scholarly journals Abiotic synthesis of high-molecular-weight organics from an inorganic gas mixture of carbon monoxide, ammonia, and water by 3 MeV proton irradiation

2004 ◽  
Vol 84 (8) ◽  
pp. 1410-1412 ◽  
Author(s):  
Yoshinori Takano ◽  
Akihiro Ohashi ◽  
Takeo Kaneko ◽  
Kensei Kobayashi
1989 ◽  
Vol 18 (9) ◽  
pp. 1527-1530 ◽  
Author(s):  
Kensei Kobayashi ◽  
Tairo Oshima ◽  
Hiroshi Yanagawa

e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
C.P. Stephens ◽  
R.S. Benson ◽  
X. Ling ◽  
H. Song ◽  
H.-J. Ham ◽  
...  

AbstractThe effect of low dose proton irradiation on the morphology of ultra high molecular weight polyethylene (UHMWPE) was studied. The integral proton dose was ranging from 900 Gy to 1200 Gy. The experimental data revealed that low dose proton irradiation in the presence of oxygen leads to the formation of intermolecular crosslinks in UHMWPE and that proton irradiation produces morphological changes that involve a reduction in the thickness of the interfacial region and increase in the thickness of the amorphous region. The observed morphological changes depend on the integral dose


Author(s):  
Richard B. Vallee

Microtubules are involved in a number of forms of intracellular motility, including mitosis and bidirectional organelle transport. Purified microtubules from brain and other sources contain tubulin and a diversity of microtubule associated proteins (MAPs). Some of the high molecular weight MAPs - MAP 1A, 1B, 2A, and 2B - are long, fibrous molecules that serve as structural components of the cytamatrix. Three MAPs have recently been identified that show microtubule activated ATPase activity and produce force in association with microtubules. These proteins - kinesin, cytoplasmic dynein, and dynamin - are referred to as cytoplasmic motors. The latter two will be the subject of this talk.Cytoplasmic dynein was first identified as one of the high molecular weight brain MAPs, MAP 1C. It was determined to be structurally equivalent to ciliary and flagellar dynein, and to produce force toward the minus ends of microtubules, opposite to kinesin.


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