1  non-intestinal epithelium from the bursa of Fabricius.

2 us rapidly destroyed B cells in the bursa of Fabricius.

3 opmentally regulated in the chicken bursa of Fabricius.

4 es place in GALT, such as the avian bursa of Fabricius.

5 e the cellular homolog of the avian bursa of Fabricius.

6 uring B cell development within the bursa of Fabricius, a lymphoid organ unique to birds.

7 levels are particularly high in the bursa of Fabricius and comparatively low in ovarian follicles at

8 cal changes in the large intestine, bursa of Fabricius, and cecal tonsil.

9 of the sugarcane borer, Diatraea saccharalis Fabricius, and historical and modern agricultural activi

10 especially prominent in the tongue, bursa of Fabricius, and trachea.

11 ung rabbit appendix and the chicken bursa of Fabricius are primary lymphoid organs where the B cell A

12  on epithelial cells of the chicken bursa of Fabricius, BEN is expressed in a variety of tissues duri

13 velopment; >95% of the cells in the bursa of Fabricius die without entering the secondary immune syst

14 eas IFITM1 is only expressed in the bursa of Fabricius, gastrointestinal tract, cecal tonsil, and tra

15 ulipennis Poppius and Liocoris tripustulatus Fabricius (Heteroptera: Miridae) are pests of glasshouse

16 on of B-lineage precursors into the bursa of Fabricius is unaffected, whereas development into mature

17         In follicles of the chicken bursa of Fabricius, myc induction of B-cell neoplasia requires a

18 ullorum preferentially targeted the bursa of Fabricius prior to eliciting intestinal inflammation.

19                           The avian bursa of Fabricius provides an essential microenvironment for B c

20      B cells removed from the avian bursa of Fabricius rapidly undergo cell death in culture.

21 ssion in the tongue, esophagus, and bursa of Fabricius was unaffected.