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Neutron Structure of Human Carbonic Anhydrase II: A Hydrogen-Bonded Water Network “Switch” Is Observed Between pH 7.8 and 10.0

Biochemistry

2011

English

Generation and Application of Fluorescent Anti-Human Β2-Microglobulin VHHs via Amino Modification

Theoretical Chemistry

Pharmaceutical Science

English

The Efficacy and Safety of Combination of PD-1 and CTLA-4 Inhibitors: A Meta-Analysis

Experimental Hematology and Oncology

English

Fragment-Based Discovery of 6 Azaindazoles as Inhibitors of Bacterial DNA Ligase

2014

English

Structure-Guided Synthesis and Mechanistic Studies Reveal Sweetspots on Naphthyl Salicyl Hydrazone Scaffold as Non-Nucleosidic Competitive, Reversible Inhibitors of Human Ribonucleotide Reductase

Journal of Medicinal Chemistry

Drug Discovery

Molecular Medicine

2018

English

Asymmetric 1, 4-Additions to 5-Alkoxy-2 (5h)-Furanonesenantioselective Synthesis and Absolute Configuration Determination of Β-Amino-Δ-Butyrolactones and Amino Diols

English

The Inhibition of Cellular Recovery in Human Tumour Cells by Inhibitors of Topoisomerase

British Journal of Cancer

Cancer Research

Oncology

1990

English

Defining the Molecular Basis of Amyloid Inhibitors: Human Islet Amyloid Polypeptide–Insulin Interactions

Journal of the American Chemical Society

English

Identification of Amino Acids in the Binding Pocket of the Human KDEL Receptor

Journal of Biological Chemistry

English

Nicotinamide Derivatives as a New Class of Gastric (H+/K+)-ATPase Inhibitors. III. Synthesis and Gastric Antisecretory Activity of 2-((2- And 4-Aminobenzyl, and .ALPHA.-methylbenzyl)sulfinyl)-N-(4-pyridinyl)-3-pyridinecarboxamides.

Chemical and Pharmaceutical Bulletin

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Neutron Structure of Human Carbonic Anhydrase II: A Hydrogen-Bonded Water Network “Switch” Is Observed Between pH 7.8 and 10.0

Generation and Application of Fluorescent Anti-Human Β2-Microglobulin VHHs via Amino Modification

The Efficacy and Safety of Combination of PD-1 and CTLA-4 Inhibitors: A Meta-Analysis

Fragment-Based Discovery of 6 Azaindazoles as Inhibitors of Bacterial DNA Ligase

Structure-Guided Synthesis and Mechanistic Studies Reveal Sweetspots on Naphthyl Salicyl Hydrazone Scaffold as Non-Nucleosidic Competitive, Reversible Inhibitors of Human Ribonucleotide Reductase

Asymmetric 1, 4-Additions to 5-Alkoxy-2 (5h)-Furanonesenantioselective Synthesis and Absolute Configuration Determination of Β-Amino-Δ-Butyrolactones and Amino Diols

The Inhibition of Cellular Recovery in Human Tumour Cells by Inhibitors of Topoisomerase

Defining the Molecular Basis of Amyloid Inhibitors: Human Islet Amyloid Polypeptide–Insulin Interactions

Identification of Amino Acids in the Binding Pocket of the Human KDEL Receptor

Nicotinamide Derivatives as a New Class of Gastric (H+/K+)-ATPase Inhibitors. III. Synthesis and Gastric Antisecretory Activity of 2-((2- And 4-Aminobenzyl, and .ALPHA.-methylbenzyl)sulfinyl)-N-(4-pyridinyl)-3-pyridinecarboxamides.