Fabry disease is a rare inherited condition characterized by the toxic accumulation of a fatty substance called globotriaosylceramide (Gb3) in the body’s cells. This buildup impairs organ function, especially in the kidneys and heart. The disease is also known as Anderson-Fabry disease, after...
While bilateral striopallidodentate calcinosis is commonly referred to as 'Fahr's disease' (a misnomer), there are 35 additional names used in the literature for the same condition. Secondary bilateral calcification is also reported in a variety of genetic, developmental, metabolic, infectious and ...
1) What is the molecular basis of the Long Q-T syndrome disease? (What is abnormal at the cellular, biochemical, or molecular level)? 2) What is the genetic basis of Long Q-T syndrome? What metabolic disorder (be specific) is characterized by h...
细胞里的mRNA越多,蛋白质就越多。But our discovery is a little bit different. We have found a new class of RNAs that have changed how we think about cancer detection. These are relatively small RNAs, and they don't actually...
Although molecular mimicry has yet to be unequivocally proven, in the past several years there has been a sharpening of its definition with better experimental data implicating it as a cause of neurological disease in humans. 展开 关键词:
European Molecular Biology OrganizationEmbo ReportsScully JL (2004) `What is a disease?' EBMO reports 5(7), pp 650-653Scully, J.L. 2004. What is a disease?. EMBO reports 5(7): 650–653.Leach SJ (2004) What is a disease? Disease, Disability and their definitions. European Molecular ...
EMBO reports VOL 5 | NO 7 | 2004©2004 EUROPEAN MOLECULAR BIOLOGY ORGANIZATIONviewpointviewpoint650What is a disease?Disease,disability and their definitionsJackie Leach ScullyAt first sight, the answer to “What is adisease?” is straightforward. Most ofus feel we have an intuitive grasp of...
Parkinson’s disease is a disorder wherein certain cells in the brain gradually sicken and die off. This causes problems with brain signaling and gives rise to a characteristic set of motor symptoms, namely slowed movements, rigidity, tremor, and balance problems, as well as nonmotor symptoms....
Genotyping is the technology that detects small genetic differences that can lead to major changes in phenotype, including both physical differences that make us unique and pathological changes underlying disease. It has a vast range of uses acros...
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