|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Young children s theory of mind and emotion 显示文摘 | Harris P L Johnson C N Hutton D Anddrews G Cooke T | 1989 | Cogni- tion and Emotion1989，3，： | 1 |
| 2 | Chloroplast transformation in chlamydomonas with high velocity microprojectiles 显示文摘 | Boynton J E Gillham N W Harris E H Hosler J P Johnson A M Jones A R Randolph-Anderson B L Robertson D Klein T M Shark K B Sanford J C | 1988 | Science1988，240，： | 1 |
| 3 | Mouse I-I6 Homeobox 1 (Hmxl) mutations cause cranial abnormalities and re- duced body mass显示文摘 | Munree R J Prabhu V Acland G M Johnson K R Harris B S O' Brien T P Welsh I C Neden D M Schimenti J C | 2009 | BMC Dev Biol2009，9，： | 1 |
| 4 | Tissue heterogeneity of the mammalian mitoehondrial pro- teome显示文摘 | Johnson D T Harris R A French S | 2007 | Am J Physiol Cell Physiol2007，292，2： | 1 |
| 5 | Destruction or decomposition of hypergolic chemicals in a liquid propellant testing laboratory显示文摘 | Greene Benjamin McClure Mark B Johnson Harry T | 2004 | Chemical Health and Safety2004，，： | 1 |
| 6 | Inhaled benzo (a) pyrene impairs long-term potentiation in the F1 generation rat dentate gyrus显示文摘 | Wormley DD Chirwa S Nayyar T Wu J Johnson S Brown LA Harris E Hood DB | 2004 | Cell Mol Biol ( Noisy-le-grand)2004，50，6： | 1 |
| 7 | Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10显示文摘Objective To map a mouse deafness gene, identify the underlying mutation and develop a mouse model for human deafness. Methods Genetic linkage cross and genome scan were used to map a novel mutation named hypoplasia of the membranous labyrinth (hml), which causes hearing loss in mutant mice. Results ① hml was mapped on mouse Chr 10 (~43 cM from the centromere) suggests that the homologous human gene is on 12q22-q24, which was defined on the basis of known mouse-human homologies (OMIM, 2004). ② This study has generated 25 polymorphic microsatellite markers, placed 3 known human genes in the correct order in a high-resolution mouse map and narrowed the hml candidate gene region to a 500 kb area. | Belinda S Harris Patricia F Ward-Bailey Roderick T Bronson Muriel T Davisson Kenneth R Johnson | 2004 | Journal of Pharmaceutical Analysis2004，16，1： | 0 |
| 8 | 小鼠10号染色体上致聋突变基因hml的精确定位(英文)显示文摘目的 定位小鼠致聋基因 ,识别决定其性状的有关突变 ,为人类耳聋基因研究提供动物模型。方法 利用全基因组扫描来定位名为hml可致小鼠听力丧失突变基因。结果 ①hml基因定位在小鼠 10号染色体上 ,距中心粒约4 3cM处。根据已知的鼠 人同源同线性特点 ,提示人的同源基因位于 12 q2 2 -q2 4 ;②获得了 2 5个多态性微卫星标记 ,通过高分辨的小鼠图谱将 3个已知人类基因进行了正确排列 ,并将hml侯选基因限定在一个 5 0 0kb的区域内。 | Belinda S Harris Patricia F Ward-Bailey Heping Yu Roderick T Bronson Muriel T Davisson Kenneth R Johnson | 2004 | 西安交通大学学报(医学版)2004，25，3： | 0 |
您所在的机构暂未开通此部分的功能，请联系管理员