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Frequent breakpoints of focal deletion and uniparental disomy in 22q11.1 or 11.2 segmental duplication region reveal distinct tumorigenesis in rhabdoid tumor of the kidney.
- Published in:
- Genes, Chromosomes & Cancer, 2021, v. 60, n. 8, p. 546, doi. 10.1002/gcc.22952
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- Publication type:
- Article
BRCA1 alterations with additional defects in DNA damage response genes may confer chemoresistance to BRCA-like breast cancers treated with neoadjuvant chemotherapy.
- Published in:
- Genes, Chromosomes & Cancer, 2017, v. 56, n. 5, p. 405, doi. 10.1002/gcc.22445
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- Publication type:
- Article
Meiosis error and subsequent genetic and epigenetic alterations invoke the malignant transformation of germ cell tumor.
- Published in:
- Genes, Chromosomes & Cancer, 2013, v. 52, n. 3, p. 274, doi. 10.1002/gcc.22027
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- Publication type:
- Article
Association of germline or somatic TP53 missense mutation with oncogene amplification in tumors developed in patients with Li-Fraumeni or Li-Fraumeni-like syndrome.
- Published in:
- Genes, Chromosomes & Cancer, 2011, v. 50, n. 7, p. 535, doi. 10.1002/gcc.20878
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- Publication type:
- Article
Genome-wide analysis of allelic imbalances reveals 4q deletions as a poor prognostic factor and MDM4 amplification at 1q32.1 in hepatoblastoma.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 7, p. 596, doi. 10.1002/gcc.20770
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- Publication type:
- Article
Two candidate tumor suppressor genes, MEOX2 and SOSTDC1, identified in a 7p21 homozygous deletion region in a Wilms tumor.
- Published in:
- Genes, Chromosomes & Cancer, 2009, v. 48, n. 12, p. 1037, doi. 10.1002/gcc.20705
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- Publication type:
- Article
Duplication of paternal IGF2 or loss of maternal IGF2 imprinting occurs in half of Wilms tumors with various structural WT1 abnormalities.
- Published in:
- Genes, Chromosomes & Cancer, 2008, v. 47, n. 8, p. 712, doi. 10.1002/gcc.20572
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- Publication type:
- Article
Duplication of the paternal IGF2 allele in trisomy 11 and elevated expression levels of IGF2 mRNA in congenital mesoblastic nephroma of the cellular or mixed type.
- Published in:
- Genes, Chromosomes & Cancer, 2007, v. 46, n. 10, p. 929, doi. 10.1002/gcc.20481
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- Publication type:
- Article
Anaplastic histology Wilms' tumors registered to the Japan Wilms' Tumor Study Group are less aggressive than that in the National Wilms' Tumor Study 5.
- Published in:
- 2016
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- Publication type:
- journal article
RASSF1A methylation indicates a poor prognosis in hepatoblastoma patients.
- Published in:
- Pediatric Surgery International, 2013, v. 29, n. 11, p. 1147, doi. 10.1007/s00383-013-3371-z
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- Publication type:
- Article
Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells.
- Published in:
- Journal of Human Genetics, 2005, v. 50, n. 3, p. 124, doi. 10.1007/s10038-005-0231-2
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- Publication type:
- Article
Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb.
- Published in:
- Journal of Human Genetics, 2003, v. 48, n. 4, p. 194, doi. 10.1007/s10038-003-0009-3
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- Publication type:
- Article
ATM depletion induces proteasomal degradation of FANCD2 and sensitizes neuroblastoma cells to PARP inhibitors.
- Published in:
- BMC Cancer, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12885-023-10772-y
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- Publication type:
- Article
Association of 11q loss, trisomy 12, and possible 16q loss with loss of imprinting of insulin‐like growth factor–II in Wilms tumor.
- Published in:
- Genes, Chromosomes & Cancer, 2006, v. 45, n. 6, p. 592, doi. 10.1002/gcc.20321
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- Publication type:
- Article
Paternally inherited WT1 mutation plus uniparental disomy of 11p may be an essential mechanism for development of WT1-mutated familial Wilms tumor.
- Published in:
- 2019
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- Publication type:
- case study
Outcome of renal tumors registered in Japan Wilms Tumor Study-2 (JWiTS-2): A report from the Japan Children's Cancer Group (JCCG).
- Published in:
- 2018
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- Publication type:
- journal article
Methylation of the RASSF1A promoter is predictive of poor outcome among patients with Wilms tumor.
