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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.
5 acular scarring and focal pigmentary retinal mottling; (4) congenital contractures; and (5) marked ea
6 se presented with retinal pigment epithelium mottling, a patchy pattern of hypoautofluorescent speckl
7 gouti overexpression, through a continuum of mottled agouti/yellow phenotypes with partial agouti ove
8 e with increments of added simulated quantum mottle and by determining DRR to establish lower and upp
9 ybridization we describe the distribution of mottled and toxic milk transcripts during mouse embryoni
11 enous oxygen saturation correlated with knee mottling and high central venous pressure, but these cor
14 llow macular deposits and/or macular pigment mottling, and abnormal electroretinograms demonstrating
15 apillary refill time on the index fingertip, mottling, and Pv-aCO(2) (the difference between partial
17 t nucleorhabdovirus (SYNV) and tomato yellow mottle-associated cytorhabdovirus (TYMaV) was rescued on
18 (MNK) and Wilson (WND) disease genes are the mottled (Atp7a) and toxic milk (Atp7b) genes, respective
20 thought to be a model for OHS, Atp7aMo-blo (mottled blotchy), we sequenced the entire 4.5 kb coding
22 l-established mouse model of Menkes disease, mottled-brindled (mo-br), we tested whether systemic adm
26 ive changes and improved the survival of the mottled-brindled mouse-a murine model of severe Menkes d
28 tions into recombination in cowpea chlorotic mottle bromovirus (CCMV) resulted in the recovery of an
29 ogenic RNA viruses, namely, Cowpea chlorotic mottle (CCMV) and Brome mosaic virus (BMV), are modulate
30 ited detachment from the matrix, rounding, a mottled cell membrane, and vacuolization of the cytoplas
31 Ocular findings were focal macular pigment mottling, chorioretinal atrophy with a predilection for
33 , but as mosaics-either visible (manifesting mottled coat color) in the scored generation (G2) or mas
34 5' untranslated region (UTR) of the bean pod mottle comovirus (BPMV) RNA2, and found it to be essenti
36 , retinal pigment epitelium, defects/pigment mottling, depigmentation area, subretinal haemorrhage, s
37 ia are thick (>400 m), massive (not bedded), mottled deposits containing saponite, talc-saponite, Fe-
39 panese eel (Anguilla japonica) and the giant mottled eel (A. marmorata) - can act as surrogate specie
43 sed in a Menkes copper transporter-deficient mottled fibroblast cell line defective in copper export.
44 ecks (15 patients), small flecks surrounding mottled foveal changes (3 patients), extensive chorioret
48 ouse albino locus that results in coat-color mottling has been characterized at the molecular level.
49 er-contrast nodules were detected on quantum mottle images (1-mm diameter, CD = 0.01 mm), compared wi
51 bnormalities included mild to severe pigment mottling in 27 patients (63%) and lacunar maculopathy in
52 ring, as indicated by increased agouti/black mottling in the direction of the pseudoagouti phenotype.
53 r dystrophy, with retinal pigment epithelial mottling in younger subjects, progressing to typical BEM
