Cellular and molecular aspects of clag 9
Cellular and molecular aspects of clag 9
批准号:
nhmrc : 137204
负责人:
A/Pr Donald Gardiner
金额:
$14.1万
依托单位国家:
澳大利亚
项目类别:
NHMRC Project Grants
财政年份:
2001
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2001-01-01 至 2003-12-31
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Malaria is a very important disease worldwide, causing hundreds of millions of cases and about two million deaths per year. Severe malaria including cerebral malaria is a major cause of death. It is caused by red blood cells which contain malaria parasites sticking to the lining of microscopic veins and clogging them; what happens after this is complex. The process of sticking is called cytoadherence. We have discovered a gene which is important in this process of sticking. We have called it by the acronym clag, for cytoadherence-linked asexual gene; most Australians know of Clag as a glue. Our evidence for this has been accepted for publication by the prestigious USA journal Proceedings of the National Academy of Sciences of the USA. Recent work overseas aimed at determining the entire DNA sequence of the malaria parasite has shown that clag is not alone; there are at least 9 slightly different clag genes in the malaria parasite. What do the others do? We propose two possibilities. The first is that all of them act in cytoadherence but that different clags enable the parasitised cells to stick to different things on the lining of veins. The second is that they enable the parasitised cells, or perhaps the parasites alone, to stick to other things at different stages of the complex life cycle of the parasite. The experiments that we propose should show whether either of these proposals is true.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Trafficking of the major virulence protein to the host cell surface in malaria parasite-infected erythrocytes
-
批准号:nhmrc : 602506
-
项目类别:NHMRC Project Grants
-
资助金额:$43.89万
-
财政年份:2010
-
负责人:A/Pr Donald Gardiner
-
依托单位:
Plasmodium falciparum neutral aminopeptidases: structure-function analysis for the discovery of anti-malarial drugs.
-
批准号:nhmrc : 571917
-
项目类别:NHMRC Project Grants
-
资助金额:$42.28万
-
财政年份:2009
-
负责人:A/Pr Donald Gardiner
-
依托单位:
A transgenic approach to rationale drug design in plasmodium falciparum
-
批准号:nhmrc : 496700
-
项目类别:Career Development Fellowships
-
资助金额:$28.06万
-
财政年份:2008
-
负责人:A/Pr Donald Gardiner
-
依托单位:
The clag gene family of P. falciparum; examining roles in cytoadherence, rheological properties or tissue trophism.
-
批准号:nhmrc : 199608
-
项目类别:NHMRC Project Grants
-
资助金额:$30.14万
-
财政年份:2002
-
负责人:A/Pr Donald Gardiner
-
依托单位:
Investigation of a virulence locus on chromosome 9 of Plasmodium falciparum utilising improved transfection technology
-
批准号:nhmrc : 137211
-
项目类别:NHMRC Project Grants
-
资助金额:$14.1万
-
财政年份:2001
-
负责人:A/Pr Donald Gardiner
-
依托单位:
国内基金
海外基金
登录
查看更多内容
配子生成素GGN不同位点突变损伤分子伴侣BIP及HSP90B1功能导致精子形成障碍的发病机理
-
批准号:82371616
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:姚晨成
-
依托单位:
MYRF/SLC7A11调控施万细胞铁死亡在三叉神经痛脱髓鞘病变中的作用和分子机制研究
-
批准号:82370981
-
项目类别:面上项目
-
资助金额:48.00万元
-
批准年份:2023
-
负责人:陈敏洁
-
依托单位:
PET/MR多模态分子影像在阿尔茨海默病炎症机制中的研究
-
批准号:82372073
-
项目类别:面上项目
-
资助金额:48.00万元
-
批准年份:2023
-
负责人:张淼
-
依托单位:
GREB1突变介导雌激素受体信号通路导致深部浸润型子宫内膜异位症的分子遗传机制研究
-
批准号:82371652
-
项目类别:面上项目
-
资助金额:45.00万元
-
批准年份:2023
-
负责人:刘开江
-
依托单位:
靶向PARylation介导的DNA损伤修复途径在恶性肿瘤治疗中的作用与分子机制研究
-
批准号:82373145
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:历鹏
-
依托单位:
OBSL1功能缺失导致多指(趾)畸形的分子机制及其临床诊断价值
-
批准号:82372328
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:项盈
-
依托单位:
O6-methyl-dGTP抑制胶质母细胞瘤的作用及分子机制研究
-
批准号:82304565
-
项目类别:青年科学基金项目
-
资助金额:30.00万元
-
批准年份:2023
-
负责人:李瑾
-
依托单位:
转录因子LEF1低表达抑制HMGB1致子宫腺肌病患者子宫内膜容受性低下的分子机制
-
批准号:82371704
-
项目类别:面上项目
-
资助金额:49.00万元
-
批准年份:2023
-
负责人:徐步芳
-
依托单位:
Irisin通过整合素调控黄河鲤肌纤维发育的分子机制研究
-
批准号:32303019
-
项目类别:青年科学基金项目
-
资助金额:30.00万元
-
批准年份:2023
-
负责人:职韶阳
-
依托单位:
上皮细胞黏着结构半桥粒在热激保护中的作用机制研究
-
批准号:31900545
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2019
-
负责人:傅容
-
依托单位: