Publications by authors named "Tim-Matthias Strom"

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Resistance to mesenchymal reprogramming sustains clonal propagation in metastatic breast cancer.
Massimo Saini, Laura Schmidleitner, Helena Domínguez Moreno, Elisa Donato, Mattia Falcone, Tim-Matthias Strom

Cell Rep· June 2023

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In situ metabolomics of aldosterone-producing adenomas.
Masanori Murakami, Yara Rhayem, Thomas Kunzke, Na Sun, Annette Feuchtinger, Tim Matthias Strom

JCI Insight· September 2019

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An atlas of the aging lung mapped by single cell transcriptomics and deep tissue proteomics.
Ilias Angelidis, Lukas M Simon, Isis E Fernandez, Maximilian Strunz, Christoph H Mayr, Tim-Matthias Strom

Nat Commun· February 2019

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Pollen of common ragweed (Ambrosia artemisiifolia L.): Illumina-based de novo sequencing and differential transcript expression upon elevated NO/O.
Feng Zhao, Jörg Durner, J Barbro Winkler, Claudia Traidl-Hoffmann, Tim-Matthias Strom

Environ Pollut· May 2017

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Identification of Cadherin 2 () Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy.
Bongani M Mayosi, Maryam Fish, Gasnat Shaboodien, Elisa Mastantuono, Sarah Kraus, Tim-Matthias Strom

Circ Cardiovasc Genet· April 2017

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Characterization of circular RNAs in human, mouse and rat hearts.
Stanislas Werfel, Stephan Nothjunge, Thomas Schwarzmayr, Tim-Matthias Strom, Thomas Meitinger

J Mol Cell Cardiol· September 2016

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Screening for CHCHD10 mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variant.
Nicolai Marroquin, Sebastian Stranz, Kathrin Müller, Thomas Wieland, Wolfgang P Ruf, Tim-Matthias Strom

Brain· February 2016

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Development of A Cell-Based Assay to Identify Small Molecule Inhibitors of FGF23 Signaling.
Susanne Diener, Kenji Schorpp, Tim-Matthias Strom, Kamyar Hadian, Bettina Lorenz-Depiereux

Assay Drug Dev Technol· October 2015

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Early onset hearing loss in autosomal recessive hypophosphatemic rickets caused by loss of function mutation in ENPP1.
Elisabeth Steichen-Gersdorf, Bettina Lorenz-Depiereux, Tim Matthias Strom, Nicholas J Shaw

J Pediatr Endocrinol Metab· July 2015

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Polyneuropathy, scoliosis, tall stature, and oligodontia represent novel features of the interstitial 6p deletion phenotype.
Birgit Zirn, Maja Hempel, Andreas Hahn, Bernd Neubauer, Janine Wagenstaller, Tim Matthias Strom

Am J Med Genet A· November 2008

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