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- 2005
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Mark
Prevalence estimates of recurrent balanced cytogenetic aberrations and gene fusions in unselected patients with neoplastic disorders.
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- Contribution to journal › Article
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Mark
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia.
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- Contribution to journal › Article
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Mark
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.
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- Contribution to journal › Article
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Mark
Molecular signatures in childhood acute leukemia and their correlations to expression patterns in normal hematopoietic subpopulations.
(
- Contribution to journal › Article
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Mark
Gene expression profiling of leukemic cell lines reveals conserved molecular signatures among subtypes with specific genetic aberrations
(
- Contribution to journal › Article
- 2004
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Mark
The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architecture with Large, Palindromic, Low-Copy Repeats.
(
- Contribution to journal › Article
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Mark
Structural integrity and expression of the L3MBTL gene in normal and malignant hematopoietic cells
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- Contribution to journal › Article
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Mark
Tumor karyotype predicts clinical outcome in colorectal cancer patients
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- Contribution to journal › Article
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Mark
MDS/AML-associated cytogenetic abnormalities in multiple myeloma and monoclonal gammopathy of undetermined significance: Evidence for frequent de novo occurrence and multipotent stem cell involvement of del(20q).
(
- Contribution to journal › Article
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Mark
Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies.
(
- Contribution to journal › Article
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Mark
Autologous del(20q)-positive erythroid progenitor cells, re-emerging after DLI treatment of an MDS patient relapsing after allo-SCT, can provide a normal peripheral red blood cell count.
(
- Contribution to journal › Article
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Mark
Genome characteristics of primary carcinomas, local recurrences, carcinomatoses, and liver metastases from colorectal cancer patients
(
- Contribution to journal › Article
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Mark
Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer
(
- Contribution to journal › Article
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Mark
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
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Mark
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
(
- Contribution to journal › Article
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Mark
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
(
- Contribution to journal › Article
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Mark
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).
(
- Contribution to journal › Article
- 2003
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Mark
Clinical and genetic studies of ETV6/ABL1-positive chronic myeloid leukaemia in blast crisis treated with imatinib mesylate.
(
- Contribution to journal › Article
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Mark
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article