ライフサイエンスコーパス: be joined by

1 which the zinc or free base (Fb) porphyrins are joined by a 4,4'-diphenylethyne linker and bear swal

2 The V(1) and V(0) are joined by a 60-A long and 40-A wide central stalk, c

3 roducts in which 5-, 6-, or 7-membered rings are joined by a C-C single bond.

4 ndicating that the mother cell and forespore are joined by a channel have led to the suggestion that

5 minal domain (NTD) and C-terminal domain and are joined by a charged linker region rich in serine and

6 he two peptides of the two-chain carboxylase are joined by a disulfide bond.

7 NADP(+) revealed that the two flavin domains are joined by a disulfide linkage and that the relative

8 for substantial RRE function, provided they are joined by a flexible linker that allows the two doma

9 ein (Env) of murine leukemia viruses (MuLVs) are joined by a labile disulfide bond that can be stabil

10 ns (a paired domain and a homeodomain) which are joined by a linker, and a transactivation domain enr

11 Switch regions are joined by a mechanism that requires an intact DNA da

12 a single molecule in which the two monomers are joined by a peptide linker.

13 -linked ligand dimers', in which two ligands are joined by a polymer chain of variable length.

14 In the 3CD structure, the 3C and 3D domains are joined by a poorly ordered polypeptide linker, possi

15 east longevity may be interrelated, and they are joined by a potential fourth, genetic stability.

16 Following cleavage, the DNA ends are joined by a process that is incompletely understood

17 oups of the two beta chain 82 lysyl residues are joined by a trimesyl bridge.

18 bola virus GP glycoprotein, are predicted to be joined by a disulfide bond.

19 l DARPin capping repeats were re-designed to be joined by a shared helix in such a way that rigid con

20 ephalon including the cerebral cortex before being joined by a second wave of OLPs from the lateral a

21 lex formed at the initiation codon before it is joined by a 60S subunit to form an active 80S ribosom

22 ase pair fits the Watson-Crick geometry, but is joined by a pattern of hydrogen bond donor and accept

23 Mannose residues were joined by a (1 --> 3) linkage, in contrast to the (

24 The cloned Fv fragments were joined by a newly created disulfide bond to form a

25 nt procedures such as tubal ligation are now being joined by ambulatory laparoscopic cholecystectomy.

26 nthetic polymers in which sugar repeat units are joined by amide linkages.

27 ynthesized in which glucose-derived monomers are joined by an alpha-1,2 amide linkage to give enantio

28 ain with two well-defined alpha-helices that are joined by an ordered, four-residue linker.

29 us end joining (NHEJ), but DNA ends can also be joined by an alternative error-prone mechanism termed

30 EJ deficiency, DSBs with mismatched ends can be joined by an error-prone mechanism involving joining

31 e circularly permuted molecules, the termini were joined by an eight amino acid residue insertion, an

32 The fibrous domains were joined by an extremely flexible hinge.

33 further enhanced when the two aromatic rings were joined by an oxygen or sulfur atom to form the tric

34 The uranium oxide ribbons are joined by bridging iodate ligands to yield two-dimen

35 SR) in B lymphocytes, switch (S) region DSBs are joined by C-NHEJ to form junctions either with short

36 Silver and magnetite nanoparticles are joined by carboxymethyl chitosan, useful in biologic

37 Ultimately, they are joined by cells at the back of the slug, the reargua

38 The glycopeptidyl constructs were joined by chemical ligation, followed by metal-free

39 ar phenotype to ncd; even though chromosomes are joined by chiasmata they fail to segregate at meiosi

40 ami patterns in which flat inflexible sheets are joined by creases, are primarily created for zero-th

41 To do this, AEGIS pairs are joined by different arrangements of hydrogen bond do

42 The porphyrins in each cyclic hexamer are joined by diphenylethyne linkers affording a wheel-l

43 exclusively in the form of a homodimer that is joined by disulfide bonding.

44 single break in the phosphodiester backbone was joined by DNA ligase.

45 EN-1(Rad27) in the processing of DNA ends to be joined by Dnl4/Lif1.

46 and (transiently) the notochord anlage, and is joined by dynamic expression in the left lateral plat

47 This list has recently been joined by endothelial cells (ECs) undergoing mesenc

48 ructs where gp120 and the ectodomain of gp41 are joined by flexible linkers.

49 NTF2-like and UBA) that have been thought to be joined by flexible linkers like beads on a string, wi

50 c acid polymer in which D-glutamate monomers are joined by gamma-peptidyl bonds.

51 In the Xenopus embryo, blastomeres are joined by gap junctions that allow the movement of s

52 the mammalian brain have long been known to be joined by gap junctions, which are the most common ty

53 rom chemically synthesized oligonucleotides, were joined by in vitro recombination to produce interme

54 volves a dimeric structure in which the RNAs are joined by intermolecular interactions between GACG l

55 cell mechanosensitivity; this enterprise has been joined by large-scale genetic screening in the zebr

56 ure of EccC revealed that the ATPase domains are joined by linker/pocket interactions that modulate i

57 ynthase is a homodimer in which the subunits are joined by lumenal domain disulfide bond(s).

58 omprise two or more separate components that are joined by 'mechanical' rather than covalent bonds.

59 trand breaks with non-complementary ends can be joined by mechanisms of illegitimate recombination.

60 ain uniformly plus-end-distal MTs, but these are joined by minus-end-distal MTs as the processes cont

61 sidue peptide (alpha)thioester; this segment is joined by native chemical ligation to a 66-aa Cys pep

62 Pro-Pro-Pro-Pro-Val-Pro, respectively; these are joined by oligoglycyl linkers.

63 ells may have gained additional functions or were joined by other cell types to generate the variety

64 These oligomers are joined by phosphodiester bonds in which the 3',5'-li

65 These paired DNA ends are joined by proteins of the nonhomologous end-joining

66 ation of terminal repeat (TR) sequences that are joined by random recombination upon circularization

67 The two SCR domains and the Fc fragment were joined by randomised conformational peptides.

68 These findings have been joined by reports that these patients also are sens

69 These experts were joined by representatives from several National Ins

70 omosome 2p and four genomic breakpoints that are joined by short sequences of unknown origin.

71 protein contains four principal helices that are joined by short, partially structured loops.

72 Various RNA substrate sequences may be joined by simple Watson-Crick covaration of the DNA b

73 It contains two open reading frames that are joined by splicing and code for the putative pogo tr

74 eptides are separated by 250 amino acids and are joined by the C303-C598 and C310-C629 disulfide bond

75 mately 1) suggest that two hp-12LOX monomers are joined by the catalytic domains, with the PLAT domai

76 The broken ends are joined by the DSB repair machinery, which includes t

77 ly observed zigzag units (interface II) that are joined by the reciprocal epsilon-amino-gamma-glutamy

78 the only available therapy but has recently been joined by the nucleoside analogues, the most extens

79 This has now been joined by the sequence of a candidate for the human

80 he other 21 399 atoms; the QM and MM regions are joined by two boundary atoms treated by the generali

81 Inositol trisphosphate has been joined by two other Ca-releasing messengers, cyclic

82 We find that the 337-352 salt bridge is joined by two other charged side chains, R333 and E34

83 day (E)12.5 and tracheal lymphatics at E16.5 were joined by zippers, not buttons.