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Characterization of a cryptic rearrangement in a case of mantle cell lymphoma with negative FISH studies.
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An Uncommon Case of Double-Hit Mantle Cell Lymphoma That Demonstrates a Transformation Process.
Am J Clin Pathol. 2020 Jan 1;153(1):49-57. doi: 10.1093/ajcp/aqz133.
3
CD5-negative blastoid variant mantle cell lymphoma with complex CCND1/IGH and MYC aberrations.
Ann Lab Med. 2012 Jan;32(1):95-8. doi: 10.3343/alm.2012.32.1.95. Epub 2011 Dec 20.
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Molecular cytogenetic study of a mantle cell lymphoma with a complex translocation involving the CCND1 (11q13) region.
Cancer Genet Cytogenet. 2004 Oct 1;154(1):67-71. doi: 10.1016/j.cancergencyto.2004.02.002.
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Increased complexity of t(11;14) rearrangements in plasma cell neoplasms compared with mantle cell lymphoma.
Genes Chromosomes Cancer. 2021 Oct;60(10):678-686. doi: 10.1002/gcc.22977. Epub 2021 Jun 22.
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Mantle cell lymphoma with aberrant expression of CD10.
Histopathology. 2008 Jul;53(1):20-9. doi: 10.1111/j.1365-2559.2008.03060.x. Epub 2008 Jun 2.
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CCND1-IGH Fusion-Amplification and MYC Copy Number Gain in a Case of Pleomorphic Variant Mantle Cell Lymphoma.
Am J Clin Pathol. 2016 Dec;146(6):747-752. doi: 10.1093/ajcp/aqw194. Epub 2016 Dec 27.

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Case report: Identification of atypical mantle cell lymphoma with rearrangement by next-generation sequencing.
Front Oncol. 2023 Mar 29;13:1145376. doi: 10.3389/fonc.2023.1145376. eCollection 2023.
2
Mate Pair Sequencing: Next-Generation Sequencing for Structural Variant Detection.
Methods Mol Biol. 2023;2621:127-149. doi: 10.1007/978-1-0716-2950-5_9.
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Genomic profiling for clinical decision making in lymphoid neoplasms.
Blood. 2022 Nov 24;140(21):2193-2227. doi: 10.1182/blood.2022015854.
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The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms.
Leukemia. 2022 Jul;36(7):1720-1748. doi: 10.1038/s41375-022-01620-2. Epub 2022 Jun 22.
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Current Knowledge in Genetics, Molecular Diagnostic Tools, and Treatments for Mantle Cell Lymphomas.
Front Oncol. 2021 Nov 23;11:739441. doi: 10.3389/fonc.2021.739441. eCollection 2021.
6
Increased complexity of t(11;14) rearrangements in plasma cell neoplasms compared with mantle cell lymphoma.
Genes Chromosomes Cancer. 2021 Oct;60(10):678-686. doi: 10.1002/gcc.22977. Epub 2021 Jun 22.
7
The pathologic diagnosis of mantle cell lymphoma.
Histol Histopathol. 2021 Oct;36(10):1037-1051. doi: 10.14670/HH-18-351. Epub 2021 Jun 11.
8
Molecular Pathogenesis of Mantle Cell Lymphoma.
Hematol Oncol Clin North Am. 2020 Oct;34(5):795-807. doi: 10.1016/j.hoc.2020.05.002. Epub 2020 Jul 22.
10
Cryptic insertions of the immunoglobulin light chain enhancer region near in t(11;14)-negative mantle cell lymphoma.
Haematologica. 2020 Aug;105(8):e408-e411. doi: 10.3324/haematol.2019.237073. Epub 2019 Nov 21.

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and hijack immunoglobulin light-chain enhancers in cyclin D1 mantle cell lymphoma.
Blood. 2019 Feb 28;133(9):940-951. doi: 10.1182/blood-2018-07-862151. Epub 2018 Dec 11.
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SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq).
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Mantle cell lymphoma with a novel t(11;12)(q13;p11.2): a proposed alternative mechanism of CCND1 up-regulation.
Hum Pathol. 2017 Jun;64:207-212. doi: 10.1016/j.humpath.2017.01.001. Epub 2017 Jan 27.
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The molecular pathogenesis of mantle cell lymphoma.
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CCND1 mutations increase protein stability and promote ibrutinib resistance in mantle cell lymphoma.
Oncotarget. 2016 Nov 8;7(45):73558-73572. doi: 10.18632/oncotarget.12434.
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BIMA V3: an aligner customized for mate pair library sequencing.
Bioinformatics. 2014 Jun 1;30(11):1627-9. doi: 10.1093/bioinformatics/btu078. Epub 2014 Feb 12.
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Landscape of somatic mutations and clonal evolution in mantle cell lymphoma.
Proc Natl Acad Sci U S A. 2013 Nov 5;110(45):18250-5. doi: 10.1073/pnas.1314608110. Epub 2013 Oct 21.
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CCND2 rearrangements are the most frequent genetic events in cyclin D1(-) mantle cell lymphoma.
Blood. 2013 Feb 21;121(8):1394-402. doi: 10.1182/blood-2012-08-452284. Epub 2012 Dec 18.
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An assessment of the usefulness of immunohistochemical stains in the diagnosis of hairy cell leukemia.
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