Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Ronald M. Cook"'
Autor:
Krishna K. Niyogi, Robert H. Calderon, James J. Russell, Ronald M. Cook, Alizée Malnoë, Rachel M. Dent, José G. García-Cerdán, Cynthia Gaw, Catherine de Vitry
Publikováno v:
The Journal of Biological Chemistry
Background: Photosystem II is an essential component of oxygenic photosynthesis. Results: Photosystem II is specifically decreased in rubredoxin mutants of the green alga Chlamydomonas reinhardtii, the cyanobacterium Synechocystis sp. PCC 6803, and t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dad65ae4680040c227743446d3623fd9
https://doi.org/10.1074/jbc.m113.487629
https://doi.org/10.1074/jbc.m113.487629
Publikováno v:
International Journal of Peptide and Protein Research. 6:55-58
A protected decapeptide corresponding to a section found in the last half of the protein chain of rubredoxin has been prepared by standard peptide methods.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4bb14fdfbdcb0944e5adf000b358c6c4
https://doi.org/10.1111/j.1399-3011.1974.tb02360.x
https://doi.org/10.1111/j.1399-3011.1974.tb02360.x
Publikováno v:
International Journal of Peptide and Protein Research. 4:177-180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f11d091c4b915b083c5e80606155026d
https://doi.org/10.1111/j.1399-3011.1972.tb03417.x
https://doi.org/10.1111/j.1399-3011.1972.tb03417.x
Publikováno v:
International Journal of Peptide and Protein Research. 4:101-108
A synthesis is described for the protected N-terminal nonapeptide (A11-A 19) fragment of rubredoxin, methyl Na-benzyloxycarbonyl-O-t-butyl-L-tyrosyl-L-isoleucyl-O-t-butyl-L-tyrosyl-L-t-butyl-L-aspartyl-L-prolyl-L-alanyl-L-leucyl-L-valyl-glycinate.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dc23304ca139465cccac85411a8b17f
https://doi.org/10.1111/j.1399-3011.1972.tb03405.x
https://doi.org/10.1111/j.1399-3011.1972.tb03405.x
Publikováno v:
Chemistry - A European Journal. 9:3466-3471
Fluorogenic probes dual-labeled with reporter and quencher dyes use a change in fluorescence to monitor biochemical events (e.g., substrate binding or enzyme digestion). Such events change the reporter-quencher distance, which affects fluorescence. R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de104b35385a6f1c346fe1c0f5cb660
https://doi.org/10.1002/chem.200304941
https://doi.org/10.1002/chem.200304941
Publikováno v:
Bioconjugate Chemistry. 13:1155-1158
Several fluorescence resonance energy transfer (FRET) oligonucleotide probes were made with different internal linkages between the DNA and the quencher dye. In one example, a 5'-fluorescein beta-actin-based 26-mer DNA sequence was synthesized bearin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ed78018a516a0e87eef14ec8d9e50ac
https://doi.org/10.1021/bc0200125
https://doi.org/10.1021/bc0200125
Publikováno v:
The Journal of Organic Chemistry. 65:9033-9038
5-Carboxy Tamra 1 was conjugated to 4-hydroxypiperidine with BOP and N-methylmorpholine, and the resulting 5-(N-pipyridyl-4-hydroxy)-Tamra carboxamide 2 was treated with 2-cyanoethyl tetraisopropylphosphorodiamidite to give 5-[N-pipyridyl-4-O-(2-cyan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf875832c7b80807e31dc2679822febf
https://doi.org/10.1021/jo0011134
https://doi.org/10.1021/jo0011134
Publikováno v:
Organic Process Research & Development. 5:45-49
Literature syntheses of 4,7,2‘,7‘-tetrachloro-5(and 6)-carboxy-fluorescein (“5 and 6 TET”) 1 and 4‘,5‘-dichloro-2‘,7‘-dimethoxy-5(and 6)-carboxyfluorescein (“5 and 6 JOE”) 2 are reviewed, and new, preparatively useful methods are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::82b0e6a832b24007d7154d8dc0d56ca8
https://doi.org/10.1021/op000292o
https://doi.org/10.1021/op000292o
Publikováno v:
Nucleosides and Nucleotides. 18:1809-1824
A uridine-based linker immobilized onto polystyrene beads at the 5′ terminus via a phosphodiester group and then used as a universal DNA synthesis support gives post synthesis DNA cleavage in 8 hrs or less without alkali metal salts. DNA produced w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20b2a10ea36b1083e7274f6265897c5d
https://doi.org/10.1080/07328319908044845
https://doi.org/10.1080/07328319908044845
Autor:
and Matthew H. Lyttle, Michael F. Songster, J. Howard Adams, Ronald M. Cook, Vasu Jammalamadaka, Derek Hudson
Publikováno v:
The Journal of Organic Chemistry. 63:3706-3716
Mild, efficient conditions have been developed for the preparation of 4-methylbenzhydrylamine polystyrene (MBHA) and aminomethyl polystyrene (AMPS) resins by a two-step procedure with synthons 1a and 1c. The products possess excellent swelling charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::306c1a4bf6f3ba33ba9c824cdd26a5cc
https://doi.org/10.1021/jo9802269
https://doi.org/10.1021/jo9802269