About: The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation

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About: The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation Goto Sponge NotDistinct Permalink

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scientific article published on 01 April 2001

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 2001 (uk) im April 2001 veröffentlichter wissenschaftlicher Artikel (de) article scientifique publié en 2001 (fr) artículu científicu espublizáu n'abril de 2001 (ast) scientific article published on 01 April 2001 (en)
publication date	wds:Q58481910-B461EFCE-5BE8-48F6-A269-6D070645F7BC
publication date	2001-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58481910-BE80F2A8-FFAE-483C-9A28-2D5878F8CFB5
language of work or name	English
cites work	wds:Q58481910-271FBB1E-E393-462B-AC48-465C27356D76 wds:Q58481910-3BBAC7C8-D1A0-4A5F-9AF1-0AB2A3801DBA wds:Q58481910-4F6CA2A2-88A1-49BB-905E-23EBA0296589 wds:Q58481910-99613937-583E-4F43-A029-308EF2F1371A wds:Q58481910-A93EBA29-F3BB-4423-9C8B-D8D11FFF1020 wds:Q58481910-ACB23B5F-C162-4B95-A78A-A7F139A3E95F wds:Q58481910-B6FBCA24-B90C-4689-9F61-04A2F11825A6 wds:Q58481910-CABBFF89-665A-4F64-BD08-F6340CD5413C wds:Q58481910-E52B3A38-0B59-48AF-9555-46191D4DFD24
cites work	Prognostic implications of chromosomal findings in acute lymphoblastic leukaemia at diagnosis The impact of the new fish technologies on the cytogenetics of haematological malignancies Cytogenetics adds independent prognostic information in adults with acute lymphoblastic leukaemia on MRC trial UKALL XA. MRC Adult Leukaemia Working Party. Investigation of minimal residual disease in childhood and adult acute lymphoblastic leukaemia by molecular analysis Molecular genetics, natural history and the demise of childhood leukaemia Cytogenetic studies of infant acute lymphoblastic leukemia: poor prognosis of infants with t(4;11) - a report of the Children's Cancer Group Cross-species color banding in ten cases of myeloid malignancies with complex karyotypes Multiplex fluorescence in situ hybridization and cross species color banding of a case of chronic myeloid leukemia in blastic crisis with a complex Philadelphia translocation The management of patients with leukaemia: the role of cytogenetics in this molecular era.
author name string	wds:Q58481910-431B1323-2DE7-48C6-9576-D6D3F158E9E4 wds:Q58481910-4825D9DF-8FF6-4FA0-B4A4-E62DA47DCBC2
author name string	L M Secker-Walker M Martineau
rdfs:label	The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation (en) The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation (nl)
skos:prefLabel	The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation (en) The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation (nl)
name	The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation (en) The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management. Annotation (nl)
author	wds:Q58481910-72EDC7A2-D780-472B-A0E6-B1320517B2DE
author	Christine J Harrison
title	wds:Q58481910-1CFA9012-B525-4768-B87A-25C62059EC59
title	The Leukaemia Research Fund/United Kingdom Cancer Cytogenetics Group Karyotype Database in acute lymphoblastic leukaemia: a valuable resource for patient management (en)
page(s)	wds:Q58481910-2C108A94-00F6-4100-94BD-B6180DA90C7F
page(s)	3-10
instance of	wds:Q58481910-7ACF0F55-ADDD-49E7-A3E2-13E9128FCA2A
instance of	scholarly article
main subject	wds:Q58481910-1CE83320-9587-4295-828A-9CF50E615857 wds:Q58481910-BF7F8637-C46B-4FEF-A580-435281C25AAA wds:Q58481910-E409E74C-D635-483E-936F-15FF403E5506
main subject	leukemia database Patients
PubMed ID	wds:Q58481910-BB558166-C74E-4639-8744-B3DEDABFF4E2
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11328273
PubMed ID	11328273
published in	wds:Q58481910-F83F1300-51BA-49B7-B0F7-C58A62C5E64F
published in	British Journal of Haematology
issue	wds:Q58481910-3E8F20C1-5308-425A-8284-A0AF30834FDA
volume	wds:Q58481910-F4F34FB2-E549-4171-A5D0-31753D941863
issue	1
volume	113
DOI	wds:Q58481910-F35AB003-A8C2-4758-91FA-A98072A2B1CC
