Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Shih Ying Li"'
Publikováno v:
Archives of Biochemistry and Biophysics. 319:470-480
The Ah receptor from rat liver has been purified, using a specific oligonucleotide affinity column, in order to characterize the components of the receptor and to investigate features that modulate its DNA-binding activity. The purified DNA-binding f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef00fbf1ebda67b72aa3af05aa2f13b9
https://doi.org/10.1006/abbi.1995.1319
https://doi.org/10.1006/abbi.1995.1319
Autor:
Johanna D. Stoeckler, Mallela S. P. Sarma, Palle V. P. Pragnacharyulu, Elie Abushanab, Shih-Ying Li, Chandra Vargeese
Publikováno v:
Journal of Medicinal Chemistry. 37:3844-3849
The synthesis and biological evaluation of three chain-hydroxylated (+)-erythro-9-(2S-hydroxy-3R-nonyl)adenine [(+)-EHNA] derivatives are reported. Hydroxy groups at positions 9', 8', and 8',9' (12, 25, and 16) were introduced by either epoxidation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b82585faf46a126d13313b34d26d4da
https://doi.org/10.1021/jm00048a020
https://doi.org/10.1021/jm00048a020
Autor:
Shih-Ying Li, 李世應
96
Ecological risk assessment is a tool to assess the ecosystem’s situation cause by human activity that makes the negative influence. Because in the ecological risk assessment framework doesn’t offer the conceptual model for assessor to ass
Ecological risk assessment is a tool to assess the ecosystem’s situation cause by human activity that makes the negative influence. Because in the ecological risk assessment framework doesn’t offer the conceptual model for assessor to ass
Externí odkaz:
http://ndltd.ncl.edu.tw/handle/35qge6
Autor:
John Dougherty, Shih-Ying Li
Publikováno v:
Archives of biochemistry and biophysics. 340(1)
The Ah receptor binds aryl hydrocarbons such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) with high affinity. After binding aryl hydrocarbons, the receptor releases the 90-kDa heat shock protein and forms a dimer with the Arnt protein capable of bin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cff87f0d945a1297ea7a1cac9b0cd1c6
https://pubmed.ncbi.nlm.nih.gov/9126279
https://pubmed.ncbi.nlm.nih.gov/9126279
Publikováno v:
Biochemical and Biophysical Research Communications. 119:88-94
The combination of 1.6 microM 4 beta phorbol, 12 beta myristate, 13 alpha acetate (PMA) and 1 microM A23187 produced a five-fold greater stimulation of rat hepatocyte glycogen phosphorylase activity than was seen with PMA alone. Vasopressin activatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fbd4f9a32860e8f2b8de2f790163ecd
https://doi.org/10.1016/0006-291x(84)91622-x
https://doi.org/10.1016/0006-291x(84)91622-x
Publikováno v:
Life Sciences. 28:401-406
The accumulation of cyclic AMP due to adenosine deaminase plus theophylline and either isoproterenol or ACTH in the presence of adenosine deaminase plus theophylline, was inhibited by clonidine, N6-(phenylisopropyl)-adenosine and prostaglandin E2. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c288774a6294310ef09615cbba1058c
https://doi.org/10.1016/0024-3205(81)90085-0
https://doi.org/10.1016/0024-3205(81)90085-0
Publikováno v:
Life Sciences. 27:953-961
The incorporation of radioactive phosphate into phosphatidylinositol was stimulated by epinephrine in hamster fat cells. This action was inhibited by alpha-adrenergic antagonists in the potency order: Prazosin⪢phentolamine>yohimbine. Methoxamine, b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ff864ab621069a6b92208d49ebcd6de
https://doi.org/10.1016/0024-3205(80)90105-8
https://doi.org/10.1016/0024-3205(80)90105-8
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Stoeckler, Johanna D., Rosenfield, Cathy G., Shih-Hsi, Chu, Shih-Ying, Li, Acton, Edward M., Ryan, Kenneth J., Parks, Robert E., Jr.
Publikováno v:
In Biochemical Pharmacology 1990 40(3):615-619