ライフサイエンスコーパス: mottle

1 lly transparent thin-layer electrochemistry (MOTTLE).

2 reen-film system to attain the same level of mottle.

3 of RPL3B mRNA exhibited leaf overgrowth and mottling.

4 t FAF patterns identified: granular (46.2%), mottled (34.0%), and nummular (18.1%).

5 acular scarring and focal pigmentary retinal mottling; (4) congenital contractures; and (5) marked ea

6 gouti overexpression, through a continuum of mottled agouti/yellow phenotypes with partial agouti ove

7 e with increments of added simulated quantum mottle and by determining DRR to establish lower and upp

8 ybridization we describe the distribution of mottled and toxic milk transcripts during mouse embryoni

9 enous oxygen saturation correlated with knee mottling and high central venous pressure, but these cor

10 d respiratory motion artifacts, noise due to mottle, and overall impression.

11 llow macular deposits and/or macular pigment mottling, and abnormal electroretinograms demonstrating

12 within V2 stripes, giving them an irregular, mottled appearance.

13 (MNK) and Wilson (WND) disease genes are the mottled (Atp7a) and toxic milk (Atp7b) genes, respective

14 Mottled attenuation within the aneurysmal sac was seen i

15 thought to be a model for OHS, Atp7aMo-blo (mottled blotchy), we sequenced the entire 4.5 kb coding

16 Mottled (Brindled) mice, which lack a functional ATP7A c

17 l-established mouse model of Menkes disease, mottled-brindled (mo-br), we tested whether systemic adm

18 Male mice with the Mottled-Brindled allele (Mo-brJ) accumulate copper in th

19 6R) males to female carriers of the X-linked mottled/brindled (Mobr) mutation.

20 tions into recombination in cowpea chlorotic mottle bromovirus (CCMV) resulted in the recovery of an

21 ited detachment from the matrix, rounding, a mottled cell membrane, and vacuolization of the cytoplas

22 Ocular findings were focal macular pigment mottling, chorioretinal atrophy with a predilection for

23 , but as mosaics-either visible (manifesting mottled coat color) in the scored generation (G2) or mas

24 5' untranslated region (UTR) of the bean pod mottle comovirus (BPMV) RNA2, and found it to be essenti

25 MOTTLE defines redox behavior for cytochrome c in good a

26 , retinal pigment epitelium, defects/pigment mottling, depigmentation area, subretinal haemorrhage, s

27 ia are thick (>400 m), massive (not bedded), mottled deposits containing saponite, talc-saponite, Fe-

28 Fluorosed enamel can be porous, mottled, discolored, hypomineralized, and protein-rich i

29 Mottled expression in the liver is in contrast to the pr

30 k expression is restricted to bronchi, while mottled expression is diffuse.

31 lar FAF with peripheral drusen (P<0.001) and mottled FAF with RPE depigmentation (P<0.001).

32 sed in a Menkes copper transporter-deficient mottled fibroblast cell line defective in copper export.

33 ecks (15 patients), small flecks surrounding mottled foveal changes (3 patients), extensive chorioret

34 The mottled gene is expressed in all tissues throughout embr

35 These results suggest that the mottled gene product functions primarily in the homeosta

36 ouse albino locus that results in coat-color mottling has been characterized at the molecular level.

37 er-contrast nodules were detected on quantum mottle images (1-mm diameter, CD = 0.01 mm), compared wi

38 Sixty quantum mottle images of the same size and quantum noise level w

39 bnormalities included mild to severe pigment mottling in 27 patients (63%) and lacunar maculopathy in

40 ring, as indicated by increased agouti/black mottling in the direction of the pseudoagouti phenotype.

41 r dystrophy, with retinal pigment epithelial mottling in younger subjects, progressing to typical BEM

42 Hepatic expression of both toxic milk and mottled is in the parenchyma, as opposed to blood cells.

43 Atypical for RP features included mottled macula at an early age and peripapillary sparing

44 Cucumber green mottle mosaic virus (CGMMV) was first described in 1935

45 d onto tobacco, giving rise to symptoms of a mottle-mosaic typical of the wild-type virus (the D191A,

46 phenotypic and biochemical data suggest that mottled mutants in the mouse, which range in severity an

47 Thus we provide further proof that mottled mutants will provide excellent models for MD as

48 e entire 4.5 kb coding region of three other mottled mutants, two of which are thought to be models f

49 ns included focal retinal pigment epithelial mottling near the site of chemotherapy injection (2 eyes

50 ar attenuation, optic nerve head pallor, and mottling of retinal pigment epithelium.

51 ficient to cause lethality in hemizygotes or mottling of the coat in heterozygotes, but did lead to c

52 the most common of which were focal pigment mottling of the retina and chorioretinal atrophy in 11 o

53 r the same radiation exposure, the perceived mottle on computed radiographs was significantly higher

54 y trauma, as well as mild diffuse pigmentary mottling on the trunk and proximal limbs.

