18 results on '"Matsushima C"'
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2. Formation of a thin Mn III oxide film on noble metal electrodes from a manganese solution
- Author
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Nakayama, M, Matsushima, C, and Ogura, K
- Published
- 2002
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3. Formation of a thin MnIII oxide film on noble metal electrodes from a manganese solution
- Author
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Nakayama, M, primary, Matsushima, C, additional, and Ogura, K, additional
- Published
- 2002
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4. HOUSEHOLD USES OF TIME - TRANSITIONS FROM 1960 TO 1980.
- Author
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MATSUSHIMA, C. and SUZUKI, Y.
- Abstract
Studies of time-use in Japan were reviewed by Tanaka at the Uppsala Conference,
1 followed by a review of time-input for household work given by Matsushima at the Bulgaria Conference.2 This paper will study the changes of household work with data based on past national 5-year interval surveys, the NHK (Nippon Hoso Kyokai) Japan Broadcasting Corporation surveys of 1960, 1965, 1970, (1973 interim), 1975 and 1980. The latest 1980 survey has been summarized by Nakanishi.3 [ABSTRACT FROM AUTHOR]- Published
- 1983
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5. Association of Some Porcine Muscle Characteristics with Postmortem Temperature and Plasma 17-Hydroxycorticosteroid Levels
- Author
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Matsushima, C. Y. and Topel, D. G.
- Abstract
The association of postmortem muscle temperature with chemical and physical properties of the M. longissimusand plasma 17-hydroxycorticosteroids from pigs receiving a minimum of preslaughter stress was studied. A nonsignificant narrow range of plasma 17-OHCS between the Duroc, Poland China, Hampshire and Yorkshire strains was found. Antemortem stress under the reported slaughter conditions appeared to have little influence on plasma 17-OHCS levels from the four strains. But differences between strains in the rate of pH decline and ultimate physical properties of the M. longissimuswere evident in sides held at 2° C. The Poland China strain exhibited muscles with fastest rate of glycolysis and lowest subjective color and firmness score. Retaining carcasses at 40° C. for 4 hr. postmortem accelerated the rate of pH decline and decreased water-binding capacity. Color and gross morphological changes appeared related more to changes in pH during early postmortem periods than to the ultimate pH. At the end of the 24 hr. chill period, chilled sides were darker and less exudative than those held at the higher temperature. However, muscles held at 40° C. were also adjudged slightly pale, but normal in firmness and degree of exudation. Sarcoplasmic and myofibrillar protein extractability was greatly reduced in unchilled muscles.
- Published
- 1969
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6. Influence of Induced Adrenal Insufficiency and Stress on Porcine Plasma and Muscle Characteristics
- Author
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Marple, D. N., Topel, D. G., and Matsushima, C. Y.
- Abstract
Injecting 100 mg. prednisolone daily for days resulted in atrophy of the adrenal gland. The animals were stressed 48 hr. after recieving the last prednisolone injection and then sacrificed. Susceptibility to stress was increased in the partial adrenal insufficient pigs determined by their inability to withstand 5 min. of physical exercise before slaughter. Plasma lactate levels were increased significantly (P<.05) due to the effect of the physical exercise, and blood pH at death was significantly creased among the stressed adrenal insufficient group. Initial lactic acid content of the M. longissimuswas significantly lower in group two pigs when compared to group three. No significant differences were noted among 24-hr, muscle lactate levels. The glycogen content of the M. longissimuswas significantly increased because of prednisolone injections, but the level of initial muscle glycogen did not appear to influence the ultimate amount of lactic acid produced by postmortem anerobic glycolysis. No significant differences were noted among treatments when M. longissimusvalues and color scores were examined statistically. Low levels of plasma 17-OHCS per sedid not serve to increase the rate of postmortem anerobic glycolysis. The partial adrenal insufficient pigs used in this study may be unable to adequately remove high levels of lactic acid from the blood and muscle during exhaustive exercise.
- Published
- 1969
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7. Phase 2 Trial of Veliparib, Local Irradiation and Temozolomide in Patients with Newly Diagnosed High-Grade Glioma: A Children's Oncology Group Study.
