The PML gene is linked to a megabase-scale insertion/deletion restriction fragment length polymorphism (Q71846545)

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21 October 2019

title

The PML gene is linked to a megabase-scale insertion/deletion restriction fragment length polymorphism (English)

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21 October 2019

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7 June 2024

neoplasm protein

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7 June 2024

nuclear protein

1 reference

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restriction fragment length polymorphism

7 June 2024

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7 June 2024

A. Goy

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7 June 2024

T. Passalaris

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Y. H. Xiao

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W. H. Miller

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D. S. Siegel

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A. D. Zelenetz

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language of work or name

English

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National Center for Biotechnology Information

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7 June 2024

publication date

1 March 1995

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21 October 2019

20 March 1995

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National Center for Biotechnology Information

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full work available at URL

7 June 2024

https://api.elsevier.com/content/article/PII:088875439580217A?httpAccept=text/xml

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Crossref

DOI

https://api.crossref.org/works/10.1016/0888-7543(95)80217-A

https://api.elsevier.com/content/article/PII:088875439580217A?httpAccept=text/plain

7 June 2024

1 reference

Crossref

DOI

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7 June 2024

1 reference

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21 October 2019

volume

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21 October 2019

issue

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21 October 2019

page(s)

327-333

1 reference

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Expression pattern of the RAR alpha-PML fusion gene in acute promyelocytic leukemia

21 October 2019

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A fraction of the mouse genome that is derived from islands of nonmethylated, CpG-rich DNA

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Pulsed-field gel analysis of human immunoglobulin heavy-chain constant region gene deletions reveals the extent of unmapped regions within the locus

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The role of DNA repeats and associated secondary structures in genomic instability and neoplasia

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Treatment of first relapse in acute promyelocytic leukaemia with all-trans retinoic acid.

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Localization of preferential sites of rearrangement within the BCR gene in Philadelphia chromosome-positive acute lymphoblastic leukemia

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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

7 June 2024

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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

7 June 2024

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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)

7 June 2024

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Mechanisms of illegitimate recombination

7 June 2024

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A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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Diversity of the immunoglobulin gene superfamily

7 June 2024

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

7 June 2024

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DNA duplication associated with Charcot-Marie-Tooth disease type 1A

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Genomic variability and alternative splicing generate multiple PML/RAR alpha transcripts that encode aberrant PML proteins and PML/RAR alpha isoforms in acute promyelocytic leukaemia

7 June 2024

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Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit

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Unusual organization of the human T-cell receptor beta-chain gene complex is linked to recombination hotspots

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Insertion/deletion-related polymorphisms in the human T cell receptor beta gene complex

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Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency

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7 June 2024

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Retinoic acid regulates aberrant nuclear localization of PML-RAR alpha in acute promyelocytic leukemia cells

7 June 2024

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Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man

7 June 2024

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Identifiers

DOI

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21 October 2019

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