Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 15 de 15
Filtrer
2.
Adv Sci (Weinh) ; 8(22): e2102718, 2021 Nov.
Article de Anglais | MEDLINE | ID: mdl-34590441

RÉSUMÉ

It is of importance to explore a new carbon nanomaterial possessing vital functions to fulfill the high standards for practical achievement of the electromagnetic (EM) barrier for blocking EM waves and the electrochemical (EC) barrier as a functional separator for EC energy storage. Herein, facile synthesis of a new class of carbon nanostructures, which consist of interconnected N-doped graphitic carbon nanocubes partially embedded by nickel nanoparticles, is described. The hollow interior of graphitic nanocube induces internal reflection of EM waves and confines active materials of EC energy storage. Nitrogen functionalities implanted in graphitic structure enhance electrical conductivity as well as improve chemical interaction with active materials. Furthermore, nickel nanoparticles in graphitic nanocube function as an EM wave-absorbing material and an electrocatalyst for EC energy storage. Through comprehensive assessments, remarkable performances originating from distinctive nanostructures give new insights into structural design for the carbon nanostructure-based high-performance EM and EC barriers.

3.
Cancers (Basel) ; 12(5)2020 May 25.
Article de Anglais | MEDLINE | ID: mdl-32466217

RÉSUMÉ

It is controversial as to whether papillary thyroid microcarcinoma (PTMC) has some genomic and transcriptomic characteristics that differentiate between an early-stage lesion that would eventually evolve into the larger papillary thyroid cancer (PTC), and an occult indolent cancer in itself. To investigate this, we comprehensively elucidated the genomic and transcriptomic landscapes of PTMCs of different sizes, using a large-scaled database. This study included 3435 PTCs, 1985 of which were PTMCs. We performed targeted next-generation sequencing for 221 PTCs and integrated these data with the data including The Cancer Genome Atlas (TCGA) project. The frequency of v-raf murine sarcoma viral oncogene homolog B (BRAF)V600E mutation was higher in PTMCs >0.5 cm than that in very small PTMCs (≤0.5 cm) and decreased again in PTCs >2 cm. Among PTMCs, the prevalence of mutations in rat sarcoma (RAS) and telomerase reverse transcriptase (TERT) promoter was not significantly different according to their size, but lower than in large PTCs. There was no change in the tumor mutational burden, the number of driver mutations, and transcriptomic profiles with tumor size, among PTMCs and all PTCs. Although a few genes with differential expression and TERT promoter mutations were found in a few PTMCs, our findings showed that there were no useful genomic or transcriptomic characteristics for the prediction of the future progression of PTMC.

4.
J Korean Med Sci ; 34(24): e172, 2019 Jun 24.
Article de Anglais | MEDLINE | ID: mdl-31222985

RÉSUMÉ

BACKGROUND: Non-invasive prenatal testing (NIPT) using cell-free fetal DNA from maternal plasma for fetal aneuploidy identification is expanding worldwide. The objective of this study was to evaluate the clinical utility of NIPT for the detection of trisomies 21, 18, and 13 of high-risk fetus in a large Korean population. METHODS: This study was performed retrospectively, using stored maternal plasma from 1,055 pregnant women with singleton pregnancies who underwent invasive prenatal diagnosis because of a high-risk indication for chromosomal abnormalities. The NIPT results were confirmed by karyotype analysis. RESULTS: Among 1,055 cases, 108 cases of fetal aneuploidy, including trisomy 21 (n = 57), trisomy 18 (n = 42), and trisomy 13 (n = 9), were identified by NIPT. In this study, NIPT showed 100% sensitivity and 99.9% specificity for trisomy 21, and 92.9% sensitivity and 100% specificity for trisomy 18, and 100% sensitivity and 99.9% specificity for trisomy 13. The overall positive predictive value (PPV) was 98.1%. PPVs for trisomies 21, 18, and 13 ranged from 90.0% to 100%. CONCLUSION: This study demonstrates that our NIPT technology is reliable and accurate when applied to maternal DNA samples collected from pregnant women. Further large prospective studies are needed to adequately assess the performance of NIPT.