- Author
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Karajannis MA, Onar-Thomas A, Lin T, Baxter PA, Boué DR, Cole BL, Fuller C, Haque S, Jabado N, Lucas JT Jr, MacDonald SM, Matsushima C, Patel N, Pierson CR, Souweidane MM, Thomas DL, Walsh MF, Zaky W, Leary SES, Gajjar A, Fouladi M, and Cohen KJ
- Abstract
Background: The outcome for pediatric patients with high-grade glioma (HGG) remains poor. Veliparib, a potent oral poly(adenosine diphosphate-ribose) polymerase (PARP) 1/2 inhibitor, enhances the activity of radiotherapy and DNA-damaging chemotherapy., Methods: We conducted a single-arm, non-randomized phase 2 clinical trial to determine whether treatment with veliparib and radiotherapy, followed by veliparib and temozolomide, improves progression-free survival in pediatric patients with newly diagnosed HGG without H3 K27M or BRAF mutations compared to patient level data from historical cohorts with closely matching clinical and molecular features. Following surgical resection, newly diagnosed children with non-metastatic HGG were screened by rapid central pathology review and molecular testing. Eligible patients were enrolled on Stratum 1 (IDH wild-type) or Stratum 2 (IDH mutant)., Results: Both strata were closed to accrual for futility after planned interim analyses. Among the 23 eligible patients who enrolled on Stratum 1 and received protocol therapy, the 1-year event-free survival (EFS) was 23% (standard error, SE = 9%) and 1-year overall survival (OS) was 64% (SE = 10%). Among the 14 eligible patients who enrolled on Stratum 2 and received protocol therapy, the 1-year EFS was 57% (SE = 13%) and 1-year OS was 93% (SE = 0.7%)., Conclusions: Rapid central pathology review and molecular testing for eligibility was feasible. The protocol therapy including radiation, veliparib and temozolomide was well tolerated but failed to improve outcome compared to clinically and molecularly matched historical control cohorts treated with higher doses of alkylator chemotherapy., (© The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)
- Published
- 2024
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8. Neonatal subpial hemorrhage along the medial side of the temporal lobe: Two case reports.
- Author
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Matsubara N, Kanagaki M, Ito S, Matsushima C, Ide M, Kitamura R, Nishida Y, and Akasaka Y
- Abstract
Neonatal subpial hemorrhage has been underrecognized until recently and its pathophysiology remains unclear. Advances in magnetic resonance imaging have facilitated the identification of hemorrhage within the subpial space and cohort studies recently reported its imaging and clinical features. We encountered two cases of neonatal subpial hemorrhage along the medial side of the temporal lobe. Case 1: A 1-day-old boy had repeated apneic attacks with cyanosis from 2 hours after birth at 39 weeks of gestation by vacuum extraction delivery. Computed tomography and magnetic resonance imaging showed subpial hemorrhage from the medial to caudal side of the right temporal lobe with T2 prolongation in the underlying cerebral parenchyma. Case 2: A 0-day-old boy had repeated apneic attacks with cyanosis from 3 hours after birth at 39 weeks of gestation by vaginal delivery. Subpial hemorrhage was observed from the anterior to medial side of the left temporal lobe on computed tomography and magnetic resonance imaging. On magnetic resonance imaging, the adjacent brain parenchyma showed a hyperintense signal on T2-weighted imaging. No abnormalities or signs of fetal distress were noted in the course of delivery. A mildly prolonged activated partial thromboplastin clotting time, an elevated D-dimer level, and low fibrinogen level were detected in a blood examination after birth in both cases. Both cases had subpial hemorrhage along the medial side of the temporal lobe, which suggested that an external mechanical force with fetal head molding during delivery caused subpial hemorrhage; however, other factors, including coagulopathy, may be involved in its pathophysiology., (© 2022 The Authors. Published by Elsevier Inc. on behalf of University of Washington.)
- Published
- 2022
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9. Sensitive detection of GATA1 mutations using complementary DNA-based analysis for transient abnormal myelopoiesis associated with the Down syndrome.
