Meyer C - Search Results

1

Genomic DNA-based measurable residual disease monitoring in pediatric acute myeloid leukemia: unselected consecutive cohort study.

Zaliova M, Zuna J, Winkowska L, Janotova I, Skorepova J, Lukes J, Meyer C, Marschalek R, Novak Z, Domansky J, Stary J, Sramkova L, Trka J. Zaliova M, et al. Among authors: meyer c. Leukemia. 2024 Jan;38(1):21-30. doi: 10.1038/s41375-023-02083-9. Epub 2023 Nov 24. Leukemia. 2024. PMID: 38001170 Free PMC article.

2

Diagnostic tool for the identification of MLL rearrangements including unknown partner genes.

Meyer C, Schneider B, Reichel M, Angermueller S, Strehl S, Schnittger S, Schoch C, Jansen MW, van Dongen JJ, Pieters R, Haas OA, Dingermann T, Klingebiel T, Marschalek R. Meyer C, et al. Proc Natl Acad Sci U S A. 2005 Jan 11;102(2):449-54. doi: 10.1073/pnas.0406994102. Epub 2004 Dec 30. Proc Natl Acad Sci U S A. 2005. PMID: 15626757 Free PMC article.

3

Prenatal origin of childhood AML occurs less frequently than in childhood ALL.

Burjanivova T, Madzo J, Muzikova K, Meyer C, Schneider B, Votava F, Marschalek R, Stary J, Trka J, Zuna J. Burjanivova T, et al. Among authors: meyer c. BMC Cancer. 2006 Apr 21;6:100. doi: 10.1186/1471-2407-6-100. BMC Cancer. 2006. PMID: 16630339 Free PMC article.

4

Genomic DNA of leukemic patients: target for clinical diagnosis of MLL rearrangements.

Meyer C, Kowarz E, Schneider B, Oehm C, Klingebiel T, Dingermann T, Marschalek R. Meyer C, et al. Biotechnol J. 2006 Jun;1(6):656-63. doi: 10.1002/biot.200600037. Biotechnol J. 2006. PMID: 16892314

5

A MLL-KIAA0284 fusion gene in a patient with secondary acute myeloid leukemia and t(11;14)(q23;q32).

Burmeister T, Meyer C, Thiel G, Reinhardt R, Thiel E, Marschalek R. Burmeister T, et al. Among authors: meyer c. Blood Cells Mol Dis. 2008 Sep-Oct;41(2):210-4. doi: 10.1016/j.bcmd.2008.05.005. Epub 2008 Jul 18. Blood Cells Mol Dis. 2008. PMID: 18640063

6

Covert preleukemia driven by MLL gene fusion.

Zuna J, Burjanivova T, Mejstrikova E, Zemanova Z, Muzikova K, Meyer C, Horsley SW, Kearney L, Colman S, Ptoszkova H, Marschalek R, Hrusak O, Stary J, Greaves M, Trka J. Zuna J, et al. Among authors: meyer c. Genes Chromosomes Cancer. 2009 Jan;48(1):98-107. doi: 10.1002/gcc.20622. Genes Chromosomes Cancer. 2009. PMID: 18932267

7

An interstitial deletion at 3p21.3 results in the genetic fusion of MLH1 and ITGA9 in a Lynch syndrome family.

Meyer C, Brieger A, Plotz G, Weber N, Passmann S, Dingermann T, Zeuzem S, Trojan J, Marschalek R. Meyer C, et al. Clin Cancer Res. 2009 Feb 1;15(3):762-9. doi: 10.1158/1078-0432.CCR-08-1908. Clin Cancer Res. 2009. PMID: 19188145

8

LDI-PCR: identification of known and unknown gene fusions of the human MLL gene.

Meyer C, Marschalek R. Meyer C, et al. Methods Mol Biol. 2009;538:71-83. doi: 10.1007/978-1-59745-418-6_5. Methods Mol Biol. 2009. PMID: 19277576

9

Infant acute bilineal leukemia.

Derwich K, Sedek L, Meyer C, Pieczonka A, Dawidowska M, Gaworczyk A, Wachowiak J, Konatkowska B, Witt M, Marschalek R, Szczepański T. Derwich K, et al. Among authors: meyer c. Leuk Res. 2009 Jul;33(7):1005-8. doi: 10.1016/j.leukres.2009.02.007. Epub 2009 Mar 16. Leuk Res. 2009. PMID: 19286255

10

Nebulette is the second member of the nebulin family fused to the MLL gene in infant leukemia.

Cóser VM, Meyer C, Basegio R, Menezes J, Marschalek R, Pombo-de-Oliveira MS. Cóser VM, et al. Among authors: meyer c. Cancer Genet Cytogenet. 2010 Apr 15;198(2):151-4. doi: 10.1016/j.cancergencyto.2009.12.013. Cancer Genet Cytogenet. 2010. PMID: 20362230 Free article.

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