Detection of CALR Mutation in Clonal and Nonclonal Hematologic Diseases Using Fragment Analysis and Next-Generation Sequencing

JA Gardner, JD Peterson, SA Turner… - American journal of …, 2016 - academic.oup.com
Objectives: To describe three methods used to screen for frameshift mutations in exon 9 of
the CALR gene. Methods: Genomic DNA from 47 patients was extracted from peripheral …

[HTML][HTML] A novel assay to detect calreticulin mutations in myeloproliferative neoplasms

V Rosso, J Petiti, E Bracco, R Pedrola, F Carnuccio… - Oncotarget, 2017 - ncbi.nlm.nih.gov
The myeloproliferative neoplasms are chronic myeloid cancers divided in Philadelphia
positive (Ph+), chronic myeloid leukemia, or negative: polycythemia vera (PV) essential …

[HTML][HTML] Germline JAK2 L611S mutation in a child with thrombocytosis

B Aral, M Courtois, S Ragot, V Bourgeois… - …, 2018 - ncbi.nlm.nih.gov
AB hematopoietic progenitors is theoretically associated with a risk (though possibly low) of
disease progression, underscoring the need for regular follow up. Consequently, a frequent …

Cytokine pathway variants modulate platelet production: IFNA16 is a thrombocytosis susceptibility locus in humans

DV Gnatenko, Z Liu, P Hearing, SY Sohn, Y Hu… - Blood …, 2022 - ashpublications.org
Inflammatory stimuli have divergent effects on peripheral platelet counts, although the
mechanisms of thrombocytopenic and thrombocytotic responses remain poorly understood …

Rapid, low cost and sensitive detection of Calreticulin mutations by a PCR based amplicon length differentiation assay for diagnosis of myeloproliferative neoplasms

NT Trung, DT Quyen, NX Hoan, DP Giang… - BMC Medical …, 2019 - Springer
Background Calreticulin (CALR) gene mutations are currently recommended as biomarkers
in diagnosis of patients with myeloproliferative neoplasms (MPN) with Jak2 V617F negative …

Progenitor genotyping reveals a complex clonal architecture in a subset of CALR‐mutated myeloproliferative neoplasms

S Martin, CM Wright, LM Scott - British Journal of Haematology, 2017 - Wiley Online Library
The identification of acquired CALR mutations in patients with essential thrombocythaemia
(ET) or myelofibrosis (MF) has meant that disease‐initiating mutations can now be detected …

[PDF][PDF] CALR and CD47: An insight into their roles in the disease progression of MDS and MPN

K Boasman, M Simmonds, C Rinaldi - Journal of Blood Disorders & …, 2018 - core.ac.uk
Myelodysplastic syndrome and myeloproliferative neoplasms are clonal myeloid disorders
arising from haematopoietic stem cells that have the tendency to progress into acute myeloid …

Calreticulin mutation analysis in non-mutated Janus kinase 2 essential thrombocythemia patients in Chiang Mai University: analysis of three methods and clinical …

E Rattarittamrong, A Tantiworawit, N Kumpunya… - …, 2018 - Taylor & Francis
Objectives: The primary objective was to determine the prevalence of calreticulin (CALR)
mutation in patients with non-JAK2 V617F mutated essential thrombocythemia (ET). The …

Polymerase chain reaction-restriction fragment length polymorphism method for detection of Calreticulin type-1 and type-2 mutations in myeloproliferative neoplasm

S Naseem, J Binota, N Varma, P Satyarthi… - Journal of …, 2021 - Springer
Calreticulin (CALR) mutations are included in the WHO diagnostic criteria of
Myeloproliferative Neoplasm (MPN). Presence of CALR mutation, aids in their diagnosis by …

Capricious CALR mutated clones in myeloproliferative neoplasms.

K Haslam, E Conneally… - Blood Cells, Molecules & …, 2016 - europepmc.org
Capricious CALR mutated clones in myeloproliferative neoplasms. - Abstract - Europe PMC
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