- Author
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Mizuta S, Yamane N, Mononobe S, Watanabe A, Kitamura R, Takahara T, Matsushima C, Yoshida A, Okamoto S, Tanaka K, Iwai A, Ikegawa A, Wada T, Usami I, Maihara T, Komai T, Heike T, Nishida Y, and Kobayashi K
- Subjects
- DNA, Complementary, GATA1 Transcription Factor genetics, Humans, Mutation, Down Syndrome complications, Down Syndrome diagnosis, Down Syndrome genetics, Leukemia, Megakaryoblastic, Acute complications, Leukemia, Megakaryoblastic, Acute diagnosis, Leukemia, Megakaryoblastic, Acute genetics, Leukemoid Reaction diagnosis, Leukemoid Reaction genetics
- Abstract
Introduction: GATA1 mutation plays an important role in initiating transient abnormal myelopoiesis (TAM) and in the clonal evolution towards acute megakaryoblastic leukaemia (AMKL) associated with Down syndrome (DS). This study aimed to develop and validate the clinical utility of a complementary DNA (cDNA) analysis in parallel with the conventional genomic DNA (gDNA) Sanger sequencing (Ss), as an initial screening test for GATA1 mutations., Methods: GATA1 mutations were evaluated using both gDNA and cDNA in 14 DS patients using Ss and fragment analysis (FA), respectively., Results: The detection sensitivity of conventional gDNA sequencing was limited in low blast percentage TAM (LBP-TAM); however, cDNA-based Ss readily detected all the pathognomonic GATA1 mutations. The cDNA-based FA readily detected GATA1 frameshift mutation with a reliable sensitivity ranging from 0.005% to 0.01% of clonal cells., Conclusions: GATA1 mutations are heterogeneous; therefore, we would like to propose a dual cDNA and gDNA analysis as a standard diagnostic approach, especially for LBP-TAM. cDNA-based FA promises an excellent sensitivity for detecting frameshift GATA1 mutations in the longitudinal clonal evolution towards AMKL without using a patient specific primer., (© 2021 John Wiley & Sons Ltd.)
- Published
- 2022
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10. Multiple analysis of root exudates and microbiome in rice (Oryza sativa) under low P conditions.
- Author
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Matsushima C, Shenton M, Kitahara A, Wasaki J, Oikawa A, Cheng W, Ikeo K, and Tawaraya K
- Subjects
- Exudates and Transudates, Plant Roots, Rhizosphere, Soil, Microbiota, Oryza
- Abstract
Plants release various metabolites from roots and root exudates contribute to differences in stress tolerance among plant species. Plant and soil microbes have complex interactions that are affected by biotic and abiotic factors. The purpose of this study was to examine the differences in metabolites in root exudates of rice (Oryza sativa) cultivars and their correlation with bacterial populations in the rhizosphere. Two rice cultivars (O. sativa cv. Akamai and O. sativa cv. Koshihikari) were grown in soils fertilized with 0 g P kg
-1 (- P) or 4.8 g P kg-1 (+ P). Root exudates and root-attached soil were collected at 13 and 20 days after transplanting (DAT) and their metabolites and bacterial community structure were determined. The exudation of proline, serine, threonine, valine and 4-coumarate were increased under low P conditions in both cultivars. There was a positive correlation between the concentration of pantothenate in root exudates and the representation of members of the genera Clostridium and Sporosarcina, which were negatively correlated with root dry weight. Gracilibacter, Opitutus, Pelotomaculum, Phenylobacterium and Oxobacter were positively correlated with root dry weight and presence of allantoin, 2-aminobtyrate and GlcNac. This study provides new information about the response of plants and rhizosphere soil bacteria to low P conditions., (© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)- Published
- 2021
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11. Monocyte Chemoattractant Protein-1 (MCP-1) as a Potential Therapeutic Target and a Noninvasive Biomarker of Liver Fibrosis Associated With Transient Myeloproliferative Disorder in Down Syndrome.
- Author
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Kobayashi K, Yoshioka T, Miyauchi J, Nakazawa A, Yamazaki S, Ono H, Tatsuno M, Iijima K, Takahashi C, Okada Y, Teranishi K, Matsunaga T, Matsushima C, Inagaki M, Suehiro M, Suehiro S, Nishitani M, Kubota H, Iio J, Nishida Y, Katayama T, Takada N, Watanabe K, Yamamoto T, Yasumizu R, Matsuoka K, Ohki K, Kiyokawa N, Maihara T, and Usami I
- Subjects
- Biomarkers, Cytokines analysis, Diagnosis, Differential, Humans, Infant, Newborn, Liver chemistry, Liver pathology, Liver Cirrhosis etiology, Chemokine CCL2 analysis, Down Syndrome complications, Leukemoid Reaction complications, Liver Cirrhosis diagnosis
- Abstract
Liver fibrosis is one of the common complications of transient myeloproliferative disorder (TMD) in Down syndrome (DS), but the exact molecular pathogenesis is largely unknown. We herein report a neonate of DS with liver fibrosis associated with TMD, in which we performed the serial profibrogenic cytokines analyses. We found the active monocyte chemoattractant protein-1 expression in the affected liver tissue and also found that both serum and urinary monocyte chemoattractant protein-1 concentrations are noninvasive biomarkers of liver fibrosis. We also showed a prospective of the future anticytokine therapy with herbal medicine for the liver fibrosis associated with TMD in DS.
