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B F Feng

Publications and source records attributed to B F Feng.

3 recordsLinked to original sources

Stabilized Kuramoto-Sivashinsky system.

A model consisting of a mixed Kuramoto-Sivashinsky-Korteweg-de Vries equation, linearly coupled to an extra linear dissipative equation, is proposed. The model applies to a description of surface waves on multilayered liquid films. The extra equation makes it possible to stabilize the zero solution in the model, thus opening the way to the existence of stable solitary pulses. By means of perturbation theory, treating the dissipation and the instability-generating gain in the model (but not the linear coupling between the two waves) as small perturbations, and making use of the balance equation for the net momentum, we demonstrate that the perturbations may select two steady-state solitons from their continuous family existing in the absence of the dissipation and gain. In this case, the selected pulse with the larger value of the amplitude is expected to be stable, provided that the zero solution is stable. The prediction is completely confirmed by direct simulations. If the integration domain is not very large, some pulses are stable even when the zero background is unstable. An explanation for the latter finding is proposed. Furthermore, stable bound states of two and three pulses are found numerically.

Journal Article↗

Hepatitis C virus in human B lymphocytes transformed by Epstein-Barr virus in vitro by in situ reverse transcriptase-polymerase chain reaction.

AIM: To study persistence and replication of hepatitis C virus (HCV) in patients' peripheral blood mononuclear cells (PBMC) cultured in vitro. METHODS: Epstein Barr virus (EBV) was used to transform the hepatitis C virus from a HCV positive patient to permanent lymphoblastoid cell lines (LCL). Positive and negative HCV RNA strands of the cultured cells and growth media were detected by reverse transcriptase-polymerase chain reaction (RT-PCR) each month. Core and NS5 proteins of HCV were further tested using immunohistochemical SP method and in situ RT-PCR. RESULTS: HCV RNA positive strands were consistently detected the cultured cells for one year. The negative-strand RNA in LCL cells and the positive-strand RNA in supernatants were observed intermittently. Immunohistochemical results medicated expression of HCV NS3 and C proteins in LCL cytoplasm mostly. The positive signal of PCR product was dark blue and mainly localized to the LCL cytoplasm. The RT-PCR signal was eliminated by overnight RNase digestion but not DNase digestion. CONCLUSION: HCV may exist and remain functional in a cultured cell line for a long period.

B-Lymphocytes↗