ライフサイエンスコーパス: improperly

1 ingle nucleotide polymorphisms may be folded improperly.

2 eral but not all mRNA export mutants produce improperly 3' processed transcripts at the nonpermissive

3 bsurface are discussed, including sealing of improperly abandoned wells and remediation of hydraulic

4 y regions in cap rocks, such as fractures or improperly abandoned wells, are important considerations

5 In a stam-1 mutant, both LOV-1 and PKD-2 improperly accumulate at the ciliary base.

6 d treatment of malignancies where EGFR-TK is improperly activated.

7 phase initiation in mitotic cells containing improperly aligned chromosomes and increases the probabi

8 HPC and M-HPC due to steric clashes with the improperly aligned methyl group on the C2 carbon, result

9 strands and cells within those strands were improperly aligned.

10 both KvLQT1 and HERG, and L51H is processed improperly and interacts with neither channel.

11 enorhabditis elegans has been elusive due to improperly annotated transcription start sites (TSSs).

12 family, because if this concept is presented improperly (as implied above), it can suggest that it is

13 in rpn5Delta cells, proteasome subunits are improperly assembled and/or localized.

14 ubules and outer dense fibers and accumulate improperly assembled fibrous sheath proteins.

15 required for the formation of the storage of improperly assembled NPCs (SINC) compartment.

16 d, malformed NPCs accumulate in a storage of improperly assembled nuclear pore complexes compartment,

17 elicits premature germination of spores with improperly assembled protective layers resulting in the

18 the endoplasmic reticulum (ER), misfolded or improperly assembled proteins are exported to the cytopl

19 use individual GABA(B) receptor subunits and improperly assembled receptor complexes are not function

20 he protein that may allow the mutant form to improperly associate with other monomer subunits.

21 venting chromosome segregation in cells with improperly attached chromosomes [1, 2 and 3].

22 w studies show that Aurora B kinase corrects improperly attached chromosomes by recruiting molecules

23 rization and error-correction mechanisms for improperly attached chromosomes.

24 Improperly attached kinetochores activate the spindle as

25 nt must detect the presence of unattached or improperly attached kinetochores and must then inhibit p

26 The spindle checkpoint senses unattached or improperly attached kinetochores during mitosis, inhibit

27 ult in recruitment of Mad1:Mad2 complexes to improperly attached kinetochores.

28 ces between SAC activation by unattached and improperly attached kinetochores.

29 C. dubliniensis isolates may have been improperly characterized as atypical Candida albicans du

30 apitulate canonical cellular hierarchies and improperly classify major neuronal cell types.

31 Mitotic chromosomes are improperly condensed in mutants, and polytene chromosome

32 f root hair cells in Arabidopsis thaliana is improperly controlled in root hair-defective rhd4-1 muta

33 t analytically and show that the practice of improperly controlling for covariates is the norm in the

34 of causality, and the ecological groups are improperly delineated with regard to the hypothesis.

35 how significant, interpretable deviations in improperly developed brains.

36 efects in the head or tail region of larvae, improperly developed gonad in adult worms and embryonic

37 -function mutations in MET1 and CMT3 develop improperly, display altered planes and numbers of cell d

38 jacent environments if Fluv from CWs will be improperly disposed after usage.

39 Improperly distanced reference strains generate CGMs tha

40 The proportion of spermatocyst bundles with improperly elongated spermatid nuclei explains 71% of th

41 target for microbial immune evasion and, if improperly engaged, a trigger point for various clinical

42 the true FDR well, or at least, it does not improperly favor or disfavor any particular method.

43 tertiary structure, causing the enzyme to be improperly folded and retained within the cell.

44 indicating that these mutant receptors were improperly folded and/or processed and thus retained int

45 only three or five transmembrane domains are improperly folded and/or processed.

46 on of the aberrant tubulins, indicating that improperly folded beta-tubulin is degraded by the protea

47 r quality control by preventing transport of improperly folded glycoproteins out of the ER.

48 Furthermore, these improperly folded K(+) channels are translocated out of

49 Improperly folded membrane proteins are retained in the

50 ction in the periplasm to degrade damaged or improperly folded membrane proteins.

51 Improperly folded or denatured proteins tend to aggregat

52 Accumulation of improperly folded polypeptides in the endoplasmic reticu

53 nerally function as molecular chaperones for improperly folded protein substrates.

54 Many mutations are structural and produce improperly folded protein, explaining their effect in pa

55 level of heme loading is probably not due to improperly folded protein.

56 biogenesis and the resulting accumulation of improperly folded proteins in the endoplasmic reticulum

57 Improperly folded proteins in the endoplasmic reticulum

58 The accumulation of improperly folded proteins within the endoplasmic reticu

59 uble forms as well as in inclusion bodies as improperly folded proteins.

60 inal half of this domain was consistent with improperly folded receptor sequences.

61 cellular compartments indicated that GFP is improperly folded when localized outside of the cytoplas

62 eing used to study structure/function may be improperly folded.

63 during stress when kinases are denatured or improperly folded.

64 dal axon membrane, typically associated with improperly formed paranodes, and in unmyelinated segment

65 isrupting even minor pauses can give rise to improperly formed proteins and human disease.

66 Thus, the improperly held exon cannot access the correct AG, but c

67 Moreover, LacY also folds improperly in proteoliposomes prepared without YidC.

68 CR6 on the Vgamma3(+) gammadeltaT cells also improperly increased their distribution in dermis of the

69 ing the ability to synthesize ppGpp or polyP improperly initiate chromosome replication, proteolyze t

70 The outer hair cells of the cochlea are improperly innervated and express neuronal markers that

71 duplication defects: The newly formed SPB is improperly inserted into the nuclear envelope (NE), prev

72 Connexin43 (Cx43) and zona occludens-1 are improperly localized in Akap9 mutant testes, and Cx43 fa

73 tructure of the fusome and periodically show improperly localized oocytes, stl mutants do not alter o

74 ective root hair morphology, EYFP-RabA4b was improperly localized or was absent from the tips of root

75 structural and functional characteristics of improperly localized poles, we investigated the connecti

76 heir podosome arrays were loosely packed and improperly localized within the cell.

