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6 e with tumors expressing this profile, which we designated acini-like tumors, had a significantly low
7 the discovery of a novel AFX isoform, which we designated AFX zeta, in which the first 16 amino acid
13 DivIB comprises three discrete domains that we designate alpha, beta, and gamma from the N to C term
17 ed cationic lipid-PLGA hybrid nanoparticles; we designated antigen-adsorbed (out), antigen-encapsulat
19 WWG-ethanolamide, in which n = 4 or 8, which we designate as "N-anchored" and "C-anchored" peptides,
21 d, short-armed Liaoning dromaeosaurid, which we designate as a new genus and species, Zhenyuanlong su
24 ally folded thermodynamic intermediates that we designate as F (most folded) and I (intermediately fo
27 e identified approximately 135 proteins that we designate as long-lived asymmetrically retained prote
28 ved with the Rad1-Rad10-Rad14 complex, which we designate as nucleotide excision repair factor-1, NEF
31 s via modulating auxin homeostasis for which we designate as reset, not to be confused with the gravi
32 , and argue that this layer structure, which we designate as smectic-fA phase, is thermodynamically s
35 ocated in the periplasmic domain, in regions we designate as the lower part of the large external cle
36 ow that the N-terminal region of gp41, which we designate as the neurotoxic domain, induces iNOS prot
37 he first example of a class of proteins that we designate as trypanokines, i.e., factors secreted by
38 ndomized to receive electrical shocks (which we designated as "experimental shocks") immediately befo
39 lated rats received additional shocks (which we designated as "rescue shocks") after 8 mins of chest
40 and characterization of a novel protein that we designated as calcineurin/NFAT-activating and immunor
42 les, mitochondria, and lipid droplets, which we designated as granule-containing vesicles (GCVs) and
43 at the base of the isolated stem-loop, which we designated as high-frequency recombination sites 1 an
44 atecholamine-O-methyltransferase (COMT) that we designated as low pain sensitivity (LPS), average pai
45 histocompatibility complex (MHC) gene, which we designated as MHC Q1b, whose expression decreases in
47 e discovered a 29-bp consensus sequence that we designated as the Clock-Associated Transcriptional Ac
48 allowed us to discover a novel compound that we designate aspercryptin and to propose a biosynthetic
50 ified the putative two-component system that we designated Bacillus anthracis respiratory response (B
51 to either K332 in L5, forming a product that we designated band 1, or to the major outer membrane pro
53 a novel 399 bp repetitive DNA element (which we designate beta) 9bp upstream of a seryl-tRNA(CAG) gen
56 ew member of the alpha-CA gene family, which we designate carbonic anhydrase-related protein XI (CA-R
61 Adjacent to the cepR2 gene is a gene that we designate cepS, which encodes an AraC-type transcript
63 ng a 27-kDa protein of unknown function that we designated COLD-REGULATED GENE 27 (COR27; At5g42900).
65 olecular transfer between E1 and Ubc9, which we designate "cross-sumoylation." Rhes binds directly to
69 variants with R5-tropic-like V3 loops, which we designated "dual-R," use CCR5 much more efficiently t
70 A distinct superfamily of kinases, which we designated DxTN after its sequence signature, appears
76 ve domain in laminin-gamma3 domain IV, which we designate F5 peptide, and show that the overexpressio
81 three members in Arabidopsis thaliana, which we designated GALACTAN SYNTHASE1, (GALS1), GALS2 and GAL
83 on the deduced amino acid sequence identity we designated GAPC1 and GAPC2 as group I (97% identical)
93 dispersed innate type 2 helper cells, which we designate Ih2 cells, play an integral role in type 2
96 code distinct but paralogous proteins, which we designate interferon-lambda1 (IFN-lambda1), IFN-lambd
97 were confined to a short DNA sequence, which we designated ipeX for inhibition of porin expression, a
100 (NAP1) and to a human homologue of NAP1, and we designate it hNAP2 (human nucleosome assembly protein
103 natural ligand for the cortactin SH3 domain, we designated it CortBP1 for cortactin-binding protein 1
110 ique mixed-domain lamellar morphology, which we designate LAMP Transmission electron microscopy indic
112 han any other member of the family and which we designate mammalian inositol phosphate multikinase (m
115 al evidence that the FLJ10193 protein, which we designate Med25, is a bona fide subunit of the mammal
116 n rare-cleaving nuclease architecture, which we designate 'megaTAL', in which the DNA binding region
118 here that a mouse Mps1p ortholog (esk, which we designate mMps1p) regulates centrosome duplication.
121 d protein encoded by the FLJ10914 ORF, which we designate MRGBP, as a new component of the TRRAP/TIP6
122 es: Muscle RING Finger 1 (MuRF1), and a gene we designate Muscle Atrophy F-box (MAFbx), the latter be
123 The homology of the predicted protein, which we designated NAG (neuroblastoma amplified gene), to a C
127 promoters were located upstream of loci that we designated nipAB and nipC, which correspond to hcp-hc
128 t encoding a G protein-coupled receptor that we designated NmU-R2 based on its homology to NmU-R1.
