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Do Humans Possess a Second Sense of Hearing?

机译：人类会带来第二种听觉吗？

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来源
《American Scientist》 |2015年第5期|348-355|共8页
作者
Todd Neil;
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作者单位

Sheffield Mus Dept, Sheffield, S Yorkshire, England|Univ Manchester, Percept, Manchester M13 9PL, Lancs, England;

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收录信息美国《科学引文索引》(SCI);
原文格式 PDF
正文语种 eng
中图分类
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专利

1. Mechanism of a novel missense mutation, p.V174M, of the human connexin31 (GJB3) in causing nonsyndromic hearing loss [J] . LiT.-C., KuanY.-H., KoT.-Y., Biochemistry and Cell Biology . 2014,第4期

机译：人类连接蛋白31（GJB3）的新型错义突变p.V174M引起非综合征性听力损失的机制
2. Mechanism of Two Novel Human GJC3 Missense Mutations in Causing Non-Syndromic Hearing Loss [J] . SuC.-C., LiS.-Y., YenY.-C., Cell biochemistry and biophysics . 2013,第2期

机译：两种新型人类GJC3错义突变引起非综合征性听力损失的机制
3. Mechanism of Two Novel Human GJC3 Missense Mutations in Causing Non-Syndromic Hearing Loss [J] . Ching-Chyuan Su, Shuan-Yow Li, Yung-Chang Yen, Cell Biochemistry and Biophysics . 2013,第2期

机译：两种新型人类GJC3错义突变导致非综合征性听力损失的机制
4. Puppet show for entertaining hearing-impaired, together with normal-hearing people — A novel application of human sensing technology to inclusive education [C] . Goseki Masafumi, Adachi Takayuki, Mizoguchi Hiroshi, 2012 First International Conference on Innovative Engineering Systems . 2012

机译：与正常听觉者一起娱乐听觉障碍的木偶表演—人类感应技术在全纳教育中的新颖应用
5. Dictyostelium discoideum possess a highly diverged presenilin/gamma-secretase that accurately processes human amyloid precursor protein and is required for growth and correct cell fate determination. [D] . McMains, Vanessa C. 2010

机译：盘基网柄菌拥有高度分化的早老素/γ-分泌酶，可准确加工人淀粉样蛋白前体蛋白，是生长和正确确定细胞命运所必需的。
6. Lack of collagen α6(IV) chain in mice does not cause severe-to-profound hearing loss or cochlear malformation a distinct phenotype from nonsyndromic hearing loss with COL4A6 missense mutation [O] . Shaoying Tang, Tomoko Yonezawa, Yukihide Maeda, 2021

机译：小鼠中缺乏胶原蛋白α6（iv）链不会造成严重致力于深刻的听力损失或耳蜗畸形从非合成症听力损失与COL4A6畸形突变的不同表型
7. Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84 [O] . H. Shahin, M. Rahil, A. A. Rayan, 2010

机译：人类听力损失中立体膜蛋白基因PTPRQ的无意义突变DFNB84

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