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Page 1
Translational Read-Through Therapy of RPGR Nonsense Mutations.
Int J Mol Sci. 2020 Nov 10;21(22):8418. doi: 10.3390/ijms21228418.
Int J Mol Sci. 2020.
PMID: 33182541
Free PMC article.
Development of the NOGGO GIS v1 Assay, a Comprehensive Hybrid-Capture-Based NGS Assay for Therapeutic Stratification of Homologous Repair Deficiency Driven Tumors and Clinical Validation.
Willing EM, Vollbrecht C, Vössing C, Weist P, Schallenberg S, Herbst JM, Schatz S, Jóri B, Bataillon G, Harter P, Salutari V, Martin AG, Vergote I, Colombo N, Roeper J, Berg T, Berger R, Kah B, Noettrup TJ, Falk M, Arndt K, Polten A, Ray-Coquard I, Selzam F, Pirngruber J, Schmidt S, Hummel M, Tiemann M, Horst D, Sehouli J, Pujade-Lauraine E, Tiemann K, Braicu EI, Heukamp LC.
Willing EM, et al. Among authors: vossing c.
Cancers (Basel). 2023 Jun 30;15(13):3445. doi: 10.3390/cancers15133445.
Cancers (Basel). 2023.
PMID: 37444554
Free PMC article.
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The Major Ciliary Isoforms of RPGR Build Different Interaction Complexes with INPP5E and RPGRIP1L.
Vössing C, Atigbire P, Eilers J, Markus F, Stieger K, Song F, Neidhardt J.
Vössing C, et al.
Int J Mol Sci. 2021 Mar 30;22(7):3583. doi: 10.3390/ijms22073583.
Int J Mol Sci. 2021.
PMID: 33808286
Free PMC article.
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The Combined Therapy of Cabozantinib, Crizotinib, and Osimertinib in a Lung Cancer Patient with Acquired MET Amplification and Resistance Mutations.
Jóri B, Vössing C, Pirngruber J, Willing EM, Arndt K, Falk M, Tiemann M, Heukamp LC, Hoffknecht P.
Jóri B, et al. Among authors: vossing c.
Curr Oncol. 2023 Sep 27;30(10):8805-8814. doi: 10.3390/curroncol30100635.
Curr Oncol. 2023.
PMID: 37887535
Free PMC article.
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A novel missense variant in the EML1 gene associated with bilateral ribbon-like subcortical heterotopia leads to ciliary defects.
Markus F, Kannengießer A, Näder P, Atigbire P, Scholten A, Vössing C, Bültmann E, Korenke GC, Owczarek-Lipska M, Neidhardt J.
Markus F, et al. Among authors: vossing c.
J Hum Genet. 2021 Dec;66(12):1159-1167. doi: 10.1038/s10038-021-00947-5. Epub 2021 Jul 1.
J Hum Genet. 2021.
PMID: 34211111
Free PMC article.
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