Zobrazeno 1 - 10
of 85
pro vyhledávání: '"L. E. ORGEL"'
Autor:
Catherine Fenselau, Richard Caprioli, A. O. Nier, W. B. Hanson, A. Seiff, M. B. Mcelroy, N. W. Spencer, R. J. Duckett, T. C. D. Knight, W. S. Cook, K. Biemann, J. Oro, P. Toulmin, L. E. Orgel, D. M. Anderson, P. G. Simmonds, D. Flory, A. V. Diaz, D. R. Rushneck, J. A. Biller, Tobias Owen
Publikováno v:
Journal of Mass Spectrometry. 38:1-10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe165b3a6b010142e12e4c4b7cc2ab9b
https://doi.org/10.1002/jms.396
https://doi.org/10.1002/jms.396
Autor:
L. E. Orgel
La obra va dirigida a los estudiantes de Química inorgánica y a todos los que desean adquirir una visión general de este aspecto nuevo de la teoría de la valencia; no está escrita para los profesionales de la Química teórica. Por esto la bibli
Autor:
L. E. Orgel
Publikováno v:
Science of Aging Knowledge Environment. 2001
The ways in which the accumulation of mutations might contribute to the process of aging in higher organisms or in individual clones of cells has been discussed at length. No corresponding treatment of the consequences of transcription errors in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76df7f3aaca01488ed18b1a2c235c142
https://doi.org/10.1126/sageke.2001.1.cp8
https://doi.org/10.1126/sageke.2001.1.cp8
Autor:
G F, Joyce, L E, Orgel
Publikováno v:
The American biology teacher. 60(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b32d5736c644fb7d5bf1ed7c82e6251
https://pubmed.ncbi.nlm.nih.gov/11541103
https://pubmed.ncbi.nlm.nih.gov/11541103
Autor:
K E, Wen, L E, Orgel
Publikováno v:
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life. 31(3)
We have used amino acids activated by carbonyldiimidazole to study the enantiospecificity of peptide elongation in aqueous solution. Peptide 'primers' Glu10 and Ala3Glu10 were elongated with the enantiomers of arginine, glutamic acid, asparagine, phe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::01c8a0f944d67fa37e8a9af8964a83b6
https://pubmed.ncbi.nlm.nih.gov/11434103
https://pubmed.ncbi.nlm.nih.gov/11434103
Autor:
I A, Kozlov, L E, Orgel
Publikováno v:
Molekuliarnaia biologiia. 34(6)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6511b6c3a8730705429e4feafe8dcac8
https://pubmed.ncbi.nlm.nih.gov/11153470
https://pubmed.ncbi.nlm.nih.gov/11153470
Autor:
B C, Chu, L E, Orgel
Publikováno v:
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life. 29(5)
Monomeric cysteine residues attached to cysteine-containing peptides by disulfide bonds can be activated by carbonyldiimidazole. If two monomeric cysteine residues, attached to a 'scaffold' peptide Gly-Cys-Glyn-Cys-Glu10, (n = 0, 1, 2, 3) are activat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f131f476c7603e761da5f3f86adc2a47
https://pubmed.ncbi.nlm.nih.gov/10573686
https://pubmed.ncbi.nlm.nih.gov/10573686
Autor:
A R, Hill, L E, Orgel
Publikováno v:
Origins of life and evolution of the biosphere : the journal of the International Society for the Study of the Origin of Life. 29(2)
Unlike glutamic acid, L-gamma-carboxyglutamic acid does not oligomerize efficiently when treated with carbonyldiimidazole in aqueous solution. However, divalent ions such as Mg2+ catalyze the reaction, and lead to the formation of oligomers in good y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e6be59441ea37772cd45e5efe3623c19
https://pubmed.ncbi.nlm.nih.gov/10227198
https://pubmed.ncbi.nlm.nih.gov/10227198
Autor:
B C, Chu, L E, Orgel
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f767e03bdddf71f4e45924645defcc0e
https://pubmed.ncbi.nlm.nih.gov/8313001
https://pubmed.ncbi.nlm.nih.gov/8313001
Autor:
A R, Hill, L E, Orgel
Publikováno v:
Bioconjugate chemistry. 2(6)
Photooxidation and consequent cleavage of oligodeoxynucleotides by the uranyl ion is greatly enhanced in the presence of a terminal 5'- or 3'-phosphate group. This enhanced cleavage is confined to nearby phosphodiester bonds in the case of a 5'-phosp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::06a71868b8a7a80764e22b00b632c906
https://pubmed.ncbi.nlm.nih.gov/1805940
https://pubmed.ncbi.nlm.nih.gov/1805940