Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Christiane Bommer"'
Autor:
Theo D. Kim, Seval Türkmen, Michaela Schwarz, Gökben Koca, Hendrik Nogai, Christiane Bommer, Bernd Dörken, Peter Daniel, Philipp le Coutre
Publikováno