About: 15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia

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scientific article published on 01 March 1977

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1977 (uk) im März 1977 veröffentlichter wissenschaftlicher Artikel (de) ശാസ്ത്രപ്രബന്ധം (ml) artículu científicu espublizáu en marzu de 1977 (ast) scientific article published on 01 March 1977 (en)
publication date	wds:Q66694390-81C1F36A-FFA0-4331-818F-E460FE3B4241
publication date	1977-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q66694390-04392A19-2DF1-41B4-9CA4-749C0A183E7B
language of work or name	English
cites work	wds:Q66694390-D5DDA5A6-997E-43DA-A6DC-4176B6D152CF wds:Q66694390-E69A8C55-B83D-426E-953E-5538B7481864 wds:Q66694390-EEB0AD8B-6BB6-4E55-8502-E75D5C3A7ACA
cites work	X-Y chromosomal interchange in the aetiology of true hermaphroditism and of XX Klinefelter's syndrome Parathyroid carcinoma.A study of 70 cases Letter: Possible evidence for Xp plus in and XX Male
author name string	wds:Q66694390-64FC27D7-5597-48C2-9DC7-1A410C306C75
author name string	C Dougherty
rdfs:label	15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia (en) 15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia (nl)
skos:prefLabel	15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia (en) 15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia (nl)
name	15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia (en) 15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia (nl)
author	wds:Q66694390-79A8B15F-783D-461B-A9F3-C272FD149170 wds:Q66694390-9C37BA05-A829-4895-83CC-CE05E499342B
author	Janet Rowley Harvey Morris Golomb
title	wds:Q66694390-E3B04F84-94AA-4B0D-B8E9-210A8325D4A3
title	15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia (en)
page(s)	wds:Q66694390-1A8D5FDE-2B2C-406A-8DBF-4067EEAD722A
page(s)	549-550
instance of	wds:Q66694390-9B606C1B-B944-4C16-B932-FE5DCF116B93
instance of	scholarly article
PubMed ID	wds:Q66694390-03CD4571-6413-4965-B0E0-98617D596D6D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/65649
PubMed ID	65649
published in	wds:Q66694390-9BE356C4-8AF6-4904-88CF-BCCFA9703A6C
published in	The Lancet
issue	wds:Q66694390-58CD26AF-2FDF-495D-8866-006976180555
volume	wds:Q66694390-65D9E0F2-10E6-4CBD-B185-39461D48CDFD
issue	8010
volume	1
DOI	wds:Q66694390-BF8112A9-2F42-4FBA-BD07-0A3AC50AA787
DOI	http://dx.doi.org/10.1016/S0140-6736(77)91415-5
DOI	10.1016/S0140-6736(77)91415-5
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q66694390
is cites work of	Cellular localization, expression, and structure of the nuclear dot protein 52 Molecular analysis of simple variant translocations in acute promyelocytic leukemia The pathogenesis of acute promyelocytic leukaemia: evaluation of the role of molecular diagnosis and monitoring in the management of the disease The Potential of Vitamin D-Regulated Intracellular Signaling Pathways as Targets for Myeloid Leukemia Therapy Rearrangements and aberrant expression of the retinoic acid receptor alpha gene in acute promyelocytic leukemias Translocations of the RARalpha gene in acute promyelocytic leukemia Cellular homologs of the avian erythroblastosis virus erb-A and erb-B genes are syntenic in mouse but asyntenic in man. The cell biology of disease: Acute promyelocytic leukemia, arsenic, and PML bodies New advances in the treatment of acute promyelocytic leukemia Two distinctly regulated events, priming and triggering, during retinoid-induced maturation and resistance of NB4 promyelocytic leukemia cell line Chromosome abnormalities in acute promyelocytic leukemia (APL) Leukaemogenesis: more than mutant genes A tumor suppressor-dependent inhibitor of angiogenesis is immunologically and functionally indistinguishable from a fragment of thrombospondin A PMLRARalpha transgene initiates murine acute promyelocytic leukemia Mapping of human chromosomal regions related to neoplasia: Evidence from chromosomes 1 and 17 Chromosomal translocation t(15;17) in human acute promyelocytic leukemia fuses RARα with a novel putative transcription factor, PML Chromosomal sublocalization of human c-myb and c-fes cellular onc genes Differentiation therapy of leukemia: 3 decades of development A continuum model for tumour suppression Translocation breakpoint of acute promyelocytic leukemia lies within the retinoic acid receptor alpha locus JAML, a novel protein with characteristics of a junctional adhesion molecule, is induced during differentiation of myeloid leukemia cells Acute promyelocytic leukaemia in children Newly diagnosed acute promyelocytic leukemia History of acute promyelocytic leukemia: a tale of endless revolution Early death rate in acute promyelocytic leukemia remains high despite all-trans retinoic acid The emerging complexity of gene fusions in cancer Structure, localization and transcriptional properties of two classes of retinoic acid receptor alpha fusion proteins in acute promyelocytic leukemia (APL): structural similarities with a new family of oncoproteins Differentiation therapy Localization of nascent RNA and CREB binding protein with the PML-containing nuclear body. Treatment of acute promyelocytic leukaemia with all-trans retinoic acid and arsenic trioxide: a paradigm of synergistic molecular targeting therapy. Maturation sensitive and resistant t(15;17) NB4 cell lines as tools for APL physiopathology: nomenclature of cells and repertory of their known genetic alterations and phenotypes Cytogenetic studies in acute promyelocytic leukemia: a survey of secondary chromosomal abnormalities Onco gen: Human oncogene locations and chromosome aberrations Genome sequencing and cancer All trans retinoic acid in acute promyelocytic leukemia Vitamin A, cancer treatment and prevention: the new role of cellular retinol binding proteins Chromosome abnormalities in patients with hairy cell leukemia Ligation of the CD44 adhesion molecule reverses blockage of differentiation in human acute myeloid leukemia Molecular pathogenesis of acute promyelocytic leukaemia and APL variants Finding a role for PML in APL pathogenesis: a critical assessment of potential PML activities Acute promyelocytic leukemia: a model for the role of molecular diagnosis and residual disease monitoring in directing treatment approach in acute myeloid leukemia Associations between morphology, karyotype, and clinical features in myeloid leukemias. Role of MmTRA1b/phospholipid scramblase1 gene expression in the induction of differentiation of human myeloid leukemia cells into granulocytes The history of myeloproliferative disorders: before and after Dameshek The molecular pathogenesis of acute promyelocytic leukaemia: implications for the clinical management of the disease Simple, rapid and accurate molecular diagnosis of acute promyelocytic leukemia by loop mediated amplification technology Fluorescence in situ hybridization: a highly efficient technique of molecular diagnosis and predication for disease course in patients with myeloid leukemias New highly sensitive fluorescence in situ hybridization method to detect PML/RARA fusion in acute promyelocytic leukemia Detection of minimal residual disease Molecular cytogenetics of the acute promyelocytic leukemia-derived cell line NB4 and of four all-trans retinoic acid-resistant subclones SNP array analysis of acute promyelocytic leukemia may be of prognostic relevance and identifies a potential high risk group with recurrent deletions on chromosomal subband 1q31.3. Standardization and quality control studies of 'real-time' quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia - a Europe Against Cancer program.

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