| Rank |
Title |
Journal |
Year |
PubWeight™‹?› |
|
1
|
CARP-2 is an endosome-associated ubiquitin ligase for RIP and regulates TNF-induced NF-kappaB activation.
|
Curr Biol
|
2008
|
1.58
|
|
2
|
Pharmacogenetic impact of polymorphisms in the coding region of the UGT1A1 gene on SN-38 glucuronidation in Japanese patients with cancer.
|
Cancer Sci
|
2006
|
1.31
|
|
3
|
Homogeneous catalytic system for reversible dehydrogenation-hydrogenation reactions of nitrogen heterocycles with reversible interconversion of catalytic species.
|
J Am Chem Soc
|
2009
|
1.18
|
|
4
|
Cancer prevention by natural compounds.
|
Drug Metab Pharmacokinet
|
2004
|
1.11
|
|
5
|
Studies on the interactions between drug and estrogen. II. On the inhibitory effect of 29 drugs reported to induce gynecomastia on the oxidation of estradiol at C-2 or C-17.
|
Biol Pharm Bull
|
2003
|
0.96
|
|
6
|
Sorafenib and sunitinib, two anticancer drugs, inhibit CYP3A4-mediated and activate CY3A5-mediated midazolam 1'-hydroxylation.
|
Drug Metab Dispos
|
2011
|
0.90
|
|
7
|
A phase I study of infusional 5-fluorouracil, leucovorin, oxaliplatin and irinotecan in Japanese patients with advanced colorectal cancer who harbor UGT1A1*1/*1,*1/*6 or *1/*28.
|
Oncology
|
2012
|
0.89
|
|
8
|
Cancer prevention by bovine lactoferrin and underlying mechanisms--a review of experimental and clinical studies.
|
Biochem Cell Biol
|
2002
|
0.89
|
|
9
|
Role of human cytochrome P450 (CYP) in the metabolic activation of nitrosamine derivatives: application of genetically engineered Salmonella expressing human CYP.
|
Drug Metab Rev
|
2002
|
0.89
|
|
10
|
Antibacterial activity of akyl gallates against Bacillus subtilis.
|
J Agric Food Chem
|
2004
|
0.88
|
|
11
|
Phase I/II study of FOLFIRI in Japanese patients with advanced colorectal cancer.
|
Jpn J Clin Oncol
|
2010
|
0.88
|
|
12
|
Dehydrogenative oxidation of alcohols in aqueous media using water-soluble and reusable Cp*Ir catalysts bearing a functional bipyridine ligand.
|
J Am Chem Soc
|
2012
|
0.86
|
|
13
|
Biosynthesis of poly-gamma-glutamic acid in plants: transient expression of poly-gamma-glutamate synthetase complex in tobacco leaves.
|
J Biosci Bioeng
|
2005
|
0.86
|
|
14
|
The vacuole-targeting fungicidal activity of amphotericin B against the pathogenic fungus Candida albicans and its enhancement by allicin.
|
J Antibiot (Tokyo)
|
2009
|
0.84
|
|
15
|
Transient inhibition of cyp3a in rats by star fruit juice.
|
Drug Metab Dispos
|
2005
|
0.83
|
|
16
|
Enhancement of the fungicidal activity of amphotericin B by allicin, an allyl-sulfur compound from garlic, against the yeast Saccharomyces cerevisiae as a model system.
|
Planta Med
|
2006
|
0.83
|
|
17
|
Pharmacokinetic study of S-1 in patients in whom inulin clearance was measured.
|
Oncology
|
2012
|
0.82
|
|
18
|
A diclofenac suppository-nabumetone combination therapy for arthritic pain relief and a monitoring method for the diclofenac binding capacity of HSA site II in rheumatoid arthritis.
|
Biopharm Drug Dispos
|
2013
|
0.82
|
|
19
|
Inhibition of human cytochrome P450 1B1, 1A1 and 1A2 by antigenotoxic compounds, purpurin and alizarin.
|
Mutat Res
|
2002
|
0.82
|
|
20
|
Potent inhibition by star fruit of human cytochrome P450 3A (CYP3A) activity.
|
Drug Metab Dispos
|
2004
|
0.81
|
|
21
|
A shear stress responsive gene product PP1201 protects against Fas-mediated apoptosis by reducing Fas expression on the cell surface.
|
Apoptosis
|
2011
|
0.80
|
|
22
|
Visualization analysis of the vacuole-targeting fungicidal activity of amphotericin B against the parent strain and an ergosterol-less mutant of Saccharomyces cerevisiae.
|
Microbiology
|
2013
|
0.80
|
|
23
|
Possible application of human c-Ha-ras proto-oncogene transgenic rats in a medium-term bioassay model for carcinogens.
|
Toxicol Pathol
|
2007
|
0.80
|
|
24
|
Clinical and economic evaluation of first-line therapy with FOLFIRI or modified FOLFOX6 for metastatic colorectal cancer.
|
Jpn J Clin Oncol
|
2010
|
0.80
|
|
25
|
Molecular design of multifunctional antibacterial agents against methicillin resistant Staphylococcus aureus (MRSA).
|
Bioorg Med Chem
|
2003
|
0.80
|
|
26
|
Orally administered bovine lactoferrin induces caspase-1 and interleukin-18 in the mouse intestinal mucosa: a possible explanation for inhibition of carcinogenesis and metastasis.
|
Cytokine
|
2004
|
0.80
|
|
27
|
Antibacterial activity of polygodial.
|
Phytother Res
|
2005
|
0.80
|
|
28
|
Association of ABCC2 genotype with efficacy of first-line FOLFIRI in Japanese patients with advanced colorectal cancer.