Sujet(s)
Aberrations des chromosomes , Syndrome de Down/diagnostic , Syndrome de Patau/diagnostic , Adulte , Aneuploïdie , Études cas-témoins , Acides nucléiques acellulaires/métabolisme , Syndrome de Down/génétique , Femelle , Humains , Caryotype , Mâle , Adulte d'âge moyen , Valeur prédictive des tests , Grossesse , Diagnostic prénatal , République de Corée , Études rétrospectives , Syndrome de Patau/génétique , Syndrome d'Edwards/diagnostic , Syndrome d'Edwards/épidémiologie , Jeune adulte
5.
Medicina (Kaunas) ; 55(5)2019 May 18.
Article de Anglais | MEDLINE | ID: mdl-31109045

RÉSUMÉ

Background and Objectives: The purpose of this retrospective study was to identify predictors of short-term outcomes associated with a lumbosacral transforaminal epidural steroid injection (TFESI). Materials and Methods: The medical records of 218 patients, who were diagnosed with lumbosacral radiculopathy and treated with a TFESI, were reviewed in this retrospective study. A mixture of corticosteroid, lidocaine, and hyaluronidase was injected during TFESI. Patients with >50% pain relief on the numerical rating scale compared with the initial visit constituted the good responder group. Demographic, clinical, MRI, and electrodiagnostic data were collected to assess the predictive factors for short-term outcomes of the TFESI. Results: A multivariate logistic regression analysis demonstrated that a shorter duration of symptoms and a positive sharp wave (PSW)/fibrillation (Fib) observed in electrodiagnostic study (EDx) increased the odds of significant improvement 2-4 weeks after the TFESI. Conclusions: Shorter duration of symptoms and PSW/Fib on EDx were predictors of favorable short-term response to TFESI.


Sujet(s)
Injections épidurales/normes , Région lombosacrale , Radiculopathie/traitement médicamenteux , Adulte , Sujet âgé , Loi du khi-deux , Programme d'études/normes , Femelle , Humains , Injections épidurales/méthodes , Modèles logistiques , Mâle , Adulte d'âge moyen , Odds ratio , Mesure de la douleur/méthodes , Radiculopathie/complications , République de Corée , Études rétrospectives
6.
PM R ; 11(7): 731-736, 2019 07.
Article de Anglais | MEDLINE | ID: mdl-30735601

RÉSUMÉ

BACKGROUND: Anal sphincter needle electromyography (EMG) is a useful tool to evaluate various neurologic lesions. However, landmark-based needle placement has risks of missing the intended target including risk of bowel penetration. Ultrasound guidance has been widely used to enhance needle placement for various interventional procedures, but it has not been previously reported for use in anal sphincter EMG. OBJECTIVE: To demonstrate the accuracy of ultrasound-guided needle insertion into the external anal sphincter (EAS). DESIGN: Observational study. SETTING: Tertiary care university hospital. PARTICIPANTS: A single live male participant and six fresh cadavers. METHODS: A preliminary study was conducted in a single live male participant to investigate the utility of ultrasonography imaging for the EAS and proper transducer location. After this preliminary study, 12 sides of the EAS in six fresh cadavers were assessed. A hooked fine wire was inserted into the EAS under ultrasound guidance. MAIN OUTCOME MEASURES: Accuracy of needle placement was assessed after cadaver dissection. RESULTS: The EAS was easily identified with ultrasound in preliminary and cadaver studies. The needle tips were located in the EAS in 11 of 12 cadavers. CONCLUSIONS: Ultrasound-guided needle EMG of the EAS is convenient and accurate in cadavers and may be useful in clinical practice. Further studies comparing ultrasound-guided and landmark-guided needle EMG of the EAS in live patients will be needed.


