Logic Ciucuits Using Solution-processed Single-walled Carbon Nanotue Transistors

This letter reports on the realization of logic circuits employing solution-processed networks of single-walled carbon nanotubes. We constructed basic logic gates (inverter, NAND and NOR) with n- and p-type field-effect transistors fabricated by solution-based chemical doping. Complementary metal-oxide-semiconductor inverters exhibited voltage gains of up to 20, which illustrates the great potential of carbon nanotube networks for printable flexible electronics.Comment: 12 PAGES, 3 FIGURE

多接合タンデム太陽電池の電気特性の評価解析法に関する研究

学位の種別:課程博士University of Tokyo(東京大学

Comprehensive Comparative Genomics and Phenotyping of Methylobacterium Species

The pink-pigmented facultative methylotrophs (PPFMs), a major bacterial group found in the plant phyllosphere, comprise two genera: Methylobacterium and Methylorubrum. They have been separated into three major clades: A, B (Methylorubrum), and C. Within these genera, however, some species lack either pigmentation or methylotrophy, which raises the question of what actually defines the PPFMs. The present study employed a comprehensive comparative genomics approach to reveal the phylogenetic relationship among the PPFMs and to explain the genotypic differences that confer their different phenotypes. We newly sequenced the genomes of 29 relevant-type strains to complete a dataset for almost all validly published species in the genera. Through comparative analysis, we revealed that methylotrophy, nitrate utilization, and anoxygenic photosynthesis are hallmarks differentiating the PPFMs from the other Methylobacteriaceae. The Methylobacterium species in clade A, including the type species Methylobacterium organophilum, were phylogenetically classified into six subclades, each possessing relatively high genomic homology and shared phenotypic characteristics. One of these subclades is phylogenetically close to Methylorubrum species; this finding led us to reunite the two genera into a single genus Methylobacterium. Clade C, meanwhile, is composed of phylogenetically distinct species that share relatively higher percent G+C content and larger genome sizes, including larger numbers of secondary metabolite clusters. Most species of clade C and some of clade A have the glutathione-dependent pathway for formaldehyde oxidation in addition to the H4MPT pathway. Some species cannot utilize methanol due to their lack of MxaF-type methanol dehydrogenase (MDH), but most harbor an XoxF-type MDH that enables growth on methanol in the presence of lanthanum. The genomes of PPFMs encode between two and seven (average 3.7) genes for pyrroloquinoline quinone-dependent alcohol dehydrogenases, and their phylogeny is distinctly correlated with their genomic phylogeny. All PPFMs were capable of synthesizing auxin and did not induce any immune response in rice cells. Other phenotypes including sugar utilization, antibiotic resistance, and antifungal activity correlated with their phylogenetic relationship. This study provides the first inclusive genotypic insight into the phylogeny and phenotypes of PPFMs

The Effect of Susceptibility of Gadolinium Contrast Media on Diffusion-weighted Imaging and the Apparent Diffusion Coefficient

京都市立病院金沢大学医薬保健研究域保健学系Rationale and Objectives: The development of parallel magnetic resonance imaging has resulted in the frequent use of diffusion-weighted imaging (DWI) in clinical medicine, which usually involves the use of contrast medium. However, gadolinium (Gd) contrast medium may have some effect on DWI and the apparent diffusion coefficient (ADC). The present study was performed to determine whether the magnetic susceptibility of contrast medium alters the DWI signal and the value of ADC in some imaging techniques. Materials and Methods: Nonfat suppression DWI, short-time inversion recovery (STIR) combination, and chemical shift selective (CHESS) combination DWI were performed to examine 10 phantoms with gadolinium-meglumine gadopentetate (Gd-DTPA) dissolved at concentrations from 0.0005 to 0.1 mmol in physiologic saline as a contrast medium. The average pixel value and ADC of each method were determined. Results: ADC showed no differences between before and after treatment with contrast medium for all imaging techniques with Gd considered distributed over the whole tumor. The signal intensity did not change on nonfat suppression or CHESS combination DWI, but deteriorated on STIR. Conclusions: ADC was not influenced by the magnetic susceptibility of contrast medium. In addition, it was suggested that the ability of tumor detection may be reduced if STIR is used as fat suppression. © 2008 AUR

