Analysis of the joining sequences of the t(15;17) translocation in human acute promyelocytic leukemia: sequence non-specific recombination between the PML and RARA genes within identical short stretches (Q48076765)

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scientific article published in January 1995

Language	Label	Description	Also known as
English	Analysis of the joining sequences of the t(15;17) translocation in human acute promyelocytic leukemia: sequence non-specific recombination between the PML and RARA genes within identical short stretches	scientific article published in January 1995

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

Analysis of the joining sequences of the t(15;17) translocation in human acute promyelocytic leukemia: sequence non-specific recombination between the PML and RARA genes within identical short stretches (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

acute promyelocytic leukemia

1 reference

based on heuristic

inferred from title

author name string

Yoshida H

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

Naoe T

2

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

Fukutani H

3

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

Kiyoi H

4

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

Kubo K

5

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

Ohno R

6

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

publication date

1 January 1995

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

12

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

37-44

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

Molecular heterogeneity of the PML gene rearrangement in acute promyelocytic leukemia: prevalence and clinical significance.

1 reference

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Bacterial assays for recombinagens

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Clonal analysis of multiple point mutations in the N-ras gene in patients with acute myeloid leukemia.

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Nonhomologous DNA end rejoining in chromosomal aberration formation

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Translocation breakpoint of acute promyelocytic leukemia lies within the retinoic acid receptor alpha locus

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A chromosomal basis of lymphoid malignancy in man.

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Parallel DNA triplexes, homologous recombination, and other homology-dependent DNA interactions

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Oncogenic conversion of transcription factors by chromosomal translocations

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Molecular analysis of both translocation products of a Philadelphia-positive CML patient

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The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor alpha gene to a novel transcribed locus

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The PML-RARα fusion mRNA generated by the t(15;17) translocation in acute promyelocytic leukemia encodes a functionally altered RAR

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Breakpoint clusters of the PML gene in acute promyelocytic leukemia: Primary structure of the reciprocal products of the PML‐RARA gene in a patient with t(15;17)

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The acute promyelocytic leukemia-specific PML-RAR alpha fusion protein inhibits differentiation and promotes survival of myeloid precursor cells

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Chromosomal translocation t(15;17) in human acute promyelocytic leukemia fuses RARα with a novel putative transcription factor, PML

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Noncomplementary DNA double-strand-break rejoining in bacterial and human cells

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Minimal residual disease status in pre-B acute lymphoblastic leukemia patients after chemotherapy and bone marrow transplantation: assessment of the anti-leukemic effects of chemotherapy and BMT

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Evidence for a 15; 17 translocation in every patient with acute promyelocytic leukemia

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Recombination between similar but not identical DNA sequences during yeast transformation occurs within short stretches of identity

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The sites of radiation induced-breakage in human lymphocyte chromosomes, determined by quinacrine fluorescence

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The double-strand-break repair model for recombination

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The use of integrating DNA vectors to analyse the molecular defects in ionising radiation-sensitive mutants of mammalian cells including ataxia telangiectasia

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Characterization of the translocation breakpoint sequences of two DEK-CAN fusion genes present in t(6;9) acute myeloid leukemia and a SET-CAN fusion gene found in a case of acute undifferentiated leukemia

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Hypervariable minisatellite DNA is a hotspot for homologous recombination in human cells

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Identifiers

10.1002/GCC.2870120107

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/7534109

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