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Peter Mombaerts

Researcher at Massachusetts Institute of Technology

Publications -  22
Citations -  8994

Peter Mombaerts is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: T-cell receptor & T cell. The author has an hindex of 21, co-authored 22 publications receiving 8678 citations. Previous affiliations of Peter Mombaerts include University of Ulm & Howard Hughes Medical Institute.

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RAG-1-deficient mice have no mature B and T lymphocytes

TL;DR: The introduction of a mutation in RAG-1 into the germline of mice via gene targeting in embryonic stem cells is described and it is shown that this mutation either activates or catalyzes the V(D)J recombination reaction of immunoglobulin and T cell receptor genes.
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Visualizing an Olfactory Sensory Map

TL;DR: A genetic approach is developed to visualize axons from olfactory sensory neurons expressing a given odorant receptor, as they project to the Olfactory bulb, which provides direct support for a model in which a topographic map of receptor activation encodes odor quality in the ofactory bulb.
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Mutations in T-cell antigen receptor genes α and β block thymocyte development at different stages

TL;DR: Analysis of mice carrying mutant T-cell antigen receptor (TCP) genes indicates that TCP-β gene rearrangement or expression is critical for the differentiation of CD4− CD8− thymocyte to CD4+CD8+ thymocytes, as well as for the expansion of the pool ofCD4+ CD8+ cells.
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Spontaneous development of inflammatory bowel disease in T cell receptor mutant mice

TL;DR: It is suggested that dysfunction of the mucosal immune system may underly the pathogenesis of some types of IBD in humans.
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T cell receptor δ gene mutant mice : independent generation of αβ T cells and programmed rearrangements of γδ TCR genes

TL;DR: The analyses of TCR γ and δ genes in the mutant mice suggest that intracellular mechanisms acting at the level of DNA rearrangement play key roles in the differential δ and γ gene rearrangements and in the generation of the highly restricted junctional sequences during fetal thymic development.