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t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders.
L'Abbate A, Tolomeo D, De Astis F, Lonoce A, Lo Cunsolo C, Mühlematter D, Schoumans J, Vandenberghe P, Van Hoof A, Palumbo O, Carella M, Mazza T, Storlazzi CT. L'Abbate A, et al. Among authors: muhlematter d. Mol Cancer. 2015 Dec 16;14:211. doi: 10.1186/s12943-015-0484-0. Mol Cancer. 2015. PMID: 26671595 Free PMC article.
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene.
Storlazzi CT, Fioretos T, Surace C, Lonoce A, Mastrorilli A, Strömbeck B, D'Addabbo P, Iacovelli F, Minervini C, Aventin A, Dastugue N, Fonatsch C, Hagemeijer A, Jotterand M, Mühlematter D, Lafage-Pochitaloff M, Nguyen-Khac F, Schoch C, Slovak ML, Smith A, Solè F, Van Roy N, Johansson B, Rocchi M. Storlazzi CT, et al. Among authors: muhlematter d. Hum Mol Genet. 2006 Mar 15;15(6):933-42. doi: 10.1093/hmg/ddl010. Epub 2006 Feb 1. Hum Mol Genet. 2006. PMID: 16452126
Polysomy 8 defines a clinico-cytogenetic entity representing a subset of myeloid hematologic malignancies associated with a poor prognosis: report on a cohort of 12 patients and review of 105 published cases.
Beyer V, Mühlematter D, Parlier V, Cabrol C, Bougeon-Mamin S, Solenthaler M, Tobler A, Pugin P, Gregor M, Hitz F, Hess U, Chapuis B, Laurencet F, Schanz U, Schmidt PM, van Melle G, Jotterand M. Beyer V, et al. Among authors: muhlematter d. Cancer Genet Cytogenet. 2005 Jul 15;160(2):97-119. doi: 10.1016/j.cancergencyto.2004.12.003. Cancer Genet Cytogenet. 2005. PMID: 15993266 Review.
Systematic screening at diagnosis of -5/del(5)(q31), -7, or chromosome 8 aneuploidy by interphase fluorescence in situ hybridization in 110 acute myelocytic leukemia and high-risk myelodysplastic syndrome patients: concordances and discrepancies with conventional cytogenetics.
Beyer V, Castagné C, Mühlematter D, Parlier V, Gmür J, Hess U, Kovacsovics T, Meyer-Monard S, Tichelli A, Tobler A, Jacky E, Schanz U, Bargetzi M, Hagemeijer A, de Witte T, van Melle G, Jotterand M. Beyer V, et al. Among authors: muhlematter d. Cancer Genet Cytogenet. 2004 Jul 1;152(1):29-41. doi: 10.1016/j.cancergencyto.2003.10.005. Cancer Genet Cytogenet. 2004. PMID: 15193439
Effect of conditioned media, nutritive elements, and mitotic synchronization on the accuracy of the cytogenetic analysis in acute nonlymphocytic leukemia patients presenting with inv(16)/t(16;16) or t(15;17).
Castagné C, Mühlematter D, van Melle G, Gachoud V, Jotterand Bellomo M. Castagné C, et al. Among authors: muhlematter d. Cancer Genet Cytogenet. 1997 Apr;94(2):106-12. doi: 10.1016/s0165-4608(96)00209-9. Cancer Genet Cytogenet. 1997. PMID: 9109938
Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia.
Storlazzi CT, Albano F, Guastadisegni MC, Impera L, Mühlematter D, Meyer-Monard S, Wuillemin W, Rocchi M, Jotterand M. Storlazzi CT, et al. Among authors: muhlematter d. Blood Cells Mol Dis. 2008 May-Jun;40(3):452-5. doi: 10.1016/j.bcmd.2007.11.004. Epub 2008 Feb 21. Blood Cells Mol Dis. 2008. PMID: 18178491 No abstract available.
Automated four-color interphase fluorescence in situ hybridization approach for the simultaneous detection of specific aneuploidies of diagnostic and prognostic significance in high hyperdiploid acute lymphoblastic leukemia.
Blandin AT, Mühlematter D, Bougeon S, Gogniat C, Porter S, Beyer V, Parlier V, Beckmann JS, van Melle G, Jotterand M. Blandin AT, et al. Among authors: muhlematter d. Cancer Genet Cytogenet. 2008 Oct 15;186(2):69-77. doi: 10.1016/j.cancergencyto.2008.06.008. Cancer Genet Cytogenet. 2008. PMID: 18940469
31 results