ChemInform Abstract: Pd-Complex-Bound Amino Acid-Based Supramolecular Gel Catalyst for Intramolecular Addition-Cyclization of Alkynoic Acids in Water.

ChemInform ◽  
2012 ◽  
Vol 43 (43) ◽  
pp. no-no
Author(s):  
Kazuki Ogata ◽  
Daisuke Sasano ◽  
Tomoya Yokoi ◽  
Katsuhiro Isozaki ◽  
Hirofumi Seike ◽  
...  
Langmuir ◽  
2016 ◽  
Vol 32 (41) ◽  
pp. 10705-10711 ◽  
Author(s):  
Yajie Wang ◽  
Pengyao Xing ◽  
Shangyang Li ◽  
Mingfang Ma ◽  
Minmin Yang ◽  
...  

2012 ◽  
Vol 41 (5) ◽  
pp. 498-500 ◽  
Author(s):  
Kazuki Ogata ◽  
Daisuke Sasano ◽  
Tomoya Yokoi ◽  
Katsuhiro Isozaki ◽  
Hirofumi Seike ◽  
...  

Soft Matter ◽  
2016 ◽  
Vol 12 (1) ◽  
pp. 141-148 ◽  
Author(s):  
Jie Liu ◽  
Fengyang Xu ◽  
Ziling Sun ◽  
Yue Pan ◽  
Jian Tian ◽  
...  

A novel gelator from a glycoamino acid derivative was discovered to perform supramolecular self-assembly and gel–crystal transition upon ageing.


2014 ◽  
Vol 16 (13) ◽  
pp. 6041 ◽  
Author(s):  
Subhasish Roy ◽  
Dibakar Kumar Maiti ◽  
Shrabani Panigrahi ◽  
Durga Basak ◽  
Arindam Banerjee

2016 ◽  
Vol 61 (2) ◽  
Author(s):  
Qiangliang Yu ◽  
Dongmei Li ◽  
Meirong Cai ◽  
Feng Zhou ◽  
Weimin Liu

Author(s):  
M.K. Lamvik ◽  
L.L. Klatt

Tropomyosin paracrystals have been used extensively as test specimens and magnification standards due to their clear periodic banding patterns. The paracrystal type discovered by Ohtsuki1 has been of particular interest as a test of unstained specimens because of alternating bands that differ by 50% in mass thickness. While producing specimens of this type, we came across a new paracrystal form. Since this new form displays aligned tropomyosin molecules without the overlaps that are characteristic of the Ohtsuki-type paracrystal, it presents a staining pattern that corresponds to the amino acid sequence of the molecule.


Author(s):  
A. J. Tousimis

The elemental composition of amino acids is similar to that of the major structural components of the epithelial cells of the small intestine and other tissues. Therefore, their subcellular localization and concentration measurements are not possible by x-ray microanalysis. Radioactive isotope labeling: I131-tyrosine, Se75-methionine and S35-methionine have been successfully employed in numerous absorption and transport studies. The latter two have been utilized both in vitro and vivo, with similar results in the hamster and human small intestine. Non-radioactive Selenomethionine, since its absorption/transport behavior is assumed to be the same as that of Se75- methionine and S75-methionine could serve as a compound tracer for this amino acid.


Author(s):  
Chi-Ming Wei ◽  
Margaret Hukee ◽  
Christopher G.A. McGregor ◽  
John C. Burnett

C-type natriuretic peptide (CNP) is a newly identified peptide that is structurally related to atrial (ANP) and brain natriuretic peptide (BNP). CNP exists as a 22-amino acid peptide and like ANP and BNP has a 17-amino acid ring formed by a disulfide bond. Unlike these two previously identified cardiac peptides, CNP lacks the COOH-terminal amino acid extension from the ring structure. ANP, BNP and CNP decrease cardiac preload, but unlike ANP and BNP, CNP is not natriuretic. While ANP and BNP have been localized to the heart, recent investigations have failed to detect CNP mRNA in the myocardium although small concentrations of CNP are detectable in the porcine myocardium. While originally localized to the brain, recent investigations have localized CNP to endothelial cells consistent with a paracrine role for CNP in the control of vascular tone. While CNP has been detected in cardiac tissue by radioimmunoassay, no studies have demonstrated CNP localization in normal human heart by immunoelectron microscopy.


1979 ◽  
Vol 7 (1) ◽  
pp. 261-262
Author(s):  
E. V. ROWSELL

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