戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1  intravenously in a peripheral vessel in the left arm.
2 and a lump in the subcutaneous tissue of the left arm.
3 d to receive laser treatment on the right or left arm.
4 t redness, swelling, and burning pain in his left arm.
5 as significantly greater for the nondominant left arm.
6 The next day, he experienced numbness in his left arm.
7 of its consequence, that is the force on the left arm.
8  of LoxP by cleaving the upper strand on the left arm.
9 h resulted in a dense hemianaesthesia of her left arm.
10  and were able to distinguish a right from a left arm.
11 hibited the best classification rates in the left arm.
12  long Schizosaccharomyces pombe chromosome I left arm.
13 f-touch, in which the right hand strokes the left arm.
14 t occupies the previous position of the real left arm after a delay of 60-90 s.
15     Furthermore, the origin of the FLA (Free Left Arm) Alu family can be traced back to the very begi
16 eted reinnervation surgery on a woman with a left arm amputation at the humeral neck.
17 airpin structure involving 10 repeats on its left arm and a G-rich region on its right arm.
18  and that the protected site encompasses the left arm and center of DSE1.
19 from a necrotic skin lesion on the patient's left arm and demonstrated angioinvasive features on hist
20 ment with worsening headache and progressive left arm and left leg weakness.
21 ch focusing on the characterization of both "left-arm" and "right-arm" HL interchain disulfide peptid
22 of a mirror placed at the midline facing the left arm, and obscuring the right).
23 otides in the right arm of IRII, but not the left arm, are absolutely required for termination of RC
24 e of arterial axis variants in the right and left arm arterial axes of individual patients are lackin
25 hs, in the right leg at 4 months, and in the left arm at 12 months.
26 tructure in which LoxP was oriented with the left arm bound by the cleaving Cre subunit suggested a p
27 unit preferentially associates with the LoxP left arm, directing the first strand exchange to that si
28 entally and found that this advantage of the left arm disappeared in left-handed human participants.
29  subjects learned to stabilize the perturbed left arm during right-arm movements by predicting and ac
30 holine micelles as LD mimic reveals that the left arm forms a concise hydrophobic core comprising try
31                                          The left-arm handgrip dynamometry displayed the highest corr
32 e mole larger than 3 mm in diameter on their left arms (hazard ratio = 1.37, 95% confidence interval
33  In contrast, MAT alpha cells inactivate the left arm, including HML, and thus preferentially recombi
34  vein with the right arm injection than with left arm injection (53 of 70, 76% vs 30 of 58, 52%, P <.
35 ontrast material injection and for right and left arm injection.
36 t subclavian artery was necessary to relieve left arm ischemia in another patient.
37 ponse patterns were similar across right and left arm movements to identical targets (extrinsic coord
38 similar neural representations for right and left arm movements.
39              Cre preferred to react with the left arm of a LoxP suicide substrate, but at a similar r
40 show that dormant replication origins on the left arm of budding yeast chromosome III become activate
41 ype rDNA lose the DeltaRFB allele and distal left arm of chromosome 1 during vegetative propagation.
42 a high-resolution meiotic linkage map of the left arm of chromosome 1, one of Tetrahymena's five chro
43 quencing was conducted for trisomics for the left arm of chromosome 2 (2L) and compared with the norm
44 atellite and the terminal HeT-A array in the left arm of chromosome 2 (2L), is sensitive to its conte
45 d and characterized in the 24F region on the left arm of chromosome 2 in Drosophila.
46 tic subunit in the Drosophila genome, on the left arm of chromosome 2.
47               The D. simulans alleles on the left arm of chromosome 3 are largely recessive, allowing
48 nd Est-6, separated by nearly 1000 kb on the left arm of chromosome 3 of Drosophila melanogaster.
49 r (RE) that controls recombination along the left arm of chromosome III (III-L).
50 script levels encoded by all 65 genes on the left arm of chromosome III and 185 transcription factor
51 t, is the initiating event in activating the left arm of chromosome III for donor selection.
52 the structure of approximately 45 kbp of the left arm of chromosome III in a and alpha cells in logar
53 ferences in recombinational frequency of the left arm of chromosome III in yeast a and alpha cells.
54 is established in part by RE, a locus on the left arm of chromosome III that activates the surroundin
55 cells inhibit recombination along the entire left arm of chromosome III, including HML, whereas MATa
56 PS2 are located approximately 30 kb from the left arm of chromosome III, well removed from HML, HMR,
57 r (RE) that controls recombination along the left arm of chromosome III.
58 E), located between HMLalpha and MATa on the left arm of chromosome III.
59 o differences in chromatin structure for the left arm of chromosome III.
60 hat regulates recombination along the entire left arm of chromosome III.
61 r, that controls recombination of the entire left arm of chromosome III.
62               MATa cells activate the entire left arm of chromosome III; thus MATa preferentially rec
63 introduced into the native SUC2 locus on the left arm of chromosome IX.
64 a 405-kb region comprising nearly all of the left arm of chromosome VII in Saccharomyces cerevisiae.
65 myces cerevisiae, here we replace the native left arm of chromosome XII (chrXIIL) with a linear artif
66  is located adjacent to the PLB1 gene on the left arm of chromosome XIII and which we refer to as PLB
67              The PNG1 gene was mapped to the left arm of chromosome XVI by genetic approaches and its
68  nT1 breakpoint was previously mapped to the left arm of LGIV, where egl-18/elt-6 are located.
69 the contribution of 14 adjacent genes on the left arm of lp54 to the overall infectivity of B. burgdo
70 ated the ability of different regions of the left arm of Saccharomyces cerevisiae chromosome V to par
71  replication terminus (psiL1) located on the left arm of the chromosome of Bacillus subtilis and with
72 single basepair change is located within the left arm of the LysR recognition motif (5'-TGCAA-N7-TTGC
73                                    Since the left arm of the stem-loop structure must represent an im
74           The cluster maps at 65A 5-6 on the left arm of the third chromosome, in agreement with the
75 ging the DR2-type and core-type sites on the left arm of the tranpsoson.
76 ng to either of its two binding sites on the left arm of the transposon.
77                                          The left arm of the Xfas53 genome has over 90% nucleotide id
78          Analysis of a 131-kb segment of the left arm of yeast chromosome XIV beginning 157 kb from t
79 ting of an isochromosome composed of the two left arms of chromosome 5, were associated with azole re
80   Two regions of the genome, one each on the left arms of the second and third chromosomes, showed si
81       It is located in the 65F region of the left arm on the third chromosome, approx. 500 bp 5' of t
82 ed theory, this poorer generalization of the left arm originated from a difference in parameters char
83  intermittent dizziness, and numbness in the left arm over the course of 3 months.
84 severe chest pain, difficulty breathing, and left arm pain) and in one participant in the placebo gro
85 gulation difficulties, 4 (9%) a sensation of left arm paresthesia, and 3 (7%) sympathetic flight/frig
86  a PD >20 mm Hg in 514 (6.5%) patients and a left arm preponderance (82%).
87           Lys86 and Lys201 interact with the left arm scissile adenine base differently than in struc
88 re present, along with the existence of free left arm sequences.
89 tive with an altered right-arm sequence, the left arm showed these changes, suggesting that the selec
90 adically experiences a supernumerary 'ghost' left arm that occupies the previous position of the real
91 to a new joint configuration of the right or left arm to investigate the coordinate systems in which
92 eplication and gyrase cleavage; and (ii) the left arm was not required for efficient Mu replication,
93 received a transfusion through a PICC in the left arm were significantly more likely to develop a dee
94  our study also revealed a region on the far left arm where recombination is obligatory.