chromosome disease 中文意思是什麼
chromosome disease
解釋
染色體病- chromosome : n. 【生物學】染色體。
- disease : n. 1. 病，疾病；【植物；植物學】病害。2. （精神等的）病態，弊病。3. （酒等的）變質；（食物等的）腐敗。4. 〈廢語〉不安。
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8p22 of human chromosome is an region with abundant disease - related genes. it is said that it is susceptible loci of hypertension and schizophrenia. the region is also the loci of oncogene and tumor su - pressor gene
人染色體8p22區是疾病基因富含區域，有報道說該區域是高血壓、精神分裂癥等疾病的易感位點，也是癌基因和抑癌基因的研究熱點。 -
When the researchers performed a detailed genetic comparison of affected and disease - free family members, they found that a specific segment of chromosome 12 was the most likely genomic hiding place for this unknown factor
當研究人員對受影響的和未受影響的家族成員進行詳細的遺傳對比時，發現染色體12的一個特殊區段最可能是該未知因素的基因組藏匿部位。 -
8p22 of human chromosome is an region rich in disease - related genes and is also the susceptible loci of oncogenes and tumor suppressor genes
人染色體8p22區是一個富含疾病基因的區域，是癌基因和抑癌基因的研究熱點。 -
Especially for the study of chinese y chromosome diversity, disease distribution, the origin of the nationality han, and flow disciplines, the distribution data and areas of the top 300 common chinese names would provide new clues and information which have the highest valuation in research and practical use
尤其是中國人前300個常見姓氏的數據和分佈地區，對于研究中國人y染色體多樣性疾病的分佈漢民族源和流以及其他學科領域，都有可能提供新的線索和參考，具有極高的研究和實際使用的價值。 -
The article related research achievenment on the molecular genetics of mental disease and spirits obstruction, expounds the molecular genetics basis and the mechanism of result in mental disease from chromosome aberration, gene mutation, dynamic mutation and genetic heterogeneity, etc
文章綜述了當前對精神病和精神障礙的分子遺傳學研究成果，從染色體畸變、基因突變、遺傳的異質性等方面闡明精神病發生的復雜的遺傳背景和機制。 -
In addition, he has made significant contributions to the mapping and annotation of human chromosome 7, and, identification of many other disease genes
除此以外，在斷定人類第七組染色體以及許多其他疾病基因，作出了重大的突破。 -
Professor tsui is a discoverer of the gene for cystic fibrosis and has made significant contributions to the mapping and annotation of human chromosome 7 and identification of many other disease genes
徐教授斷定了囊狀纖維的缺陷基因。此外，在鑒定人類第七組染色體及許多其他疾病基因亦作出了重大的突破。 -
In 2001, wilson and his colleagues cloned another two members - human wnk1 gene and wnk4 gene which were located on chromosome 12 and 17, respectively. the two genes are disease - causing genes responsible for a mendelian hypertension. the disease - causing mutations are the large deletions in the first intron in wnk1 gene, causing increased expression in leukocytes
2001年， wilson等克隆了此家族的另兩個成員? ?人的wnk1和wnk4基因，分別位於12號和17號染色體，這兩個基因是一種孟德爾遺傳型高血壓病的致病基因，致病突變分別是wnk1基因第一內含子的大片段缺失，導致患者白細胞的基因表達量提高5倍左右。
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