Physician
Otolaryngology (ENT)
Dr. Scott R. Phillips, MD
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Scott Phillips practices Otolaryngology (ENT). He went to medical school at Indiana University School of Medicine. Indiana University School of Medicine has a rank of 45 in research and a 47 in primary care He over the years received 2 awards: "Fellow (FACS)" and "Fellow (FAAO-HNS)". Scott Phillips is a published doctor as well. He has 43 publications published. The latest was: Crystal structure of intact elongation factor EF-Tu from Escherichia coli in GDP conformation at 2.05 A resolution. He accepts Medicare payments and is registered with Medicare.gov.
Publications
- Drosophila rolling blackout displays lipase domain-dependent and -independent endocytic functions downstream of dynamin.
- Neuronal loss of Drosophila NPC1a causes cholesterol aggregation and age-progressive neurodegeneration.
- The pathologies associated with functional titration of phosphatidylinositol transfer protein alpha activity in mice.
- Conformational dynamics of the major yeast phosphatidylinositol transfer protein sec14p: insight into the mechanisms of phospholipid exchange and diseases of sec14p-li...
- Specific and nonspecific membrane-binding determinants cooperate in targeting phosphatidylinositol transfer protein beta-isoform to the mammalian trans-Golgi network.
- The diverse biological functions of phosphatidylinositol transfer proteins in eukaryotes.
- Phosphatidylinositol transfer protein function in the yeast Saccharomyces cerevisiae.
- Phosphatidylinositol transfer protein function in the mouse.
- Structural and kinetic studies of a series of mutants of galactose oxidase identified by directed evolution.
- Mice lacking phosphatidylinositol transfer protein-alpha exhibit spinocerebellar degeneration, intestinal and hepatic steatosis, and hypoglycemia.
- Genetic ablation of phosphatidylinositol transfer protein function in murine embryonic stem cells.
- Crystal structure of the precursor of galactose oxidase: an unusual self-processing enzyme.
- Conserved tyrosine-369 in the active site of Escherichia coli copper amine oxidase is not essential.
- Phosphatidylinositol transfer proteins and protein kinase C make separate but non-interacting contributions to the phosphorylation state necessary for secretory compet...
- Crystal structure of the Holliday junction resolving enzyme T7 endonuclease I.
- Direct and indirect readout in mutant Met repressor-operator complexes.
- Leishmania pyruvate kinase: the crystal structure reveals the structural basis of its unique regulatory properties.
- Visualization of dioxygen bound to copper during enzyme catalysis.
- The structure of pyruvate kinase from Leishmania mexicana reveals details of the allosteric transition and unusual effector specificity.
- Yeast Sec14p deficient in phosphatidylinositol transfer activity is functional in vivo.
- The active site base controls cofactor reactivity in Escherichia coli amine oxidase: x-ray crystallographic studies with mutational variants.
- Polyanionic inhibitors of phosphoglycerate mutase: combined structural and biochemical analysis.
- Sulphate ions observed in the 2.12 A structure of a new crystal form of S. cerevisiae phosphoglycerate mutase provide insights into understanding the catalytic mechanism.
- Crystal structure of intact elongation factor EF-Tu from Escherichia coli in GDP conformation at 2.05 A resolution.
- Crystal structure of restriction endonuclease BglI bound to its interrupted DNA recognition sequence.
- A phosphatidylinositol 3-kinase and phosphatidylinositol transfer protein act synergistically in formation of constitutive transport vesicles from the trans-Golgi netw...
- The 2.3 A X-ray crystal structure of S. cerevisiae phosphoglycerate mutase.
- Crystal structure of the Saccharomyces cerevisiae phosphatidylinositol-transfer protein.
- Crystallization and preliminary X-ray diffraction studies of the Saccharomyces cerevisiae phospholipid-transfer protein Sec14p.
- Essential role for diacylglycerol in protein transport from the yeast Golgi complex.
- Catalytic mechanism of the quinoenzyme amine oxidase from Escherichia coli: exploring the reductive half-reaction.
- A carboxy terminal domain of the hMSH-2 gene product is sufficient for binding specific mismatched oligonucleotides.
- Crystal structure of a quinoenzyme: copper amine oxidase of Escherichia coli at 2 A resolution.
- X-ray crystallographic studies of cofactors in galactose oxidase.
- Structure and mechanism of galactose oxidase. The free radical site.
- Crystal structure of a free radical enzyme, galactose oxidase.
- Built by association: structure and function of helix-loop-helix DNA-binding proteins.
- The beta-ribbon DNA recognition motif.
- Preliminary studies of two active site mutants of galactose oxidase.
- Pheromone binding to two rodent urinary proteins revealed by X-ray crystallography.
- Crystallographic refinement of the three-dimensional structure of the FabD1.3-lysozyme complex at 2.5-A resolution.
- Genetic background alters the severity and onset of neuromuscular disease caused by the loss of ubiquitin-specific protease 14 (usp14).
Schools
University Of Cincinnati College Of Medicine
Grant Med Center
Doctors Specialties
- Family Medicine
- Otolaryngology (ENT)
Accepted Insurances
- Aetna HMO
- Choice Plus POS II
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Coventry Health America PPO
- First Health (Coventry Health Care) PPO
- Choice Care PPO
- MultiPlan PPO
- PHCS Network PPO
Awards
- Fellow (FACS)
- Fellow (FAAO-HNS)
Education
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San Antonio Uniformed Services Health Education Consortium -
Indiana University School of Medicine
Drug Facts
| NPI NUMBER | 1437126687 | |
| NPPES Provider LastName | PHILLIPS | |
| NPPES Provider FirstName | SCOTT | |
| NPPES Provider ZIPCode | 431109585 | |
| NPPES Provider State | OH | |
| Specialty Description | Family Practice | |
| Total Claim Count | 4259.0 | |
| Distinct Opioid Count | 3.0 | |
| Opioid Claim Count | 104.0 | |
| Percent Opioid Claims | 2.44 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1437126687 |
| Last Name Of The Provider | PHILLIPS |
| First Name Of The Provider | SCOTT |
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