overlap during development. Abnormal vision during these overlapping critical periods, because of cataracts or misalignment of the two eyes for example, is the cause of amblyopia. Amblyopia is a prevalent visual disorder in children and can present with any of several visual problems including lower visual acuity and impaired depth perception. Yet, how depth perception is affected by abnormal vision has remained elusive. In the proposed research, we investigate the circuit basis for the development and plasticity of depth perception in the mouse. The development of stereoscopic vision is much slower than other characteristics of vision and relies on complex properties of binocular disparity. Disparity between the eyes is what produces the perception of depth. We will characterize multiple dimensions of its development and plasticity by taking advantage of a natural depth discrimination task that depends on binocular vision. Over this same period, we will measure with two-photon microscopy how complex disparity properties are refined in the visual cortex and area LM (a secondary binocular visual area), as well as how and when they are sensitive to abnormal vision. Understanding the properties of binocular depth perception and the development of those properties will provide a foundation for developing therapeutic approaches to treat developmental visual disorders such as amblyopia that cause stereovision deficits.
摘要 视觉系统的功能特性对正常视力的破坏最敏感 发展的“关键时期”。有趣的是,几种功能特性的临界期,如眼睛 主导性和敏锐性,在发展过程中重叠。在这些重叠的关键时期,视力异常, 例如,由于白内障或两只眼睛的错位,是导致弱视的原因。弱视是一种 儿童普遍存在的视力障碍,可出现包括视力低下在内的任何一种视力问题 视力和深度知觉受损。然而,视觉异常是如何影响深度知觉的,这一问题一直存在。 难以捉摸。在提出的研究中,我们研究了深度发展和可塑性的电路基础。 老鼠的感知能力。立体视觉的发展比其他特征要慢得多 视觉和依赖于双眼视差的复杂属性。眼睛之间的视差是产生 对深度的感知。我们将通过以下方式来表征其发展和可塑性的多个维度 依靠双目视觉的自然深度辨别任务的优势。在同一时期,我们 将用双光子显微镜测量复杂的视差特性是如何在视觉皮质和 Lm区(次级双目视觉区域),以及他们如何以及何时对异常视力敏感。 了解双目深度知觉的特性以及这些特性的发展将提供 开发治疗弱视等发育性视觉障碍的治疗方法的基础 这会导致立体视觉缺陷。

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 }}

Aaron W McGee其他文献

Aaron W McGee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('Aaron W McGee', 18)}}的其他基金

Dissecting the role of aggrecan and perineuronal nets in visual plasticity
剖析聚集蛋白聚糖和神经周围网络在视觉可塑性中的作用
  • 批准号:
    10753758
  • 财政年份:
    2023
  • 资助金额:
    $ 39.89万
  • 项目类别:
Deciphering Inhibition of Visual Plasticity by NgR1
解读 NgR1 对视觉可塑性的抑制
  • 批准号:
    8463201
  • 财政年份:
    2012
  • 资助金额:
    $ 39.89万
  • 项目类别:
Deciphering Inhibition of Visual Plasticity by NgR1
解读 NgR1 对视觉可塑性的抑制
  • 批准号:
    8841366
  • 财政年份:
    2012
  • 资助金额:
    $ 39.89万
  • 项目类别:
Deciphering Inhibition of Visual Plasticity by NgR1
解读 NgR1 对视觉可塑性的抑制
  • 批准号:
    9982965
  • 财政年份:
    2012
  • 资助金额:
    $ 39.89万
  • 项目类别:
Deciphering Inhibition of Visual Plasticity by NgR1
解读 NgR1 对视觉可塑性的抑制
  • 批准号:
    8295849
  • 财政年份:
    2012
  • 资助金额:
    $ 39.89万
  • 项目类别:
Deciphering Inhibition of Visual Plasticity by NgR1
解读 NgR1 对视觉可塑性的抑制
  • 批准号:
    9060941
  • 财政年份:
    2012
  • 资助金额:
    $ 39.89万
  • 项目类别:
Deciphering Inhibition of Visual Plasticity by NgR1
解读 NgR1 对视觉可塑性的抑制
  • 批准号:
    9754152
  • 财政年份:
    2012
  • 资助金额:
    $ 39.89万
  • 项目类别:
Deciphering Inhibition of Visual Plasticity by NgR1
解读 NgR1 对视觉可塑性的抑制
  • 批准号:
    8658088
  • 财政年份:
    2012
  • 资助金额:
    $ 39.89万
  • 项目类别:
Regulation of Anatomical Plasticity and Perceptual Learning by NgR1
NgR1 对解剖可塑性和知觉学习的调节
  • 批准号:
    8320118
  • 财政年份:
    2011
  • 资助金额:
    $ 39.89万
  • 项目类别:
Regulation of Anatomical Plasticity and Perceptual Learning by NgR1
NgR1 对解剖可塑性和知觉学习的调节
  • 批准号:
    8227408
  • 财政年份:
    2011
  • 资助金额:
    $ 39.89万
  • 项目类别:

