Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Hui Emma Zhang"'
Autor:
Hui Chen, Gerard Li, Yik Lung Chan, Hui Emma Zhang, Mark D. Gorrell, Carol A. Pollock, Sonia Saad, Brian G. Oliver
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Tobacco smoking increases the risk of metabolic disorders due to the combination of harmful chemicals, whereas pure nicotine can improve glucose tolerance. E-cigarette vapour contains nicotine and some of the harmful chemicals found in cigarette smok
Externí odkaz:
https://doaj.org/article/6daccfcfd4374bfc99055b30083d175c
Autor:
Cecy R Xi, Arianna Di Fazio, Naveed Ahmed Nadvi, Karishma Patel, Michelle Sui Wen Xiang, Hui Emma Zhang, Chandrika Deshpande, Jason K K Low, Xiaonan Trixie Wang, Yiqian Chen, Christopher L D McMillan, Ariel Isaacs, Brenna Osborne, Ana Júlia Vieira de Ribeiro, Geoffrey W McCaughan, Joel P Mackay, W Bret Church, Mark D Gorrell
Publikováno v:
Molecules, Vol 25, Iss 22, p 5392 (2020)
Proteases catalyse irreversible posttranslational modifications that often alter a biological function of the substrate. The protease dipeptidyl peptidase 4 (DPP4) is a pharmacological target in type 2 diabetes therapy primarily because it inactivate
Externí odkaz:
https://doaj.org/article/fa9dcf2606954561b940299e84274b4d
Autor:
Gerard Li, Hui Chen, Carol A. Pollock, Sonia Saad, Brian G. Oliver, Hui Emma Zhang, Mark D. Gorrell, Yik Lung Chan
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
Frontiers in Physiology
Frontiers in Physiology
Tobacco smoking increases the risk of metabolic disorders due to the combination of harmful chemicals, whereas pure nicotine can improve glucose tolerance. E-cigarette vapour contains nicotine and some of the harmful chemicals found in cigarette smok
Autor:
Michelle Sui Wen Xiang, James G. Kench, Hui Emma Zhang, Jiali Carrie Huang, Stefanie Wetzel, Mark D. Gorrell, Geoffrey W. McCaughan, Wengen Wu, Ben Roediger, Linxuan Jiang, William W. Bachovchin, James M. Henderson, Jack H. Lai
Publikováno v:
Cancers, Vol 13, Iss 5495, p 5495 (2021)
Cancers
Volume 13
Issue 21
Cancers
Volume 13
Issue 21
Simple Summary This study reported, for the first time, on the expression and activity of the dipeptidyl peptidase 4 (DPP4) family during the development of hepatocellular carcinoma (HCC). We also demonstrated that the pan-DPP inhibitory compound ARI
Autor:
Hui Emma Zhang, Quintin Lee, Mark D. Gorrell, Christopher J. Jolly, Adam Cook, Ben Roediger, Margaret G. Gall, Geoffrey W. McCaughan
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-10 (2019)
Scientific Reports
Scientific Reports
The ubiquitous intracellular protease dipeptidyl peptidase 9 (DPP9) has roles in antigen presentation and B cell signaling. To investigate the importance of DPP9 in immune regeneration, primary and secondary chimeric mice were created in irradiated r
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1865:993-1002
Hepatocellular carcinoma (HCC) represents ~90% of all cases of primary liver cancer and occurs predominantly in patients with underlying chronic liver disease and cirrhosis. Establishing appropriate animal models for HCC is required for basic and tra
Publikováno v:
Frontiers in Bioscience. 24:1-17
Fibroblast activation protein (FAP) belongs to the dipeptidyl peptidase IV (DPP4; CD26) gene family. Other related genes in this family of enzyme include DPP4, 8 and 9. The FAP serine protease has the rare property of both dipeptidyl peptidase and en
Autor:
Arianna Di Fazio, W. Bret Church, Michelle Sui Wen Xiang, Xin Maggie Wang, Cecy R. Xi, Hui Emma Zhang, Charles G. Bailey, Geoffrey W. McCaughan, Chandrika N. Deshpande, Yiqian Chen, Naveed A. Nadvi, Mehdi Sharifi Tabar, Mark D. Gorrell
Publikováno v:
Protein expression and purification. 181
Fibroblast activation protein alpha (FAP) is a cell-surface expressed type II glycoprotein that has a unique proteolytic activity. FAP has active soluble forms that retain the extracellular portion but lack the transmembrane domain and cytoplasmic ta
Autor:
Ana Julia Vieira de Ribeiro, Cecy R. Xi, Ariel Isaacs, Christopher L. D. McMillan, Arianna Di Fazio, K. Patel, Michelle Sui Wen Xiang, Mark D. Gorrell, Geoffrey W. McCaughan, Chandrika N. Deshpande, W. Bret Church, Joel P. Mackay, Brenna Osborne, Naveed A. Nadvi, Hui Emma Zhang, Yiqian Chen, Xiaonan Trixie Wang, Jason Low
Publikováno v:
Molecules
Molecules, Vol 25, Iss 5392, p 5392 (2020)
Volume 25
Issue 22
Molecules, Vol 25, Iss 5392, p 5392 (2020)
Volume 25
Issue 22
Proteases catalyse irreversible posttranslational modifications that often alter a biological function of the substrate. The protease dipeptidyl peptidase 4 (DPP4) is a pharmacological target in type 2 diabetes therapy primarily because it inactivate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5967ba4b1c4b2fd7da292bf6872c7dff
https://doi.org/10.20944/preprints202009.0390.v2
https://doi.org/10.20944/preprints202009.0390.v2
Autor:
Cecy Xi, Arianna Arianna Di Fazio, Naveed Nadvi, Karishma Patel, Michelle Xiang, Hui Emma Zhang, Chandrika Deshpande, Jason Low, Xiaonan Trixie Wang, Yiqian Chen, Brenna Osborne, Ana Julia Vieira de Ribeiro, Geoffrey McCaughan, Bret Church, Joel Mackay, Mark Gorrell
Proteases catalyse irreversible posttranslational modifications that often alter a biological function of the substrate. The protease dipeptidyl peptidase 4 (DPP4) is a pharmacological target in type 2 diabetes therapy primarily because it inactivate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03cf9e8b14599de6680f037b14ba15a6
https://doi.org/10.20944/preprints202009.0390.v1
https://doi.org/10.20944/preprints202009.0390.v1