ライフサイエンスコーパス: concatamer

1 vored formation of ACh-binding sites between concatamers.

2 high-molecular-weight head-to-tail circular concatamers.

3 pies/diploid genome in presumed head-to-tail concatamers.

4 sm which generates long, palindromic, duplex concatamers.

5 cle fibers where it persists as head-to-tail concatamers.

6 ge between VWF dimers, to form ultralong VWF concatamers.

7 activation was verified by using kappaB-Sp1 concatamers (-295 to -286) in a thymidine kinase promote

8 For the first time, these concatamers allow analysis of functional properties of a

9 genomic fragments, vector or the transposon concatamer and then presents the clipped sequence reads

10 ing circle replication of the large circular concatamers and the recombinational activity of the tail

11 derstanding both the biogenesis of ultralong concatamers at acidic pH and flow-regulated changes in c

12 A TASK-3-TASK-1 concatamer channel was comparatively zinc insensitive.

13 s at acidic pH and flow-regulated changes in concatamer conformation in plasma at alkaline pH that tr

14 A 46-bp concatamer containing the TAAT element, tested separatel

15 The lengths of von Willebrand factor (VWF) concatamers correlate with hemostatic potency.

16 Further, in multicopy plasmid concatamers, each intron could only silence a single pro

17 e mechanisms by which these large multimeric concatamers form remain to be defined.

18 s used to evaluate the frequency of circular concatamer formation by intermolecular recombination of

19 to the formation of intermolecular circular concatamers in a head-to-tail orientation through trans-

20 merization." Expressed NMDARs containing NR1 concatamers in which the NR1 C termini are "uncoupled" d

21 We expressed (alpha4beta2)2 concatamers in Xenopus oocytes with free accessory subun

22 ngements, generated by constructing cofactor concatamers, indicated a preferential heptamer configura

23 ormone (PTH) gene, a pause site found in the concatamer junction (CJ) of replicating T7 DNA, and term

24 scription normally at a class II pause site (concatamer junction) but are deficient in termination at

25 We describe DOSCATs (DOuble Standard conCATamers), novel calibration standards based on QconC

26 the identity of a minor supercoiled dimeric concatamer observed by both approaches.

27 However, the transcriptional activity of a concatamer of the Ets site alone did not increase with i

28 eened a mouse cDNA expression library with a concatamer of the sequence CCATTAGPyGA and found a new h

29 We prepared concatamers of alpha4 and beta2 subunits for human nicot

30 Thus, peptides including concatamers of heparin-binding consensus sequences may e

31 Concatamers of MSE2 were necessary and sufficient to pro

32 DNA affinity chromatography using concatamers of the latter resulted in > 20,000-fold puri

33 esis of artificial QconCAT proteins that are concatamers of tryptic peptides for several proteins.

34 ication and are artificial proteins that are concatamers of tryptic peptides for several proteins.

35 e ds-linear genomes that persisted stably as concatamers or monomeric circles.

36 l-characterized (15)N-labeled quantification concatamer (QconCAT) carrying prototypic tryptic peptide

37 Quantification concatamer (QconCAT) internal standards were originally

38 ose, a stable isotope-labeled quantification concatamer (QconCAT) of PICALM was designed, expressed,

39 post-infection, into non-rearranged circular concatamers ranging in size between about 9 and 15 copie

40 Coexpression of mutant and wild-type concatamers resulted in expression of either Het(betaalp

41 These concatamers should enable selection of drugs specific fo

42 eta) transfections contained less beta-alpha concatamer than wild type but more than both Het(betaalp

43 2S-beta2S-alpha1) and tandem (beta2S-alpha1) concatamers to target selectively alpha1(A322D) to each

44 Assembly of AChRs from concatamers was less efficient, but function was much mo

45 Using these concatamers, we investigate the requirements for loading

46 Furthermore, these large circular concatamers were capable of expressing both GFP- and Alk

47 When concatamers were expressed alone, dipentameric AChRs wer

48 ted a specific GABA binding site, pentameric concatamers were used.

49 ed formation of ACh-binding sites within the concatamer, whereas linkage between the C terminus of al

50 integrated as an intact, tandem head to tail concatamer with a median copy number of 6 with variable

51 Furthermore, expression of trimeric concatamers with His --> Ala mutations at some but not a

52 Coexpression of concatamers with monomeric beta2, beta4, or alpha4 subun