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Jan Erikson

Researcher at Wistar Institute

Publications -  82
Citations -  8525

Jan Erikson is an academic researcher from Wistar Institute. The author has contributed to research in topics: T cell & B cell. The author has an hindex of 45, co-authored 82 publications receiving 8148 citations.

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Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells

TL;DR: Using a DNA probe that is specific for the complete gene (c-myc), different somatic cell hybrids possessing varying numbers of human chromosomes were analyzed by the Southern blotting technique and results indicate that the human c- myc gene is located on chromosome 8.
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Commensal Bacteria Calibrate the Activation Threshold of Innate Antiviral Immunity

TL;DR: It is demonstrated that antibiotic-treated ABX mice exhibit impaired innate and adaptive antiviral immune responses and substantially delayed viral clearance after exposure to systemic LCMV or mucosal influenza virus, indicating that commensal-derived signals provide tonic immune stimulation that establishes the activation threshold of the innate immune system required for optimal antiviral immunity.
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Translocation and Rearrangements of the c-myc Oncogene Locus in Human Undifferentiated B-Cell Lymphomas

TL;DR: It is shown in this study that the c- myc locus is rearranged in 5 out of 15 cell lines from patients with undifferentiated B-cell lymphomas, and that the rearrangement involves a region at the 5' side of an apparently intact c-myc gene.
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Transcriptional activation of the translocated c-myc oncogene in Burkitt lymphoma

TL;DR: The translocation of a c-myc oncogene to the heavy chain locus on human chromosome 14 is apparently sufficient for its transcriptional activation and may be an essential step in the pathway leading to neoplasia.
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Gene for alpha-chain of human T-cell receptor: location on chromosome 14 region involved in T-cell neoplasms

TL;DR: The locus for the alpha-chain T-cells receptor may participate in oncogene activation in T-cell tumors through translocations and inversions detectable in human T- cell leukemias and lymphomas.