DOI	http://dx.doi.org/10.1046/J.1365-2141.2001.02643.X
DOI	10.1046/J.1365-2141.2001.02643.X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58481910
is cites work of	Temporal changes in the incidence and pattern of central nervous system relapses in children with acute lymphoblastic leukaemia treated on four consecutive Medical Research Council trials, 1985-2001. Outcome after first relapse in childhood acute lymphoblastic leukaemia - lessons from the United Kingdom R2 trial Intrachromosomal amplification of chromosome 21 (iAMP21) may arise from a breakage-fusion-bridge cycle. Prognostic effect of chromosomal abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: results from the UK Medical Research Council ALL97/99 randomised trial Three distinct subgroups of hypodiploidy in acute lymphoblastic leukaemia Long-term follow-up of the United Kingdom medical research council protocols for childhood acute lymphoblastic leukaemia, 1980-2001 Adolescent and young adult cancer survival Molecular cytogenetic characterization of TCF3 (E2A)/19p13.3 rearrangements in B-cell precursor acute lymphoblastic leukemia. Outcome in children with Down's syndrome and acute lymphoblastic leukemia: role of IKZF1 deletions and CRLF2 aberrations Classification of pediatric acute lymphoblastic leukemia by gene expression profiling Amplification of AML1 on a duplicated chromosome 21 in acute lymphoblastic leukemia: a study of 20 cases. Strong association of the HLA-DP6 supertype with childhood leukaemia is due to a single allele, DPB1*0601. Disruption of ETV6 in intron 2 results in upregulatory and insertional events in childhood acute lymphoblastic leukaemia. A novel translocation, t(14;19)(q32;p13), involving IGH@ and the cytokine receptor for erythropoietin Unique characteristics of adolescent and young adult acute lymphoblastic leukemia, breast cancer, and colon cancer Molecular cytogenetics in haematological malignancy: current technology and future prospects Comparative expressed sequence hybridization studies of high-hyperdiploid childhood acute lymphoblastic leukemia. Prenatal origin of hyperdiploid acute lymphoblastic leukemia in identical twins. Amplification of the ABL gene in T-cell acute lymphoblastic leukemia PTPN11 mutations in childhood acute lymphoblastic leukemia occur as a secondary event associated with high hyperdiploidy. Clinical features, cytogenetics and outcome in acute lymphoblastic and myeloid leukaemia of infancy: report from the MRC Childhood Leukaemia working party ETV6/RUNX1 fusion at diagnosis and relapse: Some prognostic indications Translating microarray data for diagnostic testing in childhood leukaemia Early response to induction is predictive of survival in childhood Philadelphia chromosome positive acute lymphoblastic leukaemia: results of the Medical Research Council ALL 97 trial Variable breakpoints target PAX5 in patients with dicentric chromosomes: a model for the basis of unbalanced translocations in cancer Successful treatment without cranial radiotherapy of children receiving intensified chemotherapy for acute lymphoblastic leukaemia: results of the risk-stratified randomized central nervous system treatment trial MRC UKALL XI (ISRC TN 16757172). MLL translocations with concurrent 3' deletions: interpretation of FISH results. Abnormalities of the der(12)t(12;21) in ETV6-RUNX1 acute lymphoblastic leukemia. Derivative chromosome 9 deletions are a significant feature of childhood Philadelphia chromosome positive acute lymphoblastic leukaemia t(14;19)(q32;q13): A recurrent translocation in B-cell precursor acute lymphoblastic leukemia Cytogenetic analysis in childhood acute lymphoblastic leukemia: experience at a single institution in Korea Is trisomy 5 a distinct cytogenetic subgroup in acute lymphoblastic leukemia? Cytogenetics of long-term survivors of ETV6-RUNX1 fusion positive acute lymphoblastic leukemia Cytogenetics in childhood acute lymphoblastic leukemia in Taiwan: a single-institutional experience.

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