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1 AG-containing membranes provides a molecular explanation for why 1) DAG alone is sufficient to activa
2 sponse and tandem duplication and provide an explanation for why a large proportion of the RLK/Pelle
3 ecognized by MAb 2158 and offer a structural explanation for why a mismatched mutation at position 18
4      Through a modeling approach, we propose explanations for why a translation attenuation (TA) mech
5 oxyanion hole becomes smaller, providing one explanation for why acylation may be less efficient foll
6                       Our results provide an explanation for why agr mutants show reduced virulence i
7  the water pulse and provides an alternative explanation for why ALD growth rates for this system dec
8  are imposed on mate search, and provides an explanation for why Allee effects are often observed in
9                        We provide a physical explanation for why allostery is related to dihedral com
10 ncapsulation mechanism provides a convincing explanation for why almonds have a low metabolizable ene
11                          We discuss possible explanations for why amusics might be impaired at percei
12 idity models can be rejected or supported as explanations for why and how these three disorders overl
13 ogenic model discussed here also provides an explanation for why angioedema can occur at multiple sit
14                                  Mechanistic explanations for why antibiotics differ in their optimal
15               These findings also provide an explanation for why antihormonal therapy fails to preven
16                                  We offer an explanation for why ARB epidemics have fast and slow pha
17 al malaria, and the results offer a possible explanation for why artemether provides less advantage t
18           This model provides a mathematical explanation for why average axon turning angles in gradi
19 ate our hypothesis, also suggest a potential explanation for why axonal microtubules deteriorate in n
20 nsing (DS), have been suggested as competing explanations for why bacterial cells use the local conce
21 l Niche Conservatism hypothesis is a leading explanation for why biodiversity increases towards the e
22 riven reporter activity providing a possible explanation for why bipolars do not express opsin.
23  targets with >100 muM affinity, offering an explanation for why both MRG15 CD and Pf1 PHD1 domains a
24 e vicinity of the acyl linkage, providing an explanation for why carbapenems inhibit OXA-1.
25               These data provide a molecular explanation for why caveolin-3 levels are down-regulated
26               Our model provides a molecular explanation for why certain mutations of Mettl3 and Mett
27  buried in CheA-long (CheA(L)), providing an explanation for why CheA(L) fails to bind CheZ.
28         The results also provide a potential explanation for why cochlear-implant users and hearing-i
29  are large aggregates, suggesting a possible explanation for why disease pathology does not always co
30      This interaction provides a mechanistic explanation for why disruption of either FGF or BMP sign
31 particularly in the short term, may offer an explanation for why domesticators and breeders have real
32 n and its antiapoptotic function provides an explanation for why eIF2alpha kinase deficiency in disea
33 er modeling of chromosomes, and suggests new explanations for why elucidating the functional signific
34 ted HePTP/PP2A activity provides a molecular explanation for why ERK activity is sensitive to membran
35 oms as adaptive fail to provide parsimonious explanations for why even mild depressive symptoms impai
36  transplanted animals, providing a potential explanation for why exogenous IL-7 did not increase GVHD
37 eakest Allee effects and may thus provide an explanation for why extinctions due to Allee effects are
38 NA damage induced by HPV16 E7, providing one explanation for why FA patients are predisposed to HPV-a
39             Finally, the findings provide an explanation for why figure-ground cues modulate the resp
40 n levels in fluorosed enamel and provides an explanation for why fluorosed enamel has a higher than n
41 sm in gammadelta T cells but also provide an explanation for why gammadelta T cells are less dependen
42 ences in these contacts provide a structural explanation for why GluR2 L483Y and GluR3 L507Y are nond
43          Moreover, they provide a functional explanation for why granule cells have approximately fou
44 m the target lysine and provide a structural explanation for why H3T3 phosphorylation and H3K9 acetyl
45          Our findings may provide a rational explanation for why H5N1 viruses at present rarely infec
46                         Our results offer an explanation for why HER2 inhibition blocks the growth of
47     This study uncovers a previously unknown explanation for why HLA-B*27 and HLA-B*57 allele groups
48                  Our results also suggest an explanation for why I164L is detected in Southeast Asia
49                    These data may provide an explanation for why IAPs have evolved with multiple BIR
50 eptor after loss of sex steroids provides an explanation for why IL-6 is important for skeletal homeo
51 onses illustrate the need for a more unified explanation for why immunity is compromised in neonates.
