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1 ISH analyses confirmed previous findings; EtOH withdrawa
2 ISH and FISH take 3 d to perform, whereas IF/FISH takes
3 ISH and IF revealed SN1 and SN2 expression in the gangli
4 ISH arises more commonly from normal and high-normal BP
5 ISH for precursor 45S and mature 28S rRNA was accomplish
6 ISH performed on human malignant tumors revealed strong
7 ISH risks were higher than in those with high-normal BP
8 ISH risks were similar to those with high-normal BP and
9 = 2.0, average HER2 copies >/= 4.0; group 2 (ISH-positive): ratio >/= 2.0, copies < 4.0; group 3 (ISH
10 tive): ratio >/= 2.0, copies < 4.0; group 3 (ISH-positive): ratio < 2.0, copies >/= 6.0; group 4 (ISH
11 gh-normal BP (130 to 139/85 to 89 mm Hg); 3) ISH; 4) isolated diastolic hypertension (SBP <140 mm Hg
12 tive): ratio < 2.0, copies >/= 6.0; group 4 (ISH-equivocal): ratio < 2.0, copies >/= 4.0 and < 6.0; a
14 this study, a novel nonisotopic nucleic acid ISH method using catalyzed signal amplification and colo
17 tive HER2 tests, defined as IHC 0/1+ with an ISH ratio >/= 2.0, in eight pathology centers across Can
22 imary breast cancer were analyzed by IHC and ISH; HER2 and chromosome 17 centromere (CEP17) counts we
23 ion, we identified and characterized JHF and ISH disease-causing mutations in the capillary morphogen
27 zed reporter deposition-Ng-autometallography ISH) and a conventional indirect alkaline phosphatase me
30 H-labeled cells was more restricted than AVT ISH labeling and was limited to regions of the preoptic
31 he SQuISH protocol against a riboprobe-based ISH procedure by comparing the mRNA expression levels in
32 e 10-17-fold higher with the riboprobe-based ISH than with the SQuISH procedure and the relative abun
33 ely 1.5-fold higher with the riboprobe-based ISH than with the SQuISH procedure, although the relativ
34 ol for studying in situ hybridization-based (ISH) expression patterns in the Allen Brain Atlas, a gen
35 ole procedure takes only 3 days and, because ISH conditions are the same for each probe tested, allow
36 he quality of each probe is evaluated before ISH using a RNA probe quantification (dot blot) assay.
37 duced mixed expired NO and suggest that both ISH and allergen-induced bronchoconstriction share patho
38 iduals with atopic asthma who underwent both ISH challenge and allergen challenge, and compared these
42 tin receptor gene expression in rat brain by ISH using a probe complementary to mRNA for all leptin r
44 ytic cycle of infection were not detected by ISH; and (4) subsets of neurons were selectively vulnera
49 spectively analyzed RAR-beta mRNA levels (by ISH using a digoxigenin-labeled antisense riboprobe) in
50 ial 16S rRNA expression was also measured by ISH, and the results revealed that there was localizatio
53 centages of hepatocytes were HCV-positive by ISH that correlated with hepatocyte ultrastructural chan
54 ion (HER2 copy number or HER2/CEP17 ratio by ISH based on counting at least 20 cells within the area)
55 ened for trial entry, 40.8% were in ASCO-CAP ISH group 1, 0.7% in group 2; 0.5% in group 3, 4.1% in g
61 eased sensitivity compared with conventional ISH and was shown to be specific for HTLV-1 tax DNA.
