Haferlach C - Search Results

1

Recurrent mutations in multiple components of the cohesin complex in myeloid neoplasms.

Kon A, Shih LY, Minamino M, Sanada M, Shiraishi Y, Nagata Y, Yoshida K, Okuno Y, Bando M, Nakato R, Ishikawa S, Sato-Otsubo A, Nagae G, Nishimoto A, Haferlach C, Nowak D, Sato Y, Alpermann T, Nagasaki M, Shimamura T, Tanaka H, Chiba K, Yamamoto R, Yamaguchi T, Otsu M, Obara N, Sakata-Yanagimoto M, Nakamaki T, Ishiyama K, Nolte F, Hofmann WK, Miyawaki S, Chiba S, Mori H, Nakauchi H, Koeffler HP, Aburatani H, Haferlach T, Shirahige K, Miyano S, Ogawa S. Kon A, et al. Among authors: haferlach t, haferlach c. Nat Genet. 2013 Oct;45(10):1232-7. doi: 10.1038/ng.2731. Epub 2013 Aug 18. Nat Genet. 2013. PMID: 23955599

2

Insight into the molecular pathogenesis of myeloid malignancies.

Haferlach T, Bacher U, Haferlach C, Kern W, Schnittger S. Haferlach T, et al. Among authors: haferlach c. Curr Opin Hematol. 2007 Mar;14(2):90-7. doi: 10.1097/MOH.0b013e3280168490. Curr Opin Hematol. 2007. PMID: 17255785 Review.

3

Translocations as a mechanism for homozygous deletion of 13q14 and loss of the ATM gene in a patient with B-cell chronic lymphocytic leukemia.

Herholz H, Kern W, Schnittger S, Haferlach T, Dicker F, Haferlach C. Herholz H, et al. Among authors: haferlach t, haferlach c. Cancer Genet Cytogenet. 2007 Apr 1;174(1):57-60. doi: 10.1016/j.cancergencyto.2006.11.006. Cancer Genet Cytogenet. 2007. PMID: 17350468

4

Trisomy 13 is strongly associated with AML1/RUNX1 mutations and increased FLT3 expression in acute myeloid leukemia.

Dicker F, Haferlach C, Kern W, Haferlach T, Schnittger S. Dicker F, et al. Among authors: haferlach t, haferlach c. Blood. 2007 Aug 15;110(4):1308-16. doi: 10.1182/blood-2007-02-072595. Epub 2007 May 7. Blood. 2007. PMID: 17485549 Free article.

5

A case of chronic myeloproliferative syndrome followed by precursor T-cell acute lymphoblastic leukemia.

Bacher U, Haferlach T, Kern W, Harich HD, Schnittger S, Haferlach C. Bacher U, et al. Among authors: haferlach t, haferlach c. Cancer Genet Cytogenet. 2007 May;175(1):52-6. doi: 10.1016/j.cancergencyto.2006.12.007. Cancer Genet Cytogenet. 2007. PMID: 17498558

6

A comparative study of molecular mutations in 381 patients with myelodysplastic syndrome and in 4130 patients with acute myeloid leukemia.

Bacher U, Haferlach T, Kern W, Haferlach C, Schnittger S. Bacher U, et al. Among authors: haferlach t, haferlach c. Haematologica. 2007 Jun;92(6):744-52. doi: 10.3324/haematol.10869. Haematologica. 2007. PMID: 17550846 Free article.

7

Feasibility of using the combined MDS-EVI1/EVI1 gene expression as an alternative molecular marker in acute myeloid leukemia: a report of four cases.

Weisser M, Haferlach C, Haferlach T, Schnittger S. Weisser M, et al. Among authors: haferlach t, haferlach c. Cancer Genet Cytogenet. 2007 Aug;177(1):64-9. doi: 10.1016/j.cancergencyto.2007.05.003. Cancer Genet Cytogenet. 2007. PMID: 17693194

8

Monitoring of minimal residual disease in acute myeloid leukemia.

Kern W, Haferlach C, Haferlach T, Schnittger S. Kern W, et al. Among authors: haferlach t, haferlach c. Cancer. 2008 Jan 1;112(1):4-16. doi: 10.1002/cncr.23128. Cancer. 2008. PMID: 18000811 Free article. Review.

9

Mutations of the TP53 gene in acute myeloid leukemia are strongly associated with a complex aberrant karyotype.

Haferlach C, Dicker F, Herholz H, Schnittger S, Kern W, Haferlach T. Haferlach C, et al. Among authors: haferlach t. Leukemia. 2008 Aug;22(8):1539-41. doi: 10.1038/leu.2008.143. Epub 2008 Jun 5. Leukemia. 2008. PMID: 18528419

10

Inverted duplication dup(1)(q32q21) as sole aberration in lymphoid and myeloid malignancies.

Bacher U, Schnittger S, Grüneisen A, Haferlach T, Kern W, Haferlach C. Bacher U, et al. Among authors: haferlach t, haferlach c. Cancer Genet Cytogenet. 2009 Jan 15;188(2):108-11. doi: 10.1016/j.cancergencyto.2008.09.004. Cancer Genet Cytogenet. 2009. PMID: 19100515

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