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1 Vps34, we identify Etf1, an uncharacterized type II transmembrane protein.
2 ein-like protein, and a functionally unknown type II transmembrane protein.
3 core 1 beta3-Gal-T predicts a 363-amino acid type II transmembrane protein.
4 acid residues with the characteristics of a type II transmembrane protein.
5 These results demonstrate that SMDF is a type II transmembrane protein.
6 The Apo3 ligand (Apo3L) is a 249 amino-acid, type II transmembrane protein.
7 ent to transfer the activity to an unrelated type II transmembrane protein.
10 ator on T cells (LIGHT) is a recently cloned type II transmembrane protein belonging to the TNF famil
12 family members are initially synthesized as type II transmembrane proteins, but some of these protei
13 identified on the surface of lymphoids as a type II transmembrane protein, CD38 has now been establi
14 By constructing chimeras with CD98hc and a type II transmembrane protein (CD69), we found that the
15 ntain an open reading frame that predicted a type II transmembrane protein composed of 406 amino acid
16 t the N-terminal intracellular domain of the type II transmembrane protein glycoGag is responsible fo
20 describe that ODZ1 (also known as TENM1), a type II transmembrane protein involved in fetal brain de
22 onal analysis, we report herein that CD74, a Type II transmembrane protein, is a high-affinity bindin
24 The influenza virus neuraminidase (NA), a type II transmembrane protein, is directly transported t
25 ing experiments between CD69 and the related type II transmembrane protein, NKRp1A, identified a requ
26 ends of a mouse liver cDNA library encodes a type II transmembrane protein of 393 amino acids with 90
29 ated human and mouse TPST cDNAs that predict type II transmembrane proteins of 370 amino acid residue
30 The human and mouse TPST-2 cDNAs predict type II transmembrane proteins of 377 and 376 amino acid
33 this article, we show that CPXV012, a 9-kDa type II transmembrane protein, prevents peptide transpor
35 nduced upon association with LAP1 and LULL1, type II transmembrane proteins residing in the nuclear e
36 heimer amyloid plaque component precursor, a type II transmembrane protein specifically expressed in
42 AD-metabolizing enzyme in mammals is CD38, a type II transmembrane protein that converts NAD primaril
43 omavirus is a 44-amino acid, Golgi-resident, type II transmembrane protein that efficiently transform
44 sqv-1 and showed that the SQV-1 protein is a type II transmembrane protein that functions as a UDP-gl
46 infected B cells in the gut express Sag as a type II transmembrane protein that is recognized by the
47 Using pulldowns, we here identify teneurins, type II transmembrane proteins that are also candidate s
48 TorsinB strictly depends on LAP1 and LULL1, type II transmembrane proteins that are integral parts o
50 SF attachment protein receptors (SNAREs) are type II transmembrane proteins that have critical roles
51 Fas ligand (FasL) is a potent proapoptotic type-II transmembrane protein that can cause cell death
53 IL-6R, and IL-1RII, CANDIS does not bind the type II transmembrane protein TNF-alpha, demonstrating f
55 operties of Kv4.2: dipeptidyl-peptidase-like type II transmembrane proteins typified by DPPX-S, and c
56 factor family of ligands, is a 40-kilodalton type II transmembrane protein which is cleaved to produc
57 on indicated that Joro 177 MoAb recognizes a type II transmembrane protein, which is the mouse homolo
59 crophage C-type lectin, is a 219-amino acid, type II transmembrane protein with a single extracellula
60 of the mutation in axy4-1 identified AXY4, a type II transmembrane protein with a Trichome Birefringe
62 c-122 codes for a phylogenetically conserved type II transmembrane protein with collagen repeats and
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