Different mechanism may underlie respiratory failure of myotonic and Duchenne muscular dystrophies--a pulseoxymetric and spirometric study

Respiratory failure is an important cause of death in many neuromuscular diseases. We studied the relationship between nocturnal hypoxemia and respiratory muscle weakness by nocturnal pulseoxymetry and spirometry in two major hereditary myopathies, myotonic and Duchenne muscular dystrophies (MD and DMD respectively). In DMD significant nocturnal periodic hypoxemia appears only in cases with vital capacity lower than 20% of its expected value, suggesting that % vital capacity is a useful index of early respiratory failure. In contrast there was no correlation between vital capacity and severity of hypoxemia in MD patients. Therefore, we conclude respiratory muscle weakness is a single important factor which determines the severity of respiratory failure in DMD, while another/other factor (s), such as disturbance of respiratory control or myotonia, may play an important role in MD.     

MOCVD-grown AlGaAs/GaAs HBTs with epitaxially embedded p+ layers in extrinsic base

AlGaAs/GaAs HBTs having a 300 ? base were grown by two-stage MOCVD. In the second stage, p+ layers were epitaxially embedded in the extrinsic base to make the base contact. The current through the parasitic pn interface between the emitter and the embedded p+ layers was negligible. The technique employed here makes undamaged narrow-base HBTs possible.     

Smart optical receiver with automatic decision threshold settingand retiming phase alignment

The requirements for a smart optical receiver are discussed, and a design architecture suitable for introducing ICs based on automatic decision threshold setting and retiming phase alignment using digital/analog signal processing feedback is proposed. With the proposed architecture, the decision threshold level and the retiming clock phase of received data in the decision circuit are automatically adjusted to the optimum position. This obviates the need for decision threshold level and retiming clock phase adjustments in production testing, and it reduces the power penalty (receiver sensitivity degradation) on the received optical waveform variation. The power penalty caused by temperature and supply-voltage variations and aging in installation is also reduced. The performance of the proposed architecture is estimated; the power penalty as compared with the manual optimum adjustment is less than 0.4 dB, and the robustness to avalanche photodiode multiplication factor variations and crosstalk are improved     

Non-Functionalized Gold Nanoparticles Inhibit Human Papillomavirus (HPV) Infection

The spontaneous interaction between human papillomavirus type 16 (HPV16) L1 virus-like particles (VLPs) and non-functionalized gold nanoparticles (nfGNPs) interferes with the nfGNPs’ salt-induced aggregation, inhibiting the red–blue color shift in the presence of NaCl. Electron microscopy and competition studies showed that color-shift inhibition is a consequence of direct nfGNP–VLP interaction and, thus, may produce a negative impact on the virus entry cell process. Here, an in vitro infection system based on the HPV16 pseudovirus (PsV) was used to stimulate the natural infection process in vitro. PsVs carry a pseudogenome with a reporter gene, resulting in a fluorescent signal when PsVs infect a cell, allowing quantification of the viral infection process. Aggregation assays showed that nfGNP-treated PsVs also inhibit color shift in the presence of NaCl. High-resolution microscopy confirmed nfGNP–PsV complex formation. In addition, PsVs can interact with silver nanoparticles, suggesting a generalized interaction of metallic nanoparticles with HPV16 capsids. The treatment of PsVs with nfGNPs produced viral infection inhibition at a higher level than heparin, the canonical inhibitor of HPV infection. Thus, nfGNPs can efficiently interfere with the HPV16 cell entry process and may represent a potential active component in prophylactic formulations to reduce the risk of HPV infection.