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Detection of the High-Level Aminoglycoside Resistance Gene aph(2")-Ib in Enterococcus faecium

Antimicrobial Agents and Chemotherapy, 2000-10, Vol.44 (10), p.2876-2879

2000

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Aminoglycoside Resistance Genesaph(2")-Ib and aac(6′)-Im Detected Together in Strains of both Escherichia coli andEnterococcus faecium

Antimicrobial Agents and Chemotherapy, 2001-10, Vol.45 (10), p.2691-2694

2001

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Novel tricyclic inhibitors of farnesyl protein transferase. Biochemical characterization and inhibition of Ras modification in transfected Cos cells

The Journal of biological chemistry, 1995-12, Vol.270 (51), p.30611-30618

1995

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Aminoglycoside resistance genes aph(2)-Ib and aac(6')-Im detected together in strains of both escherichia coli and Enterococcus faecium

Antimicrobial agents and chemotherapy, 2001-10, Vol.45 (10), p.2691-2694

2001

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Novel Tricyclic Inhibitors of Farnesyl Protein Transferase

The Journal of biological chemistry, 1995-12, Vol.270 (51), p.30611-30618

1995

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Discovery of novel nonpeptide tricyclic inhibitors of ras farnesyl protein transferase

Bioorganic & medicinal chemistry, 1997-01, Vol.5 (1), p.101-113

1997

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A cembranolide diterpene farnesyl protein transferase inhibitor from the marine soft coral Lobophytum cristagalli

Bioorganic & medicinal chemistry letters, 1996-04, Vol.6 (7), p.909-912

1996

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Differential regulation of phosphoinositide and phosphatidylcholine hydrolysis by protein kinase C-β1 overexpression : Effects on stimulation by α-thrombin, guanosine 5'-O-(thiotriphosphate), and calcium

The Journal of biological chemistry, 1992-05, Vol.267 (14), p.9826-9830

1992

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Characterization of Site-Specific Mutants Altered at Protein Kinase C β1Isozyme Autophosphorylation Sites

Proceedings of the National Academy of Sciences - PNAS, 1993-07, Vol.90 (13), p.6130-6134

1993

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Novel tricyclic aminoacetyl and sulfonamide inhibitors of Ras farnesyl protein transferase

Bioorganic & medicinal chemistry letters, 1996-12, Vol.6 (24), p.2977-2982

1996

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Indolocarbazoles. 1. Total synthesis and protein kinase inhibiting characteristics of compounds related to K-252c

Bioorganic & medicinal chemistry letters, 1993-08, Vol.3 (8), p.1537-1542

1993

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Inhibition of protein kinase c by the tyrosine kinase inhibitor erbstatin

Biochemical pharmacology, 1990-11, Vol.40 (9), p.2129-2135

1990

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Characterization of site-specific mutants altered at protein kinase C (beta)1 isozyme autophosphorylation sites

Proceedings of the National Academy of Sciences - PNAS, 1993-07, Vol.90 (13), p.6130

1993

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Detection of the High-Level Aminoglycoside Resistance Gene aph(2")-Ib in Enterococcus faecium

Aminoglycoside Resistance Genesaph(2")-Ib and aac(6′)-Im Detected Together in Strains of both Escherichia coli andEnterococcus faecium

Novel tricyclic inhibitors of farnesyl protein transferase. Biochemical characterization and inhibition of Ras modification in transfected Cos cells

Aminoglycoside resistance genes aph(2)-Ib and aac(6')-Im detected together in strains of both escherichia coli and Enterococcus faecium

Novel Tricyclic Inhibitors of Farnesyl Protein Transferase

Structure−Activity Relationship of 3-Substituted N-(Pyridinylacetyl)-4- (8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)- piperidine Inhibitors of Farnesyl-Protein Transferase: Design and Synthesis of in Vivo Active Antitumor Compounds

Discovery of novel nonpeptide tricyclic inhibitors of ras farnesyl protein transferase

A cembranolide diterpene farnesyl protein transferase inhibitor from the marine soft coral Lobophytum cristagalli

Inhibitors of Farnesyl Protein Transferase. 4-Amido, 4-Carbamoyl, and 4-Carboxamido Derivatives of 1-(8-Chloro-6,11-dihydro-5H-benzo[5,6]- cyclohepta[1,2-b]pyridin-11-yl)piperazine and 1-(3-Bromo-8-chloro-6,11- dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-yl)piperazine

Differential regulation of phosphoinositide and phosphatidylcholine hydrolysis by protein kinase C-β1 overexpression : Effects on stimulation by α-thrombin, guanosine 5'-O-(thiotriphosphate), and calcium

Characterization of Site-Specific Mutants Altered at Protein Kinase C β1Isozyme Autophosphorylation Sites

Novel tricyclic aminoacetyl and sulfonamide inhibitors of Ras farnesyl protein transferase

Indolocarbazoles. 1. Total synthesis and protein kinase inhibiting characteristics of compounds related to K-252c

Inhibition of protein kinase c by the tyrosine kinase inhibitor erbstatin

Characterization of site-specific mutants altered at protein kinase C (beta)1 isozyme autophosphorylation sites

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