Publikationen 2007

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Dürig J, Bug S, Klein-Hitpass L, Boes T, Jöns T, Martín-Subero J, Harder L, Baudis M, Dührsen U, Siebert R: Combined SNP-based genomic mapping and global gene expresssion profiling identifies novel chromosomal imbalances, mechanisms and candidate genes important in the pathogenesis of T-PLL with inv(14)(q11q32). Leukemia 21:2153-2163 (2007).

Nebral K, König M, Harder L, Siebert R, Haas O, Strehl S: Identification of PML as novel PAX5 fusion partner in childhood acute lymphoblastic leukemia. Br J Haematol 139:269-274 (2007).

Starczynowski DT, Trautmann H, Pott C, Harder L, Arnold N, Africa JA, Leeman JR, Siebert R, Gilmore TD: Mutation of an IKK phosphorylation site within the transactivation domain of REL in two patients with human B-cell lymphoma enhances REL´s in vitro transforming activity. Oncogene 26:2685-2694 (2007).

Martín-Subero JI, Gesk S, Calasanz MJ, Harder L, Siebert R: Present and future of cytogenetic diagnostics in lymphomas. Haematologica 92 (Extra 1):151-155 (2007).

Fickelscher I, Liehr T, Watts K, Bryant V, Barber JCK, Heidemann S, Siebert R, Hertz JM, Tümer Z, Thomas NS: The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneity. Am J Hum Genet 81:847-856 (2007).

Martin-Subero JI, Ibbotson R, Klapper W, Michaux L, Callet-Bauchu E, Berger F, Calasanz MJ, De Wolf-Peeters C, Dyer MJ, Felman P, Gardiner A, Gascoyne RD, Gesk S, Harder L, Horsman DE, Kneba M, Kuppers R, Majid A, Parry-Jones N, Ritgen M, Salido M, Sole F, Thiel G, Wacker HH, Oscier D, Wlodarska I, Siebert R: A comprehensive genetic and histopathologic analysis identifies two subgroups of B-cell malignancies carrying a t(14;19)(q32;q13) or variant BCL3-translocation. Leukemia 21:1532-1544 (2007).

Metzke-Heidemann S, Harder L, Gesk S, Grimm W, Siebert R: The short arm of chromosome 18 is a recurrent integration site of a supernumerary BCR/ABL gene fusion in chronic myeloid leukemia. Cancer Genet Cytogen 179:156-158 (2007).

Sellmann L, Gesk S, Walter C, Ritgen M, Harder L, Martın-Subero JI, Schroers R, Siemer D, Nückel H, Dyer MJS, Dührsen U, Siebert R, Dürig J, Küppers R: Trisomy 19 is associated with trisomy 12 and mutated IGHV genes in B-chronic lymphocytic leukaemia. Br J Haematol 138:217–220 (2007).

Weniger MA, Gesk S, Ehrlich S, Martin-Subero JI, Dyer MJS, Siebert R, Möller P, Barth TFE: Gains of REL in primary mediastinal B-cell lymphoma coincide with nuclear accumulation of REL protein. Genes Chrom Cancer 46:406-415 (2007).

Grebe S, Ichida F, Grabitz R, Bültmann B, Heidemann S, von Kaisenberg CS. Reversed pulmonary artery flow in isolated noncompaction of the ventricular myocardium. Fetal Diagn Ther; 22:29–32 (2007).

Zhou Y, Ye H, Martin-Subero JI, Gesk S, Hamoudi R, Lu YJ, Wang R, Shipley J, Siebert R, Isaacson PG, Dogan A, Du MQ: The pattern of genomic gains in salivary gland MALT lymphomas. Haematologica 92:921-927 (2007).

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