Walden E. Bjørn-Yoshimoto

发表

5-HT2C Receptor Structures Reveal the Structural Basis of GPCR Polypharmacology

David E. Gloriam, John D. McCorvy, Bryan L. Roth, 2018, Cell.

Identification and Structure-Activity Relationship Study of Imidazo[1,2-a]pyridine-3-amines as First Selective Inhibitors of Excitatory Amino Acid Transporter Subtype 3 (EAAT3).

L. Bunch, Walden E. Bjørn-Yoshimoto, Peng Wu, 2019, ACS chemical neuroscience.

Design and Synthesis of 2,3- trans-Proline Analogues as Ligands for Ionotropic Glutamate Receptors and Excitatory Amino Acid Transporters.

K. Hansen, L. Bunch, D. Pickering, 2019, ACS chemical neuroscience.

or A Review of the Numerous Benefits Versus the Biosecurity Concerns of Conotoxin Research

M. Yandell, L. Ellgaard, B. Olivera, 2020 .

Reconstructing the Origins of the Somatostatin and Allatostatin-C Signaling Systems Using the Accelerated Evolution of Biodiverse Cone Snail Toxins

K. Chase, B. Olivera, T. L. Koch, 2022, Molecular biology and evolution.

Postendocytic Sorting of Constitutively Internalized Dopamine Transporter in Cell Lines and Dopaminergic Neurons*

A. Newman, U. Gether, T. N. Jørgensen, 2010, The Journal of Biological Chemistry.

New 4-Functionalized Glutamate Analogues Are Selective Agonists at Metabotropic Glutamate Receptor Subtype 2 or Selective Agonists at Metabotropic Glutamate Receptor Group III.

J. Pin, T. Gefflaut, L. Bunch, 2016, Journal of medicinal chemistry.

Bioavailability Studies and in vitro Profiling of the Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitor UCPH‐102

C. Bundgaard, J. Bastlund, L. Bunch, 2016, ChemMedChem.

New Insight into the Structure–Activity Relationships of the Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitors UCPH‐101 and UCPH‐102

L. Bunch, S. W. Hansen, B. Abrahamsen, 2016, ChemMedChem.

Curses or Cures: A Review of the Numerous Benefits Versus the Biosecurity Concerns of Conotoxin Research

M. Yandell, J. McIntosh, L. Ellgaard, 2020, Biomedicines.

Improving heterologous production of phenylpropanoids in Saccharomyces cerevisiae by tackling an unwanted side reaction of Tsc13, an endogenous double-bond reductase

Katherina Garcia Vanegas, H. Jenssen, Nicolaas A A Buijs, 2016, FEMS yeast research.

Reconstructing the Origins of a Neuropeptide Signaling System Using the Accelerated Evolution of Biodiverse Cone Snail Venoms

K. Chase, B. Olivera, T. L. Koch, 2021 .

The importance of the excitatory amino acid transporter 3 (EAAT3)

Walden E. Bjørn-Yoshimoto, S. Underhill, 2016, Neurochemistry International.

Excitatory amino acid transporters: recent insights into molecular mechanisms, novel modes of modulation and new therapeutic possibilities.

L. Bunch, C. Fahlke, Walden E. Bjørn-Yoshimoto, 2015, Current opinion in pharmacology.

β-Sulfonamido Functionalized Aspartate Analogues as Excitatory Amino Acid Transporter Inhibitors: Distinct Subtype Selectivity Profiles Arising from Subtle Structural Differences.

L. Bunch, Niels Bisballe, Jacob C. Hansen, 2016, Journal of medicinal chemistry.

Somatostatin venom analogs evolved by fish-hunting cone snails: From prey capture behavior to identifying drug leads

B. Ueberheide, C. Hill, B. Olivera, 2021, bioRxiv.

Identification of a New Class of Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitors Followed by a Structure-Activity Relationship Study.

L. Bunch, B. Abrahamsen, Mette N. Erichsen, 2016, Journal of medicinal chemistry.