Liehr T - Search Results

1

Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrations.

Kinne RW, Kunisch E, Beensen V, Zimmermann T, Emmrich F, Petrow P, Lungershausen W, Hein G, Braun RK, Foerster M, Kroegel C, Winter R, Liesaus E, Fuhrmann RA, Roth A, Claussen U, Liehr T. Kinne RW, et al. Among authors: liehr t. Genes Chromosomes Cancer. 2003 Sep;38(1):53-67. doi: 10.1002/gcc.10242. Genes Chromosomes Cancer. 2003. PMID: 12874786

2

Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.

Liehr T, Starke H, Beensen V, Kähler C, Harbich M, Brude E, Ziegler M, Claussen U. Liehr T, et al. Int J Mol Med. 1999 Jan;3(1):11-4. doi: 10.3892/ijmm.3.1.11. Int J Mol Med. 1999. PMID: 9864379

3

Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3.

Liehr T, Kuhlenbäumer G, Wulf P, Taylor V, Suter U, Van Broeckhoven C, Lupski JR, Claussen U, Rautenstrauss B. Liehr T, et al. Genomics. 1999 May 15;58(1):106-8. doi: 10.1006/geno.1999.5803. Genomics. 1999. PMID: 10331954 No abstract available.

4

Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.

Starke H, Schreyer I, Kähler C, Fiedler W, Beensen V, Heller A, Nietzel A, Claussen U, Liehr T. Starke H, et al. Among authors: liehr t. Prenat Diagn. 1999 Dec;19(12):1169-74. Prenat Diagn. 1999. PMID: 10590438 Review.

5

Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias.

Heller A, Chudoba I, Bleck C, Senger G, Claussen U, Liehr T. Heller A, et al. Among authors: liehr t. Int J Oncol. 2000 Mar;16(3):461-8. Int J Oncol. 2000. PMID: 10675476

6

Insulin-like growth factor serum concentrations reflect insufficient growth in a hypoplastic infant with partial trisomy 9q in the 12th week of life.

Hübler A, Seidel J, Kauf E, Schramm D, Beensen V, Heller A, Liehr T, Zintl F. Hübler A, et al. Among authors: liehr t. J Pediatr Endocrinol Metab. 2000 Apr;13(4):445-50. doi: 10.1515/jpem.2000.13.4.445. J Pediatr Endocrinol Metab. 2000. PMID: 10777002

7

Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.

Heller A, Seidel J, Hübler A, Starke H, Beensen V, Senger G, Rocchi M, Wirth J, Chudoba I, Claussen U, Liehr T. Heller A, et al. Among authors: liehr t. J Med Genet. 2000 Jul;37(7):529-32. doi: 10.1136/jmg.37.7.529. J Med Genet. 2000. PMID: 10882757 Free PMC article.

8

Genetic imbalances in 26 cases of penile squamous cell carcinoma.

Alves G, Heller A, Fiedler W, Campos MM, Claussen U, Ornellas AA, Liehr T. Alves G, et al. Among authors: liehr t. Genes Chromosomes Cancer. 2001 May;31(1):48-53. doi: 10.1002/gcc.1117. Genes Chromosomes Cancer. 2001. PMID: 11284035

9

Regional localization of 10 mariner transposon-like ESTs by means of FISH--evidence for a correlation with fragile sites.

Liehr T, Reiter LT, Lupski JR, Murakami T, Claussen U, Rautenstrauss B. Liehr T, et al. Mamm Genome. 2001 Apr;12(4):326-8. doi: 10.1007/s003350010276. Mamm Genome. 2001. PMID: 11309667 No abstract available.

10

A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients.

Bleichert A, Fiedler W, Claussen U, Ernst G, Loncarevic IF, Heller A, Liehr T, Kunert C, von Eggeling F. Bleichert A, et al. Among authors: liehr t. Int J Mol Med. 2001 Jun;7(6):591-5. doi: 10.3892/ijmm.7.6.591. Int J Mol Med. 2001. PMID: 11351270

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