Profile of Christine Petit.
作者信息
Davis Tinsley H
出版信息
Proc Natl Acad Sci U S A. 2017 Aug 1;114(31):8132-8134. doi: 10.1073/pnas.1711360114. Epub 2017 Jul 24.
Abstract
摘要
相似文献
1
Profile of Christine Petit.克里斯汀·佩蒂简介。
Proc Natl Acad Sci U S A. 2017 Aug 1;114(31):8132-8134. doi: 10.1073/pnas.1711360114. Epub 2017 Jul 24.
2
Christine Petit: interdisciplinary geneticist.克里斯汀·佩蒂：跨学科遗传学家。
Lancet. 2012 Apr 7;379(9823):1291. doi: 10.1016/S0140-6736(12)60545-5.
3
Christine Petit, MD, PhD, head of an Institut Pasteur-Inserm unit, wins Bristol-Myers Squibb Neuroscience Research Award: recognized for discovering the molecular basis of hearing and the genetic causes of deafness.巴斯德研究所与法国国家健康与医学研究院联合研究单位负责人克里斯汀·佩蒂特医学博士、哲学博士荣获百时美施贵宝神经科学研究奖：因其发现听力的分子基础和耳聋的遗传病因而获认可。
Neuroscientist. 2005 Dec;11(6):595-6. doi: 10.1177/107385840501100612.
4
Immediate transition from a petit mal absence into a grand mal seizure. Case report.
Eur Neurol. 1976;14(1):11-6. doi: 10.1159/000114721.
5
[Functional relation between petit mal epilepsy and sleep].[小儿癫痫与睡眠之间的功能关系]
EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb. 1983 Sep;14(3):154-9.
6
[Centrencephalic myoclonic-astatic petit mal. Clinical and electroencephalographic long-term follow-up study in 52 patients (author's transl)].[中央脑性肌阵挛-无动性癫痫小发作。52例患者的临床与脑电图长期随访研究（作者译）]
EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb. 1978 Jun;9(2):86-96.
7
[Intraveneous therapy of petit mal status with diazepame and clonazepame (author's transl)].地西泮和氯硝西泮静脉治疗癫痫小发作持续状态（作者译）
EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb. 1977 Jun;8(2):82-8.
8
An anatomical study of the transversus abdominis plane block: location of the lumbar triangle of Petit and adjacent nerves.腹横肌平面阻滞的解剖学研究： Petit 腰三角及相邻神经的位置
Anesth Analg. 2009 Sep;109(3):981-5. doi: 10.1213/ane.0b013e3181ae0989.
9
A context analysis of psychological states prior to petit mal EEF paroxysms.
J Nerv Ment Dis. 1975 Apr;160(4):282-98. doi: 10.1097/00005053-197504000-00007.
10
Effect of incorporation of antioxidants on the chemical, rheological, and sensory properties of probiotic petit suisse cheese.添加抗氧化剂对益生菌小瑞士干酪化学、流变学和感官特性的影响。
J Dairy Sci. 2016 Mar;99(3):1762-1772. doi: 10.3168/jds.2015-9701. Epub 2016 Jan 21.
本文引用的文献
1
Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction.听觉皮层中间神经元的发育需要钙黏蛋白来运作毛细胞的机电转导。
Proc Natl Acad Sci U S A. 2017 Jul 25;114(30):7765-7774. doi: 10.1073/pnas.1703408114. Epub 2017 Jul 13.
2
Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes.通过过氧化物酶体适应性增殖受损对声音暴露的超易感性。
Cell. 2015 Nov 5;163(4):894-906. doi: 10.1016/j.cell.2015.10.023.
3
The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells.原钙黏蛋白-15的CD2亚型是成熟听觉毛细胞中顶连接复合体的重要组成部分。
EMBO Mol Med. 2014 Jul;6(7):984-92. doi: 10.15252/emmm.201403976.
4
Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane.Stereocilin 将外毛细胞纤毛彼此连接，并连接到盖膜上。
J Comp Neurol. 2011 Feb 1;519(2):194-210. doi: 10.1002/cne.22509.
5
Stereocilin-deficient mice reveal the origin of cochlear waveform distortions.缺乏立体纤毛蛋白的小鼠揭示了耳蜗波形畸变的起源。
Nature. 2008 Nov 13;456(7219):255-8. doi: 10.1038/nature07380. Epub 2008 Oct 8.
6
Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning.耳蜗毛细胞中踝关节连接复合体的分子特征及其在毛束功能中的作用。
J Neurosci. 2007 Jun 13;27(24):6478-88. doi: 10.1523/JNEUROSCI.0342-07.2007.
7
Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse.otoferlin在一种人类耳聋形式中存在缺陷，它对于听觉带状突触处的胞吐作用至关重要。
Cell. 2006 Oct 20;127(2):277-89. doi: 10.1016/j.cell.2006.08.040.
8
Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle.肌球蛋白VIIa、harmonin和钙黏蛋白23，三种协作塑造感觉毛细胞束的Usher I型基因产物。
EMBO J. 2002 Dec 16;21(24):6689-99. doi: 10.1093/emboj/cdf689.
9
Anosmin-1, defective in the X-linked form of Kallmann syndrome, promotes axonal branch formation from olfactory bulb output neurons.在X连锁型卡尔曼综合征中存在缺陷的anosmin-1蛋白，可促进嗅球输出神经元形成轴突分支。
Cell. 2002 Apr 19;109(2):217-28. doi: 10.1016/s0092-8674(02)00713-4.
10
Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling.由于连接蛋白-26基因缺陷导致的儿童期常见耳聋形式DFNB1的临床特征：对遗传咨询的意义。
Lancet. 1999 Apr 17;353(9161):1298-303. doi: 10.1016/S0140-6736(98)11071-1.
Zotero 插件