Andrew Dundee Ferguson M.D.
Cardiologist | Interventional Cardiology
550 S Landmark Ave Bloomington IN, 47403About
Dr. Andrew Ferguson is a cardiologist practicing in Bloomington, IN. Dr. Ferguson specializes in diagnosing, monitoring, and treating diseases or conditions of the heart and blood vessels and the cardiovascular system. These conditions include heart attacks, heart murmurs, coronary heart disease, and hypertension. Dr. Ferguson also practices preventative medicine, helping patients maintain a heart-healthy life.
Education and Training
Tulane Univ Sch of Med, New Orleans La 2002
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Structural basis of gating by the outer membrane transporter FecA.
- TonB-dependent receptors-structural perspectives.
- Metal import through microbial membranes.
- The ER protein folding sensor UDP-glucose glycoprotein-glucosyltransferase modifies substrates distant to local changes in glycoprotein conformation.
- A novel cysteine-rich domain of Sep15 mediates the interaction with UDP-glucose:glycoprotein glucosyltransferase.
- NMR structures of the selenoproteins Sep15 and SelM reveal redox activity of a new thioredoxin-like family.
- Expression, purification and crystallization of human 5-lipoxygenase-activating protein with leukotriene-biosynthesis inhibitors.
- What's all the FLAP about?: 5-lipoxygenase-activating protein inhibitors for
- Structural basis of CX-4945 binding to human protein kinase CK2.
- Biochemical characterization of human SET and MYND domain-containing protein 2 methyltransferase.
- Structural basis of substrate methylation and inhibition of SMYD2.
- Structure-based drug design on membrane protein targets: human integral membrane protein 5-lipoxygenase-activating protein.
- Structural approaches to obtain kinase selectivity.
- X-ray crystal structures of Escherichia coli RNA polymerase with switch region binding inhibitors enable rational design of squaramides with an improved fraction unbound to human plasma protein.
- SAR and Structural Analysis of Siderophore-Conjugated Monocarbam Inhibitors of Pseudomonas aeruginosa PBP3.
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