Biomedical subjects
J M SMITH
Publications and source records attributed to J M SMITH.
STAPHYLOCOCCUS AUREUS STRAINS ASSOCIATED WITH THE HEDGEHOG, ERINACEUS EUROPAEUS.
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DERMATOPHYTE LESIONS IN THE HEDGEHOG AS A RESERVOIR OF PENICILLIN-RESISTANT STAPHYLOCOCCI.
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A CONDUCTIVITY TECHNIQUE FOR RAPID MEASUREMENT OF IN VITRO DIALYZER PERFORMANCE.
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SYNAPSES IN THE LATERAL GENICULATE NUCLEUS OF THE PRIMATE.
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PANCREATIC BIOPSY IN THE DIAGNOSIS OF ZOLLINGER-ELLISON SYNDROME.
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A NATURAL RESERVOIR OF PENICILLIN-RESISTANT STRAINS OF STAPHYLOCOCCUS AUREUS.
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ULTRASTRUCTURAL FEATURES OF THE LATERAL GENICULATE NUCLEUS OF THE CAT.
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THE SIZE OF NERVE FIBERS SUPPLYING CEREBRAL CORTEX.
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RINGWORM IN THE SOLOMON ISLANDS.
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INDUCTION OF TOLERANCE TO SKIN GRAFTS IN MICE WITH DISRUPTED LIVER AND KIDNEY CELLS.
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HEDGEHOG RINGWORM IN THE NORTH ISLAND OF NEW ZEALAND.
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USE OF TAPE RECORDED HEART SOUNDS TO DETECT HEART DISEASE IN CHILDREN.
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PRODUCTION OF IMMUNOLOGICAL TOLERANCE IN MICE AFTER REPEATED INJECTIONS OF DISRUPTED SPLEEN CELLS.
1. Tolerance of male skin isografts has been regularly produced in female mice of the C57B1 strain sublines 1, 4, and 6 during adult life by repeated injection of completely disrupted spleen cells derived from male donors. The tolerant state is long-lasting since such grafts have remained in place more than 9 months. 2. Prolonged survival of homotransplants of skin has regularly been produced in DBA/2 mice during adult life by repeated injections of completely disrupted spleen cells from Balb/C donors. When injections of disrupted spleen cell material are continued over a sufficiently long period, permanent acceptance of the skin homografts may be obtained between these strains. 3. Immunological tolerance across even the strong H-2 histocompatibility barrier was obtained in the neonatal period and during adult life by repeated injection of disrupted spleen cell preparations. The tolerant state has been revealed by both mammary adenocarcinoma and skin homografting across this strong histocompatibility barrier. 4. In contradistinction to the tolerant state produced by injection of intact spleen cells in neonatal animals or during adult life or that produced by parabiotic union, the tolerance produced by repeated injection of disrupted spleen cell preparations cannot be transferred to syngenic neonatal mice with spleen cells of the tolerant animal. 5. The implications of these findings in transplantation biology and in consideration of the basic nature of tolerance are discussed.
A GENETIC THEORY OF INFLAMMATORY POLYARTHRITIS.
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Prolonged treatment with prednisolone in children with asthma.
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THYMECTOMY IN NEWBORN AND ADULT MICE.
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