55 Hepatic expression of both toxic milk and mottled is in the parenchyma, as opposed to blood cells.
56 ToMoLCV genomic DNA developed typical tomato mottle leaf curl disease symptoms, thereby fulfilling Ko
57 olecular and biological properties of tomato mottle leaf curl virus (ToMoLCV) from Brazil and establi
61 d onto tobacco, giving rise to symptoms of a mottle-mosaic typical of the wild-type virus (the D191A,
62 phenotypic and biochemical data suggest that mottled mutants in the mouse, which range in severity an
64 e entire 4.5 kb coding region of three other mottled mutants, two of which are thought to be models f
66 resent in all patients (wedge-shaped, n = 3; mottled, n = 9; mixed pattern, n = 6).Conclusions: Physi
67 ns included focal retinal pigment epithelial mottling near the site of chemotherapy injection (2 eyes
69 ficient to cause lethality in hemizygotes or mottling of the coat in heterozygotes, but did lead to c
70 the most common of which were focal pigment mottling of the retina and chorioretinal atrophy in 11 o
71 r the same radiation exposure, the perceived mottle on computed radiographs was significantly higher
73 i) perfusion defect 'pattern' (wedge-shaped, mottled or amorphous), ii) presence of PT and CT obstruc
74 indings (capillary refill time >2 secs, knee mottling, or cool extremities), central venous pressure,
75 tortuosity, retinal pigment epithelium (RPE) mottling/other changes, macular atrophy/puckering/epiret
76 the SA group, six in the SMA group), diffuse mottled perfusion abnormalities (six in the SA group, fi
78 e, expression of the Wilson cDNA rescued the mottled phenotype as evidenced by a reduction in copper
79 H1069Q mutant Wilson cDNA did not rescue the mottled phenotype, and immunofluorescence studies showed
80 that a rare subtype, referred to as EBS with mottled pigmentation (MP), is also a disorder of these k
81 , such as epidermolysis bullosa simplex with mottled pigmentation (mutation P25L in the V1 domain of
82 fancy, and development of remarkable diffuse mottled pigmentation on the trunk and proximal extremiti
83 ify the gene mutation(s) accountable for the mottled pigmentation phenotype in a patient with suspect
84 trates the first clinically well-documented, mottled pigmentation phenotype related to a novel EXPH5
91 osterior pole without atrophy; 7 (17.5%) had mottled retinal pigment epithelial changes; 2 (5%) had m
92 a normal fundus appearance but later develop mottled retinal pigment epithelium change along the arca
95 and salmon, suggesting that brook trout and mottled sculpin either use salmon tissue to differing de
96 uctive success among different age groups of mottled sculpin, Cottus bairdi, from a natural populatio
99 ex or nonspecific retinal pigment epithelium mottling to mild hypopigmentary changes on fundus examin
106 Previously, two generations of bean pod mottle virus (BPMV; genus Comovirus) vectors have been d
107 he in vitro assembly of the Cowpea chlorotic mottle virus (CCMV) and observed that assembly with vira
108 scent protein (GFP) and the cowpea chlorotic mottle virus (CCMV) are able to perform catalysis after
110 The N-proximal region of cowpea chlorotic mottle virus (CCMV) capsid protein (CP) contains an argi
111 on conditions, for example, cowpea chlorotic mottle virus (CCMV) capsid protein (CP) has been shown t
112 he comparable sequence from Cowpea Chlorotic Mottle Virus (CCMV) could also substitute for the BMV su
113 chanism by which virions of cowpea chlorotic mottle virus (CCMV) disassemble and allow for translatio
117 fied capsid protein (CP) of cowpea chlorotic mottle virus (CCMV) is capable of packaging both purifie
118 en capsid proteins (CPs) of cowpea chlorotic mottle virus (CCMV) is controlled by the solution pH.
121 sed with the coordinates of cowpea chlorotic mottle virus (CCMV) used to generate hypothetical struct
122 s (TMV), M13 bacteriophage, cowpea chlorotic mottle virus (CCMV), and cowpea mosaic virus (CPMV).
123 rions but not by virions of cowpea chlorotic mottle virus (CCMV), another unenveloped virus similar i
124 movirus genus, specifically cowpea chlorotic mottle virus (CCMV), are T = 3 icosahedral particles.
