Min S Chang
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Explore the profile of Min S Chang including associated specialties, affiliations and a list of published articles.
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16
Citations
237
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Recent Articles
1.
Williams C, Zhang B, Smith J, Jayagopal A, Barrett C, Pino C, et al.
J Clin Invest
. 2011 Sep;
121(10):4056-69.
PMID: 21911938
The acquisition of a mesenchymal phenotype is a critical step in the metastatic progression of epithelial carcinomas. Adherens junctions (AJs) are required for suppressing this epithelial-mesenchymal transition (EMT) but less...
2.
Russ P, Pino C, Williams C, Bader D, Haselton F, Chang M
PLoS One
. 2011 Feb;
6(1):e14563.
PMID: 21283798
Blood vessel epicardial substance (Bves) is a transmembrane adhesion protein that regulates tight junction (TJ) formation in a variety of epithelia. The role of TJs within epithelium extends beyond the...
3.
Jayagopal A, Yang J, Haselton F, Chang M
Invest Ophthalmol Vis Sci
. 2010 Sep;
52(1):588-93.
PMID: 20861479
Purpose: To investigate the role of tight junction (TJ)-associated signaling pathways in the proliferation of uveal melanoma. Methods: Human uveal melanoma cell lines overexpressing the TJ molecule blood vessel epicardial...
4.
Russ P, Kupperman A, Presley S, Haselton F, Chang M
Invest Ophthalmol Vis Sci
. 2009 Jul;
51(1):223-30.
PMID: 19628742
Purpose: Blood vessel epicardial substance (Bves) is a novel adhesion molecule that regulates tight junction (TJ) formation. TJs also modulate RhoA signaling, which has been implicated in outflow regulation. Given...
5.
Rodila R, Kim G, Fan L, Chang M, Zhang J, Wu H, et al.
J Chromatogr B Analyt Technol Biomed Life Sci
. 2008 Aug;
872(1-2):128-32.
PMID: 18692445
ABT-263 is under development for treatment of cancer. In order to support clinical trials, an analytical method for ABT-263 quantification in human urine became necessary. Due to the extremely poor...
6.
Kawaguchi M, Hager H, Wada A, Koyama T, Chang M, Bader D
PLoS One
. 2008 May;
3(5):e2261.
PMID: 18493308
While Blood vessel epicardial substance (Bves) confers adhesive properties, the molecular mechanism of regulating this activity is unknown. No predicted functional motifs in this highly conserved integral membrane protein, other...
7.
Zhang J, Reimer M, Ji Q, Chang M, El-Shourbagy T, Burke S, et al.
Anal Bioanal Chem
. 2007 Feb;
387(8):2745-56.
PMID: 17294173
During stent development, accurate monitoring of the drug concentration in animal tissues can provide critical information on how the drug is released into the circulation and the surrounding tissues. To...
8.
Chang M, Kim E, El-Shourbagy T
Rapid Commun Mass Spectrom
. 2006 Nov;
21(1):64-72.
PMID: 17133627
The capabilities and limitations of 384-well formatted sample preparation technologies applied to regulated bioanalysis were evaluated by developing two assays for the simultaneous quantitation of lopinavir and ritonavir, the active...
9.
Chang M, Kim E, El-Shourbagy T
Rapid Commun Mass Spectrom
. 2006 Jun;
20(14):2190-200.
PMID: 16791866
Cross-contamination among wells of a high-throughput, high-density assay is a risk that cannot be detected or controlled by the performance of calibration standards and quality control samples. In the current...
10.
Carr R, Andre A, Chen P, Grabowski B, Chang M, Locke C, et al.
Nephron Clin Pract
. 2006 Mar;
103(3):c100-5.
PMID: 16534233
Background/aims: Paricalcitol is highly protein bound, extensively metabolized and eliminated primarily by hepatobiliary excretion. This study was designed to determine if hepatic disease alters the pharmacokinetics or affects the safety...