相似海外基金

Hormone therapy, age of menopause, previous parity, and APOE genotype affect cognition in aging humans.
激素治疗、绝经年龄、既往产次和 APOE 基因型会影响老年人的认知。
  • 批准号:
    495182
  • 财政年份:
    2023
  • 资助金额:
    $ 39.89万
  • 项目类别:
Investigating how alternative splicing processes affect cartilage biology from development to old age
研究选择性剪接过程如何影响从发育到老年的软骨生物学
  • 批准号:
    2601817
  • 财政年份:
    2021
  • 资助金额:
    $ 39.89万
  • 项目类别:
    Studentship
RAPID: Coronavirus Risk Communication: How Age and Communication Format Affect Risk Perception and Behaviors
RAPID:冠状病毒风险沟通:年龄和沟通方式如何影响风险认知和行为
  • 批准号:
    2029039
  • 财政年份:
    2020
  • 资助金额:
    $ 39.89万
  • 项目类别:
    Standard Grant
Neighborhood and Parent Variables Affect Low-Income Preschool Age Child Physical Activity
社区和家长变量影响低收入学龄前儿童的身体活动
  • 批准号:
    9888417
  • 财政年份:
    2019
  • 资助金额:
    $ 39.89万
  • 项目类别:
The affect of Age related hearing loss for cognitive function
年龄相关性听力损失对认知功能的影响
  • 批准号:
    17K11318
  • 财政年份:
    2017
  • 资助金额:
    $ 39.89万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Affect regulation and Beta Amyloid: Maturational Factors in Aging and Age-Related Pathology
影响调节和 β 淀粉样蛋白:衰老和年龄相关病理学中的成熟因素
  • 批准号:
    9320090
  • 财政年份:
    2017
  • 资助金额:
    $ 39.89万
  • 项目类别:
Affect regulation and Beta Amyloid: Maturational Factors in Aging and Age-Related Pathology
影响调节和 β 淀粉样蛋白:衰老和年龄相关病理学中的成熟因素
  • 批准号:
    10166936
  • 财政年份:
    2017
  • 资助金额:
    $ 39.89万
  • 项目类别:
Affect regulation and Beta Amyloid: Maturational Factors in Aging and Age-Related Pathology
影响调节和 β 淀粉样蛋白:衰老和年龄相关病理学中的成熟因素
  • 批准号:
    9761593
  • 财政年份:
    2017
  • 资助金额:
    $ 39.89万
  • 项目类别:
How age dependent molecular changes in T follicular helper cells affect their function
滤泡辅助 T 细胞的年龄依赖性分子变化如何影响其功能
  • 批准号:
    BB/M50306X/1
  • 财政年份:
    2014
  • 资助金额:
    $ 39.89万
  • 项目类别:
    Training Grant
Inflamm-aging: What do we know about the effect of inflammation on HIV treatment and disease as we age, and how does this affect our search for a Cure?
炎症衰老:随着年龄的增长,我们对炎症对艾滋病毒治疗和疾病的影响了解多少?这对我们寻找治愈方法有何影响?
  • 批准号:
    288272
  • 财政年份:
    2013
  • 资助金额:
    $ 39.89万
  • 项目类别:
    Miscellaneous Programs
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了