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Author Correction to: Endemic Burkitt lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility.
Leukemia. 2021 Apr;35(4):1224. doi: 10.1038/s41375-021-01140-5.
Leukemia. 2021.
PMID: 33526862
Free PMC article.
No abstract available.
Endemic Burkitt Lymphoma in second-degree relatives in Northern Uganda: in-depth genome-wide analysis suggests clues about genetic susceptibility.
Gouveia MH, Otim I, Ogwang MD, Wang M, Zhu B, Cole N, Luo W, Hicks B, Jones K, Oehl-Huber K, Ayers LW, Pittaluga S, Legason ID, Nabalende H, Kerchan P, Kinyera T, Kawira E, Brubaker G, Levin AG, Guertler L, Kim J, Stewart DR, Adde M, Magrath I, Bergen AW, Reynolds SJ, Yeager M, Bhatia K, Adeyemo AA, Prokunina-Olsson L, Dean M, Shriner D, Rotimi CN, Chanock S, Siebert R, Mbulaiteye SM.
Gouveia MH, et al. Among authors: oehl huber k.
Leukemia. 2021 Apr;35(4):1209-1213. doi: 10.1038/s41375-020-01052-w. Epub 2020 Oct 13.
Leukemia. 2021.
PMID: 33051549
Free PMC article.
No abstract available.
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A child with neuroblastoma and metachronous anaplastic sarcoma of the kidney: Underlying DICER1 syndrome?
Apellaniz-Ruiz M, Colón-González G, Perlman EJ, Bouron-Dal Soglio D, Sabbaghian N, Oehl-Huber K, Siebert R, Foulkes WD.
Apellaniz-Ruiz M, et al. Among authors: oehl huber k.
Pediatr Blood Cancer. 2020 Dec;67(12):e28488. doi: 10.1002/pbc.28488. Epub 2020 Jun 22.
Pediatr Blood Cancer. 2020.
PMID: 32568472
No abstract available.
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Evidence for a low-penetrant extended phenotype of rhabdoid tumor predisposition syndrome type 1 from a kindred with gain of SMARCB1 exon 6.
Kordes U, Mautner VF, Oyen F, Hagel C, Hartmann C, Heuser M, Frühwald M, Hasselblatt M, Oehl-Huber K, Siebert R, Schneppenheim R, Schüller U.
Kordes U, et al. Among authors: oehl huber k.
Pediatr Blood Cancer. 2021 Oct;68(10):e29185. doi: 10.1002/pbc.29185. Epub 2021 Jun 8.
Pediatr Blood Cancer. 2021.
PMID: 34101994
No abstract available.
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Transposable element insertion as a mechanism of SMARCB1 inactivation in atypical teratoid/rhabdoid tumor.
Thomas C, Oehl-Huber K, Bens S, Soschinski P, Koch A, Nemes K, Oyen F, Kordes U, Kool M, Frühwald MC, Hasselblatt M, Siebert R.
Thomas C, et al. Among authors: oehl huber k.
Genes Chromosomes Cancer. 2021 Aug;60(8):586-590. doi: 10.1002/gcc.22954. Epub 2021 May 8.
Genes Chromosomes Cancer. 2021.
PMID: 33896072
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Acquired resistance to DZNep-mediated apoptosis is associated with copy number gains of AHCY in a B-cell lymphoma model.
Akpa CA, Kleo K, Oker E, Tomaszewski N, Messerschmidt C, López C, Wagener R, Oehl-Huber K, Dettmer K, Schoeler A, Lenze D, Oefner PJ, Beule D, Siebert R, Capper D, Dimitrova L, Hummel M.
Akpa CA, et al. Among authors: oehl huber k.
BMC Cancer. 2020 May 14;20(1):427. doi: 10.1186/s12885-020-06937-8.
BMC Cancer. 2020.
PMID: 32408898
Free PMC article.
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Mantle cell lymphomas with concomitant MYC and CCND1 breakpoints are recurrently TdT positive and frequently show high-grade pathological and genetic features.
Aukema SM, Croci GA, Bens S, Oehl-Huber K, Wagener R, Ott G, Rosenwald A, Kluin PM, van den Berg E, Bosga-Bouwer AG, Hoogendoorn M, Hoster E, Bittmann I, Nagel I, Murga Penas EM, Kreuz M, Bausinger J, Belder W, Oschlies I, Dyer MJS, Jayne S, Siebert R, Klapper W.
Aukema SM, et al. Among authors: oehl huber k.
Virchows Arch. 2021 Jul;479(1):133-145. doi: 10.1007/s00428-021-03022-8. Epub 2021 Feb 2.
Virchows Arch. 2021.
PMID: 33528622
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