55 indings (capillary refill time >2 secs, knee mottling, or cool extremities), central venous pressure,

56 the SA group, six in the SMA group), diffuse mottled perfusion abnormalities (six in the SA group, fi

57 Human Menkes disease and the murine Mottled phenotype are X-linked diseases that result from

58 e, expression of the Wilson cDNA rescued the mottled phenotype as evidenced by a reduction in copper

59 H1069Q mutant Wilson cDNA did not rescue the mottled phenotype, and immunofluorescence studies showed

60 that a rare subtype, referred to as EBS with mottled pigmentation (MP), is also a disorder of these k

61 , such as epidermolysis bullosa simplex with mottled pigmentation (mutation P25L in the V1 domain of

62 fancy, and development of remarkable diffuse mottled pigmentation on the trunk and proximal extremiti

63 ify the gene mutation(s) accountable for the mottled pigmentation phenotype in a patient with suspect

64 trates the first clinically well-documented, mottled pigmentation phenotype related to a novel EXPH5

65 ecular basis of patient's skin fragility and mottled pigmentation phenotype.

66 BS resulting from EXPH5 mutations to the EBS-mottled pigmentation subtype.

67 in EXPH5 responsible for an EBS subtype with mottled pigmentation.

68 Five radiologists assessed the mottle present in the computed radiographs and screen-fi

69 Thus, MOTTLE provides a robust analytical tool for the dissect

70 In addition, MOTTLE reproduces the redox-driven transformation of hem

71 osterior pole without atrophy; 7 (17.5%) had mottled retinal pigment epithelial changes; 2 (5%) had m

72 a normal fundus appearance but later develop mottled retinal pigment epithelium change along the arca

73 i.e., brook trout [Salvelinus fontinalis] or mottled sculpin [Cottus bairdii]).

74 Congener patterns of mottled sculpin differed from those of brook trout and s

75 and salmon, suggesting that brook trout and mottled sculpin either use salmon tissue to differing de

76 uctive success among different age groups of mottled sculpin, Cottus bairdi, from a natural populatio

77 nistration of contrast material (n = 8) or a mottled spleen (n = 2) were seen at CT.

78 One of the mottled spleens had target lesions on an early (arterial

79 ex or nonspecific retinal pigment epithelium mottling to mild hypopigmentary changes on fundus examin

80 In Desmodium yellow mottle tymovirus, amino termini from the A and B subunit

81 melid specific nanobodies against Broad bean mottle virus (BBMV).

82 Bean pod mottle virus (BPMV) is a bipartite, positive-sense (+) R

83 Bean pod mottle virus (BPMV) is one of the most important pathoge

84 ses, Cowpea mosaic virus (CPMV) and Bean pod mottle virus (BPMV).

85 Previously, two generations of bean pod mottle virus (BPMV; genus Comovirus) vectors have been d

86 he in vitro assembly of the Cowpea chlorotic mottle virus (CCMV) and observed that assembly with vira

87 scent protein (GFP) and the cowpea chlorotic mottle virus (CCMV) are able to perform catalysis after

88 in a single protein cage of cowpea chlorotic mottle virus (CCMV) at neutral pH.

89 The N-proximal region of cowpea chlorotic mottle virus (CCMV) capsid protein (CP) contains an argi

90 on conditions, for example, cowpea chlorotic mottle virus (CCMV) capsid protein (CP) has been shown t

91 he comparable sequence from Cowpea Chlorotic Mottle Virus (CCMV) could also substitute for the BMV su

92 chanism by which virions of cowpea chlorotic mottle virus (CCMV) disassemble and allow for translatio

93 Cowpea chlorotic mottle virus (CCMV) forms highly elastic icosahedral pro

94 Cowpea chlorotic mottle virus (CCMV) has long been studied as a model sys

95 fied capsid protein (CP) of cowpea chlorotic mottle virus (CCMV) is capable of packaging both purifie

96 en capsid proteins (CPs) of cowpea chlorotic mottle virus (CCMV) is controlled by the solution pH.

97 Cowpea chlorotic mottle virus (CCMV) is used as a template that undergoes

98 Cowpea chlorotic mottle virus (CCMV) undergoes a well-studied reversible

99 sed with the coordinates of cowpea chlorotic mottle virus (CCMV) used to generate hypothetical struct

100 s (TMV), M13 bacteriophage, cowpea chlorotic mottle virus (CCMV), and cowpea mosaic virus (CPMV).

