624 related articles for article (PubMed ID: 1101168)
1. Cells involved in the immune response. XXIX Establishment of optimal conditions for the primary and secondary immune responses by rabbit lymphoid cells in vitro.
Richter M; Behelak Y
Pathol Microbiol (Basel); 1975; 42(2):73-91. PubMed ID: 1101168
[TBL] [Abstract][Full Text] [Related]
2. Antibody formation in mouse bone marrow. V. The response to the thymus-independent antigen Ecsherichia coli lipopolysaccharide.
Benner R; van Oudenaren
Immunology; 1976 Jan; 30(1):49-57. PubMed ID: 765265
[TBL] [Abstract][Full Text] [Related]
3. Cells involved in the immune response. IV. The response of normal and immune rabbit bone marrow and lymphoid tissue lymphocytes to antigens in vitro.
Singhal SK; Richter M
J Exp Med; 1968 Nov; 128(5):1099-128. PubMed ID: 4176224
[TBL] [Abstract][Full Text] [Related]
4. The cells involved in cell-mediated and transplantation immunity in the normal outbred rabbit. X. The organ sources of the stimulator and responder cells in the mixed leukocyte culture reaction.
Milthorp P; Richter M
Immunology; 1979 Jan; 36(1):13-24. PubMed ID: 154469
[TBL] [Abstract][Full Text] [Related]
5. The influence of cyclophosphamide on antibody formation in the mouse.
Willers JM; Sluis E
Ann Immunol (Paris); 1975 Apr; 126(3):267-79. PubMed ID: 1101799
[TBL] [Abstract][Full Text] [Related]
6. Cells involved in the immune response. XXXI. The role of the spleen in the primary and secondary immune responses in the normal adult outbred rabbit: the initial localization of memory cells to the spleen and their subsequent dissemination to the thymus and peripheral lymph nodes.
Richter M; Berry M; Barron P
Clin Immunol Immunopathol; 1986 Jan; 38(1):101-10. PubMed ID: 3510099
[TBL] [Abstract][Full Text] [Related]
7. IgA responses in xid mice: oral antigen primes Peyer's patch cells for in vitro immune responses and secretory antibody production.
Kiyono H; Mosteller LM; Eldridge JH; Michalek SM; McGhee JR
J Immunol; 1983 Dec; 131(6):2616-22. PubMed ID: 6227659
[TBL] [Abstract][Full Text] [Related]
8. Demonstration of organ differences in peripheral B cell populations through the use of deficient fetal bovine serum.
Campbell SM; Kagnoff MF; Watson J
J Immunol; 1975 Mar; 114(3):992-6. PubMed ID: 803537
[TBL] [Abstract][Full Text] [Related]
9. Cells involved in the immune response. XXVII. The demonstration of appendix-specific antigens in the rabbit.
Colas de la Noue H; Richter M
Immunology; 1974 Sep; 27(3):421-6. PubMed ID: 4137568
[TBL] [Abstract][Full Text] [Related]
10. Cells involved in the immune response. II. The response of normal rabbit hemopoietic and lymphopoietic cells to phytohemagglutinin in vitro.
Singhal SK; Daguillard F; Richter M
Int Arch Allergy Appl Immunol; 1968; 34(2):119-27. PubMed ID: 5667373
[No Abstract] [Full Text] [Related]
11. Distribution of plaque-forming cells in the mouse for a protein antigen. Evidence for highly active parathymic lymph nodes following intraperitoneal injection of hen lysozyme.
Hill SW
Immunology; 1976 Jun; 30(6):895-906. PubMed ID: 800396
[TBL] [Abstract][Full Text] [Related]
12. Interaction between cells of Peyer's patches and cells of bone marrow origin in the immune response.
Knudson KC; France CM; Coppola ED; Miller HC; Jones TL
J Immunol; 1975 Apr; 114(4):1428-30. PubMed ID: 1090677
[No Abstract] [Full Text] [Related]
13. Cells involved in the immune response. XXXIII. Antibody-forming cells in the popliteal lymph nodes in the immunized splenectomized rabbit following intravenous immunization and their subsequent dissemination to the thymus.
Berry M; Barron P; Richter M
Clin Immunol Immunopathol; 1986 Sep; 40(3):456-65. PubMed ID: 3731541
[TBL] [Abstract][Full Text] [Related]
14. Immunologic suppression after oral administration of antigen. I. Specific suppressor cells formed in rat Peyer's patches after oral administration of sheep erythrocytes and their systemic migration.
Mattingly JA; Waksman BH
J Immunol; 1978 Nov; 121(5):1878-83. PubMed ID: 361892
[TBL] [Abstract][Full Text] [Related]
15. Immunology of the lower respiratory tract. II. The plaque-forming response of canine lymphoid tissues to sheep erythrocytes after intrapulmonary or intravenous immunization.
Kaltreider HB; Kyselka L; Salmon SE
J Clin Invest; 1974 Aug; 54(2):263-70. PubMed ID: 4603168
[TBL] [Abstract][Full Text] [Related]
16. Functional characteristics of Peyer's patch lymphoid cells. IV. Effect of antigen feeding on the frequency of antigen-specific B cells.
Kagnoff MF
J Immunol; 1977 Mar; 118(3):992-7. PubMed ID: 300396
[TBL] [Abstract][Full Text] [Related]
17. Murine bone marrow IgA responses to orally administered sheep erythrocytes.
Alley CD; Kiyono H; McGhee JR
J Immunol; 1986 Jun; 136(12):4414-9. PubMed ID: 3519768
[TBL] [Abstract][Full Text] [Related]
18. Cells involved in the immune response. XXII. The demonstration of thymus-specific antigens in the rabbit.
Colas de la Noue H; Koperstych S; Richter M
Immunology; 1972 Nov; 23(5):655-64. PubMed ID: 4117948
[TBL] [Abstract][Full Text] [Related]
19. Cells involved in the immune response. V. The migration of antigen-reactive immunocompetent cells out of the bone marrow following antigen administration.
Abdou NI; Richter M
Int Arch Allergy Appl Immunol; 1969; 35(4):330-4. PubMed ID: 5781768
[No Abstract] [Full Text] [Related]
20. Cells involved in cell-mediated and transplantation immunity. 3. The organ source(s) of the cells in the normal rabbit which mediate a reaction of cellular immunity in vitro.
Behelak Y; Richter M
Cell Immunol; 1972 Apr; 3(4):542-58. PubMed ID: 4401910
[No Abstract] [Full Text] [Related]
[Next] [New Search]