- Published
- 2017
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12. Synthesis of Recombinant Mouse Crystallin Proteins and in Vitro Measurement of Their Refractivity.
- Author
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Furuyama A, Matsushima C, Yokoi T, Ueda M, and Tamiya E
- Abstract
The eye lens is an organ that focuses light onto the retina and is reported to have a high refractive index in vertebrates. An analysis of refractivity was conducted using recombinant mouse Crystallin proteins produced in Escherichia coli ( E. coli ) compared with bovine serum albumin (BSA) and other commercially available proteins. Not only did we measure the refractivity but for one of the crystallins, Cryba1, we also confirmed that it responds uniquely to its environmental conditions. The crystallin showed high refractivity, as expected, and we confirmed that the electrical charge of the Cryba1 molecule influences its refractivity.
- Published
- 2017
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13. Identification of Phosphoinositide-Binding Protein PATELLIN2 as a Substrate of Arabidopsis MPK4 MAP Kinase during Septum Formation in Cytokinesis.
- Author
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Suzuki T, Matsushima C, Nishimura S, Higashiyama T, Sasabe M, and Machida Y
- Subjects
- Amino Acid Sequence, Arabidopsis cytology, Arabidopsis physiology, Arabidopsis Proteins genetics, Carrier Proteins genetics, Carrier Proteins metabolism, Cytokinesis, Genes, Reporter, Mitogen-Activated Protein Kinases metabolism, Phosphorylation, Plant Roots cytology, Plant Roots genetics, Plant Roots physiology, Protein Domains, Proteomics, Arabidopsis genetics, Arabidopsis Proteins metabolism, MAP Kinase Signaling System, Mitogen-Activated Protein Kinases genetics, Phosphatidylinositols metabolism
- Abstract
The phosphorylation of proteins by protein kinases controls many cellular and physiological processes, which include intracellular signal transduction. However, the underlying molecular mechanisms of such controls and numerous substrates of protein kinases remain to be characterized. The mitogen-activated protein kinase (MAPK) cascade is of particular importance in a variety of extracellular and intracellular signaling processes. In plant cells, the progression of cytokinesis is an excellent example of an intracellular phenomenon that requires the MAPK cascade. However, the way in which MAPKs control downstream processes during cytokinesis in plant cells remains to be fully determined. We show here that comparisons, by two-dimensional difference gel electrophoresis, of phosphorylated proteins from wild-type Arabidopsis thaliana and mutant plants defective in a MAPK cascade allow identification of substrates of a specific MAPK. Using this method, we identified the PATELLIN2 (PATL2) protein, which has a SEC14 domain, as a substrate of MPK4 MAP kinase. PATL2 was concentrated at the cell division plane, as is MPK4, and had binding affinity for phosphoinositides. This binding affinity was altered after phosphorylation of PATL2 by MPK4, suggesting a role for the MAPK cascade in the formation of cell plates via regeneration of membranes during cytokinesis., (© The Author 2016. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists.)
- Published
- 2016
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14. Comparison of the mesophilic cellulosome-producing Clostridium cellulovorans genome with other cellulosome-related clostridial genomes.
- Author
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Tamaru Y, Miyake H, Kuroda K, Nakanishi A, Matsushima C, Doi RH, and Ueda M
- Subjects
- Bacterial Proteins metabolism, Cellulosomes genetics, Clostridium enzymology, Clostridium cellulovorans enzymology, Genome Size, Molecular Sequence Data, Bacterial Proteins genetics, Cellulosomes enzymology, Clostridium genetics, Clostridium cellulovorans genetics, Genome, Bacterial
- Abstract
Clostridium cellulovorans, an anaerobic and mesophilic bacterium, degrades native substrates in soft biomass such as corn fibre and rice straw efficiently by producing an extracellular enzyme complex called the cellulosome. Recently, we have reported the whole-genome sequence of C. cellulovorans comprising 4220 predicted genes in 5.10 Mbp [Y. Tamaru et al., (2010) J. Bacteriol., 192: 901–902]. As a result, the genome size of C. cellulovorans was about 1 Mbp larger than that of other cellulosome-producing clostridia, mesophilic C. cellulolyticum and thermophilic C. thermocellum. A total of 57 cellulosomal genes were found in the C. cellulovorans genome, and they coded for not only carbohydrate-degrading enzymes but also a lipase, peptidases and proteinase inhibitors. Interestingly, two novel genes encoding scaffolding proteins were found in the genome. According to KEGG metabolic pathways and their comparison with 11 Clostridial genomes, gene expansion in the C. cellulovorans genome indicated mainly non-cellulosomal genes encoding hemicellulases and pectin-degrading enzymes. Thus, by examining genome sequences from multiple Clostridium species, comparative genomics offers new insight into genome evolution and the way natural selection moulds functional DNA sequence evolution. Our analysis, coupled with the genome sequence data, provides a roadmap for constructing enhanced cellulosome-producing Clostridium strains for industrial applications such as biofuel production.
