Development and maintenance of ear innervation and function: lessons from mutations in mouse and man.
作者信息
Fritzsch B, Beisel K
机构信息
Department of Biomedical Sciences, Creigton University, Omaha, NE 68178, USA.
出版信息
Am J Hum Genet. 1998 Nov;63(5):1263-70. doi: 10.1086/302126.
Abstract
摘要
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本文引用的文献
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Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.三种长QT综合征基因的基因组结构：KVLQT1、HERG和KCNE1。
Genomics. 1998 Jul 1;51(1):86-97. doi: 10.1006/geno.1998.5361.
3
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.非传统肌球蛋白MYO15突变与人类非综合征性耳聋DFNB3的关联。
Science. 1998 May 29;280(5368):1447-51. doi: 10.1126/science.280.5368.1447.
4
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.人类α-肌动蛋白基因的突变会导致常染色体显性非综合征性听力障碍。
Nat Genet. 1998 May;19(1):60-2. doi: 10.1038/ng0598-60.
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New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.导致长QT综合征的KVLQT1钾通道新突变。
Circulation. 1998 Apr 7;97(13):1264-9. doi: 10.1161/01.cir.97.13.1264.
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Development of the mouse inner ear and origin of its sensory organs.小鼠内耳的发育及其感觉器官的起源。
J Neurosci. 1998 May 1;18(9):3327-35. doi: 10.1523/JNEUROSCI.18-09-03327.1998.
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neurogenin1 is essential for the determination of neuronal precursors for proximal cranial sensory ganglia.神经生成素1对于确定近端颅感觉神经节的神经元前体至关重要。
Neuron. 1998 Mar;20(3):469-82. doi: 10.1016/s0896-6273(00)80988-5.
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The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.长QT综合征的分子遗传学：导致昏厥和猝死的基因
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Transplacental uptake of glucose is decreased in embryonic lethal connexin26-deficient mice.在胚胎致死性连接蛋白26缺陷型小鼠中，葡萄糖的经胎盘摄取减少。
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The development of the vertebrate inner ear.脊椎动物内耳的发育。
Mech Dev. 1998 Feb;71(1-2):5-21. doi: 10.1016/s0925-4773(97)00155-x.
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