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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.
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- 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.
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- 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.
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- 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.
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- 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
Molecular Regulation of Autophagy and Asymmetric Cell Division by Cancer Stem Cell Marker CD133.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 5, p. 819, doi. 10.3390/cells12050819
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- Publication type:
- Article
Identification and characterization of a 500-kb homozygously deleted region at 1p36.2-p36.3 in a neuroblastoma cell line.
- Published in:
- Oncogene, 2000, v. 19, n. 37, p. 4302, doi. 10.1038/sj.onc.1203786
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- Publication type:
- Article
High expression of Survivin, mapped to 17q25, is significantly associated with poor prognostic factors and promotes cell survival in human neuroblastoma.
- Published in:
- Oncogene, 2000, v. 19, n. 5, p. 617, doi. 10.1038/sj.onc.1203358
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- Publication type:
- Article
p73 at chromosome 1p36.3 is lost in advanced stage neuroblastoma but its mutation is infrequent.
- Published in:
- Oncogene, 1999, v. 18, n. 4, p. 1061, doi. 10.1038/sj.onc.1202390
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- Publication type:
- Article
Mutations/deletions of the WT1 gene, loss of heterozygosity on chromosome arms 11p and 11q, chromosome ploidy and histology in Wilms' tumors in Japan.
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- International Journal of Cancer, 2001, v. 94, n. 3, p. 396, doi. 10.1002/ijc.1475
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- Publication type:
- Article
Disomy 1 with terminal 1 p deletion is frequent in mass-screening-negative/late-presenting neuroblastomas in young children, but not in mass-screening-positive neuroblastomas in infants.
- Published in:
- International Journal of Cancer, 1999, v. 80, n. 1, p. 54, doi. 10.1002/(SICI)1097-0215(19990105)80:1<54::AID-IJC11>3.0.CO;2-G
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- Publication type:
- Article
Analysis of Asymmetric Cell Division Using Human Neuroblastoma Cell Lines as a Model System.
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- Symmetry (20738994), 2021, v. 13, n. 10, p. 1907, doi. 10.3390/sym13101907
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- Publication type:
- Article
Renal primitive neuroectodermal tumor: An immunohistochemical and cytogenetic analysis.
- Published in:
- Pathology International, 1996, v. 46, n. 4, p. 292, doi. 10.1111/j.1440-1827.1996.tb03613.x
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- Publication type:
- Article
Chromosome Abnormalities, Clinical Features and Molecular Mechanism in Leukemia.
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- Pathology International, 1991, v. 41, n. 10, p. 713, doi. 10.1111/j.1440-1827.1991.tb03342.x
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- Publication type:
- Article
Recycling endosomal CD133 functions as an inhibitor of autophagy at the pericentrosomal region.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-39229-8
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- Publication type:
- Article
The Role of MYCN in Symmetric vs. Asymmetric Cell Division of Human Neuroblastoma Cells.
- Published in:
- Frontiers in Oncology, 2020, v. 11, p. N.PAG, doi. 10.3389/fonc.2020.570815
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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.
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- 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
Extracellular NM23 Protein as a Therapeutic Target for Hematologic Malignancies.
- Published in:
- Advances in Hematology, 2012, p. 1, doi. 10.1155/2012/879368
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- Publication type:
- Article
Abnormalities of the FHIT Transcripts in Osteosarcoma and Ewing Sarcoma.
- Published in:
- Cancer Science, 1998, v. 89, n. 9, p. 887, doi. 10.1111/j.1349-7006.1998.tb00645.x
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- Publication type:
- Article
Deletion of WT1 and WIT1 Genes and Loss of Heterozygosity on Chromosome 11p in Wilms Tumors in Japan.
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- Cancer Science, 1993, v. 84, n. 6, p. 616, doi. 10.1111/j.1349-7006.1993.tb02021.x
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- Publication type:
- Article
c- erbB-2 and c- erbA-1 ( ear-1) Gene Amplification and c- erbB-2 Protein Expression in Japanese Breast Cancers: Their Relationship to the Histology and Other Disease Parameters.
