Fröhling S - Search Results

1

Deregulation of signaling pathways in acute myeloid leukemia.

Scholl C, Gilliland DG, Fröhling S. Scholl C, et al. Among authors: frohling s. Semin Oncol. 2008 Aug;35(4):336-45. doi: 10.1053/j.seminoncol.2008.04.004. Semin Oncol. 2008. PMID: 18692684 Review.

2

Design and validation of DNA probe sets for a comprehensive interphase cytogenetic analysis of acute myeloid leukemia.

Fischer K, Scholl C, Sàlat J, Fröhling S, Schlenk R, Bentz M, Stilgenbauer S, Lichter P, Döhner H. Fischer K, et al. Among authors: frohling s. Blood. 1996 Nov 15;88(10):3962-71. Blood. 1996. PMID: 8916963 Free article.

3

Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias.

Fischer K, Fröhling S, Scherer SW, McAllister Brown J, Scholl C, Stilgenbauer S, Tsui LC, Lichter P, Döhner H. Fischer K, et al. Among authors: frohling s. Blood. 1997 Mar 15;89(6):2036-41. Blood. 1997. PMID: 9058725 Free article.

4

Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders.

Döhner K, Brown J, Hehmann U, Hetzel C, Stewart J, Lowther G, Scholl C, Fröhling S, Cuneo A, Tsui LC, Lichter P, Scherer SW, Döhner H. Döhner K, et al. Among authors: frohling s. Blood. 1998 Dec 1;92(11):4031-5. Blood. 1998. PMID: 9834205 Free article.

5

Comparison of cytogenetic and molecular cytogenetic detection of chromosome abnormalities in 240 consecutive adult patients with acute myeloid leukemia.

Fröhling S, Skelin S, Liebisch C, Scholl C, Schlenk RF, Döhner H, Döhner K; Acute Myeloid Leukemia Study Group, Ulm. Fröhling S, et al. J Clin Oncol. 2002 May 15;20(10):2480-5. doi: 10.1200/JCO.2002.08.155. J Clin Oncol. 2002. PMID: 12011125

6

Development of a real-time RT-PCR assay for the quantification of the most frequent MLL/AF9 fusion types resulting from translocation t(9;11)(p22;q23) in acute myeloid leukemia.

Scholl C, Breitinger H, Schlenk RF, Döhner H, Fröhling S, Döhner K; AML Study Group Ulm. Scholl C, et al. Among authors: frohling s. Genes Chromosomes Cancer. 2003 Nov;38(3):274-80. doi: 10.1002/gcc.10284. Genes Chromosomes Cancer. 2003. PMID: 14506704

7

Acute myeloid leukemia with deletion 9q within a noncomplex karyotype is associated with CEBPA loss-of-function mutations.

Fröhling S, Schlenk RF, Krauter J, Thiede C, Ehninger G, Haase D, Harder L, Kreitmeier S, Scholl C, Caligiuri MA, Bloomfield CD, Döhner H, Döhner K. Fröhling S, et al. Genes Chromosomes Cancer. 2005 Apr;42(4):427-32. doi: 10.1002/gcc.20152. Genes Chromosomes Cancer. 2005. PMID: 15645492

8

Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis.

Levine RL, Wadleigh M, Cools J, Ebert BL, Wernig G, Huntly BJ, Boggon TJ, Wlodarska I, Clark JJ, Moore S, Adelsperger J, Koo S, Lee JC, Gabriel S, Mercher T, D'Andrea A, Fröhling S, Döhner K, Marynen P, Vandenberghe P, Mesa RA, Tefferi A, Griffin JD, Eck MJ, Sellers WR, Meyerson M, Golub TR, Lee SJ, Gilliland DG. Levine RL, et al. Among authors: frohling s. Cancer Cell. 2005 Apr;7(4):387-97. doi: 10.1016/j.ccr.2005.03.023. Cancer Cell. 2005. PMID: 15837627 Free article.

9

Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics: interaction with other gene mutations.

Döhner K, Schlenk RF, Habdank M, Scholl C, Rücker FG, Corbacioglu A, Bullinger L, Fröhling S, Döhner H. Döhner K, et al. Among authors: frohling s. Blood. 2005 Dec 1;106(12):3740-6. doi: 10.1182/blood-2005-05-2164. Epub 2005 Jul 28. Blood. 2005. PMID: 16051734 Free article.

10

Genetics of myeloid malignancies: pathogenetic and clinical implications.

Fröhling S, Scholl C, Gilliland DG, Levine RL. Fröhling S, et al. J Clin Oncol. 2005 Sep 10;23(26):6285-95. doi: 10.1200/JCO.2005.05.010. J Clin Oncol. 2005. PMID: 16155011 Review.

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