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SUZ12 is a candidate target of the non-canonical WNT pathway in the progression of chronic myeloid leukemia.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 107, doi. 10.1002/gcc.20722
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- Article
Large intragenic deletions of the NF2 gene: Breakpoints and associated phenotypes.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 171, doi. 10.1002/gcc.20733
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- Article
RBSP3 is frequently altered in premalignant cervical lesions: Clinical and prognostic significance.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 155, doi. 10.1002/gcc.20726
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- Article
Modeling interactions between leukemia-specific chromosomal changes, somatic mutations, and gene expression patterns during progression of core-binding factor leukemias.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 182, doi. 10.1002/gcc.20732
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- Publication type:
- Article
Clinical and molecular features in patients with atypical teratoid rhabdoid tumor or malignant rhabdoid tumor.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 176, doi. 10.1002/gcc.20729
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- Article
Hematopoietic immortalizing function of the NKL-subclass homeobox gene TLX1.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 119, doi. 10.1002/gcc.20725
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- Article
Hereditary gastrointestinal stromal tumors sharing the KIT Exon 17 germline mutation p.Asp820Tyr develop through different cytogenetic progression pathways.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 91, doi. 10.1002/gcc.20720
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- Publication type:
- Article
Genome-wide scan identifies a copy number variable region at 3q26 that regulates PPM1L in APC mutation-negative familial colorectal cancer patients.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 99, doi. 10.1002/gcc.20724
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- Publication type:
- Article
Distinct MHC gene expression patterns during progression of melanoma.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 144, doi. 10.1002/gcc.20728
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- Publication type:
- Article
Frequent deletion of CDKN2A and recurrent coamplification of KIT, PDGFRA, and KDR in fibrosarcoma of bone-An array comparative genomic hybridization study.
- Published in:
- Genes, Chromosomes & Cancer, 2010, v. 49, n. 2, p. 132, doi. 10.1002/gcc.20727
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- Publication type:
- Article