ライフサイエンスコーパス: right arm

1 e direction for movements executed using his right arm.

2 al in <8% of cases and is more common in the right arm.

3 Of the 50 patients with tremor in the right arm, 32% had distal postural tremor, 36% had dista

4 w that deletion of the distal portion of the right arm abolishes efficient binding, cleavage, and sup

5 sulting in mild cognitive changes and slight right arm and face weakness.

6 thermal pain primarily to either the left or right arm and studied the acquisition of conditioned Pav

7 ween the representation of the action of the right arm and the representation of its consequence, tha

8 These observations implicated the right arm as the unique feature of the SGS.

9 o moderate hemiparesis in either the left or right arm because of contralateral stroke and healthy co

10 elative to biceps and trapezius for left and right arm, clearly demonstrate different proficiencies b

11 m-onset segmental dystonia and one had focal right-arm dystonia.

12 0-470) also carries portions of the left and right arms flanking the core, which probably play roles

13 cated with only varying the width (d) of the right arm from 200 nm to 1000 nm.

14 jects with chronic stroke producing moderate right arm/hand weakness received 3 weeks therapy that em

15 Left/right arm histamine skin response ratios were altered in

16 the characterization of both "left-arm" and "right-arm" HL interchain disulfide peptides and observed

17 Possible roles for the SGS right arm in Mu replication are addressed.

18 cide substrate, but at a similar rate to the right arm, indicating that the first strand to be exchan

19 sphate-dependent change in protection in the right arm, indicating that this arm likely forms the T s

20 ore frequently into the azygos vein with the right arm injection than with left arm injection (53 of

21 tly seen at CT when high injection rates and right arm injections are used.

22 s showed that (i) approximately 40 bp of the right arm is required, in addition to core sequences, fo

23 his is consistent with work showing that the right arm is specialized for trajectory control while th

24 In BAMC cells, deletion of the right arm markedly reduced the expression of luciferase

25 o a rightward optical shift by recalibrating right arm movements leftward.

26 d to stabilize the perturbed left arm during right-arm movements by predicting and actively opposing

27 s had extensive overlapping deletions of the right arm of chromosome 15.

28 Mutations on the right arm of chromosome 2 (which contains approximately

29 mutations in genes in the 45A region on the right arm of chromosome 2 that are involved in oogenesis

30 chromocenter and to the 49 CD region on the right arm of chromosome 2.

31 elomere-associated sequence, or TAS), on the right arm of chromosome 3 (3R-TAS).

32 Because the right arm of chromosome 3 also affects the hydrocarbon p

33 A region on the right arm of chromosome 3 contains QTL that affect both

34 We carried out a clonal screen on the right arm of chromosome 3 for female sterile mutations u

35 that an approximately 209-kbp portion of the right arm of chromosome 5 contains at least five spatial

36 tode Caenorhabditis elegans that maps to the right arm of chromosome III.

37 ator sequences integrated at two loci on the right arm of chromosome IV and a Lac repressor-GFP fusio

38 a copy of the CAN1 gene integrated onto the right arm of chromosome VIII did show expected increases

39 sence of ribosomal DNA (rDNA) repeats on the right arm of chromosome XII makes it the longest in the

40 e, which codes for spermine synthase, on the right arm of chromosome XII of Saccharomyces cerevisiae

41 was cloned, sequenced, and localized on the right arm of chromosome XVI.

42 We also demonstrate that nucleotides in the right arm of IRII, but not the left arm, are absolutely

43 spersed monosomic and disomic regions in the right arm of linkage groups 2 and 5.

44 Results delimited the B77 FISH locus to the right arm of the D-subgenome chromosome 14 (14R) and the

45 d bioinformatics approach to the base of the right arm of the Drosophila melanogaster second chromoso

46 d on the basis of its ability to bind to the right arm of the Escherichia coli origin of chromosomal

47 The sequence of the right arm of the hairpin must be located downstream of t

48 logue, DFak56, which maps to band 56D on the right arm of the second chromosome.

49 genetically map AgMuc1 to division 7A of the right arm of the second chromosome.

50 Genetic studies have implicated the right arm of the SGS as a key structural feature for pro

51 even weak gyrase sites, if supplied with the right arm of the SGS, could promote Mu replication.

52 of translation, as it forms the base of the right arm of the stem-loop structure that is required fo

53 cytogenetically and physically mapped to the right arm of the third chromosome at 100C3 in STS Dm2514

54 ratio of the two tricosene isomers, with the right arm of the third chromosome having the largest eff

55 nd three-factor crosses located pag-3 to the right arm of the X chromosome between unc-3 and unc-7.

56 ular cross-section of the cell, the left and right arms of the chromosome form separate, parallel str

57 This analysis revealed that the left and right arms of the interrupted dyad display a high degree

58 omly assigned to escape from the left or the right arm, one of which contained a smooth floor and the

59 sed anisotropic bending signals, with the Mu right arm possessing an unusually extended set of such s

60 comparing systolic pressures in the left and right arm, predicts total and CVD mortality independent

61 ectional replication into two equal left and right arms (replichores).

62 ermore, in an SGS derivative with an altered right-arm sequence, the left arm showed these changes, s

63 ase site with the properties imparted by the right arm sequences.

64 The right arm served as a control.

65 e or the replicators distal to ARS310 on the right arm showed that both groups of replicators contrib

66 The right arm was then cooled to 10 degrees C for approximat

67 The SGS right arm was used to replace one arm of the strong pSC1

68 t represent an imperfect reverse copy of the right arm, we propose that the ribosomal shunt has evolv

69 experienced recurrent transient episodes of right arm weakness and expressive aphasia.

70 ptive and visual cues to the location of the right arm were put into conflict (by placing the arms at

71 I, overlapping clones covering 140 kb of the right arm were tested for their ability to promote extra

72 ed axes for movements made with the left and right arms were mirror symmetric about the midsagittal p

73 Meeting organizers thus felt the time was right, armed with new quantitative approaches, to call a