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MEKK2 Kinase Association With 14-3-3 Protein Regulates Activation of C-Jun N-Terminal Kinase

Journal of Biological Chemistry

Biochemistry

Cell Biology

Molecular Biology

2013

English

3. Log-Multiplicative Association Models as Latent Variable Models for Nominal and/or Ordinal Data

Sociological Methodology

English

3-Substituted 1-Naphthamidomethyl-C-Galactosyls Interact With Two Unique Sub-Sites for High-Affinity and High-Selectivity Inhibition of Galectin-3

Theoretical Chemistry

Pharmaceutical Science

English

N-((1-Benzyl-1h-1,2,3-Triazol-4-Yl)methyl)arylamide as a New Scaffold That Provides Rapid Access to Antimicrotubule Agents: Synthesis and Evaluation of Antiproliferative Activity Against Select Cancer Cell Lines

Journal of Medicinal Chemistry

Drug Discovery

Molecular Medicine

2010

English

Symmetrical Bis-Tertiary Amines as Novel CXCR4 Inhibitors

European Journal of Medicinal Chemistry

English

Glycosaminoglycans Analogs From Marine Invertebrates: Structure, Biological Effects, and Potential as New Therapeutics

Frontiers in Cellular and Infection Microbiology

English

New Betulinic Acid Derivatives as Potent Proteasome Inhibitors

Bioorganic and Medicinal Chemistry Letters

Clinical Biochemistry

Pharmaceutical Science

Drug Discovery

2011

English

Design and Synthesis of Macrocyclic Peptidyl Hydroxamates as Peptide Deformylase Inhibitors

Bioorganic and Medicinal Chemistry Letters

Clinical Biochemistry

Pharmaceutical Science

Drug Discovery

2008

English

The Long Day Leaf as a Source of Cold Hardiness Inhibitors

English

Small Molecule Inhibitors of Metabolic Enzymes Repurposed as a New Class of Anthelmintics

ACS Infectious Diseases

Infectious Diseases

2018

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

MEKK2 Kinase Association With 14-3-3 Protein Regulates Activation of C-Jun N-Terminal Kinase

3. Log-Multiplicative Association Models as Latent Variable Models for Nominal and/or Ordinal Data

3-Substituted 1-Naphthamidomethyl-C-Galactosyls Interact With Two Unique Sub-Sites for High-Affinity and High-Selectivity Inhibition of Galectin-3

N-((1-Benzyl-1h-1,2,3-Triazol-4-Yl)methyl)arylamide as a New Scaffold That Provides Rapid Access to Antimicrotubule Agents: Synthesis and Evaluation of Antiproliferative Activity Against Select Cancer Cell Lines

Symmetrical Bis-Tertiary Amines as Novel CXCR4 Inhibitors

Glycosaminoglycans Analogs From Marine Invertebrates: Structure, Biological Effects, and Potential as New Therapeutics

New Betulinic Acid Derivatives as Potent Proteasome Inhibitors

Design and Synthesis of Macrocyclic Peptidyl Hydroxamates as Peptide Deformylase Inhibitors

The Long Day Leaf as a Source of Cold Hardiness Inhibitors

Small Molecule Inhibitors of Metabolic Enzymes Repurposed as a New Class of Anthelmintics