101 rions but not by virions of cowpea chlorotic mottle virus (CCMV), another unenveloped virus similar i

102 ber mosaic virus (CMV), and Cowpea chlorotic mottle virus (CCMV), in infections of a common host, Nic

103 dentity (34% similarity) to cowpea chlorotic mottle virus (CCMV), the core structures of these two me

104 y well-studied plant virus, cowpea chlorotic mottle virus (CCMV), we demonstrate the synthesis of vir

105 lacement using the model of cowpea chlorotic mottle virus (CCMV), which BMV closely resembles.

106 epatitis B virus (HBV), and cowpea chlorotic mottle virus (CCMV)-to assess both the range of pathway

107 s of the icosahedral virus, cowpea chlorotic mottle virus (CCMV).

108 avenae subsp. citrulli (Aac), Chilli veinal mottle virus (ChiVMV, potyvirus), Watermelon silver mott

109 e subsp. citrulli (Aac), chilli vein-banding mottle virus (CVbMV, potyvirus), watermelon silver mottl

110 so induced by the NIa proteinase from pepper mottle virus (PepMoV), which has the same cleavage speci

111 Red clover mottle virus (RCMV) is a member of the comoviruses, a gr

112 Rice yellow mottle virus (RYMV) and southern bean mosaic virus, cowp

113 The translocation of rice yellow mottle virus (RYMV) within tissues of inoculated and sys

114 ve-sense RNA genome of Sweet potato feathery mottle virus (SPFMV) (genus Potyvirus, family Potyvirida

115 In sweet potato feathery mottle virus (SPFMV), another out-of-frame element (PISP

116 es bean dwarf mosaic virus (BDMV) and tomato mottle virus (ToMoV) were exchanged, and the resultant p

117 virus (CVbMV, potyvirus), watermelon silver mottle virus (WSMoV, tospovirus serogroup IV) and melon

118 virus (ChiVMV, potyvirus), Watermelon silver mottle virus (WSMoV, tospovirus serogroup IV), and Melon

119 ted tripartite RNA viruses, cowpea chlorotic mottle virus and cucumber mosaic virus.

120 icrobial source tracking markers pepper mild mottle virus and HF183 Bacteroides were respectively 2.9

121 d our analysis on the T = 3 cowpea chlorotic mottle virus and our estimate for the nanoindentation mo

122 ed by the capsid protein of cowpea chlorotic mottle virus and the anionic polymer poly(styrene sulfon

123 ndentation nanomechanics of Cowpea Chlorotic Mottle Virus capsid show that the capsid's physical prop

124 der large deformations, the Cowpea Chlorotic Mottle Virus capsid transitions to the collapsed state w

125 of both native and swollen cowpea chlorotic mottle virus capsids are generated from x-ray crystal st

126 of the virusoid associated with rice yellow mottle virus codes for a 16-kDa highly basic protein usi

127 with Tomato yellow leaf curl virus or Tomato mottle virus exhibited delayed viral DNA accumulation an

128 roperties of capsids of the cowpea chlorotic mottle virus have been examined at pH 4.8 by nanoindenta

129 Desmodium yellow mottle virus is a 28 nm diameter, T=3 icosahedral plant

130 the capsid protein (CP) of cowpea chlorotic mottle virus is optimal when there is a significant exce

131 ecific AVP1 overexpression (Commelina Yellow Mottle Virus promoter [pCOYMV]::AVP1) elicited similar p

132 he self-assembly of CP from cowpea chlorotic mottle virus with RNA molecules ranging in length from 1

133 trate the quantitative detection of Bean pod mottle virus, a pathogen of great agricultural importanc

134 ith quantitative studies of cowpea chlorotic mottle virus, hepatitis B virus, and simian virus 40 ass

135 es like the spinach latent virus and the elm mottle virus, in animal viruses like the hepatitis E vir

136 AFM experiments on cowpea chlorotic mottle virus, known to undergo a pH-controlled swelling

137 infection of Nicotiana benthamiana by tomato mottle virus, suggested that oncogenic suppression by Os

138 xperiments with the related cowpea chlorotic mottle virus, the unfused 2a core segment showed the sam

139 al structure of the related cowpea chlorotic mottle virus, we show that the modified residues are spa

140 Cabbage Leaf Curl Virus (CaLCuV) and Tomato mottle virus.

141 -induced gene silencing mediated by Bean pod mottle virus.

142 poliovirus, rhinovirus, and cowpea chlorotic mottle virus.

143 a closely related tritimovirus (Oat necrotic mottle virus; ONMV) with no known vector.

144 ing polyproteins containing the tobacco vein mottling virus (TVMV) Nla proteinase along with two othe

145 sistance to multiple pathogens: tobacco vein mottling virus, tobacco etch virus, black shank fungus P

146 computed radiographs, the perceived level of mottle was inversely related to radiation exposure.

147 Similarly, noise due to mottle was not identified on the transverse source image