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1 interact with the epsilon subunit, while the even-numbered, acidic residues gammaAsp204, gammaGlu208,
2 ar saturated diacylphosphatidylcholines with even-numbered acyl chains of lengths from 18 to 24 carbo
3 ,14-dimethylnonadeca-12,14-dienoic acid with even-numbered alkyl moiety.
4 sion between states involves movement of the even-numbered alpha-helices across the surfaces of the o
5  enzyme into two distinct conformations: for even-numbered analogues, the cob(II)alamin remains proxi
6 is known that small gold cluster anions with even-numbered atoms can molecularly chemisorb O(2) via o
7 sulfates dissociate to produce predominantly even-numbered B(n), C(n), Y(n), and Z(n) ions, and that
8 splay global aromatic ring currents, whereas even-numbered belts, with 80, 100, or 120 pai-electrons,
9 liana) seed oil have a cis-double bond on an even-numbered carbon.
10 ple mosaic blocks in the crystals containing even-numbered chains, identified by selected-area electr
11 -head orientation, the knot products contain even-numbered crossings.
12           These cocrystals contain aliphatic even-numbered dicarboxylic acids of increasing chain len
13 es leading to the octamer are populated with even-numbered, dimeric and tetrameric, PA intermediates.
14 e sufficient for activation of both odd- and even-numbered engrailed stripes.
15  from Atro mutant germ-line mothers lack the even-numbered (ftz-dependent) engrailed stripes and show
16 rane domain receptor with the N terminus and even-numbered loops facing the endoplasmic reticulum lum
17                                 The bias for even-numbered measurements was reduced when using automa
18 fference in the periodic packing of odd- and even-numbered n-alkane solids results in odd-even variat
19  exhibit up to 30 times slower dynamics than even-numbered n-alkanes near their respective melting po
20  synthesizes cellotetraosyl units and higher even-numbered oligomeric units and that a separate glyco
21                                       Linear even numbered oligomers were obtained in acetone under r
22 e from off-state dimers, it was thought that even-numbered oligomers should dominate, and that heptam
23 ing milligram quantities of unusual odd- and even-numbered oligosaccharides, greatly increasing the d
24 changes, and show that the patterning of the even-numbered parasegment boundaries relies on Opa-depen
25 ed expression of Tc-wg and Tc-en at odd- and even-numbered parasegmental boundaries, respectively.
26  repression, but is expressed throughout the even-numbered parasegments due to the loss of repression
27  that drive expression in either the odd- or even-numbered parasegments has not been defined for any
28 d-numbered parasegments and wingless (wg) in even-numbered parasegments.
29 ge in seven stripes that serve to define the even-numbered parasegments.
30 o give rise to the minor stripes seen in the even-numbered parasegments.
31 y for transcription of the engrailed gene in even-numbered parasegments.
32                                      Whereas even-numbered probes (at positions B24 and B26) contact
33 ellular Bdellovibrio, accommodating odd- and even-numbered progeny formation by non-binary division.
34               In POPC/OG mixed micelles, the even-numbered residues facing the hydrocarbon show an in
35 ic acid decorations are exclusively found on even-numbered residues in most of the glucuronoxylan pol
36 -224 of triadin form a beta-strand, with the even-numbered residues in the strand interacting with ch
37  of triadin binding to calsequestrin are the even-numbered residues Lys(210), Lys(212), Glu(214), Lys
38  of strand beta1 of the nth molecule and the even-numbered residues of strand beta2 of the (n - 1)th
39                For both strands studied, the even-numbered residues were found to be exposed to the h
40 SFRP2, a WNT antagonist, is expressed in the even-numbered rhombomeres and that over-expression of cS
41  in three segregated streams adjacent to the even-numbered rhombomeres into the branchial arches, and
42 stinct regions of the neural tube, including even-numbered rhombomeres of the hindbrain.
43 nto distinct exiting streams adjacent to the even-numbered rhombomeres.
44  ephrins results in sorting to boundaries in even-numbered rhombomeres.
45 ced by 'gain-of-function' Msx2 expression in even-numbered rhombomeres.
46 ting intermingling of cells between odd- and even-numbered rhombomeres.
47 rs with complementary loops designed to form even-numbered rings were active in DNA packaging, wherea
48 ihedral angle is approximately 0 degrees for even-numbered rings, but deviates from 0 degrees for rin
49 nts and loops insert efficiently if the next even-numbered segment in the sequence is present.
50  individually or when combined with the next even-numbered segment in the tetracycline resistance pro
51 of different adhesive properties of odd- and even-numbered segments (rhombomeres), but an adhesion mo
52 estigate the differential ability of odd and even-numbered segments to generate neural crest cells, w
53 t, the distal element expresses both odd and even-numbered stripes and also drives inappropriate expr
54          The proximal element expresses only even-numbered stripes and mediates repression by Even-sk
55 patterns shifted to early/large outbreaks in even-numbered years and late/small outbreaks in odd-numb
56 zinc fingers are atypical and similar to the even-numbered zinc fingers of ZFY and ZFX proteins in hu