1,600 research outputs found

    The Conformations and Vibrational Spectra Including Matrix Isolation of 1,3-Dibromo-2,2-dimethylpropane

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    The IR spectra of 1,3-Dibromo-2,2-dimethylpropane as a liquid and as two crystalline solids obtained at low temperature and at high pressure were recorded. Additional IR spectra of this com-. pound, matrix isolated in argon and nitrogen at 14 K, were obtained using nozzle temperatures of 300, 450 and 700 K. Raman spectra including polarization measurements were recorded at various temperatures between 340 and 230 K. Crystalline solids were obtained by freezing the liquid and by shock freezing the vapour at 85 K with subsequent annealing.The GG and AG conformes were present in the low temperature and in the high pressure crystals, respectively, and the enthalpy differences were 5.6 (liquid) and 4.2 kJ mol-1 (vapour) with GG being the more stable. An additional conformer AA was detected in the liquid and in the matrix isolated spectra, being approximately 6.4 and 6.5 kJ mol-1 less stable than GG in the liquid and vapour, respectively, Vibrational assignments of the GG and AG spectra are presented, supported by a normal coordinate analysis

    Atopic conditions and brain tumor risk in children and adolescents—an international case-control study (CEFALO)

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    In this study, atopic conditions were not associated with risk of brain tumors in children and adolescents or of glioma in particular. Results are not consistent with findings for adult glioma, possibly explained by a different distribution of histological subtypes. Only a few studies on atopic conditions and pediatric brain tumors are currently available, and the evidence is conflictin

    Is the incidence of meningiomas underestimated? A regional survey

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    We assessed the undercount of meningiomas in a population-based cancer registry. A comprehensive material was formed by compiling hospital sources with the Finnish Cancer Registry database. The completeness of each source ranged 62–69%. The corrected age-standardised meningioma incidence was 2.9/100 000 for men and 13.0/100 000 for women, a third higher than the cancer registry figures

    Recent Research on EMF and Health Risk, Twelfth report from SSM's Scientific Council on Electromagnetic Fields, 2017

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    Background: The Swedish Radiation Safety Authority's (SSM) Scientific Council on Electromagnetic Fields monitors current research on potential health risks with a correlation to exposure to electromagnetic fields, and provides the Authority with advice on assessing possible health risks. The Council gives guidance when the Authority must give an opinion on policy matters when scientific testing is necessary. The Council is required to submit a written report each year on the current research and knowledge situation. Objective: The report has the objective of covering the previous year's research in the area of electromagnetic fields (EMF). The report gives the Swedish Radiation Safety Authority an overview and provides an important basis for risk assessment. Results: The present annual report is the twelfth in this series and covers studies published from October 2015 up to and including March 2017. The report covers different areas of EMF (static, low frequency, intermediate, and radio frequency fields) and different types of studies such as biological, human and epidemiological studies. No new health risks have been identified. Whether mobile phone use causes brain tumours or not was mainly addressed using time trends studies in the last two years. The results were not entirely consistent but mainly point towards a lack of association. Some cell and animal studies indicate that EMF exposure may cause oxidative stress even at low exposure levels. It is unclear what relevance this may have when it comes to direct health effects in humans. A striking result was that some studies showed a stronger association between memory functions and radio wave exposure than other usage variables. The annual report also has a section covering other relevant scientific reports published recently

    Mobile phones and head tumours. The discrepancies in cause-effect relationships in the epidemiological studies - how do they arise?

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    The uncertainty about the relationship between the use of mobile phones (MPs: analogue and digital cellulars, and cordless) and the increase of head tumour risk can be solved by a critical analysis of the methodological elements of both the positive and the negative studies. Results by Hardell indicate a cause/effect relationship: exposures for or latencies from 65 10 years to MPs increase by up to 100% the risk of tumour on the same side of the head preferred for phone use (ipsilateral tumours) - which is the only one significantly irradiated - with statistical significance for brain gliomas, meningiomas and acoustic neuromas. On the contrary, studies published under the Interphone project and others produced negative results and are characterised by the substantial underestimation of the risk of tumour. However, also in the Interphone studies a clear and statistically significant increase of ipsilateral head tumours (gliomas, neuromas and parotid gland tumours) is quite common in people having used MPs since or for 65 10 years. And also the metaanalyses by Hardell and other Authors, including only the literature data on ipsilateral tumours in people having used MPs since or for 65 10 years - and so also part of the Interphone data - still show statistically significant increases of head tumours

