Search Results - "Gao, G.P"

Study of a compact ring monopole UWB antenna with band-notched characteristic by Yang, M. K., Gao, G.P., Niu, S. F., Zhang, J. S.

“…In this article, a printed ring shaped monopole ultra‐wideband antenna with band‐notched feature is presented and investigated. To get the band‐notched…”
Get full text

New Candidate Vaccines against Blood-Stage Plasmodium falciparum Malaria: Prime-Boost Immunization Regimens Incorporating Human and Simian Adenoviral Vectors and Poxviral Vectors Expressing an Optimized Antigen Based on Merozoite Surface Protein 1 by Goodman, Anna L, Epp, C, Moss, D, Holder, A.A, Wilson, J.M, Gao, G.P, Long, C.A, Remarque, E.J, Thomas, A.W, Ammendola, V, Colloca, S, Dicks, M.D.J, Biswas, S, Seibel, D, van Duivenvoorde, L.M, Gilbert, S.C, Hill, A.V.S, Draper, S.J

“…Although merozoite surface protein 1 (MSP-1) is a leading candidate vaccine antigen for blood-stage malaria, its efficacy in clinical trials has been limited…”
Get full text

Induction of CD8+ T cells to an HIV-1 antigen upon oral immunization of mice with a simian E1-deleted adenoviral vector by Pinto, A.R., Fitzgerald, J.C., Gao, G.P., Wilson, J.M., Ertl, H.C.J.

“…An E1-deleted adenoviral recombinant derived from the chimpanzee serotype 6 expressing a codon-optimized truncated form of gag of human immunodeficiency virus…”
Get full text

Canavan disease : mutations among Jewish and non-Jewish patients by RAJINDER KAUL, GAO, G. P, ALOYA, M, KUPPAREDDI BALAMURUGAN, PETROSKY, A, MICHALS, K, MATALON, R

“…Canavan disease is an autosomal recessive leukodystrophy caused by the deficiency of aspartoacylase (ASPA). Sixty-four probands were analyzed for mutations in…”
Get full text

T Helper Cell-Independent Antibody Responses to the Transgene Product of an E1-Deleted Adenoviral Vaccine Require NK1.1 T Cells by Xiang, Z.Q., Gao, G.P., Li, Y., Wilson, J.M., Ertl, H.CJ

“…Mice lacking CD4+ T cells due to a knock-out mutation respond to vaccination with a replication-defective adenoviral recombinant expressing the glycoprotein of…”
Get full text

Canavan disease: genomic organization and localization of human ASPA to 17p13-ter and conservation of the ASPA gene during evolution by Kaul, R, Balamurugan, K, Gao, G P, Matalon, R

“…Canavan disease, or spongy degeneration of the brain, is a severe leukodystrophy caused by the deficiency of aspartoacylase (ASPA). Recently, a missense…”
Get more information