- Published
- 2011
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15. Relationship between retinal vein occlusion and carotid artery lesions.
- Author
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Matsushima C, Wakabayashi Y, Iwamoto T, Yamauchi Y, Usui M, and Iwasaki T
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- Aged, Aged, 80 and over, Carotid Arteries diagnostic imaging, Carotid Stenosis diagnostic imaging, Carotid Stenosis physiopathology, Female, Fluorescein Angiography, Humans, Male, Middle Aged, Retinal Vein Occlusion physiopathology, Ultrasonography, Doppler, Visual Acuity, Carotid Stenosis complications, Retinal Vein Occlusion etiology
- Abstract
Purpose: To investigate the relationship between retinal vein occlusion (RVO) and carotid artery lesions., Methods: For patients with RVO who presented to the Ophthalmology Department of Tokyo Medical University Hospital between 2000 and 2003, carotid artery evaluation was possible on 58 eyes of 57 patients aged 51 years to 88 years (mean, 70.1 years). Thirty-nine patients (40 eyes) had central RVO (CRVO), and 18 patients (18 eyes) had branch RVO (BRVO). The observation period ranged from 6 months to 28 months (mean, 14 months). A diagnostic ultrasound device was used to detect carotid artery lesions., Results: Carotid artery lesions were detected in 19 (49%) of 39 patients with CRVO and in 4 (22%) of 18 patients with BRVO. In CRVO, 6 eyes without carotid artery lesions but no eye with carotid artery lesions had good decimal visual acuity of >or=0.8 (P < 0.05). Fluorescein angiographic findings identified a significantly (P < 0.01) higher incidence of the ischemic type in cases with carotid lesions (15 eyes; 79%) than in cases without carotid lesions (8 eyes; 40%)., Conclusions: The findings suggest that the presence of a carotid artery lesion has a considerable association with the development and prognosis of CRVO.
- Published
- 2007
- Full Text
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16. The Caenorhabditis elegans ADAMTS family gene adt-1 is necessary for morphogenesis of the male copulatory organs.
- Author
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Kuno K, Baba C, Asaka A, Matsushima C, Matsushima K, and Hosono R
- Subjects
- ADAM Proteins, ADAMTS1 Protein, Amino Acid Sequence, Animals, Animals, Genetically Modified, Base Sequence, Caenorhabditis elegans Proteins biosynthesis, Cattle, Cosmids, Extracellular Matrix metabolism, Gene Deletion, Genes, Reporter, Green Fluorescent Proteins, Humans, Luminescent Proteins metabolism, Male, Mice, Models, Genetic, Molecular Sequence Data, Mutation, Phenotype, Physical Chromosome Mapping, Promoter Regions, Genetic, Protein Structure, Tertiary, Recombinant Fusion Proteins metabolism, Reverse Transcriptase Polymerase Chain Reaction, Sequence Homology, Amino Acid, Caenorhabditis elegans chemistry, Caenorhabditis elegans genetics, Caenorhabditis elegans Proteins genetics, Caenorhabditis elegans Proteins physiology, Disintegrins genetics, Genitalia, Male physiology, Metalloendopeptidases genetics
- Abstract
Remodeling of the extracellular matrix (ECM) is pivotal for various biological processes, including organ morphology and development. The Caenorhabditis elegans male tail has male-specific copulatory organs, the rays and the fan. Ray morphogenesis, which involves a rapid remodeling of the ECM, is an important model of morphogenesis, although its mechanism is poorly understood. ADAMTS (a disintegrin-like and metalloproteinase with thrombospondin type I motifs) is a novel metalloproteinase family that is thought to be an important regulator for ECM remodeling during development and pathological states. We report here that a new C. elegans ADAMTS family gene, adt-1, plays an important regulatory role in ray morphogenesis. Inactivation of the adt-1 gene resulted in morphological changes in the rays as well as the appearance of abnormal protuberances around the rays. In addition, mating ability was remarkably impaired in adt-1 deletion mutant males. Furthermore, we found that the green fluorescent protein reporter driven by the adt-1 promoter was specifically expressed throughout the rays in the male tail. We hypothesize that ADT-1 controls the ray extension process via remodeling of the ECM in the cuticle.