    The Potential Involvement of E-cadherin and β-catenins in Meningioma

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    To investigate the potential involvements of E-cadherin and β-catenin in meningioma.Immunohistochemistry staining was performed on samples from patients with meningioma. The results were graded according to the positive ratio and intensity of tissue immunoreactivity. The expression of E-cadherin and β-catenin in meningioma was analyzed by its relationship with WHO2007 grading, invasion, peritumoral edema and postoperative recurrence.The positive rates of E-cadherin in meningioma WHO I, II, III were 92.69%, 33.33% and 0, respectively, (P<0.05); while the positive rates of β-catenin in meningioma WHO I, II, III were 82.93%, 33.33% and 20.00%, respectively, (P<0.05). The positive rate of E-cadherin in meningioma without invasion (94.12%) was higher than that with invasion (46.67%) (P<0.05). The difference in the positive rate of β-catenin between meningioma without invasion (88.24%) and meningioma with invasion (33.33%, P<0.05) was also statically significant. The positive rates of E-cadherin in meningioma with peritumoral edema 0, 1, 2, 3 were 93.75%, 85.71%, 60.00% and 0 respectively, (P<0.05); the positive rates of β-catenin in meningioma with peritumoral edema 0, 1, 2, 3 were 87.50%, 85.71%, 30.00% and 0 respectively, (P<0.01). The positive rates of E- cadherin in meningioma with postoperative recurrence were 33.33%, and the positive rate with postoperative non-recurrence was 90.00% (P<0.01). The positive rates of β-catenin in meningioma with postoperative recurrence and non-recurrence were 11.11%, 85.00%, respectively (P<0.01).The expression levels of E- cadherin and β-catenin correlated closely to the WHO 2007 grading criteria for meningioma. In atypical or malignant meningioma, the expression levels of E-cadherin and β-catenin were significantly lower. The expression levels of E- cadherin and β-catenin were also closely correlated with the invasion status of meningioma, the size of the peritumoral edema and the recurrent probabilities of the meningioma, all in an inverse correlationship. Taken together, the present study provided novel molecular targets in clinical treatments to meningioma

    British Journal of Cancer advance online publication

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    There is public concern that use of mobile phones could increase the risk of brain tumours. If such an effect exists, acoustic neuroma would be of particular concern because of the proximity of the acoustic nerve to the handset. We conducted, to a shared protocol, six population-based case -control studies in four Nordic countries and the UK to assess the risk of acoustic neuroma in relation to mobile phone use. Data were collected by personal interview from 678 cases of acoustic neuroma and 3553 controls. The risk of acoustic neuroma in relation to regular mobile phone use in the pooled data set was not raised (odds ratio (OR) ÂĽ 0.9, 95% confidence interval (CI): 0.7 -1.1). There was no association of risk with duration of use, lifetime cumulative hours of use or number of calls, for phone use overall or for analogue or digital phones separately. Risk of a tumour on the same side of the head as reported phone use was raised for use for 10 years or longer (OR ÂĽ 1.8, 95% CI: 1.1 -3.1). The study suggests that there is no substantial risk of acoustic neuroma in the first decade after starting mobile phone use. However, an increase in risk after longer term use or after a longer lag period could not be ruled out

    British Journal of Cancer advance online publication

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    There is public concern that use of mobile phones could increase the risk of brain tumours. If such an effect exists, acoustic neuroma would be of particular concern because of the proximity of the acoustic nerve to the handset. We conducted, to a shared protocol, six population-based case -control studies in four Nordic countries and the UK to assess the risk of acoustic neuroma in relation to mobile phone use. Data were collected by personal interview from 678 cases of acoustic neuroma and 3553 controls. The risk of acoustic neuroma in relation to regular mobile phone use in the pooled data set was not raised (odds ratio (OR) ÂĽ 0.9, 95% confidence interval (CI): 0.7 -1.1). There was no association of risk with duration of use, lifetime cumulative hours of use or number of calls, for phone use overall or for analogue or digital phones separately. Risk of a tumour on the same side of the head as reported phone use was raised for use for 10 years or longer (OR ÂĽ 1.8, 95% CI: 1.1 -3.1). The study suggests that there is no substantial risk of acoustic neuroma in the first decade after starting mobile phone use. However, an increase in risk after longer term use or after a longer lag period could not be ruled out
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