Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

31 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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
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.
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
Determination of cutoff values to detect small aneuploid clones by interphase fluorescence in situ hybridization: the Poisson model is a more appropriate approach. Should single-cell trisomy 8 be considered a clonal defect?
Castagné C, Mühlematter D, Beyer V, Parlier V, van Melle G, Jotterand M. Castagné C, et al. Among authors: muhlematter d. Cancer Genet Cytogenet. 2003 Dec;147(2):99-109. doi: 10.1016/s0165-4608(03)00189-4. Cancer Genet Cytogenet. 2003. PMID: 14623458
Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia.
van der Reijden BA, Martinet D, Dauwerse JG, Giles RH, Wessels JW, Beverstock GC, Smit B, Mühlematter D, Jotterand Bellomo M, Gabert J, Lafage-Pochitaloff M, Reiffers J, Bilhou-Nabera C, van Ommen GJ, Hagemeijer A, Breuning MH. van der Reijden BA, et al. Among authors: muhlematter d. Leukemia. 1996 Sep;10(9):1459-62. Leukemia. 1996. PMID: 8751463
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.
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
Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered.
van der Reijden BA, Dauwerse HG, Giles RH, Jagmohan-Changur S, Wijmenga C, Liu PP, Smit B, Wessels HW, Beverstock GC, Jotterand-Bellomo M, Martinet D, Mühlematter D, Lafage-Pochitaloff M, Gabert J, Reiffers J, Bilhou-Nabera C, van Ommen GJ, Hagemeijer A, Breuning MH. van der Reijden BA, et al. Among authors: muhlematter d. Oncogene. 1999 Jan 14;18(2):543-50. doi: 10.1038/sj.onc.1202321. Oncogene. 1999. PMID: 9927211
G-CSF-induced remission in two cases of acute myeloid leukemia.
Benz R, Goede JS, Parlier V, Mühlematter D, Jotterand M, Fehr J. Benz R, et al. Among authors: muhlematter d. Leuk Res. 2008 Jul;32(7):1148-52. doi: 10.1016/j.leukres.2007.11.020. Epub 2007 Dec 31. Leuk Res. 2008. PMID: 18166225
31 results