- Published in:
- Pediatric Blood & Cancer, 2012, v. 59, n. 3, p. 499, doi. 10.1002/pbc.24093
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- Publication type:
- Article
Establishment and characterization of a novel MDM2/MYCN-co-amplified neuroblastoma cell line, NBN-SHIM, established from a late recurrent stage MS tumor.
- Published in:
- Human Cell, 2024, v. 37, n. 5, p. 1602, doi. 10.1007/s13577-024-01106-6
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- Publication type:
- Article
Blastemal predominant type Wilms tumor in Japan: Japan Children's Cancer Group.
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- Pediatrics International, 2019, v. 61, n. 4, p. 351, doi. 10.1111/ped.13811
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- Publication type:
- Article
Management of pediatric renal tumor: Past and future trials of the Japan Wilms Tumor Study Group.
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- Pediatrics International, 2015, v. 57, n. 5, p. 828, doi. 10.1111/ped.12787
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- Publication type:
- Article
Promoter hypermethylation of the RASSF1A gene predicts the poor outcome of patients with hepatoblastoma.
- Published in:
- Pediatric Blood & Cancer, 2007, v. 49, n. 3, p. 240, doi. 10.1002/pbc.21031
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- Publication type:
- Article
Alterations of the genes involved in the PI3K and estrogen-receptor pathways influence outcome in human epidermal growth factor receptor 2-positive and hormone receptor-positive breast cancer patients treated with trastuzumab-containing neoadjuvant chemotherapy
- Published in:
- BMC Cancer, 2013, v. 13, n. 1, p. 1, doi. 10.1186/1471-2407-13-241
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- Publication type:
- Article
Alterations of the genes involved in the PI3K and estrogen-receptor pathways influence outcome in human epidermal growth factor receptor 2-positive and hormone receptor-positive breast cancer patients treated with trastuzumab-containing neoadjuvant chemotherapy.
- Published in:
- 2013
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- Publication type:
- journal article
Combined BubR1 protein down-regulation and RASSF1A hypermethylation in Wilms tumors with diverse cytogenetic changes.
- Published in:
- Molecular Carcinogenesis, 2008, v. 47, n. 9, p. 660, doi. 10.1002/mc.20412
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- Publication type:
- Article
Loss of p53 suppresses replication stress-induced DNA damage in ATRX-deficient neuroblastoma.
- Published in:
- Oncogenesis, 2021, v. 10, n. 11, p. 1, doi. 10.1038/s41389-021-00363-6
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- Publication type:
- Article
Pretreatment Hemoglobin Levels and Platelet-to-Lymphocyte Ratio Predict Survival Benefit from Pembrolizumab in Advanced Urothelial Carcinoma.
- Published in:
- Cancer Diagnosis & Prognosis, 2023, v. 3, n. 2, p. 230, doi. 10.21873/cdp.10206
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- Publication type:
- Article
The methylation status of RASSF1A promoter predicts responsiveness to chemotherapy and eventual cure in hepatoblastoma patients.
- Published in:
- International Journal of Cancer, 2008, v. 123, n. 5, p. 1117, doi. 10.1002/ijc.23613
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- Publication type:
- Article
Development of an osteosarcoma model with MYCN amplification and TP53 mutation in hiPS cell‐derived neural crest cells.
- Published in:
- Cancer Science, 2023, v. 114, n. 5, p. 1898, doi. 10.1111/cas.15730
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- Publication type:
- Article
Polycomb EZH1 regulates cell cycle/5‐fluorouracil sensitivity of neuroblastoma cells in concert with MYCN.
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- Cancer Science, 2022, v. 113, n. 12, p. 4193, doi. 10.1111/cas.15555
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- Publication type:
- Article
Clinical prognostic value of DNA methylation in hepatoblastoma: Four novel tumor suppressor candidates.
- Published in:
- Cancer Science, 2016, v. 107, n. 6, p. 812, doi. 10.1111/cas.12928
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- Publication type:
- Article
Different incidences of epigenetic but not genetic abnormalities between Wilms tumors in Japanese and Caucasian children.
- Published in:
- Cancer Science, 2012, v. 103, n. 6, p. 1129, doi. 10.1111/j.1349-7006.2012.02269.x
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- Publication type:
- Article
Yolk sac tumor but not seminoma or teratoma is associated with abnormal epigenetic reprogramming pathway and shows frequent hypermethylation of various tumor suppressor genes.
- Published in:
- Cancer Science, 2009, v. 100, n. 4, p. 698, doi. 10.1111/j.1349-7006.2009.01102.x
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- Publication type:
- Article