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Welcome to the Pubget Medical Subject Headings (MESH) browser. Click on a topic or subtopic below to explore related papers. In the gold box is the most recent paper about the current MESH term, and below are 20 related papers.
Protein Array Analysis (0):
Recent article
Protein Array Analysis
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
| < More recent | Older article > |
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Hepatology (52)1 2010
Abstract
We found that Wisteria floribunda agglutinin (WFA) is the best probe to differentiate intrahepatic cholangiocarcinoma (ICC) lesions from normal bile duct epithelia (BDE) (P < 0.0001). The subsequent histochemical study confirmed ICC-specific WFA staining on 165 tissue specimens. On the other hand, t...
|
PMID: 20578261
PDF is available here.
PDF is available here.
Abstract
EAT products are altered in both obesity and CAD and induce atherogenic changes in relevant target cells....
|
PMID: 20395594
PDF is available here.
PDF is available here.
Abstract
We aimed to evaluate the feasibility of fecal miRNAs as biomarkers for colorectal neoplasia screening.
Total RNA was extracted from freshly collected stool samples from 8 healthy volunteers and 29 samples collected via fecal occult blood testing from subjects with normal colonoscopie...
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PMID: 20551304
PDF is available here.
PDF is available here.
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
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PMID: 20564482
PDF is available here.
PDF is available here.
Abstract
Atomic force microscopy (AFM) with bias control is employed to fabricate oxidized nanopatterns on a silicon surface with a feature size as low as 50 nm. Nanopatterns made by a Pt/Ir coating probes have larger feature size than these made by the probe without, but the patterning speed is fast, 0.1 s...
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PMID: 21128448
PDF is available here.
PDF is available here.
Nanomedicine (5)5 2010
Abstract
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
|
PMID: 20564482
PDF is available here.
PDF is available here.
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
|
PMID: 20564482
PDF is available here.
PDF is available here.
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
|
PMID: 20564482
PDF is available here.
PDF is available here.
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
|
PMID: 20564482
PDF is available here.
PDF is available here.
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
|
PMID: 20564482
PDF is available here.
PDF is available here.
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
|
PMID: 20564482
PDF is available here.
PDF is available here.
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
|
PMID: 20564482
PDF is available here.
PDF is available here.
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
|
PMID: 20564482
PDF is available here.
PDF is available here.
Abstract
Biomolecules, including protein A, albumin, and immunoglobulin G, are spotted on top of a nanoporous substrate by using a continuous-flow microspotter (CFM) system, which normally produces spots 3 to 4 orders of magnitude more sensitive than conventional biomolecule printing methods....
|
PMID: 20564482
PDF is available here.
PDF is available here.