65 Both are believed to be allelic disorders; ISH is distinguished from JHF by its more severe phenoty
66 16 positive (p16+), 115 (48%) were HPV16 DNA ISH positive (ISH16+), and 134 (56%) were positive for a
70 publicly available collection of Drosophila ISH images, and show that our method achieves excellent
76 lasma EBV-DNA is highly concordant with EBER-ISH in HL and suggest that it may have prognostic utilit
78 available collection of Drosophila embryonic ISH images from the Berkeley Drosophila Genome Project,
80 t SPEX(2), an automatic system for embryonic ISH image processing, which can extract, transform, comp
81 munohistochemistry for p16, and fluorescence ISH for EGFR gene copy number were performed on tissue m
82 gene searches, colorimetric and fluorescent ISH image viewers, graphical displays of ISH, microarray
83 digoxigenin-labeled RNA ISH; RNA fluorescent ISH (FISH); and protein immunofluorescence (IF)-RNA FISH
91 descriptors to capture local statistics from ISH images and used the bag-of-words approach to build i
92 ypt sections double labeled using histone H3 ISH and BrdUrd, 92% of 1572 labeled cells exhibited both
94 red in single-labeled sections by histone H3 ISH tightly correlated with that found by in vivo BrdUrd
97 2% (23 of 95), and 19.0% (27 of 142) and HPV ISH was positive in 6.5% (six of 93), 14.6% (15 of 103),
98 sis (JHF) and infantile systemic hyalinosis (ISH) are autosomal recessive syndromes of unknown etiolo
99 refore, using Ventana in situ hybridisation (ISH), quantitative PCR assays and biomarkers of producti
103 ts distribution using in situ hybridization (ISH) and immunohistochemistry (IHC) combined with light
104 sion were assessed by in situ hybridization (ISH) and immunohistochemistry on tissue microarrays and
106 llel approaches, dual in situ hybridization (ISH) and neurotoxic lesions of DA neurons by using 6-hyd
107 culture, we performed in situ hybridization (ISH) and polymerase chain reaction (PCR) to detect KSHV
108 nd data type [such as in situ hybridization (ISH) and supporting histology, microarray, RNA sequencin
109 stochemistry (IHC) or in situ hybridization (ISH) as a predictor of benefit from anti-HER2 therapy.
110 uate a commercialized in situ hybridization (ISH) assay for detecting human papillomavirus (HPV) DNA,
111 ethods, by DFA, by an in situ hybridization (ISH) assay, specifically designed to detect L. pneumophi
112 Real-time RT-PCR and in situ hybridization (ISH) assays confirmed these miRNA expression profiles in
113 culture-independent, in situ hybridization (ISH) assays for the detection of MAC in culture, sputum,
114 ody mRNA patterns via in situ hybridization (ISH) calls for development of accurate and automatic ima
115 he mRNA of a gene via in situ hybridization (ISH) during the development of a Drosophila melanogaster
118 und to be positive by in situ hybridization (ISH) for HSV-1 latency-associated transcripts (LAT), the
121 DNA sequences before in situ hybridization (ISH) for localization or used ISH with radioactively-lab
123 unohistochemistry and in situ hybridization (ISH) for neutrophil and macrophage markers, cell adhesio
124 novel method of mRNA in situ hybridization (ISH) for the detection of transcriptionally active HR-HP
125 s high-resolution 3-D in situ hybridization (ISH) gene expression patterns in multiple developing sta
126 ion and complementary in situ hybridization (ISH) gene expression studies targeting selected genes in
129 NA is undetectable by in situ hybridization (ISH) in 50% of non-small-cell lung cancers (NSCLC).
130 us system (CNS) using in situ hybridization (ISH) in combination with a genetic knock-in approach.
132 Detection of RNAs by in situ hybridization (ISH) is a well-established technique that permits the st
135 sing a newly modified in situ hybridization (ISH) method for detecting hepatitis C virus (HCV) RNA.