- Published in:
- Cancer Science, 1990, v. 81, n. 6/7, p. 620, doi. 10.1111/j.1349-7006.1990.tb02618.x
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- Publication type:
- Article
Establishment and Characterization of a Small Round Cell Sarcoma Cell Line, SCCH-196, with t(11;22)(q24;q12).
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- Cancer Science, 1989, v. 80, n. 9, p. 861, doi. 10.1111/j.1349-7006.1989.tb01727.x
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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
MYND-less splice variants of AML1MTG8 (RUNX1CBFA2T1) are expressed in leukemia with t(8;21).
- Published in:
- Genes, Chromosomes & Cancer, 2005, v. 43, n. 1, p. 45, doi. 10.1002/gcc.20165
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- Publication type:
- Article
Characterization of genomic breakpoints in MLL and CBP in leukemia patients with t(11;16).
- Published in:
- Genes, Chromosomes & Cancer, 2004, v. 41, n. 3, p. 257, doi. 10.1002/gcc.20077
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- Publication type:
- Article
Chromosomes that show partial loss or gain in near-diploid tumors coincide with chromosomes that show whole loss or gain in near-triploid tumors: Evidence suggesting the involvement of the same genes in the tumorigenesis of high- and low-risk neuroblastomas
- Published in:
- Genes, Chromosomes & Cancer, 2003, v. 36, n. 2, p. 139, doi. 10.1002/gcc.10151
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- Publication type:
- Article
11q23 balanced chromosome aberrations in treatment-related myelodysplastic syndromes and acute leukemia: Report from an International Workshop.
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- Genes, Chromosomes & Cancer, 2002, v. 33, n. 4, p. 362, doi. 10.1002/gcc.10046
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- Publication type:
- Article
Mechanism and relevance of ploidy in neuroblastoma.
- Published in:
- Genes, Chromosomes & Cancer, 2000, v. 29, n. 2, p. 89, doi. 10.1002/1098-2264(2000)9999:9999<::AID-GCC1021>3.0.CO;2-Y
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- Publication type:
- Article
11p15 translocations involving the NUP98 gene in childhood therapy-related acute myeloid leukemia/myelodysplastic syndrome.
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- Genes, Chromosomes & Cancer, 1999, v. 26, n. 3, p. 215, doi. 10.1002/(SICI)1098-2264(199911)26:3<215::AID-GCC5>3.0.CO;2-1
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- Publication type:
- Article
Correlation of chromosome abnormalities with presence or absence of WT1 deletions/mutations in Wilms tumor.
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- Genes, Chromosomes & Cancer, 1999, v. 25, n. 1, p. 26, doi. 10.1002/(SICI)1098-2264(199905)25:1<26::AID-GCC4>3.0.CO;2-Z
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- Publication type:
- Article
Mixed-lineage leukemia with t(10;11)(p13;q21): An analysis of AF10-CALM and CALM-AF10 fusion mRNAs and clinical features.
- Published in:
- Genes, Chromosomes & Cancer, 1999, v. 25, n. 1, p. 33, doi. 10.1002/(SICI)1098-2264(199905)25:1<33::AID-GCC5>3.0.CO;2-3
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- Publication type:
- Article
Hematologic malignancies with the t(10;11)(p13;q21) have the same molecular event and a variety of morphologic or immunologic phenotypes.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 3, p. 253, doi. 10.1002/(SICI)1098-2264(199711)20:3<253::AID-GCC5>3.0.CO;2-1
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- Publication type:
- Article
Novel MLL-CBP fusion transcript in therapy-related chronic myelomonocytic leukemia with a t(11;16) (q23;p13) chromosome translocation.
