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Huichen Feng

Researcher at University of Pittsburgh

Publications -  38
Citations -  6547

Huichen Feng is an academic researcher from University of Pittsburgh. The author has contributed to research in topics: Merkel cell polyomavirus & Cell culture. The author has an hindex of 26, co-authored 35 publications receiving 6083 citations. Previous affiliations of Huichen Feng include University of Hong Kong.

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Journal ArticleDOI

Human Merkel cell polyomavirus infection II. MCV is a common human infection that can be detected by conformational capsid epitope immunoassays

TL;DR: It is demonstrated that Merkel cell polyomavirus is a widespread but previously unrecognized human infection and MCC patients have a markedly elevated MCV IgG response compared with control patients.
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Establishment of two immortalized nasopharyngeal epithelial cell lines using SV40 large T and HPV16E6/E7 viral oncogenes

TL;DR: Two immortalized NP cell lines are established using SV40T and HPV16E6/E7 oncogenes and showed that these two cell lines contained multiple genetic alterations, some of which have been described in NPC, which provide a possible cell model system for studying the mechanisms involved in the tumorigenesis of NPC.
Journal Article

Significance of MAD2 expression to mitotic checkpoint control in ovarian cancer cells.

TL;DR: It is suggested that the steady-state amount of MAD2 inside cells may represent a molecular switch for mitotic checkpoint control and provide a novel insight into the molecular basis of CIN in ovarian carcinoma and has implications for effective use of checkpoint-targeting drugs.
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Merkel Cell Polyomavirus Small T Antigen Controls Viral Replication and Oncoprotein Expression by Targeting the Cellular Ubiquitin Ligase SCFFbw7

TL;DR: SCF(Fbw7) knockdown mimics sT-mediated stabilization of LT, but this knockdown is insufficient to fully reconstitute the transforming activity of a mutant LSD sT protein.
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Survivin Is a Therapeutic Target in Merkel Cell Carcinoma

TL;DR: Genetic data can be applied to help identify the cause of a cancer and thus point the way to new targets that can be exploited therapeutically, as well as identifying the molecular pathway that is activated in MCC cells by this virus.