Liehr T - Search Results

1

Unbalanced chromosome 1 abnormalities leading to partial trisomy 1q in four infants with Down syndrome and acute megakaryocytic leukemia.

Silva ML, Pombo-de-Oliveira MS, Raimondi SC, Mkrtchyan H, Abdelhay E, de Figueiredo AF, de Souza MT, Garcia DR, de Ventura EM, de Sousa AM, Liehr T. Silva ML, et al. Among authors: liehr t. Mol Cytogenet. 2009 Feb 19;2:7. doi: 10.1186/1755-8166-2-7. Mol Cytogenet. 2009. PMID: 19228396 Free PMC article.

2

New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcome.

Macedo Silva ML, Land M, Heller A, Abdelhay E, do Socorro Pombo-de-Oliveira M, Ribeiro R, Alves G, Lerner D, Liehr T. Macedo Silva ML, et al. Among authors: liehr t. Oncol Rep. 2005 Sep;14(3):663-6. Oncol Rep. 2005. PMID: 16077971

3

FISH banding in tumor cytogenetics.

Liehr T, Gross M, Karst C, Glaser M, Mrasek K, Starke H, Weise A, Mkrtchyan H, Kuechler A. Liehr T, et al. Cancer Genet Cytogenet. 2006 Jan 1;164(1):88-9. doi: 10.1016/j.cancergencyto.2005.06.013. Cancer Genet Cytogenet. 2006. PMID: 16364770 No abstract available.

4

Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.

Karst C, Gross M, Haase D, Wedding U, Höffken K, Liehr T, Mkrtchyan H. Karst C, et al. Among authors: liehr t. Int J Oncol. 2006 Apr;28(4):891-7. Int J Oncol. 2006. PMID: 16525638

5

Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo.

Macedo Silva ML, Raimondi SC, Abdelhay E, Gross M, Mkrtchyan H, de Figueiredo AF, Ribeiro RC, de Jesus Marques-Salles T, Sobral ES, Gerardin Land MP, Liehr T. Macedo Silva ML, et al. Among authors: liehr t. Cancer Genet Cytogenet. 2008 Apr 1;182(1):56-60. doi: 10.1016/j.cancergencyto.2007.12.014. Cancer Genet Cytogenet. 2008. PMID: 18328953

6

Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?

Trifonov V, Fluri S, Binkert F, Nandini A, Anderson J, Rodriguez L, Gross M, Kosyakova N, Mkrtchyan H, Ewers E, Reich D, Weise A, Liehr T. Trifonov V, et al. Among authors: liehr t. Mol Cytogenet. 2008 Apr 15;1:6. doi: 10.1186/1755-8166-1-6. Mol Cytogenet. 2008. PMID: 18471318 Free PMC article.

7

Novel complex t(V;9;22) rearrangements in three cases with chronic myeloid leukemia and a rare translocation in a case with classical Philadelphia chromosome.

Mkrtchyan H, Ghazaryan S, Avetisyan G, Hovhannisyan A, Muradyan L, Daghbashyan S, Karst C, Gross M, Hinreiner S, Aroutiounian R, Liehr T. Mkrtchyan H, et al. Among authors: liehr t. Oncol Rep. 2008 Jul;20(1):99-104. Oncol Rep. 2008. PMID: 18575724

8

Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype.

Gross M, Mkrtchyan H, Glaser M, Fricke HJ, Höffken K, Heller A, Weise A, Liehr T. Gross M, et al. Among authors: liehr t. Int J Oncol. 2009 Feb;34(2):417-23. Int J Oncol. 2009. PMID: 19148476

9

A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia.

de Jesus Marques-Salles T, Liehr T, Mkrtchyan H, Raimondi SC, Tavares de Souza M, de Figueiredo AF, Rouxinol S, Jordy Macedo FC, Abdelhay E, Santos N, Macedo Silva ML. de Jesus Marques-Salles T, et al. Among authors: liehr t. Cancer Genet Cytogenet. 2009 Feb;189(1):59-62. doi: 10.1016/j.cancergencyto.2008.10.009. Cancer Genet Cytogenet. 2009. PMID: 19167614

10

Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics.

Manvelyan M, Kempf P, Weise A, Mrasek K, Heller A, Lier A, Höffken K, Fricke HJ, Sayer HG, Liehr T, Mkrtchyan H. Manvelyan M, et al. Among authors: liehr t. Int J Mol Med. 2009 Sep;24(3):335-41. doi: 10.3892/ijmm_00000237. Int J Mol Med. 2009. PMID: 19639225

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