Results 1 to 10 of about 577,308 (213)

JAK2-V617F mutation in patients with myeloproliferative neoplasms: Association with FLT3-ITD mutation [PDF]

open access: yesSrpski Arhiv za Celokupno Lekarstvo, 2010
Introduction. An acquired somatic mutation V617F in Janus kinase 2 gene (JAK2) is the cause of uncontrolled proliferation in patients with myeloproliferative neoplasms.
Čolović Milica   +4 more
doaj   +2 more sources

Determination of the JAK2 V617F mutation in thrombosis patients

open access: yesJournal of Associated Medical Sciences, 2023
Background: Janus kinase 2 (JAK2) gene mutation causes uncontrolled myeloproliferation independent of cytokines and abnormal formation of the endogenous erythroid colony.
Sutada Magmuang   +7 more
doaj   +2 more sources

CRISPR/Cas12a-Based Ultrasensitive and Rapid Detection of JAK2 V617F Somatic Mutation in Myeloproliferative Neoplasms

open access: yesBiosensors, 2021
The JAK2 V617F mutation is a major diagnostic, therapeutic, and monitoring molecular target of Philadelphia-negative myeloproliferative neoplasms (MPNs).
Miaomiao Chen   +7 more
doaj   +2 more sources

Clinical characteristics of a patient with de novo acute promyelocytic leukemia with JAK2 v617f mutation

open access: yesHematology, 2022
Background: The V617F mutation of Janus-associated kinase 2 (JAK2) is common in myeloproliferative neoplasms (MPN). JAK2 V617F mutation can be detected in patients with de novo acute myeloid leukemia (AML), but de novo acute promyelocytic leukemia (APL ...
Yi-zhi Jiang   +8 more
doaj   +1 more source

Impact of JAK2 V617F mutation on hemogram variation in patients with non-reactive elevated platelet counts. [PDF]

open access: yesPLoS ONE, 2013
BACKGROUND: Non-reactive platelet counts elevation occurs mainly in myeloproliferative disorders (MPDs), which have been reported to be closely associated with JAK2 V617F mutation.
Juan Zhou   +9 more
doaj   +1 more source

DIAGNOSTIC VALUE OF JAK2 V617F MUTATIONAL SCREENING IN PATIENTS WITH BUDD-CHIARI SYNDROME [PDF]

open access: yesAin Shams Medical Journal, 2019
Background: The diagnosis of underlying myeloproliferative neoplasms (MPNs) is often problematic in patients with Budd Chiari syndrome (BCS). A clonal mutation in JAK2 tyrosine kinase (JAK2V617F) occurs in a high proportion of patients with MPNs and is ...
Esraa A   +3 more
doaj   +1 more source

Clinical and laboratory relevance of JAK2 V617F and BCR-ABL co-existence in Philadelphia positive CML patients

open access: yesPakistan Journal of Pharmaceutical Sciences, 2021
Chronic Myeloid Leukaemia (CML) is characterized by BCR-ABL1 mutation. A number of research studies have published reports of concomitant JAK2-V617F mutation in BCR-ABL positive Chronic Myeloid Leukaemia.
Nasir Ahmad   +6 more
doaj   +1 more source

A Comparison of Bone Marrow Morphology and Peripheral Blood Findings in Low and High Level JAK2 V617F Allele Burden

open access: yesDiagnostics, 2023
Cases with low level JAK2 V617F mutations are increasingly detected; however, the clinical interpretation of the low allele JAK2 burden may be challenging.
Emina Babarović   +5 more
doaj   +1 more source

Frequency and characteristics of the V617F mutation in 23 cerebral venous sinus thrombosis patients with thrombocytosis

open access: yesJournal of International Medical Research, 2020
Objective To analyse the frequency and characteristics of the Janus kinase 2 ( JAK2) V617F mutation in patients with cerebral venous sinus thrombosis (CVST) with thrombocytosis.
Qiang Ma
doaj   +1 more source

Analysis of JAK2 V617F mutation in Tunisian patients with myeloproliferative neoplasms

open access: yesEuropean Journal of Inflammation, 2021
We aimed to investigate the prevalence of the JAK2 V617F mutation in Tunisian patients with myeloproliferative neoplasms (MPN) and to look for possible associations with diseases’ presentation. In this context, JAK2 V617F polymorphism was detected by PCR-
Soumaya Chadi   +7 more
doaj   +1 more source

Home - About - Disclaimer - Privacy