Harder S - Search Results

1

Deletions in the long arm of chromosome 10 in lymphomas with t(14;18): a pathogenetic role of the tumor supressor genes PTEN/MMAC1 and MXI1?

Siebert R, Gesk S, Harder S, Plötz S, Matthiesen P, Grote W, Schlegelberger B, Jandrig B, Grasmo-Wendler UH, Scherneck S, Rosenwald A, Ott G. Siebert R, et al. Among authors: harder s. Blood. 1998 Dec 1;92(11):4487-9. Blood. 1998. PMID: 9882102 Free article. No abstract available.

2

Application of interphase fluorescence in situ Hybridization for the detection of the Burkitt translocation t(8;14)(q24;q32) in B-cell lymphomas.

Siebert R, Matthiesen P, Harder S, Zhang Y, Borowski A, Zühlke-Jenisch R, Metzke S, Joos S, Weber-Matthiesen K, Grote W, Schlegelberger B. Siebert R, et al. Among authors: harder s. Blood. 1998 Feb 1;91(3):984-90. Blood. 1998. PMID: 9446660 Free article.

3

Application of interphase cytogenetics for the detection of t(11;14)(q13;q32) in mantle cell lymphomas.

Siebert R, Matthiesen P, Harder S, Zhang Y, Borowski A, Zühlke-Jenisch R, Plendl H, Metzke S, Joos S, Zucca E, Weber-Matthiesen K, Roggero E, Grote W, Schlegelberger B. Siebert R, et al. Among authors: harder s. Ann Oncol. 1998 May;9(5):519-26. doi: 10.1023/a:1008242729509. Ann Oncol. 1998. PMID: 9653493 Free article.

4

Detection of 6q deletions in breast carcinoma cell lines by fluorescence in situ hybridization.

Zhang Y, Matthiesen P, Siebert R, Harder S, Theile M, Scherneck S, Schlegelberger B. Zhang Y, et al. Among authors: harder s. Hum Genet. 1998 Dec;103(6):727-9. doi: 10.1007/s004390050899. Hum Genet. 1998. PMID: 9921911

5

A 3-cM commonly deleted region in 6q21 in leukemias and lymphomas delineated by fluorescence in situ hybridization.

Zhang Y, Matthiesen P, Harder S, Siebert R, Castoldi G, Calasanz MJ, Wong KF, Rosenwald A, Ott G, Atkin NB, Schlegelberger B. Zhang Y, et al. Among authors: harder s. Genes Chromosomes Cancer. 2000 Jan;27(1):52-8. doi: 10.1002/(sici)1098-2264(200001)27:1<52::aid-gcc7>3.0.co;2-x. Genes Chromosomes Cancer. 2000. PMID: 10564586

6

No evidence for deletions of the NBS1 gene in lymphomas.

Stumm M, von Ruskowsky A, Siebert R, Harder S, Varon R, Wieacker P, Schlegelberger B. Stumm M, et al. Among authors: harder s. Cancer Genet Cytogenet. 2001 Apr 1;126(1):60-2. doi: 10.1016/s0165-4608(00)00390-3. Cancer Genet Cytogenet. 2001. PMID: 11343781

7

Frequent allelic loss of the BCL10 gene in lymphomas with the t(11;14)(q13;q32).

Steinemann D, Siebert R, Harder S, Martin-Subero I, Kettwig G, Hinzmann B, Gesk S, Tiemann M, Merz H, Rosenthal A, Grote W, Morris SW, Schlegelberger B. Steinemann D, et al. Among authors: harder s. Leukemia. 2001 Mar;15(3):474-5. doi: 10.1038/sj.leu.2402037. Leukemia. 2001. PMID: 11237074 No abstract available.

8

Feasibility of simultaneous fluorescence immunophenotyping and fluorescence in situ hybridization study for the detection of estrogen receptor expression and deletions of the estrogen receptor gene in breast carcinoma cell lines.

Zhang Y, Siebert R, Matthiesen P, Harder S, Theile M, Scherneck S, Schlegelberger B. Zhang Y, et al. Among authors: harder s. Virchows Arch. 2000 Mar;436(3):271-5. doi: 10.1007/s004280050040. Virchows Arch. 2000. PMID: 10782886

9

Chromosome aberrations are restricted to the CD56+, CD3- tumour cell population in natural killer cell lymphomas: a combined immunophenotyping and FISH study.

Zhang Y, Wong KF, Siebert R, Matthiesen P, Harder S, Eimermacher H, Feller AC, Schlegelberger B. Zhang Y, et al. Among authors: harder s. Br J Haematol. 1999 Jun;105(3):737-42. doi: 10.1046/j.1365-2141.1999.01410.x. Br J Haematol. 1999. PMID: 10354139 Free article.

10

Detection of secondary genetic aberrations in follicle center cell derived lymphomas: assessment of the reliability of comparative genomic hybridization and standard chromosome analysis.

Viardot A, Martin-Subero JI, Siebert R, Harder S, Gesk S, Bentz M, Schlegelberger B. Viardot A, et al. Among authors: harder s. Leukemia. 2001 Jan;15(1):177-83. doi: 10.1038/sj.leu.2401969. Leukemia. 2001. PMID: 11243387

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