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| 1 | Analysis of Glyphosate, Glufosinate and Aminomethylphosphonic Acid by Capillary Electrophoresis with Indirect Fluorescence Detection显示文摘 | SARAH Y C CHIA-HUNG L | 2002 | Journal of Chromatoqraphy A2002，959，12： | 1 |
| 2 | Design of cylcohexane oxidation process using multiple neural networks显示文摘 | SARAH S Y L ALICE E S BADIE I MORSI | 2001 | J of Manufacturing Systems2001，1，： | 1 |
| 3 | Analysis of xyloglucan endotransglucosylase/hydrolase (XTH) gene families in kiwifruit and apple 显示文摘 | Ross G A Sarah L J Yar- Khing Y | 2009 | Postharvest Biology and Technology2009，51，2： | 1 |
| 4 | Cytokine-modified Mycobacterium smegmatis as a Novel anticancer immunotherapy显示文摘 | Sarah L Y Michaei M Zhu X W | 2004 | Int J Cancer2004，112，： | 1 |
| 5 | Transcutaneous vaccination with virus-like particles显示文摘 | Sarah L Y Michelle W Sarah W | 2006 | Vaccine2006，24，： | 1 |
| 6 | Methicillin-resistant Staphylococus aureus,Hwwaii,2000~2002显示文摘 | Li Fenfang Sarah Y Park Tracy L Ayers | 2005 | Emerg lnfect Dis2005，11，8： | 1 |
| 7 | Childhood trauma and risk for PTSD:Relationship to intergenerational effects of trauma,parental PTSD,and cortisol excretion显示文摘 | Rachel Y Sarah L Halligan R G | 2001 | Dev Psychopathol2001，13，3： | 1 |
| 8 | Methicillin-resistant staphylococcus aureus, Hawaii, 2000-2002显示文摘 | Li F Sarah Y P Ayers T L | 2005 | Emerg Infeet Dis2005，11，： | 1 |
| 9 | Non-nuclear estrogen receptor [alpha] signaling promotes cardiovascular protection but not uterine or breast cancer growth in mice显示文摘 | Chambliss Ken L Wu Qian Oltmann Sarah Konaniah Eddy S Umetani Michihisa Korach Kenneth S Thomas Gail D Mineo Chieko Yuhanna Ivan S Kim Sung Hoon Madak-Erdogan Zeynep Maggi Adriana Dineen Sean P Roland Christina L Hui David Y Brekken Rolf A | 2010 | Journal of Clinical Investigation2010，，7： | 1 |
| 10 | Analysis of glyphosate, glufosinate and aminomethylphosphonic acid by capillary electrophoresis with indirect fluorescence detection显示文摘 | SARAH Y C CHIA H L | 2002 | J Chromatoqr A2002，959，12： | 1 |
| 11 | Identification and differentiation of PDX1 β-cell progenitors within the human pancreatic epithelium显示文摘AIM:To minimize the expansion of pancreatic mesenchymal cells in vitro and confirm thatβ-cell progenitors reside within the pancreatic epithelium.METHODS:Due to mesenchymal stem cell(MSC)expansion and overgrowth,progenitor cells within the pancreatic epithelium cannot be characterized in vitro,thoughβ-cell dedifferentiation and expansion of MSC intermediates via epithelial-mesenchymal transition(EMT)may generateβ-cell progenitors.Pancreatic epithelial cells from endocrine and non-endocrine tissue were expanded and differentiated in a novel pancreatic epithelial expansion medium supplemented with growth factors known to support epithelial cell growth(dexamethasone,epidermal growth factor,3,5,3’-triiodo-l-thyronine,bovine brain extract).Cells were also infected with a single and dual lentiviral reporter prior to cell differentiation.Enhanced green fluorescent protein was controlled by the rat Insulin 1 promoter and the monomeric red fluorescent protein was controlled by the mouse PDX1 promoter.In combination with lentiviral tracing,cells expanded and differentiated in the pancreatic medium were characterized by flow cytometry(BD fluorescence activated cell sorting),immunostaining and real-time polymerase chain reaction(PCR)(7900HT Fast Realtime PCR System).RESULTS:In the presence of 10%serum MSCs rapidly expand in vitro while the epithelial cell population declines.The percentage of vimentin+cells increased from 22%±5.83%to 80.43%±3.24%(14 d)and99.00%±0.0%(21 d),and the percentage of epithelial cells decreased from 74.71%±8.34%to 26.57%±9.75%(14 d)and 4.00%±1.53%(21 d),P<0.01 for all time points.Our novel pancreatic epithelial expansion medium preserved the epithelial cell phenotype and minimized epithelial cell dedifferentiation and EMT.Cells expanded in our epithelial medium contained significantly less mesenchymal cells(vimentin+)compared to controls(44.87%±4.93%vs 95.67%±1.36%;P<0.01).During cell differentiation lentiviral reporting demonstrated that,PDX1+and insulin+cells were localized within adherent epithelial cell aggregates compared to controls.Compared to starting islets differentiated cells had at least two fold higher gene expression of PDX1,insulin,PAX4 and RFX(P<0.05).CONCLUSION:PDX1+cells were confined to adherent epithelial cell aggregates and not vimentin+cells(mesenchymal),suggesting that EMT is not a mechanism for generating pancreatic progenitor cells. | Karen L Seeberger Sarah J Anderson Cara E Ellis Telford Y Yeung Gregory S Korbutt | 2014 | World Journal of Diabetes2014，5，1： | 0 |
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