77 COS1 and Sf9 cells appeared to be misfolded, improperly localized, and proteolytically degraded.

78 t with the cortex upon shrinking and Kar3 is improperly localized, suggesting that Gpa1 is a cortical

79 channels Kv1.1 and Kv1.2 channels were often improperly located in the paranodal axon membrane, typic

80 rate that a nonfunctional circuit containing improperly matched components can evolve rapidly into a

81 Cytochrome rC(557) is an improperly matured, dimeric cytochrome c obtained from e

82 , intrinsically labile metabolites are often improperly measured or omitted from studies due to unwan

83 biorientation by unleashing chromosomes from improperly oriented microtubule attachments.

84 In addition, we occasionally observed improperly oriented mitotic spindles, residing entirely

85 okinesis defects, prolonged cell cycles, and improperly oriented mitotic spindles.

86 Invagination of these rings produced improperly oriented septa, which in turn gave rise to as

87 a result of undergoing nuclear division with improperly oriented spindles, a large percentage of cdp1

88 and the myocardial tissue that does form is improperly patterned and fails to maintain tbx5 expressi

89 Strikingly, we found that improperly patterned cells in these mice converted to th

90 brain region (r7/r8) had been deleted and/or improperly patterned.

91 al skeleton and skeletal muscle form but are improperly patterned.

92 allele, spo14-S251P, the product of which is improperly phosphorylated and fails to relocalize and re

93 are not consistent with the maps as well as improperly placed water molecules.

94 along the tubule, whereas nondividing cells improperly position their centrosomes.

95 Improperly positioned nuclei are a hallmark of numerous

96 Loss of kinesin-1 leads to improperly positioned nuclei in culture and in vivo.

97 ntaneously revert to structurally normal but improperly positioned nucleosomes, suggesting a novel me

98 nd to the enzyme with its nicotinamide group improperly positioned to allow turnover, while the affin

99 etic evidence indicates that C-13 of DHLA is improperly positioned with respect to Tyr-385 in the V34

100 er uterine segment, caesarean scars may heal improperly predisposing it to be a site of improper impl

101 osis in Idaho occurring after consumption of improperly prepared cougar jerky is described.

102 Improperly prepared machacado also may have been served

103 rad50 mutants is the result of unrepaired or improperly processed DSBs in the genome and that Rad50 a

104 of structural RNA and in the degradation of improperly processed pre-mRNA.

105 rveillance pathway that retains and degrades improperly processed precursor mRNAs within the nucleus.

106 d complex carbohydrates, an indication of an improperly processed protein.

107 to a quality-control mechanism that retains improperly processed transcripts at or near sites of tra

108 y, retain the ability to polyadenylate these improperly processed transcripts at the nonpermissive te

109 egradation of certain aberrant RNAs, such as improperly processed transcripts, which are often produc

110 nt determined that the mutant molecules were improperly processed, having been retained in the endopl

111 where Rrp3 is depleted, 35S precursor RNA is improperly processed.

112 oteins were elevated and their synthesis was improperly regulated during mGluR-LTD in FMRP-deficient

113 the control of normal cell growth, and when improperly regulated, in cellular transformation and inv

114 d growth but is a potent oncogenic factor if improperly regulated.

115 epair mechanism, is dangerous to the cell if improperly regulated.

116 or cell homeostasis and growth but lethal if improperly regulated.

117 nd breaks (DSBs) are toxic lesions, which if improperly repaired can result in cell death or genomic

118 Improperly repaired chromosomal damage can result in the

119 However, improperly repaired DSBs can cause meiotic arrest or mut

120 accurately distinguish bona fide iPSCs from improperly reprogrammed cells.

121 te mitochondrial pool through fusion between improperly retained dysfunctional/senescent and normal m

122 gy termed "mesothermic." However, rates were improperly scaled and phylogenetic, physiological, and t

123 If left improperly sealed, legacy oil and gas wells colocated wi

124 to a developmental mechanism that eliminates improperly specified cell types.

125 in culture, with a rate of approximately one improperly spliced 23S rRNA per 1.3 million copies.

126 key mediator of Purkinje cell pacemaking, is improperly spliced in RbFox2 and Rbfox1 mutant brains, l

127 Improperly spliced mRNA (SV1-CYP3A5) was found only in t

128 oforms (<5% of normal) and the appearance of improperly spliced, chimeric transcripts.

129 Unsupervised or improperly supervised insertions of the central catheter

130 Constructs generating improperly terminated transgene messenger RNAs (mRNAs) w

131 rn4 than regular constructs, suggesting that improperly terminated transgene mRNAs not only are degra

132 We propose that improperly terminated, unpolyadenylated mRNA from transg

133 lls that respond excessively and desensitize improperly to the chemokines CXCL12 and CXCL13.

134 echanism for minimizing the use of poorly or improperly translated mRNAs as templates for the product

135 he prion protein (PrP), are inefficiently or improperly translocated using only these components.

136 lating chromatin structure but are absent or improperly treated in models with rigid histone tails.

137 e with different atmospheric components, the improperly used atmospheric component should be responsi

138 We also = improperly used their figure without attribution.

139 in checkpoint pathways respond to DNA damage improperly, which in turn may enhance the rate of cancer

140 , the C-terminal phenylalanine residue packs improperly with the rest of the hydrophobic core.