1. |
Bibliography of the current world literature |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 15-16
&NA; &NA;,
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ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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2. |
Nutrition and therapeutics |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 31-59
&NA; &NA;,
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PDF (689KB)
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ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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3. |
Genetics and molecular biology |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 36-39
Paul Cullen,
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ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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4. |
Lipid metabolism |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 39-47
Jillian Davidson,
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PDF (990KB)
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ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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5. |
Cardiovascular disease and hyperlipidaemia |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 47-51
Alan Cowley,
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PDF (540KB)
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ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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6. |
Atherosclerosis: cell biology and lipoproteins |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 51-56
P Barton Duell,
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PDF (651KB)
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ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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7. |
Clinical chemistry and coagulation |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 57-59
Alan Jones,
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PDF (299KB)
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ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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8. |
Editorial |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 75-75
Scott Grundy,
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PDF (58KB)
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ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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9. |
Genetics and molecular biology |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 77-80
Helen Hobbs,
James Scott,
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PDF (386KB)
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ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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10. |
The molecular basis of abetalipoproteinemia |
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Current Opinion in Lipidology,
Volume 5,
Issue 2,
1994,
Page 81-86
Richard Gregg,
John Wetterau,
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PDF (639KB)
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摘要:
Abetalipoproteinemia is a recessive genetic disease in humans characterized by the virtual absence of apolipoprotein (apo)B and apoB-containing lipoproteins in plasma. Microsomal triglyceride transfer protein (MTP), a resident lipid transfer protein within the endoplasmic reticulum of hepatocytes and enterocytes, has been shown to be absent in enterocytes from subjects with this disease. MTP is a heterodimer of a unique large subunit and protein disulfide isomerase. It has been demonstrated that the absence of MTP in abetalipoproteinemia is secondary to mutations in the gene for the large subunit of MTP. Thus, mutations in the gene for the large subunit of MTP are a cause of abetalipoproteinemia, which indicates that the MTP is a necessary component for the assembly and secretion of apoB-containing lipoproteins from the liver and intestine.
ISSN:0957-9672
出版商:OVID
年代:1994
数据来源: OVID
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