Sujet(s)
Canal anal/physiologie , Électrodes implantées , Électromyographie/méthodes , Aiguilles , Échographie/méthodes , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Cadavre , Femelle , Volontaires sains , Humains , Mâle , Adulte d'âge moyen , Reproductibilité des résultats , Transducteurs
7.
PM R ; 11(5): 463-469, 2019 05.
Article de Anglais | MEDLINE | ID: mdl-30138721

RÉSUMÉ

BACKGROUND: The carotid artery must be avoided during stellate ganglion block. However, information on optimal neck position during the ultrasound-guided approach is limited. OBJECTIVE: To investigate the relation between the target area of the procedure and the carotid artery in different neck positions. DESIGN: Observational study. SETTING: Tertiary university. PARTICIPANTS: A total of 30 sides of the neck from 18 healthy participants were included. METHODS: An ultrasound transducer was placed at the level of the anterior tubercle of C6 with a short-axis view for measuring the distance from the tip of the C6 anterior tubercle to the margin of the carotid artery. The participants were first examined through ultrasonography in 3 different rotational neck positions (neutral, semicontralateral rotation, and full-contralateral rotation), in the supine position. After changing to the lateral decubitus position, the measurement was performed again in the same 3 neck positions. MAIN OUTCOME MEASURES: The C6 anterior tubercle to carotid distance was measured with ultrasound. RESULTS: The C6 anterior tubercle to carotid distance was the longest with full-contralateral neck rotation (P < .05). The distance was longer in the semicontralateral neck rotation compared with the neutral neck position (P < .05). Supine or decubitus positions did not affect the distance. CONCLUSIONS: We suggest that the full-contralateral neck rotation posture in either the supine or decubitus position is most beneficial for avoiding damage to the carotid artery during the ultrasound-guided stellate ganglion block. LEVEL OF EVIDENCE: Not applicable.


Sujet(s)
Bloc anesthésique du système nerveux autonome , Artère carotide commune/imagerie diagnostique , Cou , Positionnement du patient , Ganglion cervicothoracique/imagerie diagnostique , Échographie interventionnelle , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Bloc anesthésique du système nerveux autonome/effets indésirables , Indice de masse corporelle , Lésions traumatiques de l'artère carotide/étiologie , Vertèbres cervicales , Femelle , Humains , Mâle , Adulte d'âge moyen , Valeurs de référence
8.
Muscle Nerve ; 58(2): 304-306, 2018 Aug.
Article de Anglais | MEDLINE | ID: mdl-29510442

RÉSUMÉ

INTRODUCTION: The purpose of this study was to investigate the usefulness of the echogenicity (EI) ratio of the thenar to hypothenar muscle measured using ultrasonography in assessing the severity of carpal tunnel syndrome (CTS). METHODS: Fifty-nine hands of 30 patients electrodiagnostically confirmed as having CTS were classified into 3 subgroups (mild, moderate, and severe). The EI of the thenar and hypothenar muscles was measured with ultrasonography, and the EI ratio was calculated in the patients and 13 normal participants (26 hands). RESULTS: The average EI ratio was higher in the CTS group than in the control group. We also found a positive correlation between the severity of CTS and a high EI ratio measured with ultrasonography. DISCUSSION: The EI ratio of the thenar to hypothenar muscle is a useful parameter that can indicate the severity of CTS. Muscle Nerve 58: 304-306, 2018.