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- Genes, Chromosomes & Cancer, 1997, v. 20, n. 1, p. 60, doi. 10.1002/(SICI)1098-2264(199709)20:1<60::AID-GCC9>3.0.CO;2-7
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- Publication type:
- Article
Inversion of chromosome 11, inv(11)(p15q22), as a recurring chromosomal aberration associated with de novo and secondary myeloid malignancies: Identification of a P1 clone spanning the 11q22 breakpoint.
- Published in:
- Genes, Chromosomes & Cancer, 1997, v. 19, n. 3, p. 150, doi. 10.1002/(SICI)1098-2264(199707)19:3<150::AID-GCC3>3.0.CO;2-X
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- Publication type:
- Article
EWS-ERG fusion transcript produced by chromosomal insertion in a Ewing sarcoma.
- Published in:
- Genes, Chromosomes & Cancer, 1997, v. 18, n. 3, p. 228, doi. 10.1002/(SICI)1098-2264(199703)18:3<228::AID-GCC9>3.0.CO;2-3
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- Publication type:
- Article
Infrequent mutations of the TP53 gene and no amplification of the MDM2 gene in hepatoblastomas.
- Published in:
- Genes, Chromosomes & Cancer, 1996, v. 15, n. 3, p. 187, doi. 10.1002/(SICI)1098-2264(199603)15:3<187::AID-GCC8>3.0.CO;2-Z
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- Publication type:
- Article
Fusion of an ETS-family gene, EIAF, to EWS by t(17;22)(q12;q12) chromosome translocation in an undifferentiated sarcoma of infancy.
- Published in:
- Genes, Chromosomes & Cancer, 1996, v. 15, n. 2, p. 115, doi. 10.1002/(SICI)1098-2264(199602)15:2<115::AID-GCC6>3.0.CO;2-6
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- Publication type:
- Article
Letters to the editors.
- Published in:
- Genes, Chromosomes & Cancer, 1995, v. 13, n. 3, p. 225, doi. 10.1002/gcc.2870130315
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- Publication type:
- Article
There may be two tumor suppressor genes on chromosome arm Ip closely associated with biologically distinct subtypes of neuroblastoma.
- Published in:
- Genes, Chromosomes & Cancer, 1994, v. 10, n. 1, p. 30, doi. 10.1002/gcc.2870100106
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- Publication type:
- Article
Molecular assignment of a translocation breakpoint in acute myeloid leukemia with t(8;21).
- Published in:
- Genes, Chromosomes & Cancer, 1991, v. 3, n. 3, p. 163, doi. 10.1002/gcc.2870030302
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- Publication type:
- Article
Multiple methylation-free islands flank a small breakpoint cluster region on 11p13 in the t(11;14)(p13;q11) translocation.
- Published in:
- Genes, Chromosomes & Cancer, 1990, v. 1, n. 4, p. 301, doi. 10.1002/gcc.2870010407
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- Publication type:
- Article
Acute megakaryoblastic leukemia with translocation t(1;22)(p13;q13) in a 10-week-old infant.
- Published in:
- American Journal of Hematology, 1992, v. 39, n. 1, p. 56, doi. 10.1002/ajh.2830390112
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- Publication type:
- Article
Flow cytometric evidence for minimal residual disease and cytological heterogeneities in acute lymphoblastic leukemia with severe hypodiploidy.
- Published in:
- American Journal of Hematology, 1989, v. 32, n. 1, p. 42, doi. 10.1002/ajh.2830320109
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- Publication type:
- Article
DNA rearrangement and restriction fragment length polymorphism within the first BCR intron in philadelphia-positive acute leukemia.
- Published in:
- American Journal of Hematology, 1989, v. 32, n. 1, p. 24, doi. 10.1002/ajh.2830320106
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- Publication type:
- Article
A case of acute myelogenous leukemia with an 8-21 translocation, missing Y, and additional karyotypic abnormalities.
- Published in:
- American Journal of Hematology, 1978, v. 4, n. 3, p. 273, doi. 10.1002/ajh.2830040310
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- Publication type:
- Article