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1 r proteins found associated with the lamin A tail, 17 (13%) were previously described lamin A binding partners.
2      In contrast, only AraC-like transcriptional activators were previously described as regulators of the intestinal col
3        All the aberrations found in the normal breast cells were previously described in cancer literature, suggesting th
4 whose virological, immunological, and pathological features were previously described.
5 erapy (HDCT) as salvage modality for germ cell tumors (GCT) were previously described, and a score was created.
6                     Mutations at the POLTERGEIST (POL) gene were previously described as phenotypic suppressors of mutati
7 e reduction system in mammals, in which two MsrB homologues were previously described.
8                                  Rare DRB5*null individuals were previously described in African populations.
9                                     Two loci, hns and lonA, were previously described as repressors of bioluminescence in
10           Mutations in TP53, CDKN2A, HRAS, KRAS, and PIK3CA were previously described in squamous cell tumors.
11                    The two polydisperse polyvinylimidazoles were previously described by others, while the other two new
12                                     Seven of these proteins were previously described (YspA, YspB, YspC, YspD, YopE, YopN
13 g site-leucine-rich repeat genes and the protein kinase Pto were previously described.
14            DNASU and the PSI:Biology-Materials Repositories were previously described in the 2010 NAR Database Issue.
15  the barley N-glycoproteome, since only four of these sites were previously described.
16 utations of Thr-315 in the Abl kinase domain to Ile (T315I) were previously described in STI-571-resistant patients and l
17 on defects caused by Pten deletion in developing brain that were previously described as defective migration.
18 nsists of all lateral and dorsal clock neuron clusters that were previously described in Drosophila melanogaster.
19 fied mutations associated with the Mane-B017 haplotype that were previously described to be CTL epitopes restricted by Ma
20 variants Y27dD, N28F, and T94H of protein kappa IV Len that were previously described, we characterized mutants M4L, L27c
21 e possible parent-of-origin effects at the 17q11 locus that were previously described in this sample.
22 e-Botzinger complex resembles the response of neurones that were previously described under in vivo conditions.
23 s) are a type of large, layer V spindle-shaped neurons that were previously described in humans, great apes, elephants, a
24           The reactive antigens included some proteins that were previously described as immunogenic, such as the major o
25 spectrometry, revealing the same modifications of Syt1 that were previously described for Syt1 purified from brain extrac
26 onal 54 bacterial phyla and 11 archaeal phyla to those that were previously described using pyrosequencing.
27                                       Twenty-three of these were previously described (Mesulam et al., 2008) but had thei
28 enes, although the attenuating effects of only two of these were previously described.
29        We discovered ten genes with acquired mutations; two were previously described mutations that are thought to contr
30 sociated with isogenic NMI variants of attenuated virulence were previously described large deletions containing genes in
31                                        GldB and GldD, which were previously described, also appear to be lipoproteins.
32 natorial table of 23 types of ATS units, only nine of which were previously described, i.e., 14 types of alternative spli

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