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J G Belasco
Author PubWeight™ 90.31
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Title
Journal
Year
PubWeight™
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1
Two distinct destabilizing elements in the c-fos message trigger deadenylation as a first step in rapid mRNA decay.
Genes Dev
1991
7.51
2
The c-fos transcript is targeted for rapid decay by two distinct mRNA degradation pathways.
Genes Dev
1989
7.03
3
Decay of mRNA in Escherichia coli: investigation of the fate of specific segments of transcripts.
Proc Natl Acad Sci U S A
1983
6.79
4
The nonamer UUAUUUAUU is the key AU-rich sequence motif that mediates mRNA degradation.
Mol Cell Biol
1995
4.76
5
Differential expression of photosynthesis genes in R. capsulata results from segmental differences in stability within the polycistronic rxcA transcript.
Cell
1985
4.15
6
beta-Lactamase proceeds via an acyl-enzyme intermediate. Interaction of the Escherichia coli RTEM enzyme with cefoxitin.
Biochemistry
1980
3.94
7
A 5'-terminal stem-loop structure can stabilize mRNA in Escherichia coli.
Genes Dev
1992
3.15
8
Growth-rate dependent regulation of mRNA stability in Escherichia coli.
Nature
1984
3.06
9
The stability of E. coli gene transcripts is dependent on determinants localized to specific mRNA segments.
Cell
1986
2.79
10
The ompA 5' untranslated RNA segment functions in Escherichia coli as a growth-rate-regulated mRNA stabilizer whose activity is unrelated to translational efficiency.
J Bacteriol
1990
2.68
11
Control of RNase E-mediated RNA degradation by 5'-terminal base pairing in E. coli.
Nature
1992
2.53
12
An intercistronic stem-loop structure functions as an mRNA decay terminator necessary but insufficient for puf mRNA stability.
Cell
1988
2.53
13
Effect of premature termination of translation on mRNA stability depends on the site of ribosome release.
Proc Natl Acad Sci U S A
1987
2.24
14
Structure and function of a bacterial mRNA stabilizer: analysis of the 5' untranslated region of ompA mRNA.
J Bacteriol
1991
1.90
15
Multiple elements in the c-fos protein-coding region facilitate mRNA deadenylation and decay by a mechanism coupled to translation.
J Biol Chem
1994
1.90
16
mRNA stabilization by the ompA 5' untranslated region: two protective elements hinder distinct pathways for mRNA degradation.
RNA
1998
1.89
17
Regulation of proto-oncogene mRNA stability.
Biochim Biophys Acta
1992
1.84
18
RNase E autoregulates its synthesis by controlling the degradation rate of its own mRNA in Escherichia coli: unusual sensitivity of the rne transcript to RNase E activity.
Genes Dev
1995
1.74
19
An evolutionarily conserved RNA stem-loop functions as a sensor that directs feedback regulation of RNase E gene expression.
Genes Dev
2000
1.51
20
Structural model for the cooperative assembly of HIV-1 Rev multimers on the RRE as deduced from analysis of assembly-defective mutants.
Mol Cell
2001
1.46
21
The ompA 5' untranslated region impedes a major pathway for mRNA degradation in Escherichia coli.
Mol Microbiol
1994
1.39
22
Regions of RNase E important for 5'-end-dependent RNA cleavage and autoregulated synthesis.
J Bacteriol
2000
1.35
23
The destabilizing elements in the coding region of c-fos mRNA are recognized as RNA.
Mol Cell Biol
1993
1.34
24
Analysis of RNA-binding proteins by in vitro genetic selection: identification of an amino acid residue important for locking U1A onto its RNA target.
Proc Natl Acad Sci U S A
1995
1.32
25
A structural model for the HIV-1 Rev-RRE complex deduced from altered-specificity rev variants isolated by a rapid genetic strategy.
Cell
1996
1.25
26
Direct observation of substrate distortion by triosephosphate isomerase using Fourier transform infrared spectroscopy.
Biochemistry
1980
1.25
27
Importance of a 5' stem-loop for longevity of papA mRNA in Escherichia coli.
J Bacteriol
1999
1.20
28
Beta-lactamase inactivation by mechanism-based reagents.
Philos Trans R Soc Lond B Biol Sci
1980
1.17
29
Target discrimination by RNA-binding proteins: role of the ancillary protein U2A' and a critical leucine residue in differentiating the RNA-binding specificity of spliceosomal proteins U1A and U2B".
RNA
1998
1.09
30
RNA recognition by the joint action of two nucleolin RNA-binding domains: genetic analysis and structural modeling.
EMBO J
1997
1.07
31
T7 phage display: a novel genetic selection system for cloning RNA-binding proteins from cDNA libraries.
Proc Natl Acad Sci U S A
2001
1.06
32
Translation of the adhE transcript to produce ethanol dehydrogenase requires RNase III cleavage in Escherichia coli.
J Bacteriol
1996
1.02
33
Deadenylylation: a mechanism controlling c-fos mRNA decay.
Enzyme
1990
1.00
34
Degradation of pufLMX mRNA in Rhodobacter capsulatus is initiated by nonrandom endonucleolytic cleavage.
J Bacteriol
1990
1.00
35
In vitro genetic analysis of RNA-binding proteins using phage display libraries.
Methods Enzymol
1996
0.98
36
Polarization of substrate carbonyl groups by yeast aldolase: investigation by Fourier transform infrared spectroscopy.
Biochemistry
1983
0.95
37
Rapid genetic analysis of RNA-protein interactions by translational repression in Escherichia coli.
Methods Enzymol
2000
0.93
38
Comparative analysis of the plant mRNA-destabilizing element, DST, in mammalian and tobacco cells.
Plant Mol Biol
2002
0.89
39
Autoregulation of RNase E synthesis in Escherichia coli.
Nucleic Acids Symp Ser
1995
0.87
40
Critical ionization states in the reaction catalyzed by triosephosphate isomerase.
Biochemistry
1978
0.83
41
Energetics of proline racemase: double fractionation experiment, a test for concertedness and for transition-state dominance.
Biochemistry
1986
0.80
42
Energetics of proline racemase: fractionation factors for the essential catalytic groups in the enzyme-substrate complexes.
Biochemistry
1986
0.79
43
RNA-binding proteins tamed.
Nat Struct Biol
1998
0.77
44
Energetics of proline racemase: rates, fractionation factors, and buffer catalysis in the oversaturated region. Nature of the interconversion of the two forms of free enzyme.
Biochemistry
1986
0.77
45
Energetics of proline racemase: transition-state fractionation factors for the two protons involved in the catalytic steps.
Biochemistry
1986
0.76
46
Autoregulation through translation.
Curr Biol
1992
0.75