New aspects of an old theme: the genetic basis of human color vision.
作者信息
Wissinger B, Sharpe L T
机构信息
Molekulargenetisches Labor, Universitáts-Augenklinik, Tübingen, Germany.
出版信息
Am J Hum Genet. 1998 Nov;63(5):1257-62. doi: 10.1086/302127.
Abstract
摘要
相似文献
1
New aspects of an old theme: the genetic basis of human color vision.一个古老主题的新视角：人类色觉的遗传基础。
Am J Hum Genet. 1998 Nov;63(5):1257-62. doi: 10.1086/302127.
2
The genetics of normal and defective color vision.正常与缺陷色觉的遗传学
Vision Res. 2011 Apr 13;51(7):633-51. doi: 10.1016/j.visres.2010.12.002. Epub 2010 Dec 15.
3
Color vision: mice see hue too.色觉：小鼠也能辨别颜色。
Curr Biol. 2007 Jun 19;17(12):R457-60. doi: 10.1016/j.cub.2007.04.017.
4
Genetic basis of color vision.色觉的遗传基础。
Int Ophthalmol Clin. 1993 Spring;33(2):141-52. doi: 10.1097/00004397-199303320-00014.
5
The spectral sensitivities of the middle- and long-wavelength-sensitive cones derived from measurements in observers of known genotype.从中等波长敏感视锥细胞和长波长敏感视锥细胞的光谱敏感性是通过对已知基因型观察者的测量得出的。
Vision Res. 2000;40(13):1711-37. doi: 10.1016/s0042-6989(00)00021-3.
6
The molecular basis of variation in human color vision.人类色觉变异的分子基础。
Clin Genet. 2005 May;67(5):369-77. doi: 10.1111/j.1399-0004.2004.00343.x.
7
Comment on "Emergence of novel color vision in mice engineered to express a human cone photopigment".对“在经过基因工程改造以表达人类视锥色素的小鼠中出现新型色觉”的评论
Science. 2007 Oct 12;318(5848):196; author reply 196. doi: 10.1126/science.1146084.
8
Molecular genetics of human color vision.人类色觉的分子遗传学
Behav Genet. 1996 May;26(3):195-207. doi: 10.1007/BF02359380.
9
The evolution and physiology of human color vision: insights from molecular genetic studies of visual pigments.人类色觉的进化与生理学：来自视色素分子遗传学研究的见解
Neuron. 1999 Oct;24(2):299-312. doi: 10.1016/s0896-6273(00)80845-4.
10
Alouatta trichromatic color vision: cone spectra and physiological responses studied with microspectrophotometry and single unit retinal electrophysiology.三色绒毛蛛猴的色觉：用显微分光光度法和视网膜单单位电生理学研究视锥细胞光谱和生理反应。
PLoS One. 2014 Nov 18;9(11):e113321. doi: 10.1371/journal.pone.0113321. eCollection 2014.
引用本文的文献
1
Colour Vision Deficits in Children with Amblyopia: Impact of Angular Size of Stimuli on Detection.弱视儿童的色觉缺陷：刺激物视角大小对检测的影响
Vision (Basel). 2025 Jan 10;9(1):3. doi: 10.3390/vision9010003.
2
Diagnosis of colour vision deficits using eye movements.使用眼球运动诊断色觉缺陷。
Sci Rep. 2022 May 11;12(1):7734. doi: 10.1038/s41598-022-11152-5.
3
Colour vision deficiency among students in Lagos State, Nigeria.尼日利亚拉各斯州学生中的色觉缺陷
Afr Health Sci. 2019 Jun;19(2):2230-2236. doi: 10.4314/ahs.v19i2.48.
4
The science behind the quest to determine the age of bruises-a review of the English language literature.确定瘀伤年龄探索背后的科学——对英语文献的综述
Forensic Sci Med Pathol. 2007 Dec;3(4):241-51. doi: 10.1007/s12024-007-9019-3.
5
Visual and spectrophotometric observations related to histology in a small sample of bruises from cadavers.对一小份尸体瘀伤样本进行的与组织学相关的视觉和分光光度观察。
Forensic Sci Med Pathol. 2011 Sep;7(3):253-6. doi: 10.1007/s12024-010-9221-6. Epub 2011 Jan 22.
6
Homozygosity mapping of the Achromatopsia locus in the Pingelapese.Pingelapese人群中全色盲基因座的纯合性定位
Am J Hum Genet. 1999 Jun;64(6):1679-85. doi: 10.1086/302423.
本文引用的文献
1
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11.人类视杆单色性：2q11染色体上一个视锥光感受器表达候选基因的连锁分析与定位
Genomics. 1998 Aug 1;51(3):325-31. doi: 10.1006/geno.1998.5390.
2
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channel.全色盲是由编码视锥光感受器cGMP门控阳离子通道α亚基的基因突变引起的。
Nat Genet. 1998 Jul;19(3):257-9. doi: 10.1038/935.
3
Visual pigment gene structure and expression in human retinae.人类视网膜中视觉色素基因的结构与表达。
Hum Mol Genet. 1997 Jul;6(7):981-90. doi: 10.1093/hmg/6.7.981.
4
Homozygosity mapping of achromatopsia to chromosome 2 using DNA pooling.利用DNA池将全色盲基因定位到2号染色体上。
Hum Mol Genet. 1997 May;6(5):689-94. doi: 10.1093/hmg/6.5.689.
5
Individual variation in size of the human red and green visual pigment gene array.人类红色和绿色视觉色素基因阵列大小的个体差异。
Invest Ophthalmol Vis Sci. 1997 Apr;38(5):1040-3.
6
Mutations in a cyclic nucleotide-gated channel lead to abnormal thermosensation and chemosensation in C. elegans.一种环核苷酸门控通道的突变导致线虫的异常温度感觉和化学感觉。
Neuron. 1996 Oct;17(4):707-18. doi: 10.1016/s0896-6273(00)80202-0.
7
General anosmia caused by a targeted disruption of the mouse olfactory cyclic nucleotide-gated cation channel.由小鼠嗅觉环核苷酸门控阳离子通道的靶向破坏引起的一般性嗅觉丧失。
Neuron. 1996 Oct;17(4):681-93. doi: 10.1016/s0896-6273(00)80200-7.
8
Structure and function of cyclic nucleotide-gated channels.环核苷酸门控通道的结构与功能。
Annu Rev Neurosci. 1996;19:235-63. doi: 10.1146/annurev.ne.19.030196.001315.
9
Molecular genetics of human color vision.人类色觉的分子遗传学
Behav Genet. 1996 May;26(3):195-207. doi: 10.1007/BF02359380.
10
Primate photopigments and primate color vision.灵长类动物的光色素与灵长类动物的色觉。
Proc Natl Acad Sci U S A. 1996 Jan 23;93(2):577-81. doi: 10.1073/pnas.93.2.577.
Zotero 插件