Steinemann D - Search Results

1

Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndrome.

Karow A, Steinemann D, Göhring G, Hasle H, Greiner J, Harila-Saari A, Flotho C, Zenker M, Schlegelberger B, Niemeyer CM, Kratz CP. Karow A, et al. Among authors: steinemann d. Leukemia. 2007 Jun;21(6):1303-5. doi: 10.1038/sj.leu.2404651. Epub 2007 Mar 15. Leukemia. 2007. PMID: 17361219 No abstract available.

2

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. Leukemia. 2001 Mar;15(3):474-5. doi: 10.1038/sj.leu.2402037. Leukemia. 2001. PMID: 11237074 No abstract available.

3

Fluorescence in situ hybridization using the subtelomeric 11q probe as a diagnostic tool for congenital thrombocytopenia.

Göhring G, Hanke C, Kratz C, Kontny U, Steinemann D, Niemeyer CM, Schlegelberger B. Göhring G, et al. Among authors: steinemann d. Ann Hematol. 2006 Dec;85(12):883-5. doi: 10.1007/s00277-006-0177-2. Epub 2006 Sep 15. Ann Hematol. 2006. PMID: 16977432 No abstract available.

4

Uniparental disomy at chromosome 11p15.5 followed by HRAS mutations in embryonal rhabdomyosarcoma: lessons from Costello syndrome.

Kratz CP, Steinemann D, Niemeyer CM, Schlegelberger B, Koscielniak E, Kontny U, Zenker M. Kratz CP, et al. Among authors: steinemann d. Hum Mol Genet. 2007 Feb 15;16(4):374-9. doi: 10.1093/hmg/ddl458. Epub 2006 Dec 12. Hum Mol Genet. 2007. PMID: 17164262

5

Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11.

Flotho C, Steinemann D, Mullighan CG, Neale G, Mayer K, Kratz CP, Schlegelberger B, Downing JR, Niemeyer CM. Flotho C, et al. Among authors: steinemann d. Oncogene. 2007 Aug 23;26(39):5816-21. doi: 10.1038/sj.onc.1210361. Epub 2007 Mar 12. Oncogene. 2007. PMID: 17353900

6

Familial polycythemia vera with non-germline JAK2(V617F) mutation sparing the abnormal and clonal granulopoiesis.

Hussein K, Bock O, Ballmaier M, Göhring G, Steinemann D, Lehmann U, Kemper J, Buhr T, Kreipe H. Hussein K, et al. Among authors: steinemann d. Leukemia. 2007 Dec;21(12):2566-8. doi: 10.1038/sj.leu.2404846. Epub 2007 Jul 12. Leukemia. 2007. PMID: 17625610 No abstract available.

7

Chromosomal aberrations in congenital bone marrow failure disorders--an early indicator for leukemogenesis?

Göhring G, Karow A, Steinemann D, Wilkens L, Lichter P, Zeidler C, Niemeyer C, Welte K, Schlegelberger B. Göhring G, et al. Among authors: steinemann d. Ann Hematol. 2007 Oct;86(10):733-9. doi: 10.1007/s00277-007-0337-z. Epub 2007 Jul 25. Ann Hematol. 2007. PMID: 17653548

8

Copy number alterations in childhood acute lymphoblastic leukemia and their association with minimal residual disease.

Steinemann D, Cario G, Stanulla M, Karawajew L, Tauscher M, Weigmann A, Göhring G, Ludwig WD, Harbott J, Radlwimmer B, Bartram C, Lichter P, Schrappe M, Schlegelberger B. Steinemann D, et al. Genes Chromosomes Cancer. 2008 Jun;47(6):471-80. doi: 10.1002/gcc.20557. Genes Chromosomes Cancer. 2008. PMID: 18311775

9

Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome.

Steinemann D, Praulich I, Otto N, Göhring G, Niemeyer CM, Schlegelberger B. Steinemann D, et al. Br J Haematol. 2009 May;145(4):533-4. doi: 10.1111/j.1365-2141.2009.07634.x. Br J Haematol. 2009. PMID: 19298594 Free article. No abstract available.

10

A novel pedigree with heterozygous germline RUNX1 mutation causing familial MDS-related AML: can these families serve as a multistep model for leukemic transformation?

Ripperger T, Steinemann D, Göhring G, Finke J, Niemeyer CM, Strahm B, Schlegelberger B. Ripperger T, et al. Among authors: steinemann d. Leukemia. 2009 Jul;23(7):1364-6. doi: 10.1038/leu.2009.87. Epub 2009 Apr 23. Leukemia. 2009. PMID: 19387465 No abstract available.

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