Sujet(s)
Syndrome du canal carpien/imagerie diagnostique , Muscles squelettiques/imagerie diagnostique , Adulte , Sujet âgé , Électrodiagnostic , Femelle , Latéralité fonctionnelle , Humains , Traitement d'image par ordinateur , Mâle , Adulte d'âge moyen , Études rétrospectives , Échographie
9.
Ann Rehabil Med ; 37(4): 591-4, 2013 Aug.
Article de Anglais | MEDLINE | ID: mdl-24020044

RÉSUMÉ

Holmes tremor is a rare movement phenomenon, with atypical low-frequency tremor at rest and when changing postures, often related to brainstem pathology. We report a 70-year-old female patient who was presented with dystonic head and upper limb tremor after brainstem hemorrhage. The patient had experienced a sudden onset of left hemiparesis and right facial paralysis. Brain magnetic resonance imaging showed an acute hemorrhage from the brachium pontis through the dorsal midbrain on the right side. Several months later, the patient developed resting tremor of the head and left arm, which was exacerbated by a sitting posture and intentional movement. The tremor showed a regular low-frequency (1-2 Hz) for the bilateral sternocleidomastoid and cervical paraspinal muscles at rest. The patient's symptoms did not respond to propranolol or clonazepam, but gradually improved with levodopa administration. Although various remedies were attempted, overall, the results were poor. We suggest that levodopa might be a useful remedy for Holmes tremor. The curative or relieving effect of the dopaminergic agent in Holmes tremor needs more research.

10.
Ann Rehabil Med ; 37(2): 202-7, 2013 Apr.
Article de Anglais | MEDLINE | ID: mdl-23705114

RÉSUMÉ

OBJECTIVE: To investigate whether or not indirect ultrasound guidance could increase the accuracy of the glenohumeral joint injection using the superior approach. METHODS: Twelve shoulders from 7 adult cadavers were anatomically dissected after a dye injection had been performed, while the cadavers were in the supine position. Before the injection, a clinician determined the injection point using the ultrasound and the more internal axial arm rotation was compared to how it was positioned in a previous study. Injection confidence scores and injection accuracy scores were rated. RESULTS: The clinician's confidence score was high in 92% (11 of 12 shoulders) and the injection accuracy scores were 100% (12 of 12 shoulders). The long heads of the biceps tendons were not penetrated. CONCLUSION: Indirect ultrasound guidance and positioning shoulder adducted at 10° and internally rotated at 60°-70° during the superior glenohumeral joint injection would be an effective method to avoid damage to the long head of biceps tendons and to produce a highly accurate injection.

11.
Ann Rehabil Med ; 37(6): 839-47, 2013 Dec.
Article de Anglais | MEDLINE | ID: mdl-24466519

RÉSUMÉ

OBJECTIVE: To evaluate the pathophysiological mechanism of hemifacial spasm (HFS), we performed electrophysiological examinations, such as supraorbital nerve stimulation with orbicularis oris muscle recording and lateral spread tests, after suppressing the patient's central nervous system by administering intravenous diazepam. METHODS: Six patients with HFS were recruited. Supraorbital nerve stimulation with orbicularis oris muscle recording and the lateral spread test were performed, followed by intravenous application of 10 mg diazepam to achieve facial motor neuron suppression. Subsequently, we repeated the two electrophysiological experiments mentioned above at 10 and 20 minutes after the patients had received the diazepam intravenously. RESULTS: Orbicularis oris muscle responses were observed in all patients after supraorbital nerve stimulation and lateral spread tests. After the diazepam injection, no orbicularis oris muscle response to supraorbital nerve stimulation was observed in one patient, and the latencies of this response were evident as a slowing tendency with time in the remaining five patients. However, the latencies of the orbicularis oris muscle responses were observed consistently in all patients in the lateral spread test. CONCLUSION: Our results suggest that ectopic excitation/ephaptic transmission contributes to the pathophysiological mechanisms of HFS. This is because the latencies of the orbicularis oris muscle responses in the lateral spread test were observed consistently in the suppressed motor neuron in our patients.

