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Polyomaviruses
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This chapter discusses polyomaviruses, which have been the object of intense study investigating how cells become transformed into tumour cells and also other basic parameters of cellular RNA and DNA synthesis. Like papillomaviruses, the viruses of this family are widespread in the community, but unlike papillomaviruses, their disease impact is very small. The chapter highlights the polyomavirus genomes, which have compact regulatory regions and a number of overlapping genes to compensate for the small size of the genome, which is only 5.3kb coding for 68 proteins. The three regions of the genome are the non-coding region (NCCR), which contains the origin of replication (ori), and the early and late coding regions. The chapter details how polyomaviruses bind to sialic acid-containing glycoproteins and gangliosides, and enter cells by endocytosis of specialized vesicles called caveolae.
Title: Polyomaviruses
Description:
This chapter discusses polyomaviruses, which have been the object of intense study investigating how cells become transformed into tumour cells and also other basic parameters of cellular RNA and DNA synthesis.
Like papillomaviruses, the viruses of this family are widespread in the community, but unlike papillomaviruses, their disease impact is very small.
The chapter highlights the polyomavirus genomes, which have compact regulatory regions and a number of overlapping genes to compensate for the small size of the genome, which is only 5.
3kb coding for 68 proteins.
The three regions of the genome are the non-coding region (NCCR), which contains the origin of replication (ori), and the early and late coding regions.
The chapter details how polyomaviruses bind to sialic acid-containing glycoproteins and gangliosides, and enter cells by endocytosis of specialized vesicles called caveolae.
Related Results
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Abstract
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Abstract
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Abstract
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Case-control study: Unveiling human polyomaviruses and papillomavirus in Egyptian colorectal cancer patients
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Human Polyomaviruses
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Abstract
Polyomaviruses (PyVs) were discovered in the 1950s as infectious agents that pass bacterium‐tight filters and form different tumors in rodents, hence their name....

