Associate Professor, Laboratory Medicine, Yale University School of Medicine

Pathology

Dr. Michael E. Hodsdon works in the field of Pathology. He studied medicine at Washington University School of Medicine in St. Louis. Michael E. Hodsdon is a published physician. He has 40 papers published. The most current publication "The three-dimensional structure of a helix-less variant of intestinal fatty acid-binding protein."

Publications

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• Conformational dynamics of Ca2+-dependent responses in the polycystin-2 C-terminal tail.
• Use of Imipenem To Detect KPC, NDM, OXA, IMP, and VIM Carbapenemase Activity from Gram-Negative Rods in 75 Minutes Using Liquid Chromatography-Tandem Mass Spectrometry.
• Rapid detection of convallatoxin using five digoxin immunoassays.
• The number and location of EF hand motifs dictates the calcium dependence of polycystin-2 function.
• An Explicit Formulation Approach for the Analysis of Calcium Binding to EF-Hand Proteins Using Isothermal Titration Calorimetry.
• Rapid detection of carbapenemase activity through monitoring ertapenem hydrolysis in Enterobacteriaceae with LC-MS/MS.
• A Model of GAG/MIP-2/CXCR2 Interfaces and Its Functional Effects.
• An intrinsically disordered C terminus allows the La protein to assist the biogenesis of diverse noncoding RNA precursors.
• Two independent histidines, one in human prolactin and one in its receptor, are critical for pH-dependent receptor recognition and activation.
• Allosteric inhibition of macrophage migration inhibitory factor revealed by ibudilast.
• Anti-tumor effects of adenovirus containing human growth hormone sequences in a mouse model of human ovarian cancer.
• Structure of the EF-hand domain of polycystin-2 suggests a mechanism for Ca2+-dependent regulation of polycystin-2 channel activity.
• Contribution of individual histidines to the global stability of human prolactin.
• Weak self-association of human growth hormone investigated by nitrogen-15 NMR relaxation.
• Analysis of site-specific histidine protonation in human prolactin.
• Structural and functional basis of CXCL12 (stromal cell-derived factor-1 alpha) binding to heparin.
• The kinetics of binding human prolactin, but not growth hormone, to the prolactin receptor vary over a physiologic pH range.
• Mapping the binding site on CD8 beta for MHC class I reveals mutants with enhanced binding.
• Relationship between salt-bridge identity and 14-helix stability of beta3-peptides in aqueous buffer.
• Solution structure and backbone dynamics of an N-terminal ubiquitin-like domain in the GLUT4-regulating protein, TUG.
• Inhibiting HIV fusion with a beta-peptide foldamer.
• Deubiquitinating function of ataxin-3: insights from the solution structure of the Josephin domain.
• Solution structure of a beta-peptide ligand for hDM2.
• Pediatric fatality following ingestion of dinitrophenol: postmortem identification of a "dietary supplement".
• Consequences of binding an S-adenosylmethionine analogue on the structure and dynamics of the thiopurine methyltransferase protein backbone.
• Helical beta-peptide inhibitors of the p53-hDM2 interaction.
• Is there structural specificity in the reversible protein aggregates that are stored in secretory granules?
• Aggregation of human wild-type and H27A-prolactin in cells and in solution: roles of Zn(2+), Cu(2+), and pH.
• Intestinal fatty acid binding protein: the folding mechanism as determined by NMR studies.
• The three-dimensional structure of a helix-less variant of intestinal fatty acid-binding protein.
• Discrete backbone disorder in the nuclear magnetic resonance structure of apo intestinal fatty acid-binding protein: implications for the mechanism of ligand entry.
• Ligand binding alters the backbone mobility of intestinal fatty acid-binding protein as monitored by 15N NMR relaxation and 1H exchange.
• The NMR solution structure of intestinal fatty acid-binding protein complexed with palmitate: application of a novel distance geometry algorithm.
• 1H, 13C and 15N assignments and chemical shift-derived secondary structure of intestinal fatty acid-binding protein.
• Tertiary structure of thiopurine methyltransferase from Pseudomonas syringae, a bacterial orthologue of a polymorphic, drug-metabolizing enzyme.
• The tertiary structure and backbone dynamics of human prolactin.
• A PH domain within OCRL bridges clathrin-mediated membrane trafficking to phosphoinositide metabolism.
• Ayurvedic herbal medicine and lead poisoning.
• Location of the epitope for an anti-CD8alpha antibody 53.6.7 which enhances CD8alpha-MHC class I interaction indicates antibody stabilization of a higher affinity CD8 ...

Schools

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• Washington Center School of Medicine

• Yale New Haven Hospital

Doctors Specialties

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• Clinical Pathology
• Pathology

Accepted Insurances

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Education

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• Yale-New Haven Hospital
• Washington University School of Medicine in St. Louis

Hospital

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• Yale-New Haven Hospital

Helpful Reviews

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Medicare Facts

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National Provider Identifier [NPI]	1801887203
Last Name Of The Provider	HODSDON
First Name Of The Provider	MICHAEL
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