Michael J. Welch

ORCID: 0000-0001-7868-5079
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About
Contact & Profiles
Research Areas
  • Radiopharmaceutical Chemistry and Applications
  • Medical Imaging Techniques and Applications
  • Estrogen and related hormone effects
  • Medical Imaging and Pathology Studies
  • Advanced MRI Techniques and Applications
  • Chemical Reactions and Isotopes
  • Lanthanide and Transition Metal Complexes
  • Cancer, Hypoxia, and Metabolism
  • Cardiac Imaging and Diagnostics
  • Hydraulic Fracturing and Reservoir Analysis
  • Seismic Imaging and Inversion Techniques
  • Monoclonal and Polyclonal Antibodies Research
  • Asthma and respiratory diseases
  • Fluorine in Organic Chemistry
  • Drilling and Well Engineering
  • Prostate Cancer Treatment and Research
  • Metal complexes synthesis and properties
  • Rock Mechanics and Modeling
  • Inhalation and Respiratory Drug Delivery
  • HER2/EGFR in Cancer Research
  • Radioactive element chemistry and processing
  • Muon and positron interactions and applications
  • Inflammatory mediators and NSAID effects
  • Synthesis and Biological Evaluation
  • Hydrocarbon exploration and reservoir analysis

Danish Gas Technology Centre (Denmark)
2018-2024

Department of Climate Change, Energy, the Environment and Water
2023

Technical University of Denmark
2017-2023

Simmons University
2023

Office of the Chief Scientist
2022

Oil and Gas Center
2019-2020

Carbon Engineering (Canada)
2020

Norsk Hydro (Germany)
2020

Allergy and Asthma Medical Group and Research Center
2002-2018

Rady Children's Hospital-San Diego
1991-2018

Abstract We propose an in vivo method for use with positron emission tomography (PET) that results a quantitative characterization of neuroleptic binding sites using radiolabeled spiperone. The data are analyzed mathematical model describes transport, nonspecific binding, the brain. demonstrates receptor quantities B max (i.e., number sites) and K D −1 affinity) not separably ascertainable tracer methodology human subjects. have, therefore, introduced new term, potential, equivalent to...

10.1002/ana.410150302 article EN Annals of Neurology 1984-03-01

Recent evidence has defined an important role for PPARα in the transcriptional control of cardiac energy metabolism. To investigate genesis metabolic and functional derangements diabetic cardiomyopathy, mice with cardiac-restricted overexpression (MHC-PPAR) were produced characterized. The expression target genes involved fatty acid uptake oxidation pathways was increased MHC-PPAR mice. Surprisingly, glucose transport utilization reciprocally repressed hearts. Consistent gene profile,...

10.1172/jci14080 article EN Journal of Clinical Investigation 2002-01-01

Recent evidence has defined an important role for PPARα in the transcriptional control of cardiac energy metabolism. To investigate genesis metabolic and functional derangements diabetic cardiomyopathy, mice with cardiac-restricted overexpression (MHC-PPAR) were produced characterized. The expression target genes involved fatty acid uptake oxidation pathways was increased MHC-PPAR mice. Surprisingly, glucose transport utilization reciprocally repressed hearts. Consistent gene profile,...

10.1172/jci0214080 article EN Journal of Clinical Investigation 2002-01-01

Gold nanocages represent a new class of nanomaterials with compact size and tunable optical properties in the near-infrared region. They passively accumulate tumor after intravenous injection. By exposing tumors to diode laser, photothermal effect Au selectively destroys tissue minimum damage surrounding healthy tissue.

10.1002/smll.200902216 article EN Small 2010-03-11

Evidence is emerging that systemic metabolic disturbances contribute to cardiac myocyte dysfunction and clinically apparent heart failure, independent of associated coronary artery disease. To test the hypothesis perturbation lipid homeostasis in cardiomyocytes contributes dysfunction, we engineered transgenic mice with cardiac-specific overexpression fatty acid transport protein 1 (FATP1) using α-myosin heavy chain gene promoter. Two lines demonstrate 4-fold increased myocardial free (FFA)...

10.1161/01.res.0000154079.20681.b9 article EN Circulation Research 2004-12-24

PURPOSE: The purpose of this study was to investigate whether positron emission tomography (PET) with the glucose analog [ 18 F]fluorodeoxyglucose (FDG) and estrogen 16 alpha-[ F]fluoroestradiol-17 beta (FES), performed before after treatment tamoxifen, could be used detect hormone-induced changes in tumor metabolism (metabolic flare) available levels receptor (ER). In addition, we investigated these PET findings would predict hormonally responsive breast cancer. PATIENTS AND METHODS: Forty...

10.1200/jco.2001.19.11.2797 article EN Journal of Clinical Oncology 2001-06-01

Using H215O (half-life = 2.1 min) we demonstrated that a modification of the tissue autoradiographic approach permitted quantitation myocardial blood flow in open-chest dogs by direct assay and noninvasive estimation with positron-emission tomography (PET) delineated relative intact dogs. In anesthetized dogs, single-pass extraction fraction averaged 96 +/- 5% at flows 80 to 100 ml/100 g/min. This high did not differ significantly over range 12 238 Myocardial calculated after 60 sec...

10.1161/01.cir.70.4.724 article EN Circulation 1984-10-01

An understanding of the metabolic fate radiometal-labeled peptides is important due to their application in areas diagnostic imaging and targeted radiotherapy. Radioisotopes copper (64Cu, T1/2 = 12.7 h; 67Cu, 62 h) have been labeled monoclonal antibodies (mAbs) applications PET radiotherapy cancer. Copper-64-TETA-d-Phe1-octreotide ([64Cu]TETA-OC) has shown bind somatostatin receptor, both vitro vivo, this agent inhibited growth somatostatin-receptor positive tumors rats. Copper-64-TETA-OC,...

10.1021/bc990167l article EN Bioconjugate Chemistry 2000-06-23

In the diabetic heart, chronic activation of PPARα pathway drives excessive fatty acid (FA) oxidation, lipid accumulation, reduced glucose utilization, and cardiomyopathy. The related nuclear receptor, PPARβ/δ, is also highly expressed in yet its function has not been fully delineated. To address role myocardial metabolism, we generated transgenic mice with cardiac-specific expression driven by myosin heavy chain (MHC-PPARβ/δ mice). striking contrast to MHC-PPARα mice, MHC-PPARβ/δ had...

10.1172/jci32578 article EN Journal of Clinical Investigation 2007-11-21

A biodegradable positron-emitting dendritic nanoprobe targeted at α v β 3 integrin, a biological marker known to modulate angiogenesis, was developed for the noninvasive imaging of angiogenesis. The has modular multivalent core-shell architecture consisting heterobifunctional core chemoselectively functionalized with polyethylene oxide (PEO) chains that form protective shell, which imparts stealth and dictates pharmacokinetics. Each 8 branches labeling radiohalogens. Placement radioactive...

10.1073/pnas.0811757106 article EN Proceedings of the National Academy of Sciences 2009-01-08

Abstract Gold nanocages represent a novel class of nanostructures, well‐suited for biomedical applications. They can be readily prepared via the galvanic replacement reaction between silver nanocubes and chloroauric acid. Their optical resonance peaks easily precisely tuned to near‐infrared region from 650–900 nm, transparent window blood soft tissue. Furthermore, their surface conveniently conjugated with various ligands targeting cancer. In this feature article, we highlight recent...

10.1002/adfm.201001329 article EN Advanced Functional Materials 2010-10-04
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