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Fragile X mental retardation protein protects against tumour necrosis factor-mediated cell death and liver injury.
Zhuang Y, Xu HC, Shinde PV, Warfsmann J, Vasilevska J, Sundaram B, Behnke K, Huang J, Hoell JI, Borkhardt A, Pfeffer K, Taha MS, Herebian D, Mayatepek E, Brenner D, Ahmadian MR, Keitel V, Wieczorek D, Häussinger D, Pandyra AA, Lang KS, Lang PA. Zhuang Y, et al. Among authors: wieczorek d. Gut. 2020 Jan;69(1):133-145. doi: 10.1136/gutjnl-2019-318215. Epub 2019 Aug 13. Gut. 2020. PMID: 31409605 Free PMC article.
Family-based germline sequencing in children with cancer.
Kuhlen M, Taeubner J, Brozou T, Wieczorek D, Siebert R, Borkhardt A. Kuhlen M, et al. Among authors: wieczorek d. Oncogene. 2019 Feb;38(9):1367-1380. doi: 10.1038/s41388-018-0520-9. Epub 2018 Oct 10. Oncogene. 2019. PMID: 30305723 Free PMC article. Review.
Penetrance and Expressivity in Inherited Cancer Predisposing Syndromes.
Taeubner J, Wieczorek D, Yasin L, Brozou T, Borkhardt A, Kuhlen M. Taeubner J, et al. Among authors: wieczorek d. Trends Cancer. 2018 Nov;4(11):718-728. doi: 10.1016/j.trecan.2018.09.002. Epub 2018 Sep 20. Trends Cancer. 2018. PMID: 30352675 Review.
Early IFN-α signatures and persistent dysfunction are distinguishing features of NK cells in severe COVID-19.
Krämer B, Knoll R, Bonaguro L, ToVinh M, Raabe J, Astaburuaga-García R, Schulte-Schrepping J, Kaiser KM, Rieke GJ, Bischoff J, Monin MB, Hoffmeister C, Schlabe S, De Domenico E, Reusch N, Händler K, Reynolds G, Blüthgen N, Hack G, Finnemann C, Nischalke HD, Strassburg CP, Stephenson E, Su Y, Gardner L, Yuan D, Chen D, Goldman J, Rosenstiel P, Schmidt SV, Latz E, Hrusovsky K, Ball AJ, Johnson JM, Koenig PA, Schmidt FI, Haniffa M, Heath JR, Kümmerer BM, Keitel V, Jensen B, Stubbemann P, Kurth F, Sander LE, Sawitzki B; Deutsche COVID-19 OMICS Initiative (DeCOI); Aschenbrenner AC, Schultze JL, Nattermann J. Krämer B, et al. Immunity. 2021 Nov 9;54(11):2650-2669.e14. doi: 10.1016/j.immuni.2021.09.002. Epub 2021 Sep 4. Immunity. 2021. PMID: 34592166 Free PMC article.
Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities.
Wagner M, Skorobogatko Y, Pode-Shakked B, Powell CM, Alhaddad B, Seibt A, Barel O, Heimer G, Hoffmann C, Demmer LA, Perilla-Young Y, Remke M, Wieczorek D, Navaratnarajah T, Lichtner P, Klee D, Shamseldin HE, Al Mutairi F, Mayatepek E, Strom T, Meitinger T, Alkuraya FS, Anikster Y, Saltiel AR, Distelmaier F. Wagner M, et al. Among authors: wieczorek d. Am J Hum Genet. 2020 Feb 6;106(2):246-255. doi: 10.1016/j.ajhg.2020.01.002. Epub 2020 Jan 30. Am J Hum Genet. 2020. PMID: 32004447 Free PMC article.
487 results