130 iosulfate and vectorial sulfur transfer, and we designate NWMN_0026.5 as CstR (CsoR-like sulfur trans
131 hat the two components of this system, which we designate OtpA and OtpB, are not predicted to belong
133 6, 32, 38.9, 30.1, 12.7, and 75.7 kDa, which we designated p5.6, p32, p39 (NTPase), p30, p13 (VPg), a
136 Intensely orange fluorescent adducts, which we designate phytofluors, are spontaneously formed upon
142 ied type of disease involving the PrP, which we designated "protease-sensitive prionopathy" (or PSPr)
145 ts in spatially discrete micro-domains which we designate "puncta," and the relative amounts of each
147 We defined Rab-conserved sequences that we designate Rab family (RabF) motifs using the conserve
150 0836 and SMu0837 encode ABC exporters, which we designated rcrPQ (rel competence-related) genes, resp
151 ion yeast homologue of mammalian Rheb, which we designated Rhb1, was identified by genome sequencing.
153 he gene encodes a membrane-bound enzyme that we designate SCALD, for short-chain aldehyde reductase.
154 n over 125 genomes, featuring a peptide that we designate SCIFF (six cysteines in forty-five residues
155 ulates in senescent human fibroblasts, which we designated senescence-associated heterochromatic foci
156 we propose that they belong to a group which we designate SIS, for SA-independent, systemically induc
158 stationary phase and noted a protein, which we designated Snz1p (p35), that shows increased synthesi
160 eviously uncharacterized zinc-finger protein we designate TELOMERASE ACTIVATOR1 (TAC1) is overexpress
161 ons involving AR-interacting proteins, which we designate the "AR-interactome." Despite many years of
162 s a cavity masked by an acidic linker, which we designate the "FLAP." Analysis of three mutant moesin
163 e find that the NH(2)-terminal region, which we designate the actin-targeting domain, facilitates ZNF
165 a novel, full-length 6.9-kb muscle cDNA, and we designate the corresponding protein 'dysferlin'.
166 aracterized type of protein methylation, and we designate the enzyme as Rmt2 (protein arginine methyl
169 ubunit complex from the two-subunit Polzeta, we designate the four-subunit enzyme "Polzeta-d," where
170 ialidase function - and for this distinction we designate the gene and encoded protein nonA/NonA.
172 hosphotransferase system (PTS) permease, and we designate the genes encoding the permease dgaABCD (d-
179 y a global termination control system, which we designate the S box system, as most of the genes are
181 One of these is a novel sequence motif that we designate the SNOG element, because it occurs downstr
189 oth host cells were highly similar, and thus we designated the defective loci in these mutants pmi (f
192 on the phenotype displayed by its mutation, we designated the gene corresponding to Cj0643 as cbrR (
194 hly conserved in Bartonella hbp genes, which we designated the hbp family box, or "H-box." Fourth, we
195 the basis of their similarity to these loci, we designated the L. pneumophila genes helC, helB, and h
198 he phenotype of the C. jejuni Cj1242 mutant, we designated the protein Campylobacter invasion antigen
199 j1279c harbors fibronectin type III domains, we designated the protein FlpA, for fibronectin-like pro
200 rphism, CTG-->GTG (Leu-->Val), at codon 125; we designated the resulting alleles CD31.L and CD31.V, r
203 pneumophila to mammalian cells and protozoa, we designated the type IV pili CAP (for competence- and
204 ibed virus of the Flaviviridae family, which we designate "Theiler's disease-associated virus" (TDAV)
206 tionally distinct from the beta-subunits and we designate them as a gamma family of the BK channel au
211 pithelium and stroma are affected diffusely, we designated them as "atypical hyperplasia of Tag." Alt
212 Based on the characteristics of each class, we designated them as follows: 'Nonresponders' (n = 905,
220 related with the melanocyte growth kinetics; we designated these clusters the melanocyte growth arres
228 and chromosomal location of this chemokine, we designate this chemokine small inducible cytokine sub
229 Thus, by analogy to the Notch receptor, we designate this cleavage the S2 cleavage site, whereas
230 n of ADP ribosylation factor by cytohesin-1, we designate this cytokine-inducible protein Cybr (cytoh
236 motility and a hyperbiofilm phenotype; thus, we designate this gene bifA, for biofilm formation.
238 membrane organic cation transporters; hence, we designate this gene ORCTL2 (organic cation transporte
241 By analogy with related regulatory systems, we designate this leader RNA pattern the "L box." Genes
243 To distinguish the two unrelated families we designate this new class DGAT2 and refer to the M. ra
253 ypic, homeostatic, and migratory properties, we designate this subset peripheral memory (tpm) cells a
257 ns a functional cis element(s) in vitro, and we designated this element the DCE (downstream core elem
263 tants described in motheaten (me, mev) mice; we designated this new genotype as Ptpn6(meB2/meB2) and
266 lized the disease locus to a region in 3q29; we designated this region the morbid obesity 1 (MO1) loc
274 ) were lineage D2, 7 (8.4%) were a haplotype we designated "X6," and 3 (3.6%) were a haplotype we des
275 signated "X6," and 3 (3.6%) were a haplotype we designated "X7." Sequence analysis found 43 haplotype
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