Amyloid plaques are one of the characteristic structural abnormalities found in the brains of Alzheimer patients.

Another approach by several large pharmaceutical companies, tries to block the body's production of amyloid proteins.

另外几家大型制药公司采取了另一治疗方案, 即努力抑制人内粉蛋白的产生.

A build up of beta-amyloid protein.

由β - 淀粉蛋白堵塞而成的.

They alter the cleaves amyloid precursor protein.

淀粉状蛋白是一种形状经常改变的蛋白.

PIB adheres to amyloid plaques in the brain.

匹兹堡化合物B结合 在脑组织淀粉样斑点上.

Beta is the secretion of amyloid beta protein produced the key enzyme.

贝塔分泌酶是产生贝塔淀粉状蛋白的关键酶.

Amputation is indicated for those with extremities cancer and systemic amyloid degeneration.

截肢适用于肢体远端高度疑有癌变或已引起全身淀粉样变者.

Objective : To analyze the causes of misdiagnosis of amyloid nephropathy.

目的:分 析淀粉样变肾病病理误诊的原因.

Acini contain a small amount of secretions, but few have amyloid precursor.

腺泡内含有少量分泌物, 但很少有淀粉样体.

A Congo red stain will demonstrate the pink material to be amyloid.

刚果红染色淀粉样物呈粉红色.

They alter the way it cleaves amyloid precursor protein.

它们改变了这个酶切割淀粉样蛋白前体的方式.

Such collections of amyloid add to renal bulk, but diminish renal function.

淀粉样物质沉积使肾脏体积增大, 但功能下降.

What's more, the prions ramp up amyloid beta's neurotoxic effects.

而且, 朊病毒蛋白增强了,淀粉样蛋白的神经毒性.

There are also characteristic amyloid deposits that stain with Congo red.

同时有特征性刚果红染色的淀粉样沉着物.

Pathological examination of the medial rectus muscle showed positive Congo red stain compatible with amyloidosis.

病理切片检查显示阳性刚果红染色反应.

Cross's disease, familial amyloidosis, prevents the liver from breaking down a protein called transthyretin.

克罗斯患有一种其家族特有的淀粉样变性疾病, 它使肝脏无法分解一种叫做转体基因的蛋白.

Congo red stain has been performed on the myocardium in a case of amyloidosis.

淀粉样变性心肌经刚果红染色.

Objective : To improve the diagnostic competence for amyloidosis of larynx both clinically and radiologically.

目的: 提高对喉淀粉样变的临床及影像学诊断水平.

Perilymphatic distribution is noted in pneumoconiosis, sarcoidosis, amyloidosis.

淋巴管周分布的见于尘肺, 结节病, 淀粉样变性.

Objective : To explore the clinical characteristics and pathogenesis of primary systemic amyloidosis.

目的: 探讨原发性系统性淀粉样变病的临床特点和发病机制.

An uncertain proportion of patients, possibly about 10 per cent, have a third protein abnormality-amyloidosis.

还有一部分(比例不确定)病人可能占10%, 有第三种异常蛋白 —— 淀粉样变性.