Barbara Kantorova
Brno, JM 62500, Czech Republic
Last Updated: 09/26/2026
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Found 9 publications
Genetic Aetiology of Nonsyndromic Hearing Loss in Moravia-Silesia.
Journal: Medicina (Kaunas, Lithuania)
Published: March 28, 2018
Fragment analysis represents a suitable approach for the detection of hotspot c.7541_7542delCT NOTCH1 mutation in chronic lymphocytic leukemia.
Journal: Leukemia research
Published: April 04, 2017
Low-burden TP53 mutations in chronic phase of myeloproliferative neoplasms: association with age, hydroxyurea administration, disease type and JAK2 mutational status.
Journal: Leukemia
Published: November 30, 2016
Single cell analysis revealed a coexistence of NOTCH1 and TP53 mutations within the same cancer cells in chronic lymphocytic leukaemia patients.
Journal: British journal of haematology
Published: July 30, 2016
Decreased WNT3 expression in chronic lymphocytic leukaemia is a hallmark of disease progression and identifies patients with worse prognosis in the subgroup with mutated IGHV.
Journal: British journal of haematology
Published: April 06, 2016
Molecular Prognostic Markers and Their Clinical Relevance in Chronic Lymphocytic Leukemia
Journal: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti
Published: October 23, 2015
TP53 mutation analysis in chronic lymphocytic leukemia: comparison of different detection methods.
Journal: Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine
Published: August 13, 2014
Recurrent mutations refine prognosis in chronic lymphocytic leukemia.
Journal: Leukemia
Published: April 09, 2014
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Last Updated: 09/26/2026