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Titlebook: Amyloidosis; George G. Glenner,Elliott F. Osserman,Dorothea Zuc Book 1986 Plenum Press, New York 1986 Alzheimer‘s disease.Alzheimer′s dise

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發(fā)表于 2025-3-21 16:16:00 | 只看該作者 |倒序瀏覽 |閱讀模式
期刊全稱Amyloidosis
影響因子2023George G. Glenner,Elliott F. Osserman,Dorothea Zuc
視頻videohttp://file.papertrans.cn/155/154784/154784.mp4
圖書封面Titlebook: Amyloidosis;  George G. Glenner,Elliott F. Osserman,Dorothea Zuc Book 1986 Plenum Press, New York 1986 Alzheimer‘s disease.Alzheimer′s dise
影響因子From a process that from the days of Vir chow and Rokitansky, primarily stimulated the relatively narrow interest of pathologists, amyloidosis has risen full-blown as one of the most important of disease complexes. Its presence dominat:es the lesions of Alzheimer‘s disease, a disease affecting an estimated 2. 5 million people in the U. S. A. and thereby closely rivaling stroke as the third most common cause of death. If, as it has been de- scribed, Alzheimer‘s disease is the "Disease of the Century," then amy- loidosis is the Disease Complex of the Ages. It affects in one or more of its manifestations every organ of the body, and is at least as old as the afflicted Egyptian mummies of the pyramids. With an increasing percentage of older individuals amyloid of the senior population becomes increasingly more frequent. The subjects covered in this Symposium range through almost every clinical medical specialty. From an average of one paper in each of the past three Symposiums, the explosive interest in cerebral amyloidosis has led to the presentation of 12 papers on this subject in the present volume. The genetically predisposed familial amyloidotic processes, such as the polyneuropat
Pindex Book 1986
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書目名稱Amyloidosis影響因子(影響力)




書目名稱Amyloidosis影響因子(影響力)學(xué)科排名




書目名稱Amyloidosis網(wǎng)絡(luò)公開度




書目名稱Amyloidosis網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Amyloidosis被引頻次




書目名稱Amyloidosis被引頻次學(xué)科排名




書目名稱Amyloidosis年度引用




書目名稱Amyloidosis年度引用學(xué)科排名




書目名稱Amyloidosis讀者反饋




書目名稱Amyloidosis讀者反饋學(xué)科排名




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Ultrastructural Identification of AA-Type Amyloid Fibrils Using Polyclonal and Monoclonal Antibodiesremely low background, the staining quality with monoclonal antibodies was superior to that with polyclonal antibodies. Monoclonal antibodies, therefore, would seem to be well-suited for early detection of amyloid by electron microscopy.
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Heterogeneity of Human Amyloid Protein AA and SAAous as SAA, it is not excluded that AA may be derived from one or a restricted number of SAA forms. The molecular weight heterogeneity of AA and the possibility of deamidation of asparagine residues may explain that one SAA variant can be transformed to a heterogeneous mixture of AA proteins.
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K?ltetr?ger der mittelbaren Kühlung6 and 4.9. These are slightly larger than other AA-proteins and diverge from them in amino acid composition. Amyloid fibrils containing these AA-variants have a remarkable resistance to degradation by serum.
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Ausführung der Kaltluftmaschinen addition to elucidating one aspect of the pathogenesis of amyloid deposition, these results suggest a means for selective targeting of diagnostic traces and/or effector agents to amyloid deposits ..
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Pathogenetic Mechanisms and Precursor Product Relationships in Murine Amyloidosisn addition to elucidating one aspect of the pathogenesis of amyloid deposition, these results suggest a means for selective targeting of diagnostic traces and/or effector agents to amyloid deposits ..
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