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H Hua

Showing results (121-130 of 283) with videos related to

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Clinical and Experimental Rheumatology|April 19, 2012
The role of muscarinic acetylcholine receptor type 3 polypeptide (M3RP205-220) antibody in the saliva of patients with primary Sjögren's syndromeJ He, L Qiang, Y Ding, et al.
Multiple Sclerosis and Related Disorders|June 6, 2025
De-escalation of disease modifying therapies: A retrospective, observational single center studyCarolyn Goldschmidt, Jordan Glassman, Brandon Ly, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|April 5, 2005
Anteroposterior somatotopy of innocuous cooling activation focus in human dorsal posterior insular cortexLe H Hua, Irina A Strigo, Leslie C Baxter, et al.
Journal of Molecular Neuroscience : MN|September 6, 2002
Novel tricyclic pyrone compounds prevent intracellular APP C99-induced cell deathLee-Way Jin, Duy H Hua, Feng-Shiun Shie, et al.
The Journal of Organic Chemistry|July 12, 1996
Enantioselective Synthesis of Sulfur- Containing 1,2-Disubstituted Ferrocenes(1)Duy H. Hua, Nadège M. Lagneau, Yi Chen, et al.
Journal of Medicinal Chemistry|October 3, 2012
Inhibition of Acyl-CoA: cholesterol acyltransferase (ACAT), overexpression of cholesterol transporter gene, and protection of amyloid β (Aβ) oligomers-induced neuronal cell death by tricyclic pyrone moleculesLaxman Pokhrel, Izumi Maezawa, Thi D T Nguyen, et al.
Anti-Cancer Drugs|September 7, 1999
Tricyclic pyrone analogs: a new synthetic class of bifunctional anticancer drugs that inhibit nucleoside transport, microtubule assembly, the viability of leukemic cells in vitro and the growth of solid tumors in vivoE M Perchellet, J B Ladesich, M J Magill, et al.
Anti-Cancer Drugs|July 27, 2000
1,4-Anthraquinone: an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitroE M Perchellet, M J Magill, X Huang, et al.
Plos One|June 19, 2013
Bioavailability and efficacy of a gap junction enhancer (PQ7) in a mouse mammary tumor modelStephanie N Shishido, Keshar Prasain, Amanda Beck, et al.
Anti-Cancer Drugs|October 30, 2004
Antitumor triptycene bisquinones induce a caspase-independent release of mitochondrial cytochrome c and a caspase-2-mediated activation of initiator caspase-8 and -9 in HL-60 cells by a mechanism which does not involve Fas signalingElisabeth M Perchellet, Yang Wang, Rebeka L Weber, et al.
Pageof 29

Showing results (121-130 of 283) with videos related to

Sort By:
Pageof 29
Clinical and Experimental Rheumatology|April 19, 2012
The role of muscarinic acetylcholine receptor type 3 polypeptide (M3RP205-220) antibody in the saliva of patients with primary Sjögren's syndromeJ He, L Qiang, Y Ding, et al.
Multiple Sclerosis and Related Disorders|June 6, 2025
De-escalation of disease modifying therapies: A retrospective, observational single center studyCarolyn Goldschmidt, Jordan Glassman, Brandon Ly, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|April 5, 2005
Anteroposterior somatotopy of innocuous cooling activation focus in human dorsal posterior insular cortexLe H Hua, Irina A Strigo, Leslie C Baxter, et al.
Journal of Molecular Neuroscience : MN|September 6, 2002
Novel tricyclic pyrone compounds prevent intracellular APP C99-induced cell deathLee-Way Jin, Duy H Hua, Feng-Shiun Shie, et al.
The Journal of Organic Chemistry|July 12, 1996
Enantioselective Synthesis of Sulfur- Containing 1,2-Disubstituted Ferrocenes(1)Duy H. Hua, Nadège M. Lagneau, Yi Chen, et al.
Journal of Medicinal Chemistry|October 3, 2012
Inhibition of Acyl-CoA: cholesterol acyltransferase (ACAT), overexpression of cholesterol transporter gene, and protection of amyloid β (Aβ) oligomers-induced neuronal cell death by tricyclic pyrone moleculesLaxman Pokhrel, Izumi Maezawa, Thi D T Nguyen, et al.
Anti-Cancer Drugs|September 7, 1999
Tricyclic pyrone analogs: a new synthetic class of bifunctional anticancer drugs that inhibit nucleoside transport, microtubule assembly, the viability of leukemic cells in vitro and the growth of solid tumors in vivoE M Perchellet, J B Ladesich, M J Magill, et al.
Anti-Cancer Drugs|July 27, 2000
1,4-Anthraquinone: an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitroE M Perchellet, M J Magill, X Huang, et al.
Plos One|June 19, 2013
Bioavailability and efficacy of a gap junction enhancer (PQ7) in a mouse mammary tumor modelStephanie N Shishido, Keshar Prasain, Amanda Beck, et al.
Anti-Cancer Drugs|October 30, 2004
Antitumor triptycene bisquinones induce a caspase-independent release of mitochondrial cytochrome c and a caspase-2-mediated activation of initiator caspase-8 and -9 in HL-60 cells by a mechanism which does not involve Fas signalingElisabeth M Perchellet, Yang Wang, Rebeka L Weber, et al.
Pageof 29