136 ibe a whole-mount RNA in situ hybridization (ISH) method optimized for detection of the cellular and
137 er, we implemented an in situ hybridization (ISH) method to reveal the spatial distribution of miRNA
140 neity by fluorescence in situ hybridization (ISH) provides additional tissue morphology at single-cel
141 ed a highly sensitive in situ hybridization (ISH) system capable of HCV RNA and ISG mRNA detection in
144 unohistochemistry and in situ hybridization (ISH) to characterize changes in perinatal PR expression
145 restriction, we used in situ hybridization (ISH) to detect the frequency of RNA expression for nine
146 this effect, we used in situ hybridization (ISH) to determine whether leptin alters expression of hy
149 s this issue, we used in situ hybridization (ISH) to measure chemokine and cytokine mRNA expression l
150 ion was determined by in situ hybridization (ISH) using 35S-labelled riboprobes and immunohistochemis
153 histone H3 mRNA using in situ hybridization (ISH) was assessed as a measure of S-phase cells and comp
155 could be detected by in situ hybridization (ISH) with specific antisense oligonucleotide probes in l
158 ixative of choice for in situ hybridization (ISH), and specific anecdotal cautions interdicting the u
159 immunohistochemistry, in situ hybridization (ISH), and Western and Northern blotting, we found that b
160 nglion cells (GCs) by in situ hybridization (ISH), immunofluorescence (IF), and Western blotting.
161 d by a combination of in situ hybridization (ISH), immunofluorescence, and PCR for positive-strand an
170 ection of the LATs by in situ hybridization (ISH); (3) transcripts expressed during the lytic cycle o
171 tumor cell: group 1 (in situ hybridization [ISH]-positive): HER2-to-chromosome 17 centromere ratio >
174 atients with isolated systolic hypertension (ISH), but the effect of treatment of ISH on LV mass is n
178 of the spatial pattern of gene expression in ISH images, enabled by our recently developed [Formula:
180 l gene functions can be extracted from large ISH image databases such as the Allen Brain Atlas 1 and
188 tion-specific PCR in situ hybridization (MSP-ISH), which allows for the methylation status of specifi
195 (HPV) DNA, we compared the ability of a new ISH probe, Inform HPV III (Ventana Medical Systems, Tucs
197 ent ISH image viewers, graphical displays of ISH, microarray and RNA sequencing data, Brain Explorer
203 e results call into question the validity of ISH results derived by the use of other gene loci, such
205 ibroblasts derived from patients with JHF or ISH suggests that CMG2 mutations abrogate normal cell in
206 oportion of non-OP HNSCCs that were p16+ (or ISH+) increased among whites (P = .04 for trend) but not
207 Explorer also allows viewing of the original ISH images referenced from any point in a 3D data set.
211 Also, intracellular amplification by PCR-ISH significantly increased sensitivity compared with co
213 ted by PCR-driven in situ hybridization (PCR-ISH), and the number of viral genomes per cell was estim
214 When evaluated by reverse transcription-PCR-ISH, only a small proportion of experimentally infected
216 e have developed a standardized quantitative ISH (SQuISH) protocol that utilizes multiple radioactive
221 varies: whole-mount, digoxigenin-labeled RNA ISH; RNA fluorescent ISH (FISH); and protein immunofluor
222 this protocol, which is similar to other RNA ISH protocols, but optimized for whole-mount Drosophila
223 Epstein-Barr encoded RNA detection using RNA ISH with fluorescein isothiocyanate-labeled oligonucleot
224 ght-field dual-colour chromogenic and silver ISH assays with an image-based computational workflow (I
226 established a highly sensitive and specific ISH assay for the detection of HBV RNA, DNA, and cccDNA.
244 vaginal mucosa as early as 1 day p.i. by TSA-ISH and in retropharyngeal, tracheobronchial, or externa
245 signal-amplified in situ hybridization (TSA-ISH), and immunohistochemistry between days 1 and 12 pos
248 hybridization (ISH) for localization or used ISH with radioactively-labeled probes to obtain adequate
252 llow-up, younger and middle-aged adults with ISH had higher relative risk for CVD and CHD mortality t
253 men aged 60 years and older at baseline with ISH (systolic blood pressure [BP], > or = 160 mm Hg; dia
258 IHC signal distribution was consistent with ISH results, with transport of the protein to processes,
265 or CVD and CHD mortality risk for those with ISH were 1.23 (95% confidence interval [CI]: 1.03 to 1.4
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