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1.
Math Biosci Eng ; 20(6): 10007-10026, 2023 Mar 27.
Article in English | MEDLINE | ID: mdl-37322921

ABSTRACT

The electrostatics of two cylinders charged to the symmetrical or anti-symmetrical potential is investigated by using the null-field boundary integral equation (BIE) in conjunction with the degenerate kernel of the bipolar coordinates. The undetermined coefficient is obtained according to the Fredholm alternative theorem. The uniqueness of solution, infinite solution, and no solution are examined therein. A single cylinder (circle or ellipse) is also provided for comparison. The link to the general solution space is also done. The condition at infinity is also correspondingly examined. The flux equilibrium along circular boundaries and the infinite boundary is also checked as well as the contribution of the boundary integral (single and double layer potential) at infinity in the BIE is addressed. Ordinary and degenerate scales in the BIE are both discussed. Furthermore, the solution space represented by the BIE is explained after comparing it with the general solution. The present finding is compared to those of Darevski[2] and Lekner[4] for identity.

3.
Biochim Biophys Acta ; 1852(5): 851-61, 2015 May.
Article in English | MEDLINE | ID: mdl-25597880

ABSTRACT

Cofilin-1, a non-muscle isoform of actin regulatory protein that belongs to the actin-depolymerizing factor (ADF)/cofilin family is known to affect cancer development. Previously, we found that over-expression of cofilin-1 suppressed the growth and invasion of human non-small cell lung cancer (NSCLC) cells in vitro. In this study, we further investigated whether over-expression of cofilin-1 can suppress tumor growth in vivo, and performed a microRNA array analysis to better understand whether specific microRNA would be involved in this event. The results showed that over-expression of cofilin-1 suppressed NSCLC tumor growth using the xenograft tumor model with the non-invasive reporter gene imaging modalities. Additionally, cell motility and invasion were significantly suppressed by over-expressed cofilin-1, and down-regulation of matrix metalloproteinase (MMPs) -1 and -3 was concomitantly detected. According to the microRNA array analysis, the let-7 family, particularly let-7b and let-7e, were apparently up-regulated among 248 microRNAs that were affected after over-expression of cofilin-1 up to 7 days. Knockdown of let-7b or let-7e using chemical locked nucleic acid (LNA) could recover the growth rate and the invasion of cofilin-1 over-expressing cells. Next, the expression of c-myc, LIN28 and Twist-1 proteins known to regulate let-7 were analyzed in cofilin-1 over-expressing cells, and Twist-1 was significantly suppressed under this condition. Up-regulation of let-7 microRNA by over-expressed cofilin-1 could be eliminated by co-transfected Twist-1 cDNA. Taken together, current data suggest that let-7 microRNA would be involved in over-expression of cofilin-1 mediated tumor suppression in vitro and in vivo.


Subject(s)
Carcinoma, Non-Small-Cell Lung/genetics , Cell Proliferation/genetics , Cofilin 1/genetics , Lung Neoplasms/genetics , MicroRNAs/genetics , Animals , Blotting, Western , Carcinoma, Non-Small-Cell Lung/metabolism , Carcinoma, Non-Small-Cell Lung/pathology , Cell Line, Tumor , Cell Movement/genetics , Cofilin 1/metabolism , Gene Expression Profiling , Gene Expression Regulation, Neoplastic , Gene Knockdown Techniques , Humans , Lung Neoplasms/metabolism , Lung Neoplasms/pathology , Male , Mice, Inbred NOD , Mice, SCID , Microscopy, Fluorescence , Neoplasm Invasiveness , Oligonucleotide Array Sequence Analysis , Positron-Emission Tomography , Reverse Transcriptase Polymerase Chain Reaction , Time-Lapse Imaging/methods , Transplantation, Heterologous , Tumor Burden/genetics , Up-Regulation
4.
Pediatrics ; 134(2): e397-405, 2014 Aug.
Article in English | MEDLINE | ID: mdl-25022734

