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1 ies into dimeric PDE6C that is predominantly misassembled.
2 malformed peptidyl transferase center in the misassembled 50S subunits.
3 e found that the absence of Mam33 results in misassembled, aggregated ribosomes and a respiratory let
4 cies that uses synteny information to remove misassembled and misaligned regions, and sequence qualit
5 ontigs into three types (True, Uncertain and Misassembled), and then optimizes the scaffold graph bas
6 f DRiPs-derived HLA peptides are full-sized, misassembled, and surplus subunits of large protein comp
7 ed proteins that are terminally misfolded or misassembled are degraded by a ubiquitin- and proteasome
8 d in good yields, but competing formation of misassembled byproducts highlights some of the challenge
9                                          The misassembled complex arises from the surprising ability
10  cofactor by preventing formation of stable, misassembled complexes.
11 , we correctly identified 75% of extensively misassembled contigs and 100% of locally misassembled co
12 bled contigs in rice, and 77% of extensively misassembled contigs and 80% of locally misassembled con
13 nsis and between 31% and 100% of extensively misassembled contigs and between 57% and 73% of locally
14  that we detect more than 54% of extensively misassembled contigs and more than 60% of locally misass
15 sembled contigs and more than 60% of locally misassembled contigs in assemblies of F.tularensis and b
16 d contigs and between 57% and 73% of locally misassembled contigs in assemblies of loblolly pine.
17 vely misassembled contigs and 80% of locally misassembled contigs in budgerigar.
18 ely misassembled contigs and 100% of locally misassembled contigs in rice, and 77% of extensively mis
19 ior knowledge of contig location can lead to misassembled contigs, even when commonly used quality in
20 equencing technology, which may also lead to misassembled contigs.
21 criminating the native structures from their misassembled counterparts.
22 tably associate with Tg when it is misfolded/misassembled due to inhibition of its glycosylation.
23 state and excludes structures that otherwise misassemble efficiently.
24 uence in this region of the genome, which is misassembled from the two different alleles separated by
25                 This prediction suggests why misassembled hemoglobins often get trapped as hemichrome
26                                     Although misassembled homodimers can form under some conditions,
27 ty, yet mitochondria lacking Mgr1p contain a misassembled i-AAA protease and are defective for turnov
28 epetitive genomic regions are fragmented and misassembled in most contemporary genome assemblies.
29 ikely due to imperfect contig ends that were misassembled in tandem rather than as overlapping segmen
30     Many of these palindromes are missing or misassembled in the current reference assemblies of thes
31 issociation and partial monomer unfolding to misassemble into amyloid and other aggregates.
32 umulated around surface blebs, stress fibers misassembled into a spherical network surrounding the cy
33 d-type (WT) transthyretin (TTR) misfolds and misassembles into amyloid.
34 pe Gag), the "dimerizing" Gag-Zipper protein misassembles into very small particles, while the "trime
35 ding that bypassing quality control leads to misassembled, malfunctioning ribosomes with altered tran
36 ents with their host genomes and identifying misassembled metagenomic contigs.
37 nuclear envelope of aged cells suggests that misassembled NPCs are accumulated in aged cells.
38 changes are likely caused by the presence of misassembled NPCs, as we find that two NPC assembly muta
39 es lacking the tunnel domain of uL4 reveal a misassembled NPET, including an aberrantly flexible ribo
40  its absence resulted in the accumulation of misassembled OMPs.
41 ntical segmental duplications (>or=90%) were misassembled or collapsed within the working draft WGS a
42 volved in retrotranslocation of misfolded or misassembled proteins across the ER membrane for degrada
43 ative diseases feature specific misfolded or misassembled proteins associated with neurotoxicity.
44 idence for the ability of FtsH to refold the misassembled proteins.
45 mes are assemblies that contain fragments of misassembled regions (gaps).
46 the reference sequence, corrected previously misassembled regions and identified new palindromic ampl
47  assembly identified gaps and misoriented or misassembled regions in previous assemblies and produced
48 nd sequences and PacBio long reads, indicate misassembled regions.
49 iator of replication restart on collapsed or misassembled replication forks, blocks the strand displa
50                                              Misassembled scR1 has a primary degradation pathway in w
51 believed to be the accumulation of misfolded/misassembled secretory proteins in the ER, their inducti
52 he reference genome as well as for detecting misassembled sequences.
53  filamentous structures that we attribute to misassembled shell protein.
54 ently leading to formation of tubes or other misassembled structures rather than proper VLPs.
55 tion through selective removal of cells that misassemble the spore envelope.
56  collagen, and intact collagen that had been misassembled under nonphysiological pH and ionic-strengt