|
Drug Metab Pharmacokinet
|
2011
|
0.78
|
|
29
|
Antimycin A-induced cell death depends on AIF translocation through NO production and PARP activation and is not involved in ROS generation, cytochrome c release and caspase-3 activation in HL-60 cells.
|
J Antibiot (Tokyo)
|
2009
|
0.78
|
|
30
|
Simple and versatile catalytic system for N-alkylation of sulfonamides with various alcohols.
|
Org Lett
|
2010
|
0.78
|
|
31
|
Synergistic fungicidal activities of amphotericin B and N-methyl-N"-dodecylguanidine: a constituent of polyol macrolide antibiotic niphimycin.
|
J Antibiot (Tokyo)
|
2007
|
0.77
|
|
32
|
Synergistic fungicidal activities of polymyxin B and ionophores, and their dependence on direct disruptive action of polymyxin B on fungal vacuole.
|
J Antibiot (Tokyo)
|
2009
|
0.77
|
|
33
|
Imaging of heme/hemeproteins in nucleus of the living cells expressing heme-binding nuclear receptors.
|
FEBS Lett
|
2013
|
0.77
|
|
34
|
Dependence of vacuole disruption and independence of potassium ion efflux in fungicidal activity induced by combination of amphotericin B and allicin against Saccharomyces cerevisiae.
|
J Antibiot (Tokyo)
|
2010
|
0.77
|
|
35
|
Targeted yeast vacuole disruption by polyene antibiotics with a macrocyclic lactone ring.
|
Int J Antimicrob Agents
|
2009
|
0.77
|
|
36
|
Aerobic oxidative amidation of aromatic and cinnamic aldehydes with secondary amines by CuI/2-pyridonate catalytic system.
|
J Org Chem
|
2012
|
0.76
|
|
37
|
The cyclic organosulfur compound zwiebelane A from onion (Allium cepa) functions as an enhancer of polymyxin B in fungal vacuole disruption.
|
Planta Med
|
2010
|
0.76
|
|
38
|
Efficient synthesis of biazoles by aerobic oxidative homocoupling of azoles catalyzed by a copper(I)/2-pyridonate catalytic system.
|
Chem Commun (Camb)
|
2011
|
0.76
|
|
39
|
Multialkylation of aqueous ammonia with alcohols catalyzed by water-soluble Cp*Ir-ammine complexes.
|
J Am Chem Soc
|
2010
|
0.76
|
|
40
|
Morphological changes of the filamentous fungus Mucor mucedo and inhibition of chitin synthase activity induced by anethole.
|
Phytother Res
|
2011
|
0.76
|
|
41
|
Protective effects of α-tocopherol and ascorbic acid against cardol-induced cell death and reactive oxygen species generation in Staphylococcus aureus.
|
Planta Med
|
2013
|
0.76
|
|
42
|
Re: UGT1A1*28 genotype and irinotecan-induced neutropenia: dose matters.
|
J Natl Cancer Inst
|
2008
|
0.75
|
|
43
|
Synthesis of novel dendritic 2,2'-bipyridine ligands and their application to Lewis acid-catalyzed diels-alder and three-component condensation reactions.
|
J Org Chem
|
2007
|
0.75
|
|
44
|
Establishment of an apoptosis-sensitive rat mammary carcinoma cell line with a mutation in the DNA-binding region of p53.
|
Cancer Lett
|
2006
|
0.75
|
|
45
|
C-H activation on a diphosphine and hydrido-bridged diiridium complex: generation and detection of an active IrII-IrII species [(Cp*Ir)2(micro-dmpm)(micro-H)]+.
|
Dalton Trans
|
2008
|
0.75
|
|
46
|
Cooperative catalysis by iridium complexes with a bipyridonate ligand: versatile dehydrogenative oxidation of alcohols and reversible dehydrogenation-hydrogenation between 2-propanol and acetone.
|
Angew Chem Int Ed Engl
|
2012
|
0.75
|
|
47
|
Flocculating activity of cross-linked poly-gamma-glutamic acid against bentonite and Escherichia coli suspension pretreated with FeCl3 and its interaction with Fe3+.
|
J Biosci Bioeng
|
2005
|
0.75
|
|
48
|
Inhibitory activity of 1-farnesylpyridinium on the spatial control over the assembly of cell wall polysaccharides in Schizosaccharomyces pombe.
|
J Biochem
|
2006
|
0.75
|
|
49
|
Structure-activity relationship studies on UK-2A, a novel antifungal antibiotic from Streptomyces sp. 517-02. Part 5: Roles of the 9-membered dilactone-ring moiety in respiratory inhibition.
|
Bioorg Med Chem Lett
|
2006
|
0.75
|
|
50
|
[Need for pharmaceutical skill in using displacement of protein binding].
|
Yakugaku Zasshi
|
2007
|
0.75
|
|
51
|
Three-dimensional structure of the inclusion complex between phloridzin and beta-cyclodextrin.
|
Carbohydr Res
|
2002
|
0.75
|
|
52
|
Rapid induction of skin and mammary tumors in human c-Ha-ras proto-oncogene transgenic rats by treatment with 7,12-dimethylbenz[a]anthracene followed by 12-O-tetradecanoylphorbol 13-acetate.
|
Cancer Sci
|
2004
|
0.75
|
|
53
|
Selective inhibition of embryonic development in starfish by long-chain alkyl derivatives of UMP, TMP and AMP.
|
Nat Prod Res
|
2009
|
0.75
|
|
54
|
UK-2A, B, C, and D, novel antifungal antibiotics from Streptomyces sp. 517-02 VII. Membrane injury induced by C9-UK-2A, a derivative of UK-2A, in Rhodotorula mucilaginosa IFO 0001.
|
J Antibiot (Tokyo)
|
2002
|
0.75
|