ABSTRACT

BACKGROUND AND OBJECTIVES: Sleep disturbance is common in patients with atopic dermatitis (AD). However, studies have largely been questionnaire-based, and the pathophysiology remains unclear. The aims of this study were to determine objective characteristics of sleep disturbance in children with AD and explore contributing factors and clinical predictors. METHODS: Sleep parameters were measured by actigraphy and polysomnography in 72 patients with AD and 32 controls ages 1 to 18 years. Urinary 6-sulfatoxymelatonin levels, serum cytokines, and total and allergen-specific immunoglobulin E (IgE) levels were also measured. RESULTS: The patients with AD had significantly reduced sleep efficiency, longer sleep onset latency, more sleep fragmentation, and less nonrapid eye movement sleep. Results from actigraphy correlated well with those from polysomnography. The AD disease severity was associated with sleep disturbance (r = 0.55-0.7), and a Scoring Atopic Dermatitis index of ≥48.7 predicted poor sleep efficiency with a sensitivity of 83.3% and a specificity of 75% (area under the curve = 0.81, P = .001). Lower nocturnal melatonin secretion was significantly associated with sleep disturbance in the patients with AD. Other correlates of sleep disturbance included pruritus, scratching movements, higher total serum IgE levels, and allergic sensitization to dust mite and staphylococcal enterotoxins. CONCLUSIONS: Poor sleep efficiency is common in children with AD and can be predicted by the Scoring Atopic Dermatitis index. Melatonin and IgE might play a role in the sleep disturbance. Further studies are required to explore the mechanisms and clinical implications, and actigraphy could serve as a useful evaluating tool.


Subject(s)
Dermatitis, Atopic/epidemiology , Melatonin/metabolism , Sleep Wake Disorders/epidemiology , Actigraphy , Child , Child, Preschool , Comorbidity , Cross-Sectional Studies , Cytokines/analysis , Dermatitis, Atopic/metabolism , Female , Humans , Immunoglobulin E/analysis , Male , Polysomnography , Sleep Deprivation , Sleep Wake Disorders/metabolism
5.
Pediatr Neonatol ; 52(5): 290-3, 2011 Oct.
Article in English | MEDLINE | ID: mdl-22036226

ABSTRACT

Pure word deafness (PWD) is a rare disorder characterized by impaired verbal comprehension sparing discrimination and recognition of nonverbal sounds with relatively normal spontaneous speech, writing, and reading comprehension. Etiologies of this syndrome are varied, and there are rare reports about brain tumor with PWD in children. We report a case of medulloblastoma presented with PWD in a 7-year-old girl. She visited our outpatient clinic because of English dictation performance deterioration. PWD was diagnosed by the otolaryngologist after examinations. Posterior fossa tumor and obstructive hydrocephalus were shown in the magnetic resonance imaging of the brain. The diagnosis of medulloblastoma was then made by pathology.


Subject(s)
Cerebellar Neoplasms/complications , Deafness/etiology , Medulloblastoma/complications , Speech Perception , Child , Female , Humans
6.
Pediatr Neurol ; 40(2): 128-30, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19135630

ABSTRACT

Mycoplasma pneumoniae is a common cause of respiratory tract infection. Extrapulmonary manifestations of M. pneumoniae infection are also common. The present case is that of a previously healthy 4-year-old boy who displayed a novel simultaneous onset of both acute rhabdomyolysis and transverse myelitis associated with an infection of M. pneumoniae. He had no preceding symptoms or signs of respiratory tract infection. Intravenous immunoglobulin (1 g/kg per day) for 2 days was prescribed initially for the deterioration of neurologic condition. His rhabdomyolysis resolved without complication, but neurologic sequelae remained during 2 years of follow-up. Evaluation for M. pneumoniae infection is recommended in patients with idiopathic rhabdomyolysis and transverse myelitis, even if in the absence of antecedent respiratory symptoms.


Subject(s)
Mycoplasma Infections/complications , Mycoplasma pneumoniae , Myelitis, Transverse/etiology , Rhabdomyolysis/etiology , Child, Preschool , Humans , Magnetic Resonance Imaging , Male , Mycoplasma Infections/physiopathology
7.
Acta Paediatr Taiwan ; 48(4): 213-6, 2007.
Article in English | MEDLINE | ID: mdl-18265543

ABSTRACT

We report a case of dilated cardiomyopathy presented in a premature infant of 27 weeks' gestational age. A prenatal sonography revealed left ventricular enlargement. The infant presented with respiratory distress and heart failure soon after birth. Echocardiograms performed after birth showed dilated cardiomyopathy, and endocardial fibroelastosis was suspected. Heart failure progressed despite administration of inotropic agents. The infant died after fifteen days from circulatory failure. Postmortem examination confirmed the diagnosis of endocardial fibroelastosis.


Subject(s)
Cardiomyopathy, Dilated/diagnosis , Endocardial Fibroelastosis/diagnosis , Adult , Endocardial Fibroelastosis/etiology , Female , Humans , Infant, Newborn , Infant, Premature , Male , Pregnancy
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