Hall effect measurements indicate that the material has p-type conductivity with mid-10(15) carriers/cm(3) and hole mobilities in the 5-50 cm(2)/V.s range. (C) 2011 American Institute of Physics. [doi:10.1063/1.3611418]“
“Introduction: Fasciculoventricular pathways (FVPs) are rare causes
of preexcitation that do not mediate tachycardias. We report a two-center experience of pediatric patients with FVP and an www.selleckchem.com/products/anlotinib-al3818.html unexpectedly high association of complex congenital heart defects (CHDs), chromosomal anomalies, and hypertrophic cardiomyopathy.
Methods: A retrospective review of the electrophysiology database at two institutions was performed to identify patients with FVP from January 2000 to January 2011. Medical records of these patients were reviewed for clinical history and course, presence of comorbidities,
and details of intracardiac electrophysiology (EP) study.
Results: A total of 17 patients were identified. The primary indication for EP study was a preexcitation pattern on electrocardiogram. The majority of patients, 12/ 17 (71%), were found to have associated cardiac and genetic anomalies. Hypertrophic cardiomyopathy was found in 5/ 17 (29%) patients, with genetic testing in two patients demonstrating the lysosomal-associated membrane protein 2 mutation (Danon syndrome). Underlying complex CHDs were present in 3/ 17 (18%) patients. One patient (6%) was status post (s/ p) cardiac P005091 nmr transplant, one patient had hypertension, and another had Trisomy 21. Other electrophysiologic substrates mediating tachycardia were found in 3/ 17 (18%) patients. Only 5/ 17 patients (29%) click here were otherwise healthy with structurally normal hearts.
Conclusions:
In this largest reported series of FVP in children, there is an unusually high association of FVP with complex CHDs, chromosomal anomalies, and hypertrophic cardiomyopathy. Any patient with such disorders and manifest preexcitation should be evaluated with a high index of suspicion for a FVP. (PACE 2012; 35: 308-313)”
“After living cells are exposed to ionizing radiation, a variety of chemical modifications of DNA are induced either directly by ionization of DNA or indirectly through interactions with water-derived radicals. The DNA lesions include single strand breaks (SSB), base lesions, sugar damage, and apurinic/apyrimidinic sites (AP sites). Clustered DNA damage, which is defined as two or more of such lesions within one to two helical turns of DNA induced by a single radiation track, is considered to be a unique feature of ionizing radiation. A double strand break (DSB) is a type Of Clustered DNA damage, in which single strand breaks arc formed on opposite strands in close proximity. Fort-nation and repair of DSBs have been studied in great detail over the years as they have been linked to important biological endpoints, such as cell death, loss of genetic material, chromosome aberration.