52                                Our suggested explanation for why individuals report food insecurity i
53 existing literature and posits epidemiologic explanations for why investigators might have failed to
54 fication of gas5 as a 5'TOP gene provides an explanation for why it is a growth arrest specific trans
55                  The results also provide an explanation for why L. mexicana CPA/CPB-deficient mutant
56              We consider several alternative explanations for why leaves, river networks, and DLA clu
57 r initiation provide a potential mechanistic explanation for why long-term use of low doses of NSAIDs
58 hat of complete MMR deficiency, providing an explanation for why loss of heterozygosity is not requir
59  results suggest a physiologically plausible explanation for why LTD induction is experimentally diff
60     Our model offers a quantitatively robust explanation for why membrane bioenergetics are universal
61 ogen and its receptor on HBV thus provide an explanation for why men have a higher risk of HBV infect
62 nterkinetochore tension, thereby offering an explanation for why MI in mammals is so error-prone.
63                        These data provide an explanation for why MLL translocation breakpoints exclud
64                     These results provide an explanation for why mod(mdg4) exerts differential effect
65         This hypothesis provides a plausible explanation for why most gammaretrovirus recombinants, a
66 ns' metabolic theory provides a paradigmatic explanation for why most large-effect mutations are rece
67 nctions at middle promoters, and provides an explanation for why MotA can form non-specific multimers
68                     These studies provide an explanation for why mouse cells harbor two major classes
69 cale orientation map provides a parsimonious explanation for why multivariate pattern analysis method
70 rate of GP Ibalpha degradation, providing an explanation for why mutation of their genes leads to def
71 lap in skeletal muscle and CNS (providing an explanation for why mutation of ZEB-1 alone has little e
72 protection function of BRCA1, and provide an explanation for why mutations within the BRCA1 RING doma
73 mputational analyses also provide a possible explanation for why N-debenzoyl-2'-deoxy-PTX is inactive
74               These data provide a molecular explanation for why only a single mutated CAV1 allele is
75 d-selective region in vOT while providing an explanation for why other studies have found a lack of w
76 decay of the mRNA body, and this provides an explanation for why p38 MAPK regulates mRNA stability in
77 th VEGF-A upregulation offered a mechanistic explanation for why patients exhibit improved outcomes a
78 Hebbian synaptic plasticity and a functional explanation for why place cells become directionally sel
79 are localized in the chloroplast, a possible explanation for why plants have a larger immunophilin fa
80   In particular, the model provides a simple explanation for why PPC encodes reach targets in referen
81 ugh not without flaws, the model provides an explanation for why primary plastids have evolved so rar
82            The results provide a long-sought explanation for why PTAP duplications arise in PI-treate
83  IFN-gamma-induced apoptosis is not a viable explanation for why RB expression rescues DRB inducibili
84                This independence provides an explanation for why reaction times are usually so sluggi
85 nderlie viral evolution and provide a likely explanation for why relatively few types of plant DNA vi
86 the hope of distinguishing between potential explanations for why responses vary with time.
87                     These results suggest an explanation for why SDS and these mutations affect rever
88 asC and rivR mutations do not provide a full explanation for why serotype M3 strains are associated w
89       Our results provide a more mechanistic explanation for why sexual selection appears to drive ea
90                                      Current explanations for why sexual ornaments are found in both
91        This may provide a pathophysiological explanation for why signs of hemiplegic cerebral palsy a
92 of the mechanism of dissociation provides an explanation for why small molecules that bind at the AB/
93 ocks Mrc1 loading onto origins, providing an explanation for why so many mutants in DNA replication s
94 salt, temperature or osmolarity, but we lack explanations for why so many antiporters are needed and
95 ghts from this study may provide a plausible explanation for why some biogenic carbonates and carbona
96                           They also offer an explanation for why some cells are more sensitive to low
97 und in many P-element constructs provides an explanation for why some gene function is retained.
