Next generation sequencing in MPNs. Lessons from the past and prospects for use as predictors of prognosis and treatment responses

V Skov - Cancers, 2020 - mdpi.com
The myeloproliferative neoplasms (MPNs) are acquired hematological stem cell neoplasms
characterized by driver mutations in JAK2, CALR, or MPL. Additive mutations may appear in …

Molecular diagnostics of myeloproliferative neoplasms

SE Langabeer, H Andrikovics, J Asp… - European Journal of …, 2015 - Wiley Online Library
Since the discovery of the JAK 2 V617F mutation in the majority of the myeloproliferative
neoplasms (MPN) of polycythemia vera, essential thrombocythemia and primary …

Clonal evolution and clinical correlates of somatic mutations in myeloproliferative neoplasms

P Lundberg, A Karow, R Nienhold… - Blood, The Journal …, 2014 - ashpublications.org
Myeloproliferative neoplasms (MPNs) are a group of clonal disorders characterized by
aberrant hematopoietic proliferation and an increased tendency toward leukemic …

Correlation of mutation profile and response in patients with myelofibrosis treated with ruxolitinib

KP Patel, KJ Newberry, R Luthra… - Blood, The Journal …, 2015 - ashpublications.org
Although most patients with myelofibrosis (MF) derive benefit from ruxolitinib, some are
refractory, have a suboptimal response, or quickly lose their response. To identify genes that …

Prognostic impact of RAS-pathway mutations in patients with myelofibrosis

FPS Santos, B Getta, L Masarova, C Famulare… - Leukemia, 2020 - nature.com
RAS-pathway mutations are recurrent events in myeloid malignancies. However, there is
limited data on the significance of RAS-pathway mutations in patients with myelofibrosis …

Targeted next-generation sequencing identifies a subset of idiopathic hypereosinophilic syndrome with features similar to chronic eosinophilic leukemia, not otherwise …

SA Wang, W Tam, AG Tsai, DA Arber… - Modern …, 2016 - nature.com
The distinction between chronic eosinophilic leukemia, not otherwise specified and
idiopathic hypereosinophilic syndrome largely relies on clonality assessment. Prior to the …

[HTML][HTML] Clinical significance of DNA variants in chronic myeloid neoplasms: a report of the Association for Molecular Pathology

RF McClure, MD Ewalt, J Crow… - The Journal of Molecular …, 2018 - Elsevier
To address the clinical relevance of small DNA variants in chronic myeloid neoplasms
(CMNs), an Association for Molecular Pathology Working Group comprehensively reviewed …

Application of an NGS‐based 28‐gene panel in myeloproliferative neoplasms reveals distinct mutation patterns in essential thrombocythaemia, primary myelofibrosis …

S Delic, D Rose, W Kern, N Nadarajah… - British journal of …, 2016 - Wiley Online Library
Molecular routine diagnostics for BCR‐ABL 1‐negative myeloproliferative neoplasms (MPN)
currently focusses on mutations in JAK 2, CALR and MPL. In recent years, recurrent …

[HTML][HTML] New concepts on BARD1: Regulator of BRCA pathways and beyond

I Irminger-Finger, M Ratajska, M Pilyugin - The international journal of …, 2016 - Elsevier
For nearly two decades most research on BARD1 was closely linked to research on BRCA1,
the breast cancer predisposition gene. The co-expression of BARD1 and BRCA1 genes in …

[HTML][HTML] ASXL1 mutation in clonal hematopoiesis

T Fujino, T Kitamura - Experimental Hematology, 2020 - Elsevier
Recent advances in DNA sequencing technologies have enhanced our knowledge about
several diseases. Coupled with easy accessibility to blood samples, hematology plays a …