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Patterning of the mammalian cochlea.哺乳动物耳蜗的模式形成
Proc Natl Acad Sci U S A. 2000 Oct 24;97(22):11707-13. doi: 10.1073/pnas.97.22.11707.
2
Otx2 is a target of N-myc and acts as a suppressor of sensory development in the mammalian cochlea.Otx2是N - myc的一个靶点,并在哺乳动物耳蜗中作为感觉发育的抑制因子发挥作用。
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4
Jxc1/Sobp, encoding a nuclear zinc finger protein, is critical for cochlear growth, cell fate, and patterning of the organ of corti.编码一种核锌指蛋白的Jxc1/Sobp对耳蜗生长、细胞命运及柯蒂氏器的模式形成至关重要。
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Petrosal morphology and cochlear function in Mesozoic stem therians.中生代哺乳类干群的岩部形态与耳蜗功能。
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本文引用的文献

1
THE ABNORMALITIES OF THE INNER EAR IN KREISLER MICE.克赖斯勒小鼠内耳的异常情况。
J Embryol Exp Morphol. 1964 Sep;12:475-90.
2
Neurogenin 1 null mutant ears develop fewer, morphologically normal hair cells in smaller sensory epithelia devoid of innervation.神经生成素1基因敲除突变体的耳朵在较小的、无神经支配的感觉上皮中发育出数量更少、形态正常的毛细胞。
J Assoc Res Otolaryngol. 2000 Sep;1(2):129-43. doi: 10.1007/s101620010017.
3
Effects of neurotrophin and neurotrophin receptor disruption on the afferent inner ear innervation.神经营养因子和神经营养因子受体破坏对传入性内耳神经支配的影响。
Semin Cell Dev Biol. 1997;8:277-84.
4
FGF/FGFR-2(IIIb) signaling is essential for inner ear morphogenesis.成纤维细胞生长因子/成纤维细胞生长因子受体-2(IIIb型)信号传导对内耳形态发生至关重要。
J Neurosci. 2000 Aug 15;20(16):6125-34. doi: 10.1523/JNEUROSCI.20-16-06125.2000.
5
Sensory organ generation in the chicken inner ear: contributions of bone morphogenetic protein 4, serrate1, and lunatic fringe.鸡内耳感觉器官的生成:骨形态发生蛋白4、锯齿状蛋白1和类月桂酸边缘蛋白的作用
J Comp Neurol. 2000 Aug 28;424(3):509-20. doi: 10.1002/1096-9861(20000828)424:3<509::aid-cne8>3.0.co;2-q.
6
EphB2 guides axons at the midline and is necessary for normal vestibular function.EphB2引导轴突到达中线,对正常前庭功能至关重要。
Neuron. 2000 May;26(2):417-30. doi: 10.1016/s0896-6273(00)81174-5.
7
Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia.Eya1基因缺陷型小鼠无耳且无肾,并显示出器官原基的异常凋亡。
Nat Genet. 1999 Sep;23(1):113-7. doi: 10.1038/12722.
8
Altered cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness.DFN3型非综合征性耳聋小鼠模型中耳蜗纤维细胞的改变
Science. 1999 Aug 27;285(5432):1408-11. doi: 10.1126/science.285.5432.1408.
9
Dlx5 regulates regional development of the branchial arches and sensory capsules.Dlx5基因调控鳃弓和感觉囊的区域发育。
Development. 1999 Sep;126(17):3831-46. doi: 10.1242/dev.126.17.3831.
10
Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5.缺乏远端缺失相关基因Dlx5的小鼠的颅面、前庭和骨骼缺陷。
Development. 1999 Sep;126(17):3795-809. doi: 10.1242/dev.126.17.3795.

哺乳动物耳蜗的模式形成

Patterning of the mammalian cochlea.

作者信息

Cantos R, Cole L K, Acampora D, Simeone A, Wu D K

机构信息

National Institute on Deafness and Other Communication Disorders, Rockville, MD 20850, USA.

出版信息

Proc Natl Acad Sci U S A. 2000 Oct 24;97(22):11707-13. doi: 10.1073/pnas.97.22.11707.

DOI:10.1073/pnas.97.22.11707
PMID:11050199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC34339/
Abstract

The mammalian cochlea is sophisticated in its function and highly organized in its structure. Although the anatomy of this sense organ has been well documented, the molecular mechanisms underlying its development have remained elusive. Information generated from mutant and knockout mice in recent years has increased our understanding of cochlear development and physiology. This article discusses factors important for the development of the inner ear and summarizes cochlear phenotypes of mutant and knockout mice, particularly Otx and Otx2. We also present data on gross development of the mouse cochlea.

摘要

哺乳动物的耳蜗功能复杂,结构高度有序。尽管这个感觉器官的解剖结构已有详尽记录,但其发育的分子机制仍不清楚。近年来从突变体和基因敲除小鼠获得的信息增进了我们对耳蜗发育和生理学的理解。本文讨论了内耳发育的重要因素,并总结了突变体和基因敲除小鼠的耳蜗表型,特别是Otx和Otx2。我们还展示了小鼠耳蜗总体发育的数据。