Literature DB >> 19269737

Janus kinase 2 mutations in Philadelphia negative chronic myeloproliferative disorders: clinical implications.

Anna D Panani1.   

Abstract

The chronic myeloproliferative disorders (CMPD) are a group of clinically related diseases characterized by clonal hematopoiesis with increased proliferation of one or more myeloid cell lineages. The identification of JAK2 mutations (JAK2V617F and JAK2 exon 12) in patients with CMPD is of great significance in the understanding of the molecular mechanisms underlined the pathogenesis of the disease contributing also to clinical management of patients. However, the precise pathogenetic contribution of JAK2 mutation is far from being fully elucidated and it is currently under intense investigation. Testing of JAK2 mutations has made the diagnosis of CMPD more precise than ever before, while genotype-phenotype associations have been identified. Furthermore, the discovery of JAK2 mutations facilitated the development of new targeted therapies and clinical trials are currently ongoing.

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Year:  2009        PMID: 19269737     DOI: 10.1016/j.canlet.2009.02.010

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  4 in total

1.  Detection of JAK2 V617F mutation increases the diagnosis of myeloproliferative neoplasms.

Authors:  Shu-Peng Zhang; Hui Li; Ren-Sheng Lai
Journal:  Oncol Lett       Date:  2014-12-12       Impact factor: 2.967

2.  Molecular analysis of V617F mutation in Janus kinase 2 gene of breast cancer patients.

Authors:  Sajjad Karim; Imran Riaz Malik; Quratulain Nazeer; Ahmad Zaheer; Muhammad Farooq; Nasir Mahmood; Arif Malik; Muhammad Asif; Asim Mehmood; Abdul Rehman Khan; Abdul Jabbar; Muhammad Arshad; Qudsia Yousafi; Abrar Hussain; Zeenat Mirza; Muhammad Atif Iqbal; Mahmood Rasool
Journal:  Saudi J Biol Sci       Date:  2019-08-02       Impact factor: 4.219

3.  Molecular approach to diagnose BCR/ABL negative chronic myeloproliferative neoplasms.

Authors:  Michelle Maccarini Barcelos; Maria Cláudia Santos-Silva
Journal:  Rev Bras Hematol Hemoter       Date:  2011

4.  Low frequency of c-MPL gene mutations in Iranian patients with Philadelphia-negative myeloproliferative disorders.

Authors:  A Ghotaslou; F Nadali; B Chahardouli; N Alizad Ghandforosh; S H Rostami; K Alimoghaddam; A Ghavamzadeh
Journal:  Iran J Ped Hematol Oncol       Date:  2015-03-15
  4 in total

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