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1 ding plasma, nuclear, peripheral, single and multipass.
2 no acids) were obtained from 4 standardized, multipass, 24-hour dietary recalls and 2 timed 24-hour u
4 sirable, this study points to the value of a multipass APMF approach to generate AMT tag databases, w
7 lysis of the immunoglobulin VDJ region where Multipass can be combined with a model for the known rec
10 from a malaria virulence gene family, where Multipass generates 20 % more error-free sequences than
11 oundation for extremely long path length and multipass IM separations in SLIM providing greatly enhan
12 new basecalling method described here, named Multipass, implements a probabilistic framework for work
15 egulatory element binding protein, is also a multipass integral membrane protein which cleaves within
20 ave identified a previously uncharacterized, multipass membrane protein called PrsW (annotated YpdC)
23 ses in Drosophila have demonstrated that the multipass membrane protein Smoothened (Smo) is essential
27 w that mammalian APH-1 (mAPH-1), a conserved multipass membrane protein, physically associates with n
29 he dispatched gene, which encodes a putative multipass membrane protein, was initially identified in
31 of both intracellularly localized termini of multipass membrane proteins in the sorting pathway sugge
32 identified in Drosophila, defines a class of multipass membrane proteins that control cell fate and c
33 AN9 is a member of the tetraspanin family of multipass membrane proteins, but its cellular function i
34 ling is controlled by the interaction of two multipass membrane proteins, patched (Ptc) and smoothene
36 en gene of Drosophila melanogaster encodes a multipass membrane-spanning protein that negatively regu
41 ition, the predicted Ags1 protein contains a multipass transmembrane domain that might contribute to
46 Here, we show that the ank locus encodes a multipass transmembrane protein (ANK) that is expressed
47 endoproteolytically processed in vivo, is a multipass transmembrane protein and is a functional homo
48 xport of inorganic pyrophosphate through the multipass transmembrane protein ANK and generation of eP
50 d Bartscherer et al. identify Wntless/Evi, a multipass transmembrane protein in the secretory pathway
51 nt families and in isolated cases, in ANK, a multipass transmembrane protein involved in the transpor
55 lecular analysis reveals that rasp encodes a multipass transmembrane protein that has homology to a f
58 Autophagy-related gene 9 (Atg9) encodes a multipass transmembrane protein thought to act as a memb
60 ne protein, (2) type-2 membrane protein, (3) multipass transmembrane protein, (4) lipid chain-anchore
64 eptor by the FeLV Env backbone suggests that multipass transmembrane proteins may be particularly sui
66 nd glycoGag prevent the incorporation of the multipass transmembrane proteins serine incorporator 3 (
67 ining Protein S-Acyl Transferases (PATs) are multipass transmembrane proteins that catalyze S-acylati
68 1 and related Piezo2 (Fam38B) are vertebrate multipass transmembrane proteins with homologs in invert
69 evealed two genes, aph-1 and pen-2, encoding multipass transmembrane proteins, that interact strongly
71 e protein; 2), type II membrane protein; 3), multipass transmembrane proteins; 4), lipid chain-anchor
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