about
Cytotoxicity and apoptotic activities of alpha-, gamma- and delta-tocotrienol isomers on human cancer cells.Prevention of cell-surface attachment and reduction of penicillin-binding protein 2a (PBP2a) level in methicillin-resistant Staphylococcus aureus biofilms by Acalypha wilkesiana.Inhibition of penicillin-binding protein 2a (PBP2a) in methicillin resistant Staphylococcus aureus (MRSA) by combination of ampicillin and a bioactive fraction from Duabanga grandiflora.The antimalarial drug quinine interferes with serotonin biosynthesis and action.Biologically active vallesamine, strychnan, and rhazinilam alkaloids from Alstonia: Pneumatophorine, a nor-secovallesamine with unusual incorporation of a 3-ethylpyridine moiety.Hispidacine, an unusual 8,4'-oxyneolignan-alkaloid with vasorelaxant activity, and hispiloscine, an antiproliferative phenanthroindolizidine alkaloid, from Ficus hispida Linn.Antiproliferation and induction of caspase-8-dependent mitochondria-mediated apoptosis by β-tocotrienol in human lung and brain cancer cell lines.Crude Ethanol Extract of Pithecellobium ellipticum as a Potential Lipid-Lowering Treatment for HypercholesterolaemiaSearch for antibacterial agents from Malaysian rainforest and tropical plants.Acalypha wilkesiana extracts induce apoptosis by causing single strand and double strand DNA breaks.High Correlation of 2,2-diphenyl-1-picrylhydrazyl (DPPH) Radical Scavenging, Ferric Reducing Activity Potential and Total Phenolics Content Indicates Redundancy in Use of All Three Assays to Screen for Antioxidant Activity of Extracts of Plants fromInhibitory effect of Duabanga grandiflora on MRSA biofilm formation via prevention of cell-surface attachment and PBP2a production.Reply to "chloroquine, an antifungal but also a fertility drug".Cell wall perturbation sensitizes fungi to the antimalarial drug chloroquine.Reversal of ampicillin resistance in MRSA via inhibition of penicillin-binding protein 2a by Acalypha wilkesiana.Studies on the vasoconstrictor action of melatonin and putative melatonin receptor ligands in the tail artery of juvenile Wistar rats.Rilmenidine reveals differences in the pharmacological characteristics of prejunctional alpha2-adrenoceptors in the guinea-pig, rat and pig.Heterologous Expression of a Novel Drug Transporter from the Malaria Parasite Alters Resistance to Quinoline Antimalarials.Convergence of tuberculosis and diabetes mellitus: time to individualise pharmaceutical care.Arboridinine, a Pentacyclic Indole Alkaloid with a New Cage Carbon-Nitrogen Skeleton Derived from a Pericine Precursor.Contractile function of smooth muscle retained after overnight storage.Optimal methods for evaluating antimicrobial activities from plant extracts.Data on the Lignosus rhinocerotis water soluble sclerotial extract affecting intracellular calcium level in rat dorsal root ganglion cells.Airway Relaxation Effects of Water-Soluble Sclerotial Extract From Lignosus rhinocerotis.Community pharmacists' views on adverse drug reactions reporting in Malaysia: a pilot studyPharmacological studies on the inhibitory action of melatonin and putative melatonin analogues on porcine vascular smooth muscleCriofolinine and vernavosine, new pentacyclic indole alkaloids incorporating pyrroloazepine and pyridopyrimidine moieties derived from a common yohimbine precursorBronchodilator effects of Lignosus rhinocerotis extract on rat isolated airways is linked to the blockage of calcium entryAlstoscholactine and Alstolaxepine, Monoterpenoid Indole Alkaloids with γ-Lactone-Bridged Cycloheptane and Oxepane Moieties from Alstonia scholaris
P50
Q34968717-3B560F07-3CFF-4FC2-9997-F0FA2CABAEECQ35603611-E9BCD8C2-4429-49D4-BC8F-9F278834C051Q35659236-3A0975EE-53D5-4074-BB8E-324E0CAE310AQ37453950-969B23D5-3384-42F6-BCBA-AEC16667B31CQ38858460-1CC9EF8F-61F1-43B0-85C2-0C897D986ED5Q38932751-A87445D8-989F-4E85-8B6A-4BFAFB6ACC74Q38933975-383CB61D-15CE-4F9F-8D46-750A77475233Q39198784-3F202A47-F4D6-4054-BCD4-81BBCCA4F124Q39329720-05E0ACED-298C-462A-8F81-05F83FBBAD3DQ39456348-16CF9A53-A035-42AE-B40C-3BD90B3BDFCAQ40085657-B0EFE530-E7A8-4A36-9ACA-493D08D92785Q41435498-22975009-1A07-42DC-B9C8-7404A12A4636Q41790156-EF7DCC43-9DF4-4AB4-AD62-E6F13800B421Q41925517-1D7772FA-B36A-4B7D-AF07-10D1E9A40266Q42181134-3E4D86C5-8BCF-4CD7-A19B-1F9E71C35615Q43179062-2559CB74-E631-43CC-9FE1-652E15538209Q43185291-E4D9C22C-BC0C-47BC-AB92-532F6DC1B4C2Q48095893-D8B20FC7-4070-46CA-9A37-41D1DA1A3263Q51498089-F40D3F92-2C6D-426B-938B-D44FC3A146F9Q53181074-CEE81DA5-57EA-41BC-87C8-FF295DB463B8Q53475445-6D2D476B-AB1C-40EB-AAC6-CC10777925F5Q54375369-2446DCA9-6834-4C27-89D8-986117E8E9A7Q55315170-77C0B5C3-EA76-45A5-AA07-19FE65707DDDQ55344462-A0BA7536-B799-46E2-9EDC-C0089B576B9DQ56779793-98935F1C-4C6A-4F49-9456-86470AA5748FQ73579560-874D719E-0757-4FCE-BB14-DC1D1D97A9B9Q86122658-24745D85-DDAF-4C33-8FCB-1C014147187FQ88360343-367011F1-D0D6-4C9A-B170-742858F61EB2Q90447006-789C2319-EEE1-4851-9B00-C617FF3B1797
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Kang Nee Ting
@ast
Kang Nee Ting
@en
Kang Nee Ting
@es
Kang Nee Ting
@nl
type
label
Kang Nee Ting
@ast
Kang Nee Ting
@en
Kang Nee Ting
@es
Kang Nee Ting
@nl
prefLabel
Kang Nee Ting
@ast
Kang Nee Ting
@en
Kang Nee Ting
@es
Kang Nee Ting
@nl
P106
P1153
35753971600
P31
P496
0000-0002-7818-3922