Synthesis and photopolymerization kinetics of polymeric one-component type II photoinitiator containing benzophenone moiety and tertiary amine

2008 ◽  
Vol 48 (5) ◽  
pp. 884-888 ◽  
Author(s):  
Pu Xiao ◽  
Ying Wang ◽  
Mingzhi Dai ◽  
Suqing Shi ◽  
Gangqiang Wu ◽  
...  
1979 ◽  
Vol 42 (2) ◽  
pp. 530-557 ◽  
Author(s):  
C. H. Bailey ◽  
V. F. Castellucci ◽  
J. Koester ◽  
E. R. Kandel

1. To account for the similarity in the kinetics of habituation between the central and peripheral components of siphon withdrawal, we have tested the idea (52) that each centrally located mechanoreceptor sensory neuron sends two branches to siphon motor neurons; one to centrally located siphon motor neurons and a collateral branch that remains in the periphery and innervates the peripheral siphon motor neurons. 2. We have found a group of peripheral siphon motor neurons and tested the connection onto these cells by central mechanoreceptors. In addition, we have defined by various electrophysiological and morphological criteria two general classes of peripheral neurons that lie along the course of the siphon nerve. 3. One class (type I) consists of only a single cell in each animal. This peripheral neuron typically has the largest cell body found lying along the siphon nerve and is the only peripheral nerve cell that appears white when viewed under epi-illumination. The type I neuron often has a highly regular firing pattern, which occurs in the absence of spontaneous synaptic input. The three-dimensional morphology of this neuron suggests a paucity of fine processes, most of which do not arborize and may terminate in the connective tissue sheath. Fine structural observations of the peripheral white cell have revealed the presence of large densecore granules. The peripheral type I neuron is similar in most of its electrophysiological and morphological properties to central neurons postulated to be neurosecretory. The peripheral white cell is, at present, the only peripheral neuron we can identify with certainty as a unique individual. 4. The second class (type II) of peripheral neurons are siphon motor neurons for the peripheral component of the siphon-withdrawal reflex. In contrast to the type I neurons, members of the second class of peripheral neurons possess smaller, more spherical cell bodies that have varying amounts of orange pigmentation and which give rise to a relatively well-developed and arborized dendritic tree. Type II neurons feature an irregular spontaneous firing pattern that is occasionally modulated by a rich spontaneous synaptic input. Peripheral siphon motor neurons have restricted motor fields that produce contraction of the mantle floor and the base of the siphon. Most of the type II neurons were found to be electrically coupled to one another. 5. The peripheral siphon motor neurons resemble the central siphon motor neurons in that they receive a collateral synapse from centrally located mechanoreceptor sensory neurons. This peripheral sensory-to-motor synapse exhibits the same kinetics of decrement as its central counterpart, both of which parallel behavioral habituation. 6. The rich mechanoreceptor input onto the relatively isolated dendritic trees of the peripheral siphon motor neurons provide a uniquely restricted neuropil to study the sensory-to-motor synapse. The peripheral motor neurons may, therefore, be a useful simple preparation for the cellular study of behavioral plasticity.


2005 ◽  
Author(s):  
D. V. Gulyaev ◽  
A. K. Bakarov ◽  
A. V. Tsarev ◽  
K. S. Zhuravlev
Keyword(s):  
Type Ii ◽  

2018 ◽  
Vol 29 (3) ◽  
pp. 451-455 ◽  
Author(s):  
Tiantian Li ◽  
Zhilong Su ◽  
Hongjie Xu ◽  
Xuesong Jiang ◽  
Xiaodong Ma ◽  
...  

The absorption spectra of eight type I and three type II a diamonds irradiated with neutrons, electrons or y-rays have been recorded at 80 and 290°K after various heat treatments in the temperature range 0 to 900°C. It is found that heating in the range 350 to 450°C causes a general reduction in the irradiation-induced absorption owing to the recombination of those interstitials and vacancies which are near neighbours. Heating type II a diamonds at 600°C causes a large reduction in the irradiation-induced lines and new lines appear. These are probably due to pairs of identical defects, and the kinetics of their formation during isothermal heating at 600°C are presented. At higher temperatures all absorption lines in type II a diamonds disappear and only continuous absorption remains. This is probably due to amorphous or graphitic regions produced by agglomeration of defects. Type I diamonds show the same kind of absorption, but in addition show an increase in strength of the natural lines and also some new absorption lines which are not removed by heating at 900°C. It is suggested that these additional processes are due to the anchoring of vacant atomic sites and interstitial carbon atoms at crystal imperfections present only in type I diamonds.


Blood ◽  
1999 ◽  
Vol 93 (5) ◽  
pp. 1749-1756 ◽  
Author(s):  
Robert A. Brodsky ◽  
Galina L. Mukhina ◽  
Kim L. Nelson ◽  
Tracy S. Lawrence ◽  
Richard J. Jones ◽  
...  

Paroxysmal nocturnal hemoglobinuria (PNH) is a clonal stem cell disorder caused by a somatic mutation of the PIGA gene. The product of this gene is required for the biosynthesis of glycosylphosphatidylinositol (GPI) anchors; therefore, the phenotypic hallmark of PNH cells is an absence or marked deficiency of all GPI-anchored proteins. Aerolysin is a toxin secreted by the bacterial pathogen Aeromonas hydrophila and is capable of killing target cells by forming channels in their membranes after binding to GPI-anchored receptors. We found that PNH blood cells (erythrocytes, lymphocytes, and granulocytes), but not blood cells from normals or other hematologic disorders, are resistant to the cytotoxic effects of aerolysin. The percentage of lysis of PNH cells after aerolysin exposure paralleled the percentage of CD59+ cells in the samples measured by flow cytometry. The kinetics of red blood cell lysis correlated with the type of PNH erythrocytes. PNH type III cells were completely resistant to aerolysin, whereas PNH type II cells displayed intermediate sensitivity. Importantly, the use of aerolysin allowed us to detect PNH populations that could not be detected by standard flow cytometry. Resistance of PNH cells to aerolysin allows for a simple, inexpensive assay for PNH that is sensitive and specific. Aerolysin should also be useful in studying PNH biology.


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