12.
BMC Med Genomics ; 4: 82, 2011 Dec 02.
Article de Anglais | MEDLINE | ID: mdl-22133303

RÉSUMÉ

BACKGROUND: Epigenetic alteration of gene expression is a common event in human cancer. DNA methylation is a well-known epigenetic process, but verifying the exact nature of epigenetic changes associated with cancer remains difficult. METHODS: We profiled the methylome of human gastric cancer tissue at 50-bp resolution using a methylated DNA enrichment technique (methylated CpG island recovery assay) in combination with a genome analyzer and a new normalization algorithm. RESULTS: We were able to gain a comprehensive view of promoters with various CpG densities, including CpG Islands (CGIs), transcript bodies, and various repeat classes. We found that gastric cancer was associated with hypermethylation of 5' CGIs and the 5'-end of coding exons as well as hypomethylation of repeat elements, such as short interspersed nuclear elements and the composite element SVA. Hypermethylation of 5' CGIs was significantly correlated with downregulation of associated genes, such as those in the HOX and histone gene families. We also discovered long-range epigenetic silencing (LRES) regions in gastric cancer tissue and identified several hypermethylated genes (MDM2, DYRK2, and LYZ) within these regions. The methylation status of CGIs and gene annotation elements in metastatic lymph nodes was intermediate between normal and cancerous tissue, indicating that methylation of specific genes is gradually increased in cancerous tissue. CONCLUSIONS: Our findings will provide valuable data for future analysis of CpG methylation patterns, useful markers for the diagnosis of stomach cancer, as well as a new analysis method for clinical epigenomics investigations.


Sujet(s)
Méthylation de l'ADN/génétique , Tumeurs de l'estomac/génétique , Dosage biologique , Chromosomes humains/génétique , Analyse de regroupements , Ilots CpG/génétique , Muqueuse gastrique/métabolisme , Extinction de l'expression des gènes , Génome humain/génétique , Humains , Métastase lymphatique/génétique , Annotation de séquence moléculaire , ARN messager/génétique , ARN messager/métabolisme , Séquences répétées d'acides nucléiques/génétique , Analyse de séquence d'ADN , Estomac/anatomopathologie
13.
J Hypertens ; 29(5): 928-36, 2011 May.
Article de Anglais | MEDLINE | ID: mdl-21430563

RÉSUMÉ

OBJECTIVES: To compare gene expression profiles of placentas from preeclamptic and normal pregnancies. STUDY DESIGN: We performed microarray experiments to analyze genome-wide expression profiling for 10 placentas from pregnant women with preeclampsia and 10 placentas from women who experienced noncomplicated pregnancies (CON), and to identify dysregulated signaling pathways as well as genes in preeclampsia. RT-PCR, real-time RT-PCR and/or immunofluorescence analyses were performed to validate the data obtained from microarray experiments. RESULTS: Unsupervised hierarchical clustering showed heterogeneity of preeclampsia at the molecular levels, whereas expression profiles of preeclampsia are distinctly different from those of CON. A list of genes which are differentially expressed between preeclampsia and CON included well known preeclampsia markers, such as Flt-1, leptin, HTRA1 and SIGLEC6. Gene Set Enrichment Analysis, a pathway-oriented analysis method for expression profiles, provided evidence that a number of biological activities including pathways that regulate actin cytoskeleton, TGFß signaling, oxidative phosphorylation, and proteasome activity were aberrantly either up-regulated or down-regulated in preeclampsia. RT-PCR and real-time-RT-PCR for genes contributing these biological pathways (gene sets) enriched in either CON or preeclampsia reinforced that these biological processes were systemically dysregulated in preeclampsia. CONCLUSIONS: Genome-wide expression profiles of preeclampsia showed heterogeneous characteristics of preeclampsia at the molecular levels. Dysregulation of genes and biological pathways could contribute to abnormal behavior of preeclmapsia. Our results will help further understand underlying mechanisms by which preeclampsia affects placental physiology.


