(Q57319938)

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Further evidence that germline CEBPA mutations cause dominant inheritance of acute myeloid leukaemia

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title

Further evidence that germline CEBPA mutations cause dominant inheritance of acute myeloid leukaemia (English)

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1 reference

3

D Catovsky

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author name string

G S Sellick

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1

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H E Spendlove

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2

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K Pritchard-Jones

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4

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R S Houlston

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5

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publication date

5 May 2005

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published in

Leukemia

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volume

19

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issue

7

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page(s)

1276-1278

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cites work

CCAAT/enhancer binding protein alpha is a regulatory switch sufficient for induction of granulocytic development from bipotential myeloid progenitors

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403788

retrieved

21 January 2018

Familial acute myeloid leukaemia: four male members of a single family over three consecutive generations exhibiting anticipation

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403788

retrieved

21 January 2018

Loci other than 21q22.12 (RUNX1) and 16q21–23.2 cause familial AML

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403788

retrieved

21 January 2018

A dominant-negative mutant of C/EBPalpha, associated with acute myeloid leukemias, inhibits differentiation of myeloid and erythroid progenitors of man but not mouse.

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403788

retrieved

21 January 2018

CEBPA point mutations in hematological malignancies

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403788

retrieved

21 January 2018

Mutation of CEBPA in familial acute myeloid leukemia

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reference URL

https://api.crossref.org/works/10.1038%2FSJ.LEU.2403788

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7 January 2021

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DOI

10.1038/SJ.LEU.2403788

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PubMed publication ID

15902292

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(Q57319938)

Further evidence that germline CEBPA mutations cause dominant inheritance of acute myeloid leukaemia

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