Found: 12
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Cytogenomic features of Richter transformation.
- Published in:
- Molecular Cytogenetics (17558166), 2023, v. 16, n. 1, p. 1, doi. 10.1186/s13039-023-00662-0
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- Article
Cryptic MYC insertions in Burkitt lymphoma: New data and a review of the literature.
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- PLoS ONE, 2022, v. 17, n. 2, p. 1, doi. 10.1371/journal.pone.0263980
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- Article
Changes in the levels of prenylquinones and tocopherols in Calendula officinalis during vegetation.
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- Physiologia Plantarum, 1985, v. 63, n. 4, p. 425, doi. 10.1111/j.1399-3054.1985.tb02321.x
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- Article
Long-term survival of a child with refractory anaplastic large cell lymphoma following therapy with an antisense oligonucleotide, topotecan, and vinblastine.
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- Hematological Oncology, 2015, v. 33, n. 1, p. 52, doi. 10.1002/hon.1006
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- Article
A novel IGH@ gene rearrangement associated with CDKN2A/B deletion in young adult B-cell acute lymphoblastic leukemia.
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- Oncology Letters, 2016, v. 11, n. 3, p. 2117, doi. 10.3892/ol.2016.4169
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- Article
Predictive role of NKCD56<sup>bright</sup> cells in monitoring the progression of chronic lymphocytic leukemia during treatment.
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- Folia Histochemica et Cytobiologica, 2022, v. 60, n. 3, p. 203, doi. 10.5603/FHC.a2022.0023
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- Article
Spontaneously immortalized human T lymphocytes develop gain of chromosomal region 2p13–24 as an early and common genetic event.
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- Genes, Chromosomes & Cancer, 2004, v. 41, n. 2, p. 133, doi. 10.1002/gcc.20059
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- Article
Cytogenetic and Flow Cytometry Evaluation of Richter Syndrome Reveals MYC, CDKN2A, IGH Alterations With Loss of CD52, CD62L and Increase of CD71 Antigen Expression as the Most Frequent Recurrent Abnormalities.
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- American Journal of Clinical Pathology, 2015, v. 143, n. 1, p. 25, doi. 10.1309/AJCPATRQWANW2O3N
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- Article
Triple hit lymphoma z dodatkową ekspresją cykliny D1 ― cytogenetyczny opis przypadku.
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- Acta Haematologica Polonica, 2022, v. 53, n. A, p. 56
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- Article
Triple hit lymphoma z nietypową translokacją t(3;8)(q27;q24) z rearanżacją genów BCL6 i MYC ― cytogenetyczny opis przypadku.
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- Acta Haematologica Polonica, 2022, v. 53, n. A, p. 57
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- Article
Monoallelic and biallelic deletions of 13q14 in a group of CLL/SLL patients investigated by CGH Haematological Cancer and SNP array (8×60K).
- Published in:
- Molecular Cytogenetics (17558166), 2016, v. 9, p. 1, doi. 10.1186/s13039-015-0212-x
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- Article
A rare complex variant translocation t(9;22;6;17;1) in chronic myeloid leukemia: case report.
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- Nowotwory, 2020, v. 70, n. 5, p. 206, doi. 10.5603/NJO.2020.0041
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- Article