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PMID |
Sentence |
1 |
16009335
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Endothelial NO bioactivity in the aorta was reduced in diabetic NOD mice while vascular expression of ECE-1 and ECE-2 mRNA was increased compared with controls (all p<0.05).
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2 |
16009335
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ET(A) receptor blockade also restored abnormal endothelial NO bioactivity and reduced ECE-1 and ECE-2 gene expression in NOD mice to levels comparable with healthy controls (p<0.05).
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3 |
16009335
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Endothelial NO bioactivity in the aorta was reduced in diabetic NOD mice while vascular expression of ECE-1 and ECE-2 mRNA was increased compared with controls (all p<0.05).
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4 |
16009335
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ET(A) receptor blockade also restored abnormal endothelial NO bioactivity and reduced ECE-1 and ECE-2 gene expression in NOD mice to levels comparable with healthy controls (p<0.05).
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5 |
16741043
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Blood samples were analyzed for glucose levels, and renal gene expression of ECE-1, ECE-2, and prepro-ET-1 was determined using real-time polymerase chain reaction.
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6 |
16741043
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ECE-1, ECE-2, and prepro-ET-1 mRNA was detected in the kidneys of NOD and control mice.
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7 |
16741043
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Despite normal renal histology, expression of ECE-1 and prepro-ET-1 was reduced in NOD mice by approximately 50% compared with controls (P < 0.01); ECE-2 was markedly decreased by almost 90% compared with controls (P < 0.001).
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8 |
16741043
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Hyperglycemia at an early stage of autoimmune diabetes is associated with transcriptional downregulation of ECE-1, ECE-2, and prepro-ET-1 in the kidney.
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9 |
16741043
|
Blood samples were analyzed for glucose levels, and renal gene expression of ECE-1, ECE-2, and prepro-ET-1 was determined using real-time polymerase chain reaction.
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10 |
16741043
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ECE-1, ECE-2, and prepro-ET-1 mRNA was detected in the kidneys of NOD and control mice.
|
11 |
16741043
|
Despite normal renal histology, expression of ECE-1 and prepro-ET-1 was reduced in NOD mice by approximately 50% compared with controls (P < 0.01); ECE-2 was markedly decreased by almost 90% compared with controls (P < 0.001).
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12 |
16741043
|
Hyperglycemia at an early stage of autoimmune diabetes is associated with transcriptional downregulation of ECE-1, ECE-2, and prepro-ET-1 in the kidney.
|
13 |
16741043
|
Blood samples were analyzed for glucose levels, and renal gene expression of ECE-1, ECE-2, and prepro-ET-1 was determined using real-time polymerase chain reaction.
|
14 |
16741043
|
ECE-1, ECE-2, and prepro-ET-1 mRNA was detected in the kidneys of NOD and control mice.
|
15 |
16741043
|
Despite normal renal histology, expression of ECE-1 and prepro-ET-1 was reduced in NOD mice by approximately 50% compared with controls (P < 0.01); ECE-2 was markedly decreased by almost 90% compared with controls (P < 0.001).
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16 |
16741043
|
Hyperglycemia at an early stage of autoimmune diabetes is associated with transcriptional downregulation of ECE-1, ECE-2, and prepro-ET-1 in the kidney.
|
17 |
16741043
|
Blood samples were analyzed for glucose levels, and renal gene expression of ECE-1, ECE-2, and prepro-ET-1 was determined using real-time polymerase chain reaction.
|
18 |
16741043
|
ECE-1, ECE-2, and prepro-ET-1 mRNA was detected in the kidneys of NOD and control mice.
|
19 |
16741043
|
Despite normal renal histology, expression of ECE-1 and prepro-ET-1 was reduced in NOD mice by approximately 50% compared with controls (P < 0.01); ECE-2 was markedly decreased by almost 90% compared with controls (P < 0.001).
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20 |
16741043
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Hyperglycemia at an early stage of autoimmune diabetes is associated with transcriptional downregulation of ECE-1, ECE-2, and prepro-ET-1 in the kidney.
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21 |
18363935
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Neprilysin and insulin-degrading enzyme (IDE), which have been most extensively studied, are expressed both neuronally and within the vasculature.
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22 |
18363935
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Other enzymes shown capable of degrading Abetain vitro or in animal studies include plasmin; endothelin-converting enzymes ECE-1 and -2; matrix metalloproteinases MMP-2, -3 and -9; and angiotensin-converting enzyme (ACE).
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23 |
18363935
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The levels of plasmin and plasminogen activators (uPA and tPA) and ECE-2 are reported to be reduced in AD.
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24 |
18363935
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Reductions in neprilysin, IDE and plasmin in AD have been associated with possession of APOEepsilon4.
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25 |
18363935
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The level and activity of ACE are increased, the level being directly related to Abeta plaque load.
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26 |
18363935
|
Neprilysin and insulin-degrading enzyme (IDE), which have been most extensively studied, are expressed both neuronally and within the vasculature.
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27 |
18363935
|
Other enzymes shown capable of degrading Abetain vitro or in animal studies include plasmin; endothelin-converting enzymes ECE-1 and -2; matrix metalloproteinases MMP-2, -3 and -9; and angiotensin-converting enzyme (ACE).
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28 |
18363935
|
The levels of plasmin and plasminogen activators (uPA and tPA) and ECE-2 are reported to be reduced in AD.
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29 |
18363935
|
Reductions in neprilysin, IDE and plasmin in AD have been associated with possession of APOEepsilon4.
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30 |
18363935
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The level and activity of ACE are increased, the level being directly related to Abeta plaque load.
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