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Titlebook: Human Apolipoprotein Mutants 2; From Gene Structure C. R. Sirtori,G. Franceschini,G. Assmann Book 1989 Springer Science+Business Media New

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發(fā)表于 2025-3-21 16:10:43 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Human Apolipoprotein Mutants 2
副標題From Gene Structure
編輯C. R. Sirtori,G. Franceschini,G. Assmann
視頻videohttp://file.papertrans.cn/429/428941/428941.mp4
叢書名稱NATO Science Series A:
圖書封面Titlebook: Human Apolipoprotein Mutants 2; From Gene Structure  C. R. Sirtori,G. Franceschini,G. Assmann Book 1989 Springer Science+Business Media New
描述The pleasant community of Limone suI Garda provided outstanding hospitality for a second NATO ARW dealing with apolipoprotein variants, which are natures clues for the discovery of the physiological roles of apolipoproteins in lipoprotein metabolism in normal subjects and patients with specific dyslipoproteinemias. Limone, the site of discovery of the first human apolipoprotein mutant, apoA-I-Milano, provided a brilliant sunny spring venue for more than 50 participants from both sides of the ocean. The attendance at the colorful opening ceremony of the ARW was one of the largest on record. Two members of the Italian government, the Secretaries of Health and the Navy, gave the welcoming addresses. Six television networks, two with national audiences, covered the international workshop. The Limone oracles provided a montage of insights gleamed from the eyes of the clinican, the biochemist, and the molecular biologist. The cumulative information on the molecular defects in lipoprotein metabolism reviewed by this diverse group of investigators provided an ever expanding horizon of new knowledge in this fast moving and some times perplexing field. Clinical vignettes were presented on pa
出版日期Book 1989
關(guān)鍵詞DNA; Lipid; gene; gene expression; lipoprotein; metabolism; mutant; mutation; ocean; protein; protein structur
版次1
doihttps://doi.org/10.1007/978-1-4615-9549-6
isbn_softcover978-1-4615-9551-9
isbn_ebook978-1-4615-9549-6
copyrightSpringer Science+Business Media New York 1989
The information of publication is updating

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Synthesis of Apolipoprotein A-I in the Skeletal Muscle of the Developing Chicksignificance of elevated apo A-I production by the skeletal muscle of the newborn chick is still poorly understood. It has been suggested that the synthesis of apo A-I in skeletal muscle may be important for: a) the local traffic and distribution of lipids among the muscle cells and the cellular org
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The Molecular Basis of the Defect in Familial Combined Apolipoproteins AI and CIII Deficiencytions, taken together, imply that deficiency or chronic reduction in plasma HDL and apoAI levels may result in increased risk for atherosclerosis. In support of this possibility, a large number of epidemiological studies have revealed a strong inverse correlation between plasma HDL and apoAI levels
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Familial Apolipoprotein A-I, C-III and A-IV Deficiencydeficiency and trace or undetectable levels of apoA-I and apoC-III in their plasma. They also had diffuse yellow-orange planar xanthomas, and mild corneal opacification (9). Obligate heterozygotes in this kindred had levels of HDL cholesterol, apoA-I and apoC-III which were approximately 50% of norm
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Book 1989 and the molecular biologist. The cumulative information on the molecular defects in lipoprotein metabolism reviewed by this diverse group of investigators provided an ever expanding horizon of new knowledge in this fast moving and some times perplexing field. Clinical vignettes were presented on pa
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Philippa J. Talmud,June Lloyd,David Muller,David R. Collins,James Scott,Steve Humphriessich Marketingwissen in kurzer Zeit aneignen wollen..Für Leser kostenlos in der 2. Auflage: Testen Sie Ihr Wissen mit Fragen und Antwortenzum Buch in der Springer-Nature-Flashcards-App..978-3-658-30963-3
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