ライフサイエンスコーパス: misassemble

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1 cies that uses synteny information to remove misassembled and misaligned regions, and sequence qualit

2 f DRiPs-derived HLA peptides are full-sized, misassembled, and surplus subunits of large protein comp

3 ed proteins that are terminally misfolded or misassembled are degraded by a ubiquitin- and proteasome

4 d in good yields, but competing formation of misassembled byproducts highlights some of the challenge

5 The misassembled complex arises from the surprising ability

6 cofactor by preventing formation of stable, misassembled complexes.

7 , we correctly identified 75% of extensively misassembled contigs and 100% of locally misassembled co

8 bled contigs in rice, and 77% of extensively misassembled contigs and 80% of locally misassembled con

9 nsis and between 31% and 100% of extensively misassembled contigs and between 57% and 73% of locally

10 that we detect more than 54% of extensively misassembled contigs and more than 60% of locally misass

11 sembled contigs and more than 60% of locally misassembled contigs in assemblies of F.tularensis and b

12 d contigs and between 57% and 73% of locally misassembled contigs in assemblies of loblolly pine.

13 vely misassembled contigs and 80% of locally misassembled contigs in budgerigar.

14 ely misassembled contigs and 100% of locally misassembled contigs in rice, and 77% of extensively mis

15 ior knowledge of contig location can lead to misassembled contigs, even when commonly used quality in

16 equencing technology, which may also lead to misassembled contigs.

17 criminating the native structures from their misassembled counterparts.

18 tably associate with Tg when it is misfolded/misassembled due to inhibition of its glycosylation.

19 state and excludes structures that otherwise misassemble efficiently.

20 uence in this region of the genome, which is misassembled from the two different alleles separated by

21 Although misassembled homodimers can form under some conditions,

22 ty, yet mitochondria lacking Mgr1p contain a misassembled i-AAA protease and are defective for turnov

23 ikely due to imperfect contig ends that were misassembled in tandem rather than as overlapping segmen

24 issociation and partial monomer unfolding to misassemble into amyloid and other aggregates.

25 umulated around surface blebs, stress fibers misassembled into a spherical network surrounding the cy

26 d-type (WT) transthyretin (TTR) misfolds and misassembles into amyloid.

27 pe Gag), the "dimerizing" Gag-Zipper protein misassembles into very small particles, while the "trime

28 its absence resulted in the accumulation of misassembled OMPs.

29 ntical segmental duplications (>or=90%) were misassembled or collapsed within the working draft WGS a

30 volved in retrotranslocation of misfolded or misassembled proteins across the ER membrane for degrada

31 idence for the ability of FtsH to refold the misassembled proteins.

32 the reference sequence, corrected previously misassembled regions and identified new palindromic ampl

33 nd sequences and PacBio long reads, indicate misassembled regions.

34 iator of replication restart on collapsed or misassembled replication forks, blocks the strand displa

35 Misassembled scR1 has a primary degradation pathway in w

36 believed to be the accumulation of misfolded/misassembled secretory proteins in the ER, their inducti

37 he reference genome as well as for detecting misassembled sequences.

38 filamentous structures that we attribute to misassembled shell protein.

39 ently leading to formation of tubes or other misassembled structures rather than proper VLPs.

40 tion through selective removal of cells that misassemble the spore envelope.

41 collagen, and intact collagen that had been misassembled under nonphysiological pH and ionic-strengt

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