125 ber mosaic virus (CMV), and Cowpea chlorotic mottle virus (CCMV), in infections of a common host, Nic
126 dentity (34% similarity) to cowpea chlorotic mottle virus (CCMV), the core structures of these two me
127 y well-studied plant virus, cowpea chlorotic mottle virus (CCMV), we demonstrate the synthesis of vir
129 a single subgenomic RNA of Cowpea chlorotic mottle virus (CCMV), which is pathogenic to plants, is p
130 epatitis B virus (HBV), and cowpea chlorotic mottle virus (CCMV)-to assess both the range of pathway
132 avenae subsp. citrulli (Aac), Chilli veinal mottle virus (ChiVMV, potyvirus), Watermelon silver mott
134 e subsp. citrulli (Aac), chilli vein-banding mottle virus (CVbMV, potyvirus), watermelon silver mottl
137 so induced by the NIa proteinase from pepper mottle virus (PepMoV), which has the same cleavage speci
138 ome loads and detection rates of pepper mild mottle virus (PMMoV) and Carjivirus with values derived
139 4S method concurrently recovered pepper mild mottle virus (PMMoV) and human 18S ribosomal subunit rRN
140 Furthermore, the indigenous pepper mild mottle virus (PMMoV) in raw sewage at concentrations ran
141 the applicability of crAssphage, pepper mild mottle virus (PMMoV), and tobacco mosaic virus (TMV) as
145 ve-sense RNA genome of Sweet potato feathery mottle virus (SPFMV) (genus Potyvirus, family Potyvirida
147 o yellow leaf curl virus (TYLCV,) and tomato mottle virus (ToMoV) (Family: Geminiviridae, Genus: Bego
148 here the A-component of the bipartite tomato mottle virus (ToMoV) viral vector delivers siRNA constru
149 es bean dwarf mosaic virus (BDMV) and tomato mottle virus (ToMoV) were exchanged, and the resultant p
150 virus (CVbMV, potyvirus), watermelon silver mottle virus (WSMoV, tospovirus serogroup IV) and melon
151 virus (ChiVMV, potyvirus), Watermelon silver mottle virus (WSMoV, tospovirus serogroup IV), and Melon
153 icrobial source tracking markers pepper mild mottle virus and HF183 Bacteroides were respectively 2.9
154 d our analysis on the T = 3 cowpea chlorotic mottle virus and our estimate for the nanoindentation mo
155 ed by the capsid protein of cowpea chlorotic mottle virus and the anionic polymer poly(styrene sulfon
156 ndentation nanomechanics of Cowpea Chlorotic Mottle Virus capsid show that the capsid's physical prop
157 der large deformations, the Cowpea Chlorotic Mottle Virus capsid transitions to the collapsed state w
158 of both native and swollen cowpea chlorotic mottle virus capsids are generated from x-ray crystal st
159 of the virusoid associated with rice yellow mottle virus codes for a 16-kDa highly basic protein usi
160 cles (VLPs) when mixed with cowpea chlorotic mottle virus CP, independent of their length, ranging fr
161 with Tomato yellow leaf curl virus or Tomato mottle virus exhibited delayed viral DNA accumulation an
162 roperties of capsids of the cowpea chlorotic mottle virus have been examined at pH 4.8 by nanoindenta
164 the capsid protein (CP) of cowpea chlorotic mottle virus is optimal when there is a significant exce
165 ecific AVP1 overexpression (Commelina Yellow Mottle Virus promoter [pCOYMV]::AVP1) elicited similar p
166 tent with experiments using cowpea chlorotic mottle virus proteins: RNAs with more complex structure
167 , human Bacteroides (HF183), and pepper mild mottle virus were detected at least once in all wells.
168 ased by its interaction with Maize chlorotic mottle virus which causes the synergistic maize disease
169 he self-assembly of CP from cowpea chlorotic mottle virus with RNA molecules ranging in length from 1
171 trate the quantitative detection of Bean pod mottle virus, a pathogen of great agricultural importanc
172 ith quantitative studies of cowpea chlorotic mottle virus, hepatitis B virus, and simian virus 40 ass
173 es like the spinach latent virus and the elm mottle virus, in animal viruses like the hepatitis E vir
175 cinea (Psg) but more susceptible to bean pod mottle virus, soybean mosaic virus, and Fusarium virguli
176 infection of Nicotiana benthamiana by tomato mottle virus, suggested that oncogenic suppression by Os
177 xperiments with the related cowpea chlorotic mottle virus, the unfused 2a core segment showed the sam
178 al structure of the related cowpea chlorotic mottle virus, we show that the modified residues are spa
179 n carried out using CP from cowpea chlorotic mottle virus, with a wide range of sequences and lengths
184 ing polyproteins containing the tobacco vein mottling virus (TVMV) Nla proteinase along with two othe
185 sistance to multiple pathogens: tobacco vein mottling virus, tobacco etch virus, black shank fungus P
186 computed radiographs, the perceived level of mottle was inversely related to radiation exposure.
188 increased capillary refill time and/or skin mottling) were randomized to receive a 48-hour intraveno