| Item Type | Name |
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Concept
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Chromosome Banding
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Concept
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Chromosomes, Human, Pair 11
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Concept
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Chromosomes, Human, Pair 2
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Concept
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Chromosomes, Human, Pair 6
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Concept
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Chromosomes, Human, Pair 8
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Concept
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Chromosomes, Human, Pair 1
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Concept
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Chromosomes, Human, Pair 15
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Concept
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Chromosomes, Human, Pair 21
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Concept
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Chromosomes, Human, Pair 3
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Concept
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Chromosomes, Human, Pair 12
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Concept
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Chromosomes, Human, Pair 14
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Concept
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Chromosome Deletion
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Concept
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Chromosome Mapping
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Concept
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Chromosomes, Human, Pair 22
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Concept
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Chromosomes, Human, Pair 4
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Concept
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Chromosomes, Human, Pair 5
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Concept
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Chromosomes, Human, Pair 7
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Concept
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Chromosomes, Human, Pair 20
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Concept
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Chromosomes, Human, Pair 17
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Concept
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Chromosomes, Human, Pair 9
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Concept
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Chromosome Inversion
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Concept
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Philadelphia Chromosome
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Concept
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Chromosome Walking
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Concept
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Chromosome Breakpoints
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Concept
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Chromosome Disorders
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Concept
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Chromosome Aberrations
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Concept
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Chromosomes, Human, Pair 16
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Concept
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Chromosomes, Human, Pair 18
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Concept
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X Chromosome
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Concept
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Physical Chromosome Mapping
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Academic Article
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Detection of DNA rearrangements in the AML1 and ETO loci and of an AML1/ETO fusion mRNA in patients with t(8;21) acute myeloid leukemia.
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Academic Article
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pMCT108.2 is a chimaeric clone which physically maps to human chromosome bands 9q33 (D9S203) and 18q21.1 (D18S24).
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Academic Article
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Analysis of the t(6;11)(q27;q23) in leukemia shows a consistent breakpoint in AF6 in three patients and in the ML-2 cell line.
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Academic Article
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Cloning and chromosomal localization of a novel gene-encoding a human beta 2-integrin alpha subunit.
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Academic Article
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Reassignment of pEFD70.3 (D18S23) to human chromosome band 21q22.2 (D21S412) by physical mapping.
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Academic Article
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Involvement of the AML1 gene in the t(3;21) in therapy-related leukemia and in chronic myeloid leukemia in blast crisis.
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Academic Article
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Genomic organization and chromosomal localization of the gene TCF15 encoding the early mesodermal basic helix-loop-helix factor bHLH-EC2.
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Academic Article
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Myeloid leukemia after hematotoxins.
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Academic Article
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Expression and cytogenetic localization of the human SM22 gene (TAGLN).
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Academic Article
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Nineteen cases of the t(1;22)(p13;q13) acute megakaryblastic leukaemia of infants/children and a review of 39 cases: report from a t(1;22) study group.
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Academic Article
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Cloning and characterization of MST4, a novel Ste20-like kinase.
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Academic Article
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A human Hox 1 homeobox gene exhibits myeloid-specific expression of alternative transcripts in human hematopoietic cells.
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Academic Article
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Molecular cloning of the breakpoints of a complex Philadelphia chromosome translocation: identification of a repeated region on chromosome 17.
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Academic Article
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Gene expression profiles in acute myeloid leukemia with common translocations using SAGE.
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Academic Article
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Search for a third susceptibility gene for maturity-onset diabetes of the young. Studies with eleven candidate genes.
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Academic Article
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Isolation of the human peroxisomal acyl-CoA oxidase gene: organization, promoter analysis, and chromosomal localization.
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Academic Article
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Heritable fragile sites in cancer.
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Academic Article
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Molecular analysis of a t(11;14)(q23;q11) from a patient with null-cell acute lymphoblastic leukemia.
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Academic Article
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Chromosomal location and some structural features of human clathrin light-chain genes (CLTA and CLTB).
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Academic Article
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Acute myeloid leukaemia in a patient with Seckel syndrome.
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Academic Article
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Prolonged subcutaneous administration of recombinant alpha 2b interferon in patients with previously untreated Philadelphia chromosome-positive chronic-phase chronic myelogenous leukemia: effect on remission duration and survival: Cancer and Leukemia Group B study 8583.
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Academic Article
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Human glutamine: fructose-6-phosphate amidotransferase: characterization of mRNA and chromosomal assignment to 2p13.
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Academic Article
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Molecular characterization of 16p deletions associated with inversion 16 defines the critical fusion for leukemogenesis.
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Academic Article
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Blast-1 possesses a glycosyl-phosphatidylinositol (GPI) membrane anchor, is related to LFA-3 and OX-45, and maps to chromosome 1q21-23.
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Academic Article
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Structural organization and mapping of the human mitochondrial glycerol phosphate dehydrogenase-encoding gene and pseudogene.
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Academic Article
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Localization of prostate cancer metastasis-suppressor activity on human chromosome 17.
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Academic Article
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Identification and analysis of the gene encoding human PC2, a prohormone convertase expressed in neuroendocrine tissues.
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Academic Article
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Linkage and linkage disequilibrium in chromosome band 1p36 in American Chaldeans with inflammatory bowel disease.
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Academic Article
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Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias.
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Academic Article
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Recurring chromosomal abnormalities in leukemia in PML-RARA transgenic mice identify cooperating events and genetic pathways to acute promyelocytic leukemia.
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Academic Article
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Recurring chromosomal abnormalities in leukemia in PML-RARA transgenic mice parallel human acute promyelocytic leukemia.
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Academic Article
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Der(16)T(1-16) is a nonrandom secondary chromosome aberration in many types of human neoplasia, including myxoid liposarcoma, rhabdomyosarcoma and Philadelphia-chromosome-positive acute lymphoblastic-leukemia.
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Academic Article
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The spectrum of somatic mutations in high-risk acute myeloid leukaemia with -7/del(7q).
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Academic Article
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Cell intrinsic and extrinsic factors synergize in mice with haploinsufficiency for Tp53, and two human del(5q) genes, Egr1 and Apc.
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Academic Article
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Haploinsufficiency of del(5q) genes, Egr1 and Apc, cooperate with Tp53 loss to induce acute myeloid leukemia in mice.
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Academic Article
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MLL3 is a haploinsufficient 7q tumor suppressor in acute myeloid leukemia.
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Academic Article
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Overexpression and knockout of miR-126 both promote leukemogenesis.
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Academic Article
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Diagnostic evaluation of RNA sequencing for the detection of genetic abnormalities associated with Ph-like acute lymphoblastic leukemia (ALL).
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Academic Article
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Therapy-related myeloid neoplasms: when genetics and environment collide.
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Academic Article
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TRF2 and lamin A/C interact to facilitate the functional organization of chromosome ends.
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