A sensitive and reliable semi-quantitative real-time PCR assay to detect JAK2 V617F in blood. (Q54579055)

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English	A sensitive and reliable semi-quantitative real-time PCR assay to detect JAK2 V617F in blood.	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

A sensitive and reliable semi-quantitative real-time PCR assay to detect JAK2 V617F in blood. (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

author name string

Poodt J

1

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

Fijnheer R

2

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

Walsh IB

3

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

Hermans MH

4

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

publication date

1 December 2006

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

Hematological Oncology

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

24

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

4

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

227-233

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1002%2FHON.800

21 January 2018

The chronic myeloproliferative disorders: clonality and clinical heterogeneity

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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.800

7 January 2021

based on heuristic

inferred from DOI database lookup

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

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https://api.crossref.org/works/10.1002%2FHON.800

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHON.800

7 January 2021

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The JAK2 V617F activating tyrosine kinase mutation is an infrequent event in both "atypical" myeloproliferative disorders and myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1002%2FHON.800

7 January 2021

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

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Mutation studies in CD3+, CD19+ and CD34+ cell fractions in myeloproliferative disorders with homozygous JAK2(V617F) in granulocytes

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7 January 2021

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Identification of an acquired JAK2 mutation in polycythemia vera

1 reference

https://api.crossref.org/works/10.1002%2FHON.800

7 January 2021

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Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders

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7 January 2021

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Detection of JAK2 V617F as a first intention diagnostic test for erythrocytosis.

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7 January 2021

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A sensitive high-throughput method to detect activating mutations of Jak2 in peripheral-blood samples

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7 January 2021

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Dynamics of chronic myeloid leukaemia.

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Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera

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Identifiers

10.1002/HON.800

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 June 2018

http://europepmc.org/abstract/MED/17006961

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