1) Mitochondria and Human Disease
线粒体与人类疾病
2) mitochondrial diseases
线粒体疾病
1.
Nuclear genes and mitochondrial genes associated with mitochondrial diseases;
线粒体疾病与核基因-线粒体基因的表达调控
2.
MtDNA mutations were necessary for mitochondrial diseases that caused by mitochondrial dysfunction,but not sufficient to induce the pathology.
因线粒体功能缺陷导致的线粒体疾病,涉及线粒体基因组突变、核基因突变、及环境因素等复杂机制,深入阐明三者的相互作用关系具有重要的理论意义,进而指导线粒体疾病的诊断、预警、和治疗等,具有重要的潜在应用价值。
4) Lysosome And The Disease Of Human Being
溶酶体与人类疾病
5) Carnosine and human diseases
肌肽与人类疾病
6) human disease
人类疾病
1.
Identifying Genes and Functions Responsible for Human Disease Based on Gene Expression Profiles;
基于基因表达谱识别人类疾病相关基因和功能
2.
The mouse is an ideal model organism for studies of human disease, because mouse is physiologically very similar to human.
小鼠是人类疾病理想的动物模型，不仅因为小鼠在生理上与人类极为相似而且小鼠的遗传资源非常丰富，其大量的遗传变异可作为研究人类疾病的借鉴。
补充资料：肾细胞线粒体
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说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条