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Thale Kristin Olsen

Uppsala University
H指数:17
被引数:1,527

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Somatic RUNX1 exonic deletions in myelodysplastic syndrome: A rare yet high‐risk recurrent genetic aberration

骨髓增生异常综合征中体细胞RUNX1外显子缺失:一种罕见但高风险的复发遗传异常

2026-08-210
OAAI
Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression

染色体17的获得是神经母细胞瘤中的一种早期遗传异常,其中PPM1D正作为一个强候选癌基因出现,驱动肿瘤进展。

2025-06-040
PRE
Joint single-cell genetic and transcriptomic analysis reveal pre-malignant SCP-like subclones in human neuroblastoma
2024-08-311
OA
Single-cell analyses of metastatic bone marrow in human neuroblastoma reveals microenvironmental remodeling and metastatic
2024-02-153
OA
Dormant SOX9-Positive Cells Facilitate MYC-Driven Recurrence of Medulloblastoma
2022-10-1112
OAAI
The immune cell atlas of human neuroblastoma
2022-06-0140
OAAI
Single-cell transcriptomics of human embryos identifies multiple sympathoblast lineages with potential implications for neuroblastoma origin
2021-04-08104
OAAI
Infant High-Grade Gliomas Comprise Multiple Subgroups Characterized by Novel Targetable Gene Fusions and Favorable Outcomes

婴儿高级别神经胶质瘤包括多个亚组,其特征是新颖的可靶向基因融合和良好的预后

2020-07-01175
OAAI
Integrative discovery of treatments for high-risk neuroblastoma
2020-01-0348
OAAI