Wolfgang Schreiner - Dissemin

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All papers authored by Wolfgang Schreiner

This paper is made freely available by the publisher.

2020 Bernhard Roither, Chris Oostenbrink

ORCID

, Georg Pfeiler, Heinz Koelbl

ORCID

, Wolfgang Schreiner

ORCID

Pembrolizumab Induces an Unexpected Conformational Change in the CC′-loop of PD-1

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Elisabeth S. Gruber

ORCID

, Georg Oberhuber, Peter Birner, Michaela Schlederer, Michael Kenn, Wolfgang Schreiner

ORCID

ORCID

, Sebastian F. Schoppmann

ORCID

, Michael Gnant

ORCID

, William Tse, Lukas Kenner

ORCID

Erratum: Gruber, E.S.; et al. The Oncogene AF1Q is Associated with WNT and STAT Signaling and Offers a Novel Independent Prognostic Marker in Patients with Resectable Esophageal Cancer. Cells 2019, 8, 1357

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Michael Kenn, Dan Cacsire Castillo-Tong, Christian F. Singer

ORCID

, Michael Cibena

ORCID

, Heinz Kölbl, Wolfgang Schreiner

ORCID

Microarray Normalization Revisited for Reproducible Breast Cancer Biomarkers

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2019 Bernhard Roither, Chris Oostenbrink, Wolfgang Schreiner

ORCID

Molecular dynamics of the immune checkpoint Programmed Cell Death Protein I, PD-1: Conformational changes of the BC-loop upon binding of the ligand PD-L1 and the monoclonal antibody nivolumab

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Elisabeth Gruber

ORCID

, Georg Oberhuber, Peter Birner, Michaela Schlederer, Michael Kenn, Wolfgang Schreiner

ORCID

ORCID

, Sebastian Schoppmann

ORCID

, Michael Gnant

ORCID

, William Tse, Lukas Kenner

ORCID

The Oncogene AF1Q is Associated with WNT and STAT Signaling and Offers a Novel Independent Prognostic Marker in Patients with Resectable Esophageal Cancer

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This paper is made freely available by the publisher.

Rudolf Karch

ORCID

, Claudia Stocsits, Nevena Ilieva, Wolfgang Schreiner

ORCID

Intramolecular Domain Movements of Free and Bound pMHC and TCR Proteins: A Molecular Dynamics Simulation Study

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This paper is made freely available by the publisher.

2018 Michael Kenn, Dan Cacsire Castillo-Tong, Christian F. Singer, Michael Cibena, Heinz Kölbl, Wolfgang Schreiner

ORCID

Co-expressed genes enhance precision of receptor status identification in breast cancer patients

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