(Q33390143)

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T cell acute lymphoblastic leukemia arising from familial platelet disorder

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Europe PubMed Central

PubMed publication ID

26 July 2017

T cell acute lymphoblastic leukemia arising from familial platelet disorder (English)

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

based on heuristic

inferred from title

lymphoblastic leukemia

1 reference

based on heuristic

inferred from title

Masahiro Nakagawa

object named as

Masahiro Nakagawa

4

0 references

Motoshi Ichikawa

object named as

Motoshi Ichikawa

6

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author name string

Nahoko Nishimoto

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Yoichi Imai

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Koki Ueda

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Akihito Shinohara

5

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Yasuhito Nannya

7

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Mineo Kurokawa

8

1 reference

Europe PubMed Central

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26 July 2017

publication date

12 June 2010

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Europe PubMed Central

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26 July 2017

International Journal of Hematology

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Europe PubMed Central

PubMed publication ID

26 July 2017

92

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Europe PubMed Central

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26 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

194-197

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

AML-1 is required for megakaryocytic maturation and lymphocytic differentiation, but not for maintenance of hematopoietic stem cells in adult hematopoiesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of a conditional AML1-ETO oncogene bypasses embryonic lethality and establishes a murine model of human t(8;21) acute myeloid leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Runx1 deficiency predisposes mice to T-lymphoblastic lymphoma

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haploinsufficiency of AML1 results in a decrease in the number of LTR-HSCs while simultaneously inducing an increase in more mature progenitors

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Studies of a familial platelet disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20549580

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S12185-010-0612-Y

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

ResearchGate publication ID

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