neoplasm
• mice develop tumors after 15.5 weeks of age, with a complete shift towards hematopoietic neoplastic lesions (100%), mainly precursor T-cell lymphoma (85.7%)
• T-cell antigen receptor rearrangement analysis suggests either mono- or oligoclonal origin for all the thymic tumors
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endocrine/exocrine glands
• mice develop tumors after 15.5 weeks of age, with a complete shift towards hematopoietic neoplastic lesions (100%), mainly precursor T-cell lymphoma (85.7%)
• T-cell antigen receptor rearrangement analysis suggests either mono- or oligoclonal origin for all the thymic tumors
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hematopoietic system
• mice develop tumors after 15.5 weeks of age, with a complete shift towards hematopoietic neoplastic lesions (100%), mainly precursor T-cell lymphoma (85.7%)
• T-cell antigen receptor rearrangement analysis suggests either mono- or oligoclonal origin for all the thymic tumors
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immune system
• mice develop tumors after 15.5 weeks of age, with a complete shift towards hematopoietic neoplastic lesions (100%), mainly precursor T-cell lymphoma (85.7%)
• T-cell antigen receptor rearrangement analysis suggests either mono- or oligoclonal origin for all the thymic tumors
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