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1 port abnormalities of proteins of the band 3 macrocomplex.
2 ges between SHP2 and the Ras.Raf.phospho-MEK macrocomplex.
3 a high dilution of sample and, thus, protein macrocomplexes.
4 4, and PKCalpha, promoting formation of NHE3 macrocomplexes.
5 of the architecture of the TCR-CD3-pMHC-CD4 macrocomplex and point to regions of high CD4-Lck + ITAM
6 ls confirming the integrated function of the macrocomplex and the importance of its role in red cell
8 d insulin administration reconstituted these macrocomplexes and restored NHE3 expression in the BBM.
9 tool for both the protein identification in macrocomplexes and the understanding of the macrocomplex
10 t, the assembly of an eNOS-centered membrane macrocomplex, and membrane-initiated eNOS activation.
13 h assembly of major components of the band 3 macrocomplex at an early stage during erythropoiesis.
14 with the H(+)-transporting lysosomal ATPase macrocomplex but uncovered no differences in the interac
16 that prior to incorporation into the band 3 macrocomplex, CD47 associates with actin-binding protein
17 ults in formation of a Ras/Raf-1/phospho-MEK macrocomplex, extracellular signal-regulated protein kin
20 ductive films of such CHIT-NAD+-GDH-GDI-CHIT macrocomplexes (MC) were prepared on glassy carbon (GC)
22 arify the role of VG1Fs in the extracellular macrocomplex, specifically in mediating the recruitment
23 2 complex contacts many partners, creating a macrocomplex suitable for receptor targeting at the neur
26 ion, resulting in formation of the autophagy macrocomplex, which contains SLAMF1, beclin1, and the en
27 led that NHE3, NHERF1, IRBIT, and ezrin form macrocomplexes, which are perturbed under diabetic condi
28 odimerization mediates the formation of NHE3 macrocomplexes, which are required for the inhibition of
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