Jove
Visualize
联系我们

相关概念视频

Pedigree Analysis01:35

Pedigree Analysis

84.5K
Overview
84.5K
Learning Disabilities01:25

Learning Disabilities

213
Learning disabilities are cognitive disorders caused by neurological impairments that affect cognitive functions like language and reading, without indicating overall intellectual or developmental challenges. These disabilities differ from global intellectual or developmental disabilities as they are limited to distinct cognitive functions. Common learning disabilities include dysgraphia, dyslexia, and dyscalculia, each of which impacts unique aspects of learning.
Dyslexia
Dyslexia is a...
213
Intellectual Disability01:29

Intellectual Disability

117
Intellectual disability (ID) is a neurodevelopmental condition characterized by deficits in intellectual and adaptive functioning that manifest during the developmental period. This condition encompasses challenges in reasoning, memory, problem-solving, and learning, accompanied by impairments in everyday life skills, such as communication, self-care, and social interactions. Intellectual disability affects approximately 1% of the population in the United States, impacting an estimated 5...
117
Pleiotropy01:33

Pleiotropy

40.6K
Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
40.6K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Navigating a research career with a disability.

Development (Cambridge, England)·2023
Same journal

Retinoic acid and FGF signaling interact to control elongation and lineage specification in a mouse gastruloid model.

Development (Cambridge, England)·2026
Same journal

Expanding the C. elegans toolkit with gonad explants.

Development (Cambridge, England)·2026
Same journal

Nuclear Factor Y controls nutrient-adaptive epithelial growth by regulating mTOR in the Drosophila midgut.

Development (Cambridge, England)·2026
Same journal

Primordial germ cells differentially contribute to the germline in zebrafish.

Development (Cambridge, England)·2026
Same journal

Dissecting planar and vertical organiser signals in early chick neural development.

Development (Cambridge, England)·2026
Same journal

Real-time transcriptomic profiling of hPSC-derived cartilage during development identifies a key role for the extracellular matrix in homeostasis and protection.

Development (Cambridge, England)·2026
查看所有相关文章
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关实验视频

Updated: Jul 18, 2025

In Vivo Modeling of the Morbid Human Genome using Danio rerio
12:31

In Vivo Modeling of the Morbid Human Genome using Danio rerio

Published on: August 24, 2013

20.7K

残疾和发育生物学

Jack Darius Morgan1

  • 1The Green Laboratory, Centre for Craniofacial & Regenerative Biology, King's College London, London, SE1 9RT, UK.

Development (Cambridge, England)
|August 21, 2023
PubMed
概括
此摘要是机器生成的。

残疾科学家面临着重大的职业障碍,影响了他们在科学中的代表性. 本次审查强调了未得到满足的需求和可采取的措施,以提高对发展生物学中残疾研究人员的包容性.

科学领域:

  • 发育生物学是发展生物学.
  • 学术科学科学学术科学
  • 关于残疾人的研究.

更多相关视频

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
00:06

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Published on: August 20, 2019

13.7K
Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders
06:30

Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders

Published on: June 13, 2015

18.8K

相关实验视频

Last Updated: Jul 18, 2025

In Vivo Modeling of the Morbid Human Genome using Danio rerio
12:31

In Vivo Modeling of the Morbid Human Genome using Danio rerio

Published on: August 24, 2013

20.7K
In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
00:06

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

Published on: August 20, 2019

13.7K
Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders
06:30

Quantitative Analysis of Climbing Defects in a Drosophila Model of Neurodegenerative Disorders

Published on: June 13, 2015

18.8K

背景情况:

  • 由于许多障碍,残疾科学家在科学中代表性不足.
  • 残疾人包容性倡议正在增长,但发育生物学方面的具体数据很少.
  • 年轻胚胎学家网络在其2022年会议上优先考虑了残疾人包容性.

结论:

  • 解决未满足的需求对于增强残疾科学家的经验至关重要.
  • 英国发育生物学协会的资助是积极的一步.
  • 持续关注残疾人包容性对于一个更公平的科学界至关重要.