Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Cheng Yang Ng"'
Autor:
Hong Liu, Cheng Yang Ng, Qinde Liu, Tang Lin Teo, Tze Ping Loh, Moh Sim Wong, Sunil Kumar Sethi, Jun Guan Tan, Ping Ying Heng, Sharon Saw, Leslie Choong-Weng Lam, Joanne Mee-Yin Lee, Khairee Bin Khaled, Hnin Pwint Phyu, Noel Wan Ting Ong
Publikováno v:
Analytical and Bioanalytical Chemistry. 415:787-800
Urine albumin concentration and albumin-creatinine ratio are important for the screening of early-stage kidney damage. Commutable urine certified reference materials (CRMs) for albumin and creatinine are necessary for standardization of urine albumin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58725e965b5b043d267e5acf0d0f9964
https://doi.org/10.1007/s00216-022-04472-y
https://doi.org/10.1007/s00216-022-04472-y
Autor:
Katherine C. M. Chew, Chou Chai, Byorn W.L. Tan, Chao Liu, Han-Ming Shen, Ping Liao, Cheng Yang Ng, Sreedharan Sajikumar, Y. L. Lam, Bryce W.Q. Tan, Steven Yuan, Mui Cheng Liang, Tuck Wah Soong, Sheeja Navakkode, Shi Yin, Esther Wong, Sijie Tan, Yee Kit Tai, Kah-Leong Lim
Mammalian Target of Rapamycin (mTOR) is a master regulator of autophagy and lysosomes, and its downstream kinase-dependent pathways have been extensively characterized. Here, we report an unexpected kinase-independent regulation of autophagy and lyso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::07d48768b77111b5ade0e8725e745b15
https://doi.org/10.1101/2020.09.11.292607
https://doi.org/10.1101/2020.09.11.292607
Autor:
Wee Yong Ong, Yulin Lam, Mei-Lin Go, Yong Jun Chen, Francis Chee Kuan Tan, Chandra S. Verma, Chian-Ming Low, Srinivasaraghavan Kannan, Cheng Yang Ng
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Cytosolic phospholipase A2 (cPLA2) is an enzyme that releases arachidonic acid (AA) for the synthesis of eicosanoids and lysophospholipids which play critical roles in the initiation and modulation of oxidative stress and neuroinflammation. In the ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01798ee664b60960be748a5d1326f3b2
http://link.springer.com/article/10.1038/s41598-017-13996-8
http://link.springer.com/article/10.1038/s41598-017-13996-8
Publikováno v:
Chemical Communications. 53:1813-1816
Arachidonic acid derivatives equipped with either one or two fluorescent groups attached to the tip of the alkyl chains were synthesized and shown to function as inhibitor and substrate probes of cPLA2. The inhibitor probe was demonstrated to perform
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f8aed67a3b7ba9b619201fb72a95ed0
https://doi.org/10.1039/c6cc09305a
https://doi.org/10.1039/c6cc09305a
Autor:
Cheng Yang, Ng, Srinivasaraghavan, Kannan, Yong Jun, Chen, Francis Chee Kuan, Tan, Wee Yong, Ong, Mei Lin, Go, Chandra S, Verma, Chian-Ming, Low, Yulin, Lam
Publikováno v:
Scientific Reports
Cytosolic phospholipase A2 (cPLA2) is an enzyme that releases arachidonic acid (AA) for the synthesis of eicosanoids and lysophospholipids which play critical roles in the initiation and modulation of oxidative stress and neuroinflammation. In the ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::412845a062e3c67a3def68ac4a50dc21
https://pubmed.ncbi.nlm.nih.gov/29057981
https://pubmed.ncbi.nlm.nih.gov/29057981
Publikováno v:
Chemical communications (Cambridge, England). 53(11)
Arachidonic acid derivatives equipped with either one or two fluorescent groups attached to the tip of the alkyl chains were synthesized and shown to function as inhibitor and substrate probes of cPLA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::425762db94f4112e286f3d8c6c6924cb
https://pubmed.ncbi.nlm.nih.gov/28106899
https://pubmed.ncbi.nlm.nih.gov/28106899
Publikováno v:
Nature Communications
Two voltage-gated calcium channel subtypes—CaV1.2 and CaV1.3—underlie the major L-type Ca2+ currents in the mammalian central nervous system. Owing to their high sequence homology, the two channel subtypes share similar pharmacological properties
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d490e646c249c840ab3bf7bfbc055cd
https://pubmed.ncbi.nlm.nih.gov/25057870
https://pubmed.ncbi.nlm.nih.gov/25057870