D. Mühlematter

发表

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).

G. van Melle, C. Castagné, D. Mühlematter, 1997, Cancer genetics and cytogenetics.

A novel BCR‐ABL transcript e2a2 in a chronic myelogenous leukaemia patient with a duplicated Ph‐chromosome and monosomy 7

A. Tobler, D. Mühlematter, E. O. Leibundgut, 1999, British journal of haematology.

t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders

T. Mazza, M. Carella, C. L. Cunsolo, 2015, Molecular Cancer.

RT-PCR diagnosis of patients with acute nonlymphocytic leukemia and inv(16)(p13q22) and identification of new alternative splicing in CBFB-MYH11 transcripts.

A. Hagemeijer, B. V. D. Reijden, R. Giles, 1995, Blood.

MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene.

M. Rocchi, B. Johansson, A. Hagemeijer, 2006, Human molecular genetics.

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?

G. van Melle, C. Castagné, D. Mühlematter, 2003, Cancer genetics and cytogenetics.

Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome.

D. Mühlematter, M. Jotterand Bellomo, P. Beris, 1992, Cancer genetics and cytogenetics.

A high-resolution allelotype of B-cell chronic lymphocytic leukemia (B-CLL).

Rolf Jaggi, Jörg Hager, Andreas Tobler, 2002, Blood.

Poly(ADP.Ribosyl)ation of Nuclear Proteins by Oxidant Tumor Promoters

P. Cerutti, G. Krupitza, D. Mühlematter, 1989 .

Two clonal occurrences of tetrasomy 21 in an atypical chronic myeloid leukemia with wild-type RUNX1 alleles. Additional support for a gene dosage effect of chromosome 21 or RUNX1 in leukemia.

A. Tobler, H. Scott, D. Mühlematter, 2004, Haematologica.

Short-term culture of spleen lymphocytes for chromosome analysis of small rodents

M. Nabholz, D. Mühlematter, M. Jotterand Bellomo, 1990, Genetica.

Combination of broad molecular screening and cytogenetic analysis for genetic risk assignment and diagnosis in patients with acute leukemia

A. Gratwohl, A. Tichelli, T. Kühne, 2006, Leukemia.

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.

A. Hagemeijer, G. van Melle, A. Tobler, 2004, Cancer genetics and cytogenetics.

Genomic acute myeloid leukemia-associated inv(16)(p13q22) breakpoints are tightly clustered

C. Wijmenga, A. Hagemeijer, J. Gabert, 1999, Oncogene.

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.

G. van Melle, A. Tobler, M. Gregor, 2005, Cancer genetics and cytogenetics.

Detection of 16 p deletions by FISH in patients with inv(16) or t(16;16) and acute myeloid leukemia (AML)

D. Martinet, D. Mühlematter, J. Gmür, 1997, Leukemia.

Tetrasomy 8 in a patient with acute nonlymphocytic leukemia: a metaphase and interphase study with fluorescence in situ hybridization.

C. Castagné, D. Mühlematter, P. Schmidt, 1996, Cancer genetics and cytogenetics.

Effect of conditioned medium, nutritive elements and mitotic synchronization on the accuracy of the cytogenetic analysis in patients with chronic myeloid leukemia at diagnosis and during alpha-interferon therapy.

D. Martinet, C. Castagné, D. Mühlematter, 1999, Cancer genetics and cytogenetics.

[Fluorescent in-situ hybridization technique (FISH) in the diagnosis of Philadelphia translocation in chronic myeloid leukemia].

D. Martinet, D. Mühlematter, M. Jotterand Bellomo, 1996, Schweizerische medizinische Wochenschrift.

t(8;9)(p11;q32) IN ATYPICAL CHRONIC MYELOID LEUKAEMIA: A NEW CYTOGENETTC‐CLINICOPATHOLOGIC ASSOCIATION?

D. Mühlematter, P. Schmidt, M. J. Bellomo, 1992, British journal of haematology.

A non-random chromosome abnormality found in precursor-B lineage acute lymphoblastic leukaemia: dic(9;20)(p1?3;q11).

A. Hagemeijer, A. Veerman, J. Harbott, 1995, Leukemia.

Simple method for detection of MYH11 DNA rearrangements in patients with inv(16)(p13q22) and acute myeloid leukemia.

A. Hagemeijer, J. Reiffers, M. Breuning, 1996, Leukemia.

Case study of intracerebral plasmacytoma as an initial presentation of multiple myeloma.

K. Zaman, D. Mühlematter, M. Betz, 2007, Neuro-oncology.

t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders

T. Mazza, M. Carella, C. L. Cunsolo, 2015, Molecular Cancer.

Frequent clonal loss of heterozygosity but scarcity of microsatellite instability at chromosomal breakpoint cluster regions in adult leukemias.

M. Fey, A. Tobler, J. Schwaller, 1996, Blood.

Upregulation of MEL1 and FLJ42875 genes by position effect resulting from a t(1;2)(p36;p21) occurring during evolution of chronic myelomonocytic leukemia.

C. Storlazzi, F. Albano, W. Wuillemin, 2008, Blood Cells, Molecules & Diseases.

Broad molecular screening of an unclassifiable myeloproliferative disorder reveals an unexpected ETV6/ABL1 fusion transcript

A. Gratwohl, A. Tichelli, A. Chase, 2005, Leukemia.

Dicentric translocation (9;12) presenting as refractory Philadelphia chromosome-positive acute B-cell lymphoblastic leukemia.

A. Tichelli, M. Bargetzi, D. Mühlematter, 1999, Cancer genetics and cytogenetics.

Frequent clonal loss of heterozygosity but scarcity of microsatellite instability at chromosomal breakpoint cluster regions in adult leukemias

M. Fey, A. Tobler, A. Tichelli, 1996 .

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.

J. Beckmann, G. van Melle, Sarah Porter, 2008, Cancer genetics and cytogenetics.