Sujet(s)
Placenta/métabolisme , Pré-éclampsie/métabolisme , Transduction du signal , Technique de Western , Analyse de regroupements , Femelle , Technique d'immunofluorescence , Humains , Séquençage par oligonucléotides en batterie , Pré-éclampsie/physiopathologie , Grossesse , RT-PCR
14.
Neurobiol Aging ; 26(7): 1083-91, 2005 Jul.
Article de Anglais | MEDLINE | ID: mdl-15748788

RÉSUMÉ

Previous gene expression profiling studies in Drosophila have provided clues for understanding the aging process at the gene expression level. For a detailed understanding, studies of specific regions of the body are necessary. We therefore employed microarray analysis to examine gene expression changes in the Drosophila head during aging. Six hundred and eighty-four of the 5405 genes present in the microarray showed significant age-dependent changes as determined by significance analysis of microarray (SAM) (q < 0.05). The biological significance of the changes was analyzed using the gene annotations provided by the Gene Ontology Consortium. Major changes involved genes affecting energy metabolism (proton transport, energy pathways, oxidative phosphorylation) and neuronal function, especially responses to light. Genes involved in protein catabolism and several other metabolic processes also showed age-dependent changes. Most of the changes were reductions in gene expression and occurred before day 13 of adult life. After day 13, the age-dependent gene expression changes were relatively smaller than earlier life. Interestingly, the two biological processes of major gene expression changes are related to the two known environmental changes that increase life span in Drosophila: caloric restriction and light reduction. Our findings suggest that light signaling and energy metabolism may be important biological processes affected by aging and be interesting targets for the further investigation related to the longevity in Drosophila.


Sujet(s)
Vieillissement/physiologie , Régulation de l'expression des gènes/physiologie , Expression des gènes/physiologie , Tête/physiologie , Facteurs âges , Animaux , Drosophila , Analyse de profil d'expression de gènes/méthodes , Hybridation in situ/méthodes , Analyse sur microréseau/méthodes
15.
Mol Cells ; 14(1): 68-74, 2002 Aug 31.
Article de Anglais | MEDLINE | ID: mdl-12243355

RÉSUMÉ

To investigate the role of protein kinase A (PKA) (EC 2.7.1.37) in myogenesis, PKA activity was closely monitored during the differentiation of L6 rat skeletal myoblasts. As the differentiation proceeded, total PKA activity increased about 2-3 fold, and the protein levels of PKA RIalpha and Calpha subunits increased about 3-4 fold. We then looked at the effect of the specific inhibitor for PKA, N-[2-(p-bromocinnamy-lamino)-ethyl]-5-isoquinoline-sulfonamide (H89), on the differentiation of L6 myoblasts. H89 completely blocked the myotube formation and abolished the up-regulation of RIalpha and Ca. This inhibitory effect of H89 was dose-dependent and could be reversed upon removal of H89 from the culture medium. Furthermore, we demonstrated that specific inhibitors of phosphatidylinositol 3-kinase (PI3K), wortmannin, and LY294002 blocked the myotube formation and abolished the increase of PKA activity, which normally accompanied the differentiation of myoblasts. These results suggest that type I PKA may play a functional role(s) in the differentiation of myoblast as a putative downstream effector of the PI3K signaling pathway.


Sujet(s)
Différenciation cellulaire/physiologie , Cyclic AMP-Dependent Protein Kinases/métabolisme , Myoblastes squelettiques/métabolisme , Phosphatidylinositol 3-kinases/métabolisme , Sulfonamides , Androstadiènes/pharmacologie , Différenciation cellulaire/effets des médicaments et des substances chimiques , 4H-1-Benzopyran-4-ones/pharmacologie , Cyclic AMP-Dependent Protein Kinases/antagonistes et inhibiteurs , Antienzymes/pharmacologie , Isoquinoléines/pharmacologie , Morpholines/pharmacologie , Inhibiteurs des phosphoinositide-3 kinases , Wortmannine
SÉLECTION CITATIONS
DÉTAIL DE RECHERCHE
...