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1 nt across the spectrum of SILT, including in cryptopatches.
6 that the frequency of in-frame junctions in cryptopatch aggregates was at a level consistent with po
7 at if gammadelta+ IEL derive from T cells in cryptopatch aggregates, then a clonal relationship would
9 ed for NKp46(+) ILCs, whereas LTi-like ILCs, cryptopatches and ILFs were partially dependent on Notch
10 /-) mice also lacked postnatally 'imprinted' cryptopatches and isolated lymphoid follicles (ILFs), bu
13 in-frame joints was significantly reduced in cryptopatch cells isolated from TCR delta-deficient mice
14 ng that the enrichment of in-frame joints in cryptopatch cells must normally depend on expression of
15 V-J junctions present in gammadelta+ IEL and cryptopatch cells were encoded by identical nucleotide s
17 as rearranged in gammadelta+ IEL and in CD3+ cryptopatch cells, but not in CD3- cryptopatch cells.
20 ot identify a role for alpha(4) integrins in cryptopatch (CP) development; however, these studies dem
21 iously identified VCAM-1(+) stromal cells in cryptopatches (CP) and isolated lymphoid follicles (ILF)
23 of LTalpha and LTbetaR to the development of cryptopatches (CP), aggregates of T cell precursors in t
26 CCR6 is present on lymphocyte precursors in cryptopatches, expressed transiently during extrathymic
28 e adult intestine, luminal microbiota induce cryptopatches to transform into isolated lymphoid follic
29 e-inducer (LTi) cells, and LTi-like cells in cryptopatches within the adult intestinal lamina propria
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