Chromosome band 16q22-linked familial AML: exclusion of candidate genes, and possible disease risk modification by NQO1 polymorphisms (Q45034913)

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scientific article published in November 2004

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English	Chromosome band 16q22-linked familial AML: exclusion of candidate genes, and possible disease risk modification by NQO1 polymorphisms	scientific article published in November 2004

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

title

Chromosome band 16q22-linked familial AML: exclusion of candidate genes, and possible disease risk modification by NQO1 polymorphisms (English)

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

author

Olufunmilayo Olopade

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6

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Olufunmilayo I Olopade

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

Marshall Horwitz

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Marshall Horwitz

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5

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Hamish S. Scott

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Hamish S Scott

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7

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author name string

Robert Escher

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1

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Europe PubMed Central

PubMed publication ID

15334552

retrieved

8 December 2017

Antonia Jones

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2

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

Fitsum Hagos

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3

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

Catherine Carmichael

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4

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

publication date

1 November 2004

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

published in

Genes, Chromosomes and Cancer

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

volume

41

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

issue

3

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

page(s)

278-282

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Europe PubMed Central

PubMed publication ID

15334552

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8 December 2017

cites work

Transcription factors and translocations in lymphoid and myeloid leukemia

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

based on heuristic

inferred from DOI database lookup

No evidence for core-binding factor CBFbeta as a leukemia predisposing factor in chromosome 16q22-linked familial AML.

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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inferred from DOI database lookup

NAD(P)H:quinone oxidoreductase: polymorphisms and allele frequencies in Caucasian, Chinese and Canadian Native Indian and Inuit populations.

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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inferred from DOI database lookup

Susceptibility gene for familial acute myeloid leukemia associated with loss of 5q and/or 7q is not localized on the commonly deleted portion of 5q

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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inferred from DOI database lookup

NFAT signaling in vertebrate development

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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inferred from DOI database lookup

Cadherin and catenin alterations in human cancer

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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The proto-oncogene c-myc in hematopoietic development and leukemogenesis

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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A family inheriting different subtypes of acute myelogenous leukemia

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2.

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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The role of NFAT transcription factors in integrin-mediated carcinoma invasion

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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Unlike AML1, CBFbeta gene is not deregulated by point mutations in acute myeloid leukemia and in myelodysplastic syndromes

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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Oncogenic transcription factors in the human acute leukemias

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

based on heuristic

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AML1 interconnected pathways of leukemogenesis

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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A potential mechanism underlying the increased susceptibility of individuals with a polymorphism in NAD(P)H:quinone oxidoreductase 1 (NQO1) to benzene toxicity

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

based on heuristic

inferred from DOI database lookup

Implication of alternative splicing for expression of a variant NAD(P)H:quinone oxidoreductase-1 with a single nucleotide polymorphism at 465C>T.

1 reference

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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Loss of E2F4 activity leads to abnormal development of multiple cellular lineages

1 reference

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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Low NAD(P)H:quinone oxidoreductase 1 activity is associated with increased risk of acute leukemia in adults

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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The CBFbeta subunit is essential for CBFalpha2 (AML1) function in vivo

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Crossref

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https://api.crossref.org/works/10.1002%2FGCC.20084

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7 January 2021

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DOI

10.1002/GCC.20084

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Europe PubMed Central

PubMed publication ID

15334552

retrieved

8 December 2017

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release_ea26axgs35ft3n4p4kymw3mhay

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https://api.fatcat.wiki/v0/release/ea26axgs35ft3n4p4kymw3mhay

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24 November 2022

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PubMed publication ID

15334552

1 reference

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Europe PubMed Central

PubMed publication ID

15334552

retrieved

8 December 2017

 

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