98 diated by hER-alpha36 provide an alternative explanation for why some human breast cancers are resist
99 uccess as a breeder, offering one compelling explanation for why some individuals delay reproduction
100                                          The explanation for why some patients develop psychotic chan
101                        Finally, I propose an explanation for why some types of teaching are uniquely
102 protein stability in cells and provide a new explanation for why stressed cells accumulate osmolytes.
103                      There is no theoretical explanation for why such a code should exist.
104 e for G4DNA provides an additional molecular explanation for why such sequences are prevalent in the
105                     We also provide possible explanations for why suppressor tRNAs have not been iden
106         It also provides a plausible general explanation for why swimming cells tend to have strong a
107  for transcriptional activity, providing one explanation for why synergy between these factors is imp
108  large and fast movements provide a possible explanation for why the conduction pathways of a wide ra
109 ts microtubule shortening, thus providing an explanation for why the drug can counteract the phenotyp
110 lity to neutralizing antibody, suggesting an explanation for why the elicited neutralization was not
111 erlapping binding sites provides a potential explanation for why the G/C-rich Mad binding site consen
112 timulatory activity of chitosan, offering an explanation for why the largest particles were nearly de
113 ctural basis for LCR function and provide an explanation for why the LCR core regions are so extremel
114 pace than is the mature form and provides an explanation for why the leader peptide is removed from t
115        This observation provides a potential explanation for why the limb phenotypes, observed in typ
116 is fails to provide an ultimate evolutionary explanation for why the male germline would tolerate mor
117                    These findings suggest an explanation for why the necrotrophic fungus Gibberella f
118                     Here, we also propose an explanation for why the p38 inhibitors become insensitiv
119   Therefore, these results provide a simpler explanation for why the proTAME-induced mitotic arrest i
120 tors of neurogenesis and provides a possible explanation for why the Q/R editing process exists.
121 -term premorbid level, providing a potential explanation for why the risks and benefits of lowering b
122            This in turn provides a plausible explanation for why the smaller cations help stabilize t
123     Together, these studies provide a simple explanation for why the vast majority of BRCA2 mutants a
124                           We also provide an explanation for why the well-known isolated pentagon rul
125 Results of the qualitative analysis suggests explanations for why the programme worked in some contex
126 cific T cells in Hu patients and provided an explanation for why their detection has been elusive.
127 n the primary tumor, providing a biochemical explanation for why their expression specifically suppre
128 The final section discusses several possible explanations for why there are often little or no conseq
129  acetylcholine receptor (nAChR) subunits, an explanation for why these currents get smaller is not av
130 ion by beta-Trcp, thus providing a molecular explanation for why these mutations cause beta-catenin a
131 quences in the human p53 gene, providing one explanation for why these sites are mutational hot spots
132 t existing models do not provide a plausible explanation for why they are common.
133 bow joints when attempting any movement, one explanation for why they were better at the 'reach up' t
134 d exclusively to the cytoplasm, providing an explanation for why this isoform has no activity.
135 ppressed in HPV-positive cells, providing an explanation for why this microRNA is targeted in HPV-pos
136 aerobic conditions and provides a reasonable explanation for why this mutant protein is functional un
137                                     Possible explanations for why thymic selection directed to a sing
138        This difference provides a structural explanation for why Tn916Xis does not interact cooperati
139  growth factor receptor providing a possible explanation for why tumorigenesis was not altered after
140                     These results provide an explanation for why VHL heterozygous humans, but not mic
141 rovenance of this complex fold and offers an explanation for why Wnts utilize both lipid- and protein
142 malian cardiomyocytes as well as a potential explanation for why zebrafish and newts, but not mammals
143 Zoep mutant phenotype, providing a plausible explanation for why Zoep genetically interacts with spt

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