John A. Broadwater - Concepedia

Author

John A. Broadwater

University of Wisconsin–Madison

Also Known As

Broadwater, John, J.A. Broadwater, John A. Broadwater, John Broadwater

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

University of Wisconsin–Madison Boehringer Ingelheim (United States)Boehringer Ingelheim (Germany)Carnegie Mellon University

About

John A. Broadwater is an author at University of Wisconsin–Madison specializing in biochemistry, natural sciences, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	11	11	538
2	Natural Sciences	8	8	318
3	Medicine	7	7	376
4	Engineering	5	5	351
5	Public Health	1	1	32

John A. Broadwater

Publications

926

Citations

H-Index

Page 1

	Year	Citations
Peroxodiferric Intermediate of Stearoyl-Acyl Carrier Protein Δ<sup>9</sup> Desaturase: Oxidase Reactivity during Single Turnover and Implications for the Mechanism of Desaturation John A. Broadwater, Jingyuan Ai, Thomas M. Loehr, Biochemistry	1998	205
Desaturation and Hydroxylation John A. Broadwater, Edward Whittle, John Shanklin Journal of Biological Chemistry EngineeringDesiccationBiochemistryGeneticsCatalytic Specificity	2002	161
Lactose Fed-Batch Overexpression of Recombinant Metalloproteins in Escherichia coli BL21(DE3): Process Control Yielding High Levels of Metal-Incorporated, Soluble Protein Brianna Hoffman, John A. Broadwater, Peter F. Johnson, Protein Expression and Purification Escherichia Coli Bl21Soluble ProteinEngineeringBiochemistryBiological Inorganic Chemistry	1995	105
Mössbauer Studies of the Formation and Reactivity of a Quasi-Stable Peroxo Intermediate of Stearoyl-Acyl Carrier Protein Δ<sup>9</sup>-Desaturase John A. Broadwater, Catalina Achim, Eckard Münck, Biochemistry	1999	99
Circular Dichroism and Magnetic Circular Dichroism Studies of the Reduced Binuclear Non-Heme Iron Site of Stearoyl-ACP Δ<sup>9</sup>-Desaturase: Substrate Binding and Comparison to Ribonucleotide Reductase Yishan Yang, John A. Broadwater, Sabine Coates Pulver, Journal of the American Chemical Society Substrate BindingBiological Inorganic ChemistryAldo-keto ReductaseBiochemistryIron Metabolism	1999	57
Expression, purification, and physical characterization of Escherichia coli lipoyl(octanoyl)transferase Natasha M. Nesbitt, Camelia Baleanu‐Gogonea, Robert M. Cicchillo, Protein Expression and Purification BiosynthesisEngineeringEscherichia Coli LipoylBiochemistryEnzyme Catalysis	2004	39
The fundamental, versatile role of diiron enzymes in lipid metabolism John A. Broadwater, Jeffrey A. Haas, Brian G. Fox Fette Seifen Anstrichmittel Lipid PeroxidationMolecular BiologyDiiron CenterRedox BiologyOxidative Stress	1998	36
Synthesis, SAR, and Series Evolution of Novel Oxadiazole-Containing 5-Lipoxygenase Activating Protein Inhibitors: Discovery of 2-[4-(3-{(<i>R</i>)-1-[4-(2-Amino-pyrimidin-5-yl)-phenyl]-1-cyclopropyl-ethyl}-[1,2,4]oxadiazol-5-yl)-pyrazol-1-yl]-<i>N</i>,<i>N</i>-dimethyl-acetamide (BI 665915) Hidenori Takahashi, Doris Riether, Alessandra Bartolozzi, Journal of Medicinal Chemistry Drug TargetPharmacotherapyPharmaceutical ChemistryMolecular PharmacologyMedicinal Chemistry	2015	35
VHH antibody targeting the chemokine receptor CX3CR1 inhibits progression of atherosclerosis Sarah Löw, Haixia Wu, Kavita Jerath, mAbs Vascular DiseasePlaque ProgressionImmunologyPathologyImmunotherapy	2020	35
Combined PET/DCE-MRI in a Rabbit Model of Atherosclerosis Claudia Calcagno, Olivier Lairez, Julie A. Hawkins, JACC. Cardiovascular imaging Vascular DiseaseVascular ImageCardiovascular DiseaseMedical ImagingPet-mri	2018	32

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