Jove
Visualize
联系我们
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

相关概念视频

Sex-linked Disorders01:43

Sex-linked Disorders

102.9K
Like autosomes, sex chromosomes contain a variety of genes necessary for normal body function. When a mutation in one of these genes results in biological deficits, the disorder is considered sex-linked.
102.9K
X-linked Traits01:19

X-linked Traits

55.2K
In most mammalian species, females have two X sex chromosomes and males have an X and Y. As a result, mutations on the X chromosome in females may be masked by the presence of a normal allele on the second X. In contrast, a mutation on the X chromosome in males more often causes observable biological defects, as there is no normal X to compensate. Trait variations arising from mutations on the X chromosome are called “X-linked”.
55.2K
Pedigree Analysis01:35

Pedigree Analysis

85.1K
Overview
85.1K
Genetic Lingo01:11

Genetic Lingo

104.5K
Overview
104.5K
X and Y Chromosomes02:32

X and Y Chromosomes

26.7K
Among mammals, the gender of an organism is determined by the sex chromosomes. Humans have two sex chromosomes, X and Y. Every human diploid cell has 22 pairs of autosomes and one pair of sex chromosomes. A human female has two X chromosomes, while a male has one X chromosome and one Y chromosome.
The germline cells such as egg and sperm cells carry only half the number of chromosomes, i.e., 22 autosomes and one sex chromosome. All eggs have an X chromosome, while sperm cells can carry an X or...
26.7K
The Y Chromosome Determines Maleness02:19

The Y Chromosome Determines Maleness

6.8K
The Y chromosome is a sex chromosome found in several vertebrates and mammals, including humans. In addition to 22 pairs of autosomes, the human males have one X chromosome and one Y chromosome. In these organisms, the presence or absence of the Y chromosome determines the development of male traits.
Evolution
Around 300 million years ago, the two sex chromosomes diverged from two identical autosomal chromosomes. Over time, the Y chromosome has lost most of its genes, shrinking in size....
6.8K

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

Retinal Histology and Anatomical Landmarks.

Advances in experimental medicine and biology·2025
Same author

Fluorescein Angiography.

Advances in experimental medicine and biology·2025
Same author

Optical Coherence Tomography.

Advances in experimental medicine and biology·2025
Same author

Fundus Autofluorescence.

Advances in experimental medicine and biology·2025
Same author

Electrooculography.

Advances in experimental medicine and biology·2025
Same author

Glossary of Relevant Genetic and Molecular/Cell Biology.

Advances in experimental medicine and biology·2025
Same journal

Mammalian Respiratory Chain Complex Assemblies and Their Links to Mitochondria Stress-Induced Human Diseases.

Advances in experimental medicine and biology·2026
Same journal

Enzyme Assemblies in Nucleotide Metabolism: Structure, Regulation, and Disease Implications.

Advances in experimental medicine and biology·2026
Same journal

The Pyruvate Dehydrogenase Complex: A 90-Year-Old Enigma Shaping the Future of Structural Enzymology.

Advances in experimental medicine and biology·2026
Same journal

Regulation of the Anti-termination RNA Transcription Complex by Lon-Mediated Lambda N Degradation.

Advances in experimental medicine and biology·2026
Same journal

PCNA Macromolecular Complexes: PCNA Serves as a Molecular Hub Regulating Multiple Cellular Processes Inside and Outside of the Nucleus.

Advances in experimental medicine and biology·2026
Same journal

Dynamic Assemblies in Genome Maintenance.

Advances in experimental medicine and biology·2026
查看所有相关文章

相关实验视频

Updated: Sep 8, 2025

Author Spotlight: Insights and Innovations in Gene Expression Manipulation Techniques for Choroid Plexus Research
04:43

Author Spotlight: Insights and Innovations in Gene Expression Manipulation Techniques for Choroid Plexus Research

Published on: June 16, 2023

1.1K

与X相关的胆固醇血症

Ashley Zhou1, Stephen H Tsang2, Tarun Sharma3

  • 1Vagelos College of Physicians and Surgeons, New York, NY, USA.

Advances in experimental medicine and biology
|July 30, 2025
PubMed
概括
此摘要是机器生成的。

胆血症 (CHM) 是一种X系眼睛疾病,导致视力丧失. 这种情况涉及视网膜及其支层的逐渐退化.

关键词:
胆固醇血症是一种病.这是一个X-linked.

更多相关视频

Detecting Abnormalities in Choroidal Vasculature in a Mouse Model of Age-related Macular Degeneration by Time-course Indocyanine Green Angiography
10:24

Detecting Abnormalities in Choroidal Vasculature in a Mouse Model of Age-related Macular Degeneration by Time-course Indocyanine Green Angiography

Published on: February 19, 2014

13.8K
A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging
09:37

A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging

Published on: July 14, 2016

8.4K

相关实验视频

Last Updated: Sep 8, 2025

Author Spotlight: Insights and Innovations in Gene Expression Manipulation Techniques for Choroid Plexus Research
04:43

Author Spotlight: Insights and Innovations in Gene Expression Manipulation Techniques for Choroid Plexus Research

Published on: June 16, 2023

1.1K
Detecting Abnormalities in Choroidal Vasculature in a Mouse Model of Age-related Macular Degeneration by Time-course Indocyanine Green Angiography
10:24

Detecting Abnormalities in Choroidal Vasculature in a Mouse Model of Age-related Macular Degeneration by Time-course Indocyanine Green Angiography

Published on: February 19, 2014

13.8K
A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging
09:37

A Phenotyping Regimen for Genetically Modified Mice Used to Study Genes Implicated in Human Diseases of Aging

Published on: July 14, 2016

8.4K

科学领域:

  • 眼科医生 眼科 眼科
  • 遗传学 遗传学 是一个
  • 细胞生物学 细胞生物学

背景情况:

  • 冠状腺症 (CHM) 是最常见的X相关遗传性冠状腺变.
  • 它的特点是皮,视网膜色素上皮质 (RPE) 和视网膜的渐进性退化.
  • 慢性心血管疾病的患病率约为每5万至10万个人的1例.

研究的目的:

  • 为了提供关于胆固醇性病的全面概述.
  • 讨论CHM的遗传基础和临床表现.
  • 要突出当前的研究和潜在的治疗策略为CHM.

主要方法:

  • 现有关于胆固醇性病的研究的文献综述.
  • 分析与CHM相关的遗传数据.
  • 对临床试验数据和研究结果的审查.

主要成果:

  • CHM是由CHM基因的突变引起的,导致蛋白质REP-1的缺乏.
  • 临床特征包括渐进的视力丧失,夜盲和外周视野收缩.
  • 这种退化会影响胆,RPE和神经感应视网膜,最终导致失明.

结论:

  • 胆血症是一种严重的X相关的视网膜变,具有显著的视力损伤.
  • 了解CHM的分子机制对于开发有效的治疗方法至关重要.
  • 目前正在进行的研究表明,基因治疗和其他干预措施有望减缓或阻止疾病的进展.