Metzler M - Search Results

1

Cluster analysis of genomic ETV6-RUNX1 (TEL-AML1) fusion sites in childhood acute lymphoblastic leukemia.

von Goessel H, Jacobs U, Semper S, Krumbholz M, Langer T, Keller T, Schrauder A, van der Velden VH, van Dongen JJ, Harbott J, Panzer-Grümayer ER, Schrappe M, Rascher W, Metzler M. von Goessel H, et al. Among authors: metzler m. Leuk Res. 2009 Aug;33(8):1082-8. doi: 10.1016/j.leukres.2008.11.001. Epub 2008 Dec 10. Leuk Res. 2009. PMID: 19081626

2

A new fingerprint method for sequence analysis of chromosomal translocations at the genomic DNA level.

Leis T, Repp R, Borkhardt A, Metzler M, Schläger F, Harbott J, Lampert F. Leis T, et al. Among authors: metzler m. Leukemia. 1998 May;12(5):758-63. doi: 10.1038/sj.leu.2401006. Leukemia. 1998. PMID: 9593275

3

Nuclear transport of oligonucleotides in HepG2-cells mediated by protamine sulfate and negatively charged liposomes.

Welz C, Neuhuber W, Schreier H, Metzler M, Repp R, Rascher W, Fahr A. Welz C, et al. Among authors: metzler m. Pharm Res. 2000 Oct;17(10):1206-11. doi: 10.1023/a:1026410612600. Pharm Res. 2000. PMID: 11145225

4

Identification of leptin in human saliva.

Gröschl M, Rauh M, Wagner R, Neuhuber W, Metzler M, Tamgüney G, Zenk J, Schoof E, Dörr HG, Blum WF, Rascher W, Dötsch J. Gröschl M, et al. Among authors: metzler m. J Clin Endocrinol Metab. 2001 Nov;86(11):5234-9. doi: 10.1210/jcem.86.11.7998. J Clin Endocrinol Metab. 2001. PMID: 11701683 Clinical Trial.

5

Adrenomedullin, calcitonin gene-related peptide and their receptors: evidence for a decreased placental mRNA content in preeclampsia and HELLP syndrome.

Knerr I, Dachert C, Beinder E, Metzler M, Dötsch J, Repp R, Rascher W. Knerr I, et al. Among authors: metzler m. Eur J Obstet Gynecol Reprod Biol. 2002 Feb 10;101(1):47-53. doi: 10.1016/s0301-2115(01)00519-x. Eur J Obstet Gynecol Reprod Biol. 2002. PMID: 11905404

6

Late relapses evolve from slow-responding subclones in t(12;21)-positive acute lymphoblastic leukemia: evidence for the persistence of a preleukemic clone.

Konrad M, Metzler M, Panzer S, Ostreicher I, Peham M, Repp R, Haas OA, Gadner H, Panzer-Grumayer ER. Konrad M, et al. Among authors: metzler m. Blood. 2003 May 1;101(9):3635-40. doi: 10.1182/blood-2002-10-3252. Epub 2002 Dec 27. Blood. 2003. PMID: 12506024 Free article.

7

Analysis of t(9;11) chromosomal breakpoint sequences in childhood acute leukemia: almost identical MLL breakpoints in therapy-related AML after treatment without etoposides.

Langer T, Metzler M, Reinhardt D, Viehmann S, Borkhardt A, Reichel M, Stanulla M, Schrappe M, Creutzig U, Ritter J, Leis T, Jacobs U, Harbott J, Beck JD, Rascher W, Repp R. Langer T, et al. Among authors: metzler m. Genes Chromosomes Cancer. 2003 Apr;36(4):393-401. doi: 10.1002/gcc.10167. Genes Chromosomes Cancer. 2003. PMID: 12619163

8

Occurrence of an MLL/LAF4 fusion gene caused by the insertion ins(11;2)(q23;q11.2q11.2) in an infant with acute lymphoblastic leukemia.

Bruch J, Wilda M, Teigler-Schlegel A, Harbott J, Borkhardt A, Metzler M. Bruch J, et al. Among authors: metzler m. Genes Chromosomes Cancer. 2003 May;37(1):106-9. doi: 10.1002/gcc.10187. Genes Chromosomes Cancer. 2003. PMID: 12661012 No abstract available.

9

A new missense mutation of the vasopressin-neurophysin II gene in a family with neurohypophyseal diabetes insipidus.

Wolf MT, Dötsch J, Metzler M, Holder M, Repp R, Rascher W. Wolf MT, et al. Among authors: metzler m. Horm Res. 2003;60(3):143-7. doi: 10.1159/000072526. Horm Res. 2003. PMID: 12931042

10

Asymmetric multiplex-polymerase chain reaction - a high throughput method for detection and sequencing genomic fusion sites in t(4;11).

Metzler M, Brehm U, Langer T, Viehmann S, Borkhardt A, Stanulla M, Schrappe M, Harbott J, Beck JD, Rascher W, Repp R. Metzler M, et al. Br J Haematol. 2004 Jan;124(1):47-54. doi: 10.1046/j.1365-2141.2003.04740.x. Br J Haematol. 2004. PMID: 14675407 Free article.

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