Search Results - "Schubert, Jeffrey"
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Derivatization of Amino Acids and Peptides via Photoredox-Mediated Conjugate Addition
Published in Journal of organic chemistry (01-05-2020)“…Unnatural amino acids are key building blocks in therapeutically relevant peptides. Thus, the development of novel methods to increase the structural diversity…”
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Application of Next Generation Sequencing in Laboratory Medicine
Published in Annals of laboratory medicine (01-01-2021)“…The rapid development of next-generation sequencing (NGS) technology, including advances in sequencing chemistry, sequencing technologies, bioinformatics, and…”
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Photoredox Catalysis for Silyl‐Mediated C–H Alkylation of Heterocycles with Non‐Activated Alkyl Bromides
Published in European journal of organic chemistry (15-03-2020)“…The development of a Minisci reaction of electron‐deficient heteroarenes with non‐activated alkyl bromides under visible‐light photoredox catalysis is…”
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The genetic architecture of pediatric cardiomyopathy
Published in American journal of human genetics (03-02-2022)“…To understand the genetic contribution to primary pediatric cardiomyopathy, we performed exome sequencing in a large cohort of 528 children with…”
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Discovery of [11C]MK-6884: A Positron Emission Tomography (PET) Imaging Agent for the Study of M4Muscarinic Receptor Positive Allosteric Modulators (PAMs) in Neurodegenerative Diseases
Published in Journal of medicinal chemistry (12-03-2020)“…The measurement of receptor occupancy (RO) using positron emission tomography (PET) has been instrumental in guiding discovery and development of CNS directed…”
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2-Aminopyridines as Potent and Selective Na v 1.8 Inhibitors Exhibiting Efficacy in a Nonhuman Primate Pain Model
Published in ACS medicinal chemistry letters (13-06-2024)“…Herein we describe the discovery of a 2-aminopyridine scaffold as a potent and isoform selective inhibitor of the Na 1.8 sodium channel. Parallel library…”
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2‑Aminopyridines as Potent and Selective Nav1.8 Inhibitors Exhibiting Efficacy in a Nonhuman Primate Pain Model
Published in ACS medicinal chemistry letters (13-06-2024)“…Herein we describe the discovery of a 2-aminopyridine scaffold as a potent and isoform selective inhibitor of the Nav1.8 sodium channel. Parallel library…”
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Clinically relevant variants identified in thoracic aortic aneurysm patients by research exome sequencing
Published in American journal of medical genetics. Part A (01-05-2016)“…Thoracic aortic aneurysm (TAA) is a genetically heterogeneous disease involving subclinical and progressive dilation of the thoracic aorta, which can lead to…”
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Discovery, Optimization, and Biological Characterization of 2,3,6-Trisubstituted Pyridine-Containing M 4 Positive Allosteric Modulators
Published in ChemMedChem (06-05-2019)“…Herein we describe the discovery and optimization of a new series of 2,3-disubstituted and 2,3,6-trisubstituted muscarinic acetylcholine receptor 4 (M )…”
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Limited-View X-Ray Tomography Combining Attenuation and Compton Scatter Data: Approach and Experimental Results
Published in IEEE access (01-01-2019)“…X-ray inspection systems are critical in medical, non-destructive testing, and security applications, with systems typically measuring attenuation along…”
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Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma
Published in Acta neuropathologica communications (14-07-2022)“…CIC -rearranged sarcomas are newly defined undifferentiated soft tissue tumors with CIC- associated fusions, and dismal prognosis. CIC fusions activate PEA3…”
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Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity
Published in Journal of cardiovascular translational research (01-08-2017)“…Thoracic aortic aneurysm (TAA) is a genetic disease predisposing to aortic dissection. It is important to identify the genetic modifiers controlling penetrance…”
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Synthesis and Evaluation of Heterocyclic Catechol Mimics as Inhibitors of Catechol-O-methyltransferase (COMT)
Published in ACS medicinal chemistry letters (12-03-2015)“…3-Hydroxy-4-pyridinones and 5-hydroxy-4-pyrimidinones were identified as inhibitors of catechol-O-methyltransferase (COMT) in a high-throughput screen. These…”
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Discovery, Optimization, and Biological Characterization of 2,3,6‐Trisubstituted Pyridine‐Containing M4 Positive Allosteric Modulators
Published in ChemMedChem (06-05-2019)“…Herein we describe the discovery and optimization of a new series of 2,3‐disubstituted and 2,3,6‐trisubstituted muscarinic acetylcholine receptor 4 (M4)…”
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Synthesis and optimization of N-heterocyclic pyridinones as catechol-O-methyltransferase (COMT) inhibitors
Published in Bioorganic & medicinal chemistry letters (15-06-2016)“…[Display omitted] A series of N-heterocyclic pyridinone catechol-O-methyltransferase (COMT) inhibitors were synthesized. Physicochemical properties, including…”
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Evidence for β-Chlorocarbenium and β-Bromocarbenium Ions
Published in Organic letters (07-06-2007)“…Isotopic perturbation of degenerate equilibrium is used to determine whether tetramethylethylenechloronium and tetramethylethylenebromonium ions are closed…”
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Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study
Published in Journal of the American Heart Association (04-05-2021)“…Background Pediatric cardiomyopathy is a genetically heterogeneous disease with substantial morbidity and mortality. Current guidelines recommend genetic…”
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Characterization of Non-Nitrocatechol Pan and Isoform Specific Catechol-O-methyltransferase Inhibitors and Substrates
Published in ACS chemical neuroscience (15-02-2012)“…Reduced dopamine neurotransmission in the prefrontal cortex has been implicated as causal for the negative symptoms and cognitive deficit associated with…”
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Theoretical Investigation of Lone Pair Inversions, Ring Openings, and Hydride Shifts in O-Methylated Epoxides
Published in Journal of organic chemistry (30-03-2007)“…Mechanisms associated with the isomerization of the O-methylethylene oxonium ion and its tetramethyl-substituted analogue have been explored using correlated…”
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