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Items: 9

1.

Molecular characterization of the rare translocation t(3;10)(q26;q21) in an acute myeloid leukemia patient.

Jancuskova T, Plachy R, Zemankova L, Hardekopf DW, Stika J, Zejskova L, Praulich I, Kreuzer KA, Rothe A, Othman MA, Kosyakova N, Pekova S.

Mol Cytogenet. 2014 Jul 15;7:47. doi: 10.1186/1755-8166-7-47. eCollection 2014.

2.

Array-CGH in childhood MDS.

Tauscher M, Praulich I, Steinemann D.

Methods Mol Biol. 2013;973:267-78. doi: 10.1007/978-1-62703-281-0_17.

PMID:
23412796
3.

Patient-specific analysis of FLT3 internal tandem duplications for the prognostication and monitoring of acute myeloid leukemia.

Schiller J, Praulich I, Krings Rocha C, Kreuzer KA.

Eur J Haematol. 2012 Jul;89(1):53-62. doi: 10.1111/j.1600-0609.2012.01785.x. Epub 2012 May 9.

PMID:
22458420
4.

Constitutional trisomy 8p11.21-q11.21 mosaicism: a germline alteration predisposing to myeloid leukaemia.

Ripperger T, Tauscher M, Praulich I, Pabst B, Teigler-Schlegel A, Yeoh A, Göhring G, Schlegelberger B, Flotho C, Niemeyer CM, Steinemann D.

Br J Haematol. 2011 Oct;155(2):209-17. doi: 10.1111/j.1365-2141.2011.08817.x. Epub 2011 Aug 18. Review.

PMID:
21848520
5.

A rare case of t(11;22) in a mantle cell lymphoma like B-cell neoplasia resulting in a fusion of IGL and CCND1: case report.

Rocha CK, Praulich I, Gehrke I, Hallek M, Kreuzer KA.

Mol Cytogenet. 2011 Apr 1;4(1):8. doi: 10.1186/1755-8166-4-8.

6.

Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.

Praulich I, Tauscher M, Göhring G, Glaser S, Hofmann W, Feurstein S, Flotho C, Lichter P, Niemeyer CM, Schlegelberger B, Steinemann D.

Genes Chromosomes Cancer. 2010 Oct;49(10):885-900. doi: 10.1002/gcc.20797.

PMID:
20589934
7.

Mutations in the let-7 binding site - a mechanism of RAS activation in juvenile myelomonocytic leukemia?

Steinemann D, Tauscher M, Praulich I, Niemeyer CM, Flotho C, Schlegelberger B.

Haematologica. 2010 Sep;95(9):1616. doi: 10.3324/haematol.2010.024984. Epub 2010 May 11. No abstract available.

8.

Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1.

Steinemann D, Arning L, Praulich I, Stuhrmann M, Hasle H, Stary J, Schlegelberger B, Niemeyer CM, Flotho C.

Haematologica. 2010 Feb;95(2):320-3. doi: 10.3324/haematol.2009.010355. Epub 2009 Dec 16.

9.

Mutation analysis of the HAX1 gene in childhood myelodysplastic syndrome.

Steinemann D, Praulich I, Otto N, Göhring G, Niemeyer CM, Schlegelberger B.

Br J Haematol. 2009 May;145(4):533-4. doi: 10.1111/j.1365-2141.2009.07634.x. No abstract available.

PMID:
19298594

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