Low-magnesium, trans-cleavage activity by type III, tertiary stabilized hammerhead ribozymes with stem 1 discontinuities.
about
Efficient reverse genetics reveals genetic determinants of budding and fusogenic differences between Nipah and Hendra viruses and enables real-time monitoring of viral spread in small animal models of henipavirus infection.Selecting RNA aptamers for synthetic biology: investigating magnesium dependence and predicting binding affinityTopological rearrangement yields structural stabilization and interhelical distance constraints in the Kin.46 self-phosphorylating ribozyme.Organelle trafficking of chimeric ribozymes and genetic manipulation of mitochondria.Conformational heterogeneity and the determinants of tertiary stabilization in the hammerhead ribozyme from Dolichopoda cave crickets.Two Divalent Metal Ions and Conformational Changes Play Roles in the Hammerhead Ribozyme Cleavage Reaction.Robust suppression of HIV replication by intracellularly expressed reverse transcriptase aptamers is independent of ribozyme processing.Bridging the gap between theory and experiment to derive a detailed understanding of hammerhead ribozyme catalysis.Threshold occupancy and specific cation binding modes in the hammerhead ribozyme active site are required for active conformation.Effects of the trinucleotide preceding the self-cleavage site on eggplant latent viroid hammerheads: differences in co- and post-transcriptional self-cleavage may explain the lack of trinucleotide AUC in most natural hammerheadsExpanded hammerhead ribozymes containing addressable three-way junctions.Trans-cleaving hammerhead ribozymes with tertiary stabilizing motifs: in vitro and in vivo activity against a structured viroid RNALeadzyme formed in vivo interferes with tobacco mosaic virus infection in Nicotiana tabacum.Prediction of hammerhead ribozyme intracellular activity with the catalytic core fingerprint.Viroid research and its significance for RNA technology and basic biochemistry
P2860
Q30368610-B06A3DE5-E77F-42E0-947F-21950B4DED1CQ33812374-ED8F8A13-AE06-491B-BBEF-D339221CA79BQ35172248-2FEBD774-6FC8-4314-9B67-43EF46093674Q35620843-079971AB-634C-4C5E-8F70-E62BEBB2B455Q35667456-F9F37CFA-5F95-4B18-96D9-3B94620E49B0Q36455539-F702C1BE-FEE7-4ADF-802C-B04E29ECEE02Q36460462-00FE21FF-5DBA-42D1-AEF2-57BB0FD7862AQ36561838-D0D69506-8F17-437D-85A5-45A788870E2FQ37275350-FC4918E1-3C1E-419B-90BD-373908ED5C02Q39117957-E98A1BA2-4788-4A63-805A-FD4B2D60B78EQ41890831-7AE222AB-276B-49B6-848E-E3679A1C241EQ42108764-E654DFA2-95A6-40F9-B029-F3AFC64D4BF0Q43586198-FA536834-DAF2-42A9-BFCF-00820B8F2BDCQ45602209-DF3A95D9-D46B-4CE8-B8B3-C590655C0338Q57285695-69BBB2D4-C4F0-4766-8F6F-9B1C099E33D6
P2860
Low-magnesium, trans-cleavage activity by type III, tertiary stabilized hammerhead ribozymes with stem 1 discontinuities.
description
2005 nî lūn-bûn
@nan
2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Low-magnesium, trans-cleavage ...... es with stem 1 discontinuities
@nl
Low-magnesium, trans-cleavage ...... s with stem 1 discontinuities.
@ast
Low-magnesium, trans-cleavage ...... s with stem 1 discontinuities.
@en
type
label
Low-magnesium, trans-cleavage ...... es with stem 1 discontinuities
@nl
Low-magnesium, trans-cleavage ...... s with stem 1 discontinuities.
@ast
Low-magnesium, trans-cleavage ...... s with stem 1 discontinuities.
@en
prefLabel
Low-magnesium, trans-cleavage ...... es with stem 1 discontinuities
@nl
Low-magnesium, trans-cleavage ...... s with stem 1 discontinuities.
@ast
Low-magnesium, trans-cleavage ...... s with stem 1 discontinuities.
@en
P2860
P356
P1433
P1476
Low-magnesium, trans-cleavage ...... s with stem 1 discontinuities.
@en
P2093
Donald H Burke
S Travis Greathouse
P2860
P2888
P356
10.1186/1471-2091-6-14
P407
P577
2005-08-12T00:00:00Z
P5875
P6179
1028266560