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Nephroblastoma

CDCA8 regulates ATP5F1A protein stability and malignant phenotypes in wilms tumor cells: Prognostic implications and mechanistic insights

Qiang Zeng, Junfeng Tao, [ ... ], Linshan Zeng

Recruitment and polarization typing of tumor-associated macrophages is associated with tumor progression and poor prognosis in Wilms tumor patients

Zhang Wang, Liming Jin, [ ... ], Dawei He

ZSTK474 targeting PIK3R3 inhibits the Wilms’ tumor through G0 / G1 phase arrest

Maoxian Li, Jiayan Liu, [ ... ], Dawei He

Effect of radiation after surgery on the prognosis of children with Wilms tumor

Songqiang Chen, Zhisheng Wan, [ ... ], Zhenli Zhao

Performance of an offline systematic error correction strategy in pediatric patients receiving adjuvant conformal radiotherapy for Wilm’s tumor

Rashid Mussa Mruma, Nazima Dharsee, [ ... ], Geofrey Filbert Soko

Gene expression studies of WT1 mutant Wilms tumor cell lines in the frame work of published kidney development data reveals their early kidney stem cell origin

Brigitte Royer-Pokora, Wasco Wruck, James Adjaye, Manfred Beier

Characteristics and outcome of children with renal tumors in the Netherlands: The first five-year’s experience of national centralization

Prakriti Roy, Sophie E. van Peer, [ ... ], Marry M. van den Heuvel-Eibrink

Toward a methodology for evaluating DNA variants in nuclear families

Dustin B. Miller, Reid Robison, Stephen R. Piccolo

Prognostic significance of age in 5631 patients with Wilms tumour prospectively registered in International Society of Paediatric Oncology (SIOP) 93-01 and 2001

J. A. Hol, M. I. Lopez-Yurda, [ ... ], M. M. Van den Heuvel-Eibrink

Rhabdomyosarcoma and Wilms tumors contain a subpopulation of noggin producing, myogenic cells immunoreactive for lens beaded filament proteins

Jacquelyn Gerhart, Kathryn Behling, [ ... ], Mindy George-Weinstein

A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children’s Oncology Group study

Amy E. Armstrong, Samantha Gadd, [ ... ], Elizabeth J. Perlman

Establishment of a Conditionally Immortalized Wilms Tumor Cell Line with a Homozygous WT1 Deletion within a Heterozygous 11p13 Deletion and UPD Limited to 11p15

Artur Brandt, Katharina Löhers, [ ... ], Brigitte Royer-Pokora

TP53 Mutational Status Is a Potential Marker for Risk Stratification in Wilms Tumour with Diffuse Anaplasia

Mariana Maschietto, Richard D. Williams, [ ... ], Kathy Pritchard-Jones

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