(Q48188218)

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Prognostic significance of the BAALC isoform pattern and CEBPA mutations in pediatric acute myeloid leukemia with normal karyotype: a study by the Japanese Childhood AML Cooperative Study Group.

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scholarly article

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3 February 2020

Prognostic significance of the BAALC isoform pattern and CEBPA mutations in pediatric acute myeloid leukemia with normal karyotype: a study by the Japanese Childhood AML Cooperative Study Group (English)

1 reference

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3 February 2020

0 references

acute myeloid leukemia

1 reference

based on heuristic

inferred from title

childhood acute myeloid leukemia

1 reference

based on heuristic

inferred from title

3

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3 February 2020

author name string

Yasuhiro Mizushima

1

1 reference

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3 February 2020

Tomohiko Taki

2

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3 February 2020

Yoshihiro Yui

4

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3 February 2020

Yoshimi Hiraumi

5

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3 February 2020

Hiroshi Matsubara

6

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3 February 2020

Motonobu Watanabe

7

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3 February 2020

Ken-ichiro Watanabe

8

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3 February 2020

Yuri Kamitsuji

9

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3 February 2020

Yasuhide Hayashi

10

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3 February 2020

Ichiro Tsukimoto

11

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3 February 2020

Ryoji Kobayashi

12

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3 February 2020

Keizo Horibe

13

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3 February 2020

Akio Tawa

14

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3 February 2020

Tatsutoshi Nakahata

15

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3 February 2020

Souichi Adachi

16

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3 February 2020

publication date

22 May 2010

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3 February 2020

International Journal of Hematology

1 reference

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3 February 2020

91

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3 February 2020

831-837

1 reference

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3 February 2020

5

1 reference

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3 February 2020

https://scigraph.springernature.com/pub.10.1007/s12185-010-0585-x

0 references

Clinical relevance of mutations and gene-expression changes in adult acute myeloid leukemia with normal cytogenetics: are we ready for a prognostically prioritized molecular classification?

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Implications of NRAS mutations in AML: a study of 2502 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BAALC expression predicts clinical outcome of de novo acute myeloid leukemia patients with normal cytogenetics: a Cancer and Leukemia Group B Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Overexpression of the ETS-related gene, ERG, predicts a worse outcome in acute myeloid leukemia with normal karyotype: a Cancer and Leukemia Group B study

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The incidence and clinical significance of nucleophosmin mutations in childhood AML.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk assessment in patients with acute myeloid leukemia and a normal karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BAALC, a novel marker of human hematopoietic progenitor cells*1

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High meningioma 1 (MN1) expression as a predictor for poor outcome in acute myeloid leukemia with normal cytogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The prognostic value of P-glycoprotein (ABCB) and breast cancer resistance protein (ABCG2) in adults with de novo acute myeloid leukemia with normal karyotype

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The MLL partial tandem duplication in acute myeloid leukaemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): a study of the Japanese Childhood AML Cooperative Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Favorable prognostic significance of CEBPA mutations in patients with de novo acute myeloid leukemia: a study from the Acute Leukemia French Association (ALFA)

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prognostic significance of minimal residual disease detection and PML/RAR-alpha isoform type: long-term follow-up in acute promyelocytic leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Double CEBPA mutations, but not single CEBPA mutations, define a subgroup of acute myeloid leukemia with a distinctive gene expression profile that is uniquely associated with a favorable outcome

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BAALC, the human member of a novel mammalian neuroectoderm gene lineage, is implicated in hematopoiesis and acute leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular heterogeneity and prognostic biomarkers in adults with acute myeloid leukemia and normal cytogenetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Independent confirmation of a prognostic gene-expression signature in adult acute myeloid leukemia with a normal karyotype: a Cancer and Leukemia Group B study

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical implications of FLT3 mutations in pediatric AML.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the gene encoding the transcription factor CCAAT/enhancer binding protein alpha in myelodysplastic syndromes and acute myeloid leukemias

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BAALC 1-6-8 protein is targeted to postsynaptic lipid rafts by its N-terminal myristoylation and palmitoylation, and interacts with alpha, but not beta, subunit of Ca/calmodulin-dependent protein kinase II.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical outcome of de novo acute myeloid leukaemia patients with normal cytogenetics is affected by molecular genetic alterations: a concise review

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a PTH regulated gene selectively induced in vivo during PTH-mediated bone formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant-negative mutations of CEBPA, encoding CCAAT/enhancer binding protein-alpha (C/EBPalpha), in acute myeloid leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A previously unidentified alternatively spliced isoform of t(8;21) transcript promotes leukemogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pattern of FHIT gene expression in normal and leukaemic cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CEBPalpha mutations in childhood acute myeloid leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of Ikaros isoform 6 expression in acute myelomonocytic and monocytic leukemias: implications for up-regulation of the antiapoptotic protein Bcl-XL in leukemogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-terminally truncated WT1 protein with oncogenic properties overexpressed in leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CEBPA mutations in younger adults with acute myeloid leukemia and normal cytogenetics: prognostic relevance and analysis of cooperating mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tandem duplications of MLL and FLT3 are correlated with poor prognoses in pediatric acute myeloid leukemia: a study of the Japanese childhood AML Cooperative Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No nucleophosmin mutations in pediatric acute myeloid leukemia with normal karyotype: a study of the Japanese Childhood AML Cooperative Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Risk-stratified therapy and the intensive use of cytarabine improves the outcome in childhood acute myeloid leukemia: the AML99 trial from the Japanese Childhood AML Cooperative Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

BAALC expression and FLT3 internal tandem duplication mutations in acute myeloid leukemia patients with normal cytogenetics: prognostic implications.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Baalc, a marker of mesoderm and muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular monitoring of BAALC expression in patients with CD34-positive acute leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CEBPA point mutations in hematological malignancies

1 reference

https://pubmed.ncbi.nlm.nih.gov/20495894

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12185-010-0585-X

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20495894%20AND%20SRC:MED&resulttype=core&format=json

3 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20495894%20AND%20SRC:MED&resulttype=core&format=json

3 February 2020

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