N. Zinn

发表

Measuring and managing ratio compression for accurate iTRAQ/TMT quantification.

B. Kuster, M. Bantscheff, M. Savitski, 2013, Journal of proteome research.

De novo sequencing of peptides by MS/MS

W. Lehmann, N. Zinn, Martin E. Boehm, 2010, Proteomics.

Catalytic in vivo protein knockdown by small-molecule PROTACs.

I. E. Smith, Marcus Bantscheff, Kristoffer Famm, 2015, Nature chemical biology.

Biological plasticity rescues target activity in CRISPR knock outs

Wolfgang Huber, Lars M Steinmetz, Marcus Bantscheff, 2019, Nature Methods.

Systematic analysis of protein turnover in primary cells

Martin Beck, Nils Kurzawa, Holger Franken, 2018, Nature Communications.

Extended pharmacodynamic responses observed upon PROTAC-mediated degradation of RIPK2

Aditya R. Thawani, I. E. Smith, Carol A. Capriotti, 2020, Communications Biology.

Chemoproteomics-based design of potent LRRK2-selective lead compounds that attenuate Parkinson's disease-related toxicity in human neurons.

G. Drewes, M. Bantscheff, N. Ramsden, 2011, ACS chemical biology.

Discovery of a First-in-Class Gut-Restricted RET Kinase Inhibitor as a Clinical Candidate for the Treatment of IBS.

G. Joberty, N. Zinn, M. Cheung, 2018, ACS medicinal chemistry letters.

The mTORC1/4E-BP1 axis represents a critical signaling node during fibrogenesis

M. Karsdal, C. Swanton, G. Bergamini, 2019, Nature Communications.

Improved Proteomics-Based Drug Mechanism-of-Action Studies Using 16-Plex Isobaric Mass Tags.

M. Bantscheff, Toby Mathieson, N. Zinn, 2021, Journal of proteome research.

PeptideForest: Semisupervised machine learning integrating multiple search engines for peptide identification

M. Bantscheff, N. Zinn, C. Fufezan, 2022, bioRxiv.

Protein labelling with mercury tags: fundamental studies on ovalbumin derivatised with p-hydroxymercuribenzoic acid (pHMB)

N. Zinn, A. Sanz-Medel, J. Bettmer, 2008 .

Multiplexed Proteome Dynamics Profiling Reveals Mechanisms Controlling Protein Homeostasis

P. Grandi, M. Bantscheff, M. Savitski, 2018, Cell.

Discovery and Characterisation of Highly Cooperative FAK-Degrading PROTACs.

M. Bantscheff, N. Zinn, C. Chung, 2021, Angewandte Chemie.

Delayed fragmentation and optimized isolation width settings for improvement of protein identification and accuracy of isobaric mass tag quantification on Orbitrap-type mass spectrometers.

Manor Askenazi, Jarrod A Marto, Marcus Bantscheff, 2011, Analytical chemistry.

Biological plasticity rescues target activity in CRISPR knock outs

L. Steinmetz, P. Grandi, A. Michon, 2019, Nature Methods.

Extended pharmacodynamic responses observed upon PROTAC-mediated degradation of RIPK2

Aditya R. Thawani, I. E. Smith, M. Bantscheff, 2020, Communications Biology.

Discovery of GSK8612, a Highly Selective and Potent TBK1 Inhibitor.

Douglas W. Thomson, M. Bantscheff, G. Bergamini, 2019, ACS medicinal chemistry letters.

CZ415, a Highly Selective mTOR Inhibitor Showing in Vivo Efficacy in a Collagen Induced Arthritis Model.

Douglas W. Thomson, G. Bergamini, N. Zinn, 2016, ACS medicinal chemistry letters.

Mass spectrometry approaches to monitor protein-drug interactions.

G. Drewes, M. Bantscheff, C. Hopf, 2012, Methods.

Biophysical Studies on Interactions and Assembly of Full-size E 3 Ubiquitin Ligase SUPPRESSOR OF CYTOKINE SIGNALING 2 ( SOCS 2 )-ELONGIN BC-CULLIN 5-RING BOX PROTEIN 2 ( RBX 2 ) *

P. Grandi, N. Zinn, A. Konijnenberg, 2015 .

Biophysical Studies on Interactions and Assembly of Full-size E3 Ubiquitin Ligase

P. Grandi, N. Zinn, A. Konijnenberg, 2014, The Journal of Biological Chemistry.

One‐source peptide/phosphopeptide standards for accurate phosphorylation degree determination

Martin E. Böhm, W. Lehmann, U. Klingmüller, 2011, Proteomics.

Systematic analysis of protein turnover in primary cells

M. Bantscheff, M. Savitski, Toby Mathieson, 2018, Nature Communications.

Microquantification of phospholipid classes by stable isotope dilution and nanoESI mass spectrometry

W. Lehmann, N. Zinn, J. Seidler, 2016, Analytical and Bioanalytical Chemistry.

Metal ion-mobilizing additives for comprehensive detection of femtomole amounts of phosphopeptides by reversed phase LC-MS

W. Lehmann, N. Zinn, Martin E. Boehm, 2011, Amino Acids.

An integrated multiomic and quantitative label-free microscopy-based approach to study pro-fibrotic signalling in ex vivo human precision-cut lung slices

R. Pepperkok, G. Bergamini, T. Muley, 2020, European Respiratory Journal.

Multiomic and quantitative label-free microscopy-based analysis of ex vivo culture and TGFbeta1 stimulation of human precision-cut lung slices

R. Pepperkok, G. Bergamini, T. Muley, 2019, bioRxiv.

μLC coupled to ICP–SFMS with post-column isotope dilution analysis of sulfur for absolute protein quantification

N. Zinn, J. Bettmer, R. Krüger, 2008, Analytical and bioanalytical chemistry.

Author Correction: The mTORC1/4E-BP1 axis represents a critical signaling node during fibrogenesis

C. Swanton, G. Bergamini, G. Joberty, 2020, Nature Communications.

Phosphorus-based absolutely quantified standard peptides for quantitative proteomics.

Bettina Hahn, W. Lehmann, N. Zinn, 2009, Journal of proteome research.

Quantification of protein phosphorylation by microLC-ICP-MS.

W. Lehmann, N. Zinn, R. Krüger, 2009, Methods in molecular biology.

Preparation of heteroelement-incorporated and stable isotope-labeled protein standards for quantitative proteomics.

W. Lehmann, N. Zinn, A. Konopka, 2014, Methods in molecular biology.

Gel electrophoresis coupled to inductively coupled plasma-mass spectrometry using species-specific isotope dilution for iodide and iodate determination in aerosols.

N. Zinn, T. Hoffmann, J. Bettmer, 2007, Analytical chemistry.