Detection of mutations inJAK2exons 12-15 by Sanger sequencing-Reference-Cited by-同舟云学术

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Detection of mutations inJAK2exons 12-15 by Sanger sequencing

Published:2015-09-11 Issue:1 Volume:38 Page:34-41
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int. Jnl. Lab. Hem.

Author:

Alghasham N.¹,Alnouri Y.²,Abalkhail H.³,Khalil S.³

Affiliation:

1. Pathology Department; College of Medicine; Qassim University; Buraidah Saudi Arabia

2. Regional Lab and Blood Bank; King Saud Medical City; Riyadh Saudi Arabia

3. Department of Pathology and Laboratory Medicine; King Faisal Specialist Hospital and Research Centre; Riyadh Saudi Arabia

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Reference39 articles.

1. Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis;Levine;Cancer Cell,2005

2. A gain-of-function mutation of JAK2 in myeloproliferative disorders;Kralovics;N Engl J Med,2005

3. A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera;James;Nature,2005

4. Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders;Baxter;Lancet,2005

5. JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosis;Scott;N Engl J Med,2007

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Detection of the JAK2V617F in Phildelphia-negative Myeloproliferative Neoplasms patients: Comparison of the PCR-RFLP and Nucleotide sequencing;2023-12-05

2. Molecular landscape of the JAK2 gene in chronic myeloproliferative neoplasm patients from the state of Amazonas, Brazil;Biomedical Reports;2023-10-23

3. Screening of V617F mutation in JAK2 gene with acute myeloid leukemia in the Saudi population;Acta Biochimica Polonica;2022-02-21

4. Analysis of genetic variants in myeloproliferative neoplasms using a 22-gene next-generation sequencing panel;BMC Medical Genomics;2022-01-15

5. A novel mutation in the JAK2 gene (R588S) in a Chinese patient with erythrocytosis;Annals of Hematology;2020-07-31

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