找回密碼
 To register

QQ登錄

只需一步,快速開始

掃一掃,訪問微社區(qū)

打印 上一主題 下一主題

Titlebook: Genetics and Auditory Disorders; Bronya J. B. Keats,Richard R. Fay,Arthur N. Popper Book 2002 Springer Science+Business Media New York 200

[復制鏈接]
樓主: hector
21#
發(fā)表于 2025-3-25 06:37:10 | 只看該作者
Der Kampf um den verlorenen Tagusing spontaneous mouse models of mitochondrial hearing impairment, or direct investigation of the most likely biochemical pathways involved, may help not only in elucidating the pathophysiology between mtDNA mutations and hearing loss, but may also provide a paradigm for mitochondrial diseases in g
22#
發(fā)表于 2025-3-25 09:20:59 | 只看該作者
23#
發(fā)表于 2025-3-25 12:07:39 | 只看該作者
24#
發(fā)表于 2025-3-25 18:35:46 | 只看該作者
Introduction and Overview: Genetics in Auditory Science and Clinical Audiology,
25#
發(fā)表于 2025-3-25 23:46:41 | 只看該作者
26#
發(fā)表于 2025-3-26 00:37:03 | 只看該作者
Mapping and Cloning of Genes for Inherited Hearing Impairment,ssion, audiological configuration, etc.), the description of the phenotype should include documentation of the presence or absence of associated vestibular abnormalities, and/or neuroradiological findings in the inner ear. By this means, the results of the research findings will rapidly translate in
27#
發(fā)表于 2025-3-26 05:07:16 | 只看該作者
Cytogenetics and Cochlear Expressed Sequence Tags (ESTs) for Identification of Genes Involved in Henslocation. The advantage would be that, if such a chromosome rearrangement were found, it would immediately suggest the location of the deafness gene..The cochlear ESTs and libraries that exist have been extremely helpful in understanding different aspects of the molecular biology of the inner ear.
28#
發(fā)表于 2025-3-26 08:30:41 | 只看該作者
Hearing Loss and Mitochondrial DNA Mutations: Clinical Implications and Biological Lessons,using spontaneous mouse models of mitochondrial hearing impairment, or direct investigation of the most likely biochemical pathways involved, may help not only in elucidating the pathophysiology between mtDNA mutations and hearing loss, but may also provide a paradigm for mitochondrial diseases in g
29#
發(fā)表于 2025-3-26 14:23:59 | 只看該作者
Mice as Models for Human Hereditary Deafness,to fill the gap between human deafness and mouse models (Nolan et al. 2000). Large-scale, genome-wide mutagenesis programmes are starting in other countries too, including the US, so there will soon be many more mutants available. Deafness is one of the most heterogeneous diseases known in humans, a
30#
發(fā)表于 2025-3-26 17:48:56 | 只看該作者
 關于派博傳思  派博傳思旗下網(wǎng)站  友情鏈接
派博傳思介紹 公司地理位置 論文服務流程 影響因子官網(wǎng) 吾愛論文網(wǎng) 大講堂 北京大學 Oxford Uni. Harvard Uni.
發(fā)展歷史沿革 期刊點評 投稿經(jīng)驗總結 SCIENCEGARD IMPACTFACTOR 派博系數(shù) 清華大學 Yale Uni. Stanford Uni.
QQ|Archiver|手機版|小黑屋| 派博傳思國際 ( 京公網(wǎng)安備110108008328) GMT+8, 2025-10-8 02:56
Copyright © 2001-2015 派博傳思   京公網(wǎng)安備110108008328 版權所有 All rights reserved
快速回復 返回頂部 返回列表
马公市| 盖州市| 祁门县| 苍山县| 弋阳县| 阳谷县| 定州市| 民勤县| 凤山市| 马龙县| 汉川市| 黔南| 大洼县| 蕲春县| 高安市| 阜平县| 永嘉县| 阿勒泰市| 武城县| 宜春市| 肇源县| 西乌| 南江县| 鹤山市| 通化市| 巴彦淖尔市| 新兴县| 建平县| 贞丰县| 墨竹工卡县| 普洱| 吉林市| 柳州市| 安图县| 通榆县| 香格里拉县| 阜康市| 莱西市| 尼玛县| 荥经县| 义乌市|