(Q44661657)

English

MPL W515L/K mutations in 343 Chinese adults with JAK2V617F mutation-negative chronic myeloproliferative disorders detected by a newly developed RQ-PCR based on TaqMan MGB probes

scientific article published in March 2010

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

MPL W515L/K mutations in 343 Chinese adults with JAK2V617F mutation-negative chronic myeloproliferative disorders detected by a newly developed RQ-PCR based on TaqMan MGB probes (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

myeloproliferative disorders

1 reference

based on heuristic

inferred from title

author name string

Guo-Rui Ruan

1

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Bin Jiang

2

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Ling-Di Li

3

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Ji-Hong Niu

4

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Jin-Lan Li

5

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Min Xie

6

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Ya-Zhen Qin

7

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Yan-Rong Liu

8

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Xiao-Jun Huang

9

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Shan-Shan Chen

10

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

publication date

1 March 2010

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Hematological Oncology

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

28

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Europe PubMed Central

PubMed publication ID

5 December 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

33-39

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

21 January 2018

The World Health Organization (WHO) classification of the myeloid neoplasms

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Proposals and rationale for revision of the World Health Organization diagnostic criteria for polycythemia vera, essential thrombocythemia, and primary myelofibrosis: recommendations from an ad hoc international expert panel

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

A gain-of-function mutation of JAK2 in myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical profile of homozygous JAK2 617V>F mutation in patients with polycythemia vera or essential thrombocythemia

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical implications of the JAK2 V617F mutation in essential thrombocythemia.

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study.

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

JAK2 mutation in essential thrombocythaemia: clinical associations and long-term prognostic relevance

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Influence of JAK2V617F allele burden on phenotype in essential thrombocythemia

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

V617F mutation in JAK2 is associated with poorer survival in idiopathic myelofibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

The JAK2(V617F) tyrosine kinase mutation in myelofibrosis with myeloid metaplasia: lineage specificity and clinical correlates

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

JAK2 V617F mutational status predicts progression to large splenomegaly and leukemic transformation in primary myelofibrosis.

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Low JAK2V617F allele burden in primary myelofibrosis, compared to either a higher allele burden or unmutated status, is associated with inferior overall and leukemia-free survival

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

MPLW515L is a novel somatic activating mutation in myelofibrosis with myeloid metaplasia

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

MPL515 mutations in myeloproliferative and other myeloid disorders: a study of 1182 patients

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Anaemia characterises patients with myelofibrosis harbouring Mpl mutation.

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Concurrent MPL515 and JAK2V617F mutations in myelofibrosis: chronology of clonal emergence and changes in mutant allele burden over time.

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

An amphipathic motif at the transmembrane-cytoplasmic junction prevents autonomous activation of the thrombopoietin receptor.

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Characteristics and clinical correlates of MPL 515W>L/K mutation in essential thrombocythemia

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

A sensitive detection method for MPLW515L or MPLW515K mutation in chronic myeloproliferative disorders with locked nucleic acid-modified probes and real-time polymerase chain reaction.

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

MPL W515L mutation in Chinese patients with myeloproliferative diseases

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Haematopoietic cell lineage distribution of MPLW515L/K mutations in patients with idiopathic myelofibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Demonstration of MPLW515K, but not JAK2V617F, in in vitro expanded CD4+ T lymphocytes

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence for MPL W515L/K mutations in hematopoietic stem cells in primitive myelofibrosis

1 reference

https://api.crossref.org/works/10.1002%2FHON.899

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HON.899

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 December 2017

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