Y. Franke

发表

Structural Basis of Nav1.7 Inhibition by a Gating-Modifier Spider Toxin.

Hui Xu, Tianbo Li, A. Rohou, 2019 .

Chemical Genetics Reveals an RGS/G-Protein Role in the Action of a Compound

Stanley R Krystek, Terry Stouch, Lynn Bjerke, 2006, PLoS genetics.

Nanolipoprotein particles (NLPs) as a delivery platform for Fab based therapeutics.

Y. Franke, Hong Li, Inna Zilberleyb, 2020, Bioconjugate chemistry.

High‐throughput identification of conditional MHCI ligands and scaled‐up production of conditional MHCI complexes

Y. Franke, Hong Li, Sara M Wichner, 2021, Protein science : a publication of the Protein Society.

The Immunoglobulin Superfamily Receptome Defines Cancer-Relevant Networks Associated with Clinical Outcome

Athena W Wong, Steve Lianoglou, S. Turley, 2020, Cell.

Semiautomated Small-Scale Purification Method for High-Throughput Expression Analysis of Recombinant Proteins.

Athena W Wong, Christine Kugel, Y. Franke, 2019, Methods in molecular biology.

The Structural Basis for Class II Cytokine Receptor Recognition by JAK1.

Y. Franke, H. Wallweber, P. Lupardus, 2016, Structure.

Wnt antagonists bind through a short peptide to the first β-propeller domain of LRP5/6.

E. Bourhis, R. Hannoush, A. Estevez, 2011, Structure.

Nanolipoprotein particles for co-delivery of cystine-knot peptides and Fab–based therapeutics

R. Hannoush, Y. Franke, Hong Li, 2021, Nanoscale advances.

CLAMPs allow single cell tracking of KRASG12C inhibition and endow druggability to KRAS mutants

Marie Evangelista, H. Koeppen, Y. Franke, 2021 .

Chemical genetics identifies Rab geranylgeranyl transferase as an apoptotic target of farnesyl transferase inhibitors.

Petra Ross-Macdonald, Yvonne Franke, Carol O'Brien, 2005, Cancer cell.

An Allosteric Anti-tryptase Antibody for the Treatment of Mast Cell-Mediated Severe Asthma

B. Yaspan, J. Hackney, Lawren C. Wu, 2019, Cell.

Disruption of PH–kinase domain interactions leads to oncogenic activation of AKT in human cancers

Somasekar Seshagiri, Thomas D. Wu, Jeremy Stinson, 2012, Proceedings of the National Academy of Sciences.

Identification of a Helical Segment within the Intrinsically Disordered Region of the PCSK9 Prodomain.

M. Ultsch, C. Eigenbrot, Y. Franke, 2019, Journal of molecular biology.

The crystal structure of the catalytic domain of the NF-κB inducing kinase reveals a narrow but flexible active site.

Adam R. Johnson, Jianwen A. Feng, Lawren C. Wu, 2012, Structure.

Allosteric peptides bind a caspase zymogen and mediate caspase tetramerization.

Karen Stanger, R. Hannoush, Y. Franke, 2012, Nature chemical biology.

Structural basis for dual-mode inhibition of the ABC transporter MsbA

Benjamin D. Sellers, Jun Liang, Y. Franke, 2018, Nature.

Battling Btk Mutants With Noncovalent Inhibitors That Overcome Cys481 and Thr474 Mutations.

Adam R. Johnson, C. Eigenbrot, A. Estevez, 2016, ACS chemical biology.

Conformation-locking antibodies for the discovery and characterization of KRAS inhibitors

Melinda M. Mulvihill, H. Koeppen, Y. Franke, 2022, Nature Biotechnology.

Structural Basis of Nav1.7 Inhibition by a Gating-Modifier Spider Toxin

Alexis Rohou, Christopher P. Arthur, Jun Chen, 2019, Cell.

Structural basis of recognition of interferon-α receptor by tyrosine kinase 2

Y. Franke, H. Wallweber, M. Starovasnik, 2014, Nature Structural &Molecular Biology.

Structural basis of IFN receptor recognition by TYK2

Y. Franke, H. Wallweber, M. Starovasnik, 2014 .

Backbone cyclization of a recombinant cystine‐knot peptide by engineered Sortase A

Karen Stanger, R. Hannoush, Y. Franke, 2014, FEBS letters.

Structural basis of Nav1.7 inhibition by an isoform-selective small-molecule antagonist

Jun Li, Christine Tam, Daniel F. Ortwine, 2015, Science.

A two-in-one antibody against HER3 and EGFR has superior inhibitory activity compared with monospecific antibodies.

M. Sliwkowski, D. Danilenko, C. Eigenbrot, 2011, Cancer cell.

Structural Basis of Nav1.7 Inhibition by a Gating-Modifier Spider Toxin

Hui Xu, Tianbo Li, A. Rohou, 2019, Cell.

A Platform for Extracellular Interactome Discovery Identifies Novel Functional Binding Partners for the Immune Receptors B7-H3/CD276 and PVR/CD155

Athena W Wong, S. Turley, Y. Franke, 2019, Molecular & Cellular Proteomics.

Cellular uptake of a cystine-knot peptide and modulation of its intracellular trafficking

Cécile Chalouni, Karen Stanger, R. Hannoush, 2016, Scientific Reports.

Dual functionality of β-tryptase protomers as both proteases and cofactors in the active tetramer

W. Forrest, Y. Franke, C. Eigenbrot, 2018, The Journal of Biological Chemistry.

A selective peptide inhibitor of Frizzled 7 receptors disrupts intestinal stem cells

Z. Modrušan, S. Angers, R. Hannoush, 2018, Nature Chemical Biology.

Hematopoietic Progenitor Kinase-1 Structure in a Domain-Swapped Dimer.

BinQing Wei, Y. Franke, E. Day, 2019, Structure.

Bivalent antibody pliers inhibit β-tryptase by an allosteric mechanism dependent on the IgG hinge

A. Estevez, Y. Franke, C. Ciferri, 2020, Nature Communications.

An Allosteric Anti-tryptase Antibody for the Treatment of Mast Cell-Mediated Severe Asthma

B. Yaspan, J. Hackney, Y. Franke, 2020, Cell.

Allosteric peptides bind a caspase zymogen and mediate caspase tetramerization.

Karen Stanger, R. Hannoush, Y. Franke, 2012, Nature chemical biology.