'Resistance' to unrelated, DLA-nonidentical canine marrow grafts is unrestricted by the major histocompatibility complex.

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

'Resistance' to unrelated, DLA-nonidentical canine marrow grafts is unrestricted by the major histocompatibility complex.

Experimental hematology - 1 Aug 1994

Raff R F, Sandmaier B M, Graham T, Loughran T P, Pettinger M, Storb R

Abstract excerpt

Dogs undergoing rejection of unrelated, dog leukocyte antigen (DLA)-nonidentical marrow grafts show an increase in mononuclear cell counts in the peripheral blood at 1 week after transplant. Cells are of host origin and express phenotypic and morphologic characteristics of large granular lymphocy...

Topics

Animals
Bone Marrow Cells
Bone Marrow Transplantation
Cells, Cultured
Dogs
Female
Graft Rejection
Granulocytes
Histocompatibility Antigens
Histocompatibility Antigens Class I
In Vitro Techniques

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Killer Cells, Natural

Leukocytes, Mononuclear

Macrophages

Major Histocompatibility Complex

Male

Phenotype

Tissue Donors

Source

Open in PubMed

Identifiers

PMID: 8062888

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8062888-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

'Resistance' to unrelated, DLA-nonidentical canine marrow grafts is unrestricted by the major histocompatibility complex.PMID 8062888Read ↗

Donor CD8 cells prevent allogeneic marrow graft rejection in mice: potential implications for marrow transplantation in humans.Semantic proximity Read ↗

CD6+ T cell depleted allogeneic bone marrow transplantation from genotypically HLA nonidentical related donors.Semantic proximity Read ↗

Nonmyeloablative conditioning with busulfan before matched littermate bone marrow transplantation results in reversal of the disease phenotype in canine leukocyte adhesion deficiency.Semantic proximity Read ↗

Characterization of effector cells of graft vs leukemia following allogeneic bone marrow transplantation in mice inoculated with murine B-cell leukemia.Semantic proximity Read ↗

Isolation and characterization of hematopoietic progenitor cells in canine bone marrow.Semantic proximity Read ↗

Differential Elimination of Anti-Thymocyte Globulin of Fresenius and Genzyme Impacts T-Cell Reconstitution After Hematopoietic Stem Cell TransplantationSemantic proximity Read ↗

Natural killer cells activated with interleukin 2 in vitro can be adoptively transferred and mediate hematopoietic histocompatibility-1 antigen-specific bone marrow rejection in vivo.Semantic proximity Read ↗

Rejection of bone-marrow graft by recipient-derived cytotoxic T lymphocytes against minor histocompatibility antigens.Semantic proximity Read ↗

Nonmyeloablative hematopoietic stem cell transplantation corrects the disease phenotype in the canine model of leukocyte adhesion deficiency.Semantic proximity Read ↗

Peripheral blood microchimerism in human liver and renal transplant recipients: rejection despite donor-specific chimerism.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.