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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
13-14
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pubmed:dateCreated |
2011-5-3
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pubmed:abstractText |
Hereditary amyloidosis due to mutations of apolipoprotein A-I (apoA-I) is a rare disease characterized by the deposition of amyloid fibrils constituted by the N-terminal fragment of apoA-I in several organs. L75P is a variant of apoA-I associated with systemic amyloidosis predominantly involving the liver, kidneys, and testis, identified in a large number of unrelated subjects. Objective of the present paper was to evaluate the impact of the L75P apoA-I variant on HDL subpopulations and cholesterol esterification in carriers.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-11266606,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-14701812,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-15095475,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-15131802,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-15558533,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-15994445,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-1619367,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-17107880,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-17109866,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-19324996,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-20637862,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-20884842,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-21039326,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-2106917,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-3129016,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-7583561,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-7670941,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-8840853,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-9034206,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-9051205,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21458433-9125178
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
1873-3492
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pubmed:author |
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pubmed:copyrightInfo |
Copyright © 2011 Elsevier B.V. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
11
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pubmed:volume |
412
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1262-5
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pubmed:meshHeading |
pubmed-meshheading:21458433-Amyloidosis, Familial,
pubmed-meshheading:21458433-Apolipoprotein A-I,
pubmed-meshheading:21458433-Cholesterol,
pubmed-meshheading:21458433-Disease Progression,
pubmed-meshheading:21458433-Esterification,
pubmed-meshheading:21458433-Female,
pubmed-meshheading:21458433-Heterozygote,
pubmed-meshheading:21458433-Humans,
pubmed-meshheading:21458433-Lipoproteins, HDL,
pubmed-meshheading:21458433-Male,
pubmed-meshheading:21458433-Middle Aged,
pubmed-meshheading:21458433-Mutation
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pubmed:year |
2011
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pubmed:articleTitle |
Effect of the amyloidogenic L75P apolipoprotein A-I variant on HDL subpopulations.
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pubmed:affiliation |
Center Enrica Grossi Paoletti, Department of Pharmacological Sciences, Università degli Studi di Milano, Milano, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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