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Publications by Yi-Jin Chen
Mutagenesis Identifies the Critical Amino Acid Residues of Human Endonuclease G Involved in Catalysis, Magnesium Coordination, and Substrate Specificity
Journal of Biomedical Science
Cell Biology
Pharmacology
Biochemistry
Endocrinology
Clinical Biochemistry
Molecular Biology
Medicine
Metabolism
Diabetes
Related publications
Identification of Amino Acid Residues Responsible for Differences in Substrate Specificity and Inhibitor Sensitivity Between Two Human Liver Dihydrodiol Dehydrogenase Isoenzymes by Site-Directed Mutagenesis
Biochemical Journal
Biochemistry
Cell Biology
Molecular Biology
Amino Acid Residues Contributing to the Substrate Specificity of the Influenza a Virus Neuraminidase
Journal of Virology
Insect Science
Immunology
Microbiology
Virology
Amino Acid Residues Critical for the Specificity for Betaine Aldehyde of the Plant ALDH10 Isoenzyme Involved in the Synthesis of Glycine Betaine
Plant Physiology
Plant Science
Genetics
Physiology
Amino Acid Residues in the Laminin G Domains of Protein S Involved in Tissue Factor Pathway Inhibitor Interaction
Thrombosis and Haemostasis
Hematology
Alanine-Scanning Mutagenesis of Plasmatocyte Spreading Peptide Identifies Critical Residues for Biological Activity
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Mutagenesis and Derivatization of Human Vesicle Monoamine Transporter 2 (VMAT2) Cysteines Identifies Transporter Domains Involved in Tetrabenazine Binding and Substrate Transport
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Substrate-Induced Structural Alterations of Mycobacterial Mycothione Disulphide Reductase and Critical Residues Involved
FEBS Letters
Genetics
Cell Biology
Molecular Biology
Biochemistry
Structural Biology
Biophysics
Identification of Residues Involved in Substrate Specificity and Cytotoxicity of Two Closely Related Cutinases From Mycobacterium Tuberculosis
PLoS ONE
Multidisciplinary
Identification of Crucial Amino Acid Residues Involved in Agonist Signaling at the GPR55 Receptor
Biochemistry
Biochemistry