Tchinda J - Search Results

1

Aberrations of chromosomes 5 and 8 as recurrent cytogenetic events in anaplastic carcinoma of the thyroid as detected by fluorescence in situ hybridisation and comparative genomic hybridisation.

Wilkens L, Benten D, Tchinda J, Brabant G, Pötter E, Dralle H, von Wasielewski R. Wilkens L, et al. Among authors: tchinda j. Virchows Arch. 2000 Apr;436(4):312-8. doi: 10.1007/s004280050452. Virchows Arch. 2000. PMID: 10834532

2

Detection of karyotype changes in interphase cells: oligonucleotide-primed in situ labelling versus fluorescence in situ hybridization.

Werner M, Wilkens L, Nasarek A, Tchinda J, Komminoth P. Werner M, et al. Among authors: tchinda j. Virchows Arch. 1997 May;430(5):381-7. doi: 10.1007/s004280050047. Virchows Arch. 1997. PMID: 9174628

3

Significant hybridization differences in comparative genomic hybridization due to nucleotides used for DNA labelling and to DNA chosen for cohybridization.

Wilkens L, Tchinda J, Burkhardt D, Kreipe HH. Wilkens L, et al. Among authors: tchinda j. Pathobiology. 2002-2003;70(4):204-8. doi: 10.1159/000069330. Pathobiology. 2002. PMID: 12679597

4

Single- and double-color oligonucleotide primed in situ labeling (PRINS): applications in pathology.

Wilkens L, Tchinda J, Komminoth P, Werner M. Wilkens L, et al. Among authors: tchinda j. Histochem Cell Biol. 1997 Oct-Nov;108(4-5):439-46. doi: 10.1007/s004180050184. Histochem Cell Biol. 1997. PMID: 9387936 Review.

5

Applications of single-color and double-color oligonucleotide primed in situ labeling in cytology.

Werner M, Nasarek A, Tchinda J, von Wasielewski R, Komminoth P, Wilkens L. Werner M, et al. Among authors: tchinda j. Mod Pathol. 1997 Nov;10(11):1164-71. Mod Pathol. 1997. PMID: 9388069

6

Value of fluorescence in situ hybridization for detecting the bcr/abl gene fusion in interphase cells of routine bone marrow specimens.

Werner M, Ewig M, Nasarek A, Wilkens L, von Wasielewski R, Tchinda J, Nolte M. Werner M, et al. Among authors: tchinda j. Diagn Mol Pathol. 1997 Oct;6(5):282-7. doi: 10.1097/00019606-199710000-00006. Diagn Mol Pathol. 1997. PMID: 9458387

7

Analysis of hematologic diseases using conventional karyotyping, fluorescence in situ hybridization (FISH), and comparative genomic hybridization (CGH).

Wilkens L, Tchinda J, Burkhardt D, Nolte M, Werner M, Georgii A. Wilkens L, et al. Among authors: tchinda j. Hum Pathol. 1998 Aug;29(8):833-9. doi: 10.1016/s0046-8177(98)90453-1. Hum Pathol. 1998. PMID: 9712425

8

Cytogenetic aberrations in myelodysplastic syndrome detected by comparative genomic hybridization and fluorescence in situ hybridization.

Wilkens L, Burkhardt D, Tchinda J, Büsche G, Werner M, Nolte M, Ganser A, Georgii A. Wilkens L, et al. Among authors: tchinda j. Diagn Mol Pathol. 1999 Mar;8(1):47-53. doi: 10.1097/00019606-199903000-00008. Diagn Mol Pathol. 1999. PMID: 10408793

9

[Cytogenetic alterations in renal tumors. Applications for comparative genomic hybridization and fluorescence in situ hybridization].

Mertz KD, Tchinda J, Küfer R, Möller P, Rubin MA, Moch H, Perner S. Mertz KD, et al. Among authors: tchinda j. Urologe A. 2006 Mar;45(3):316-8, 320-2. doi: 10.1007/s00120-006-1004-z. Urologe A. 2006. PMID: 16465524 Review. German.

10

Frequent gains of the short arm of chromosome 9 in multiple myeloma with normal G-banded karyotype detected by comparative genomic hybridization.

Tchinda J, Volpert S, Kropff M, Berdel WE, Kienast J, Meinhardt F, Horst J. Tchinda J, et al. Am J Clin Pathol. 2004 Dec;122(6):875-82. doi: 10.1309/5KWK-P6UK-GNXX-HMYH. Am J Clin Pathol. 2004. PMID: 15539380

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