A400

KKE Pädiatrische Leukämie
IDI:(DE-He78)A400-20160331

Recent Publications

All known publications ...
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Separated-incision versus T-incision for internal hemipelvectomy related to Enneking type II + III resection: comparative outcomes in a single-center retrospective cohort.
BMC musculoskeletal disorders 26(1), 706 () [10.1186/s12891-025-08944-x]  GO DBCoverage BibTeX | EndNote: XML, Text | RIS

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CCCTC-binding factor regulates splicing factor proline and glutamine-rich to promote malignant growth of osteosarcoma.
American journal of translational research 17(2), 1495 - 1509 () [10.62347/STQK5435]  GO pmc   Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS

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Subclonal TP53 and KRAS variants combined with poor treatment response identify ultrahigh-risk pediatric patients with T-ALL.
Blood advances 9(6), 1267 - 1279 () [10.1182/bloodadvances.2024014209]  GO DBCoverage BibTeX | EndNote: XML, Text | RIS

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Role of stem-like cells in chemotherapy resistance and relapse in pediatric T-cell acute lymphoblastic leukemia.
Nature Communications 16(1), 5413 () [10.1038/s41467-025-61222-1]  GO DBCoverage BibTeX | EndNote: XML, Text | RIS

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Gene Therapy in Transfusion-Dependent Non-β0/β0 Genotype β-Thalassemia: First Real-World Experience of Beti-cel.
Blood advances 9(1), 29-38 () [10.1182/bloodadvances.2024014104]  GO BibTeX | EndNote: XML, Text | RIS

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Betibeglogene autotemcel gene therapy in patients with transfusion-dependent, severe genotype β-thalassaemia (HGB-212): a non-randomised, multicentre, single-arm, open-label, single-dose, phase 3 trial.
The lancet 404(10468), 2175 - 2186 () [10.1016/S0140-6736(24)01884-1]  GO BibTeX | EndNote: XML, Text | RIS

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Redistribution of PU.1 partner transcription factor RUNX1 binding secures cell survival during leukemogenesis.
The EMBO journal 43(24), 6291-6309 () [10.1038/s44318-024-00295-y]  GO BibTeX | EndNote: XML, Text | RIS

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The E3 ubiquitin ligase Herc1 modulates the response to nucleoside analogs in acute myeloid leukemia.
Blood advances 8(20), 5315-5329 () [10.1182/bloodadvances.2023011540]  GO BibTeX | EndNote: XML, Text | RIS

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The German sickle cell disease registry reveals a surprising risk of acute splenic sequestration and an increased transfusion requirement in patients with compound heterozygous sickle cell disease HbS/β-thalassaemia and no or low HbA expression.
European journal of haematology 113(4), 501-509 () [10.1111/ejh.14259]  GO  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

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Systematic analysis of RNA-binding proteins identifies targetable therapeutic vulnerabilities in osteosarcoma.
Nature Communications 15(1), 2810 () [10.1038/s41467-024-47031-y]  GO DBCoverage  Download fulltext Files BibTeX | EndNote: XML, Text | RIS

All known publications ...
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 Record created 2019-10-24, last modified 2022-03-18



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