- Published
- 2002
- Full Text
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17. [Carotid ultrasonographic and brain computerized tomographic findings in patients with vascular ocular syndromes].
- Author
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Iwamoto T, Matsushima C, Shimizu S, Takasaki M, Iwasaki T, and Usui M
- Subjects
- Aged, Amaurosis Fugax etiology, Female, Humans, Male, Middle Aged, Optic Neuropathy, Ischemic etiology, Retinal Artery Occlusion etiology, Retinal Vein Occlusion etiology, Risk Factors, Stroke etiology, Stroke prevention & control, Syndrome, Ultrasonography, Amaurosis Fugax diagnostic imaging, Brain diagnostic imaging, Carotid Arteries diagnostic imaging, Optic Neuropathy, Ischemic diagnostic imaging, Retinal Artery Occlusion diagnostic imaging, Retinal Vein Occlusion diagnostic imaging, Tomography, X-Ray Computed
- Abstract
To clarify the characteristics of cerebrovascular lesions in subtypes of vascular ocular syndrome, including amaurosis fugax(AF), retinal artery occlusion(RAO), and retinal vein occlusion(RVO), 93 patients with vascular ocular syndrome were studied by means of carotid ultrasonography(US) and brain computerized tomography(CT). The subjects comprised 21 patients with AF, 37 with RAO, and 35 with RVO who were sequentially given these diagnoses by the department of ophthalmology. On the basis of US findings, carotid lesions were defined as the presence of plaque or stenotic changes. CT findings were assessed for the presence and distribution of low-density areas(LDAs). Mean age was similar in each group, ranging from 64.5 to 67.4 years. The RAO group had high rates of men, hypertension, and smokers. US showed that the prevalence of carotid lesions ipsilateral to the affected eye was high in the RAO group and that severe stenosis and ulcerated plaque were present in 28.6% of the AF group and 45.9% of the RAO group. On CT examination, cerebral infarctions appeared as LDAs in about 10% of the patients in each group, and the incidence and distribution of LDAs were similar. Of 13 patients with cerebral infarction, only 2 were presumably due to carotid lesions; the others had a variety of causes. The discrepancy between US and CT findings was attributed to the small number of patients with cerebral infarction, since most patients had visual defects as an initial symptom. Our results suggest that extracranial carotid lesions, considered to be a major risk factor for stroke, should be carefully assessed in patients with AF or RAO to prevent further stroke.
- Published
- 2002
18. Structure-specific inhibition of cholesteryl ester transfer protein by azaphilones.
- Author
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Tomoda H, Matsushima C, Tabata N, Namatame I, Tanaka H, Bamberger MJ, Arai H, Fukazawa M, Inoue K, and Omura S
- Subjects
- Animals, Apolipoprotein A-I metabolism, Benzopyrans chemistry, Blotting, Western, Buffers, Cholesterol Ester Transfer Proteins, Cholesterol, HDL blood, Cholesterol, HDL metabolism, Cholesterol, LDL blood, Cholesterol, LDL metabolism, Humans, Lysine pharmacology, Mice, Mice, Transgenic, Structure-Activity Relationship, Benzopyrans pharmacology, Carrier Proteins antagonists & inhibitors, Cholesterol Esters metabolism, Glycoproteins metabolism
- Abstract
The effect of thirteen different fungal azaphilones, which have a common 6-iso-chromane-like ring, was tested on cholesteryl ester transfer protein (CETP) activity in vitro. Chaetoviridin B showed the most potent inhibitory activity with an IC50 value of < 6.2 microM, followed by sclerotiorin with an IC50 value of 19.4 microM. Rotiorin, chaetoviridin A and rubrorotiorin had moderate inhibitory activity (IC50 ; 30 approximately 40 microM), but others showed very weak or no inhibitory activity. The relationship between the structures and their inhibitory activity indicated that the presence of an electrophilic ketone(s) and/or enone(s) at both C-6 and C-8 positions in the isochromane-like ring is essential for eliciting CETP inhibitory activity. The transfer activity of both CE and TG was inhibited by sclerotiorin to approximately the same extent (IC50: 14.4 and 10.3 microM, respectively). A model of the reaction suggested that sclerotiorin reacts with a primary amine of amino acids such as lysine in the protein to form a covalent bond.
- Published
- 1999
- Full Text
- View/download PDF
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