Effects of Iodinated Contrast Agent on Diffusion Weighted Magnetic Resonance Imaging

京都市立病院金沢大学医薬保健研究域保健学系Rationale and Objectives: To evaluate the effects of iodine contrast agent on diffusion signal intensity and apparent diffusion coefficient (ADC) in diffusion-weighted imaging (DWI) studies in magnetic resonance imaging (MRI) examination just after computed tomography (CT) contrast imaging. Materials and Methods: On a 1.5 T MRI scanner, ADC was calculated from the signal intensity of DWI (b = 0 and 1000) using phantoms filled with contrast agent (0, 4.5, 6.0, 9.0, 30, and 60 mgI/mL). We evaluated the signal intensities of DWI and ADC in 10 patients (3 women, 7 men, 35-68 years old) examined by MRI study less than 40 minutes after injection of 100 mL of iopamidol (300 mgI/mL) for CT study. Results: The DWI signal increased until a CT value of 190 HU, but showed no changes above this value. The ADC decreased with increases in CT value. Less than 40 minutes after injection of iopamidol (300 mgI/mL) for CT scan, the signal intensity of DWI was significantly increased and ADC was significantly decreased. Conclusions: It is necessary to recognize the rate of decrease of ADC, because it is dependent on the density of iodine contrast agents. © 2009 AUR

Imaging parameter effects in apparent diffusion coefficient determination of magnetic resonance imaging

金沢大学医薬保健研究域保健学系京都市立病院Purpose: Although an apparent diffusion coefficient (ADC) value is often used for differential diagnosis of tumours, it varies with scanning parameters. The present study was performed to investigate the influence of imaging parameters, i.e., b value, repetition time (TR) and echo time (TE), on ADC value. Methods: The phantoms were scanned using diffusion weighted imaging (DWI) with changing b values (b = 0-3000 s/mm2), TR and TE to determine the influence on ADC. Moreover, ADC of the brain in normal volunteers was determined with varying b values (b = 0-1000 s/mm2). Results: Diffusion decay curves were obtained by biexponential fitting in all phantoms. The points where fast and slow components of the biexponential decay crossed were called turning points. The b values of turning points that crossed from the biexponential curve were different in each phantom. The b values of turning points depended on ADC of fast diffusion component. When ADC is calculated using two b values of front and back for the turning point, the ADC value may be different. Therefore, it was necessary to perform calculations by b value until the turning point to obtain the ADC value of the fast component. In addition, b ≥ 100 was recommended to avoid the influence of perfusion by blood. Furthermore, the choice of long TR and short TE was effective for accurate measurement of ADC. Conclusion: It is important to determine the turning point for measuring ADC. © 2009 Elsevier Ireland Ltd. All rights reserved

Improvement on detectability of early ischemic changes for acute stroke using nonenhanced computed tomography: Effect of matrix size

京都市立病院金沢大学医薬保健研究域保健学系Purpose: It has recently been reported that intravenous recombinant tissue plasminogen activator improves the clinical outcome after acute stroke. Computed tomography (CT) is the standard imaging method used to determine the indication for thrombolysis. However, detection of early ischemic change often results in an increase in local radiation exposure. Therefore, the effects of decreased matrix size and use of a noise reduction filter were evaluated. Materials and methods: The low contrast resolution was compared for different matrix sizes and imaging filters using a contrast-detail phantom. In addition, early ischemic change in clinical images with matrix sizes of 256 × 256 and 128 × 128 processed using three imaging filters (Gaussian, smoothing, and unsharp mask) from 11 patients within 3 h of stroke onset was evaluated by seven radiologists in a blind manner. Results: The use of images with a matrix size of 256 × 256 and processed with the Gaussian filter increased the detection of early signs of acute stroke. Conclusions: This study was performed to determine whether the converted matrix size and use of imaging filters could improve the detectability of early ischemic change on CT images in acute stroke. To reduce the dose of radiation exposure for patients, it was effective to use an optimal noise reduction filter and reasonable matrix size. In particular, changing the matrix size to 256 × 256 was the most effective for detection of early ischemic change in examinations using clinical images. © 2009 Elsevier Ireland Ltd. All rights reserved

Differentiation of hepatic tumors by use of image contrast with T2-weighted MRI

金沢大学医薬保健研究域Differentiation of hepatic tumors is often evaluated in terms of qualitative diagnostic performance. The signal intensity patterns of hepatic masses are known to differ on certain T2-weighted imaging sequences. In this study, we investigated the quantitative analysis of hepatic masses by using an index called the "T2-shine ratio." Fast-spin-echo (FSE), half-Fourier acquisition single-shot turbo spin echo (HASTE), and true-FISP sequences obtained with quick-imaging techniques during a single breath-hold were examined in 74 patients. T2-shine ratios were calculated by use of the signals of regions of interest (ROIs) placed on a tumor and peripheral tissue: the T2-shine ratio is defined as (tumor signal-liver signal)/liver signal. The rate of change in the T2-shine ratio was compared among three sequences of FSE, HASTE, and true-FISP. The T2-shine ratio of FSE deducted from HASTE was significantly higher for hepatic cysts than for other masses. The T2-shine ratio of HASTE deducted from True-FISP was less than zero for hemangioma. For the value that deducted the T2-shine ratio of HASTE from the T2-shine ratio of true-FISP, hemangiomas had a significantly lower value than did cysts and metastases (P < 0.05), but there was no significant difference from hepatocellular carcinomas (HCCs). Although liver cysts, cavernous hemangiomas, and other lesions could be differentiated, it was virtually impossible to distinguish HCCs from metastatic tumors. In conclusion, the quantitative analysis of hepatic tumors was able to differentiate among these lesions by use of the T2-shine ratio. © 2008 Japanese Society of Radiological Technology and Japan Society of Medical Physics

Characterization of the novel mutant A78T-HERG from a long QT syndrome type 2 patient: Instability of the mutant protein and stabilization by heat shock factor 1

Background:The human ether-a-go-go-related gene (HERG) encodes the α-subunit of rapidly activating delayed-rectifier potassium channels. Mutations in this gene cause long QT syndrome type 2 (LQT2). In most cases, mutations reduce the stability of the channel protein, which can be restored by heat shock (HS). Methods: We identified the novel mutant A78T-HERG in a patient with LQT2. The purpose of the current study was to characterize this mutant protein and test whether HS and heat shock factors (HSFs) could stabilize the mutant protein. A78T-HERG and wild-type HERG (WT-HERG) were expressed in HEK293 cells and analyzed by immunoblotting, immunoprecipitation, immunofluorescence, and whole-cell patch clamping. Results: When expressed in HEK293 cells, WT-HERG gave rise to immature and mature forms of the protein at 135 and 155 kDa, respectively. A78T-HERG gave rise only to the immature form, which was heavily ubiquitinated. The proteasome inhibitor MG132 increased the expression of immature A78T-HERG and increased both the immature and mature forms of WT-HERG. WT-HERG, but not A78T-HERG, was expressed on the plasma membrane. In whole-cell patch clamping experiments, depolarizing pulses evoked E4031-sensitive HERG channel currents in cells transfected with WT-HERG, but not in cells transfected with A78T-HERG. The A78V mutant, but not A78G mutant, remained in the immature form similarly to A78T. Maturation of the A78T-HERG protein was facilitated by HS, expression of HSF-1, or exposure to geranyl geranyl acetone. Conclusions: A78T-HERG was characterized by protein instability and reduced expression on the plasma membrane. The stability of the mutant was partially restored by HSF-1, indicating that HSF-1 is a target for the treatment for LQT2 caused by the A78T mutation in HERG