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Page 1
A progeroid syndrome caused by a deep intronic variant in TAPT1 is revealed by RNA/SI-NET sequencing.
EMBO Mol Med. 2023 Feb 8;15(2):e16478. doi: 10.15252/emmm.202216478. Epub 2023 Jan 18.
EMBO Mol Med. 2023.
PMID: 36652330
Free PMC article.
Conserved DNA sequence features underlie pervasive RNA polymerase pausing.
Gajos M, Jasnovidova O, van Bömmel A, Freier S, Vingron M, Mayer A.
Gajos M, et al. Among authors: freier s.
Nucleic Acids Res. 2021 May 7;49(8):4402-4420. doi: 10.1093/nar/gkab208.
Nucleic Acids Res. 2021.
PMID: 33788942
Free PMC article.
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Elevated levels of Rad51 recombination protein in tumor cells.
Raderschall E, Stout K, Freier S, Suckow V, Schweiger S, Haaf T.
Raderschall E, et al. Among authors: freier s.
Cancer Res. 2002 Jan 1;62(1):219-25.
Cancer Res. 2002.
PMID: 11782381
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NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein.
Zeitz C, Scherthan H, Freier S, Feil S, Suckow V, Schweiger S, Berger W.
Zeitz C, et al. Among authors: freier s.
Invest Ophthalmol Vis Sci. 2003 Oct;44(10):4184-91. doi: 10.1167/iovs.03-0251.
Invest Ophthalmol Vis Sci. 2003.
PMID: 14507859
Free article.
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