A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood AML.

A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood AML.

Xehetasun bibliografikoak
Egile Nagusiak:	Jaju, R, Haas, O, Neat, M, Harbott, J, Boultwood, J, Saha, V, Krings, B, Muller, U, Morris, S, Wainscoat, J, Kearney, L
Formatua:	Journal article
Argitaratua:	1998

Antzeko izenburuak

A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG)
nork: Jaju, R, et al.
Argitaratua: (1999)

A new recurrent translocation, t(5;11)(q35;p15.5), associated with del(5q) in childhood acute myeloid leukemia. The UK Cancer Cytogenetics Group (UKCCG)
nork: Jaju, R, et al.
Argitaratua: (1999)

A novel gene is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood AML.
nork: Jaju, R, et al.
Argitaratua: (2000)

A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia.
nork: Jaju, R, et al.
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Whole chromosome painting and FISH with subtelomeric probes reveals cryptic chromosome rearrangements in del(5q) leukaemias: a UK Cancer Cytogenetic Group study
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Lineage studies of 5q deletions using combined immunophenotyping and fish.
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Combined immunophenotyping and FISH for identification of cell lineages with the 5q-abnormality
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The 5q-syndrome.
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5q- syndrome.
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Combined immunophenotyping and FISH identifies the involvement of B-cells in 5q- syndrome.
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The 5q- syndrome.
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Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome.
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Advances in the 5q- syndrome.
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MOLECULAR MAPPING OF UNCHARACTERISTICALLY SMALL 5Q DELETIONS IN 2 PATIENTS WITH THE 5Q- SYNDROME - DELINEATION OF THE CRITICAL REGION ON 5Q AND IDENTIFICATION OF A 5Q- BREAKPOINT
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Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint.
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Narrowing the critical deleted region in the 5q-syndrome.
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P445: CRYPTIC TRANSLOCATION T(5;11)(Q35;P15) RESULTING IN NUP98::NSD1 GENE FUSION IN ADULTS WITH DE NOVO ACUTE MYELOID LEUKEMIA (AML)
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Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome.
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MOLECULAR DELINEATION OF THE CRITICAL REGION OF THE 5Q-CHROMOSOME IN THE 5Q-SYNDROME
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Narrowing and genomic annotation of the critical region of the 5q-syndrome.
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ISOLATION OF NOVEL CDNA CLONES MAPPING TO THE CRITICAL REGION OF THE 5Q-CHROMOSOME IN THE 5Q-SYNDROME
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Characterization of 6q abnormalities in childhood acute myeloid leukemia and identification of a novel t(6;11)(q24.1;p15.5) resulting in a NUP98-C6orf80 fusion in a case of acute megakaryoblastic leukemia.
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Molecular analysis of the 5q-syndrome
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The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.
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Isolation and analysis of novel candidate genes mapping to the critical region of the 5q-syndrome.
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Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC gene.
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Haploinsufficiency of ribosomal proteins and p53 activation in anemia: Diamond-Blackfan anemia and the 5q- syndrome.
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Novel genes mapping to the critical region of the 5q- syndrome.
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Allelic loss of IRF1 in myelodysplasia and acute myeloid leukemia: retention of IRF1 on the 5q- chromosome in some patients with the 5q- syndrome.
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Molecular characterization of the chromosome 9q deletion in AML.
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RECENT ADVANCES IN THE 5Q- SYNDROME
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Molecular diagnosis of the 5q deletion in malignant myeloid disorders.
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Activation of the mTOR pathway by the amino acid (L)-leucine in the 5q- syndrome and other ribosomopathies.
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Transcription mapping of the 5q- syndrome critical region: cloning of two novel genes and sequencing, expression, and mapping of a further six novel cDNAs.
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NRAS, FLT3 and TP53 mutations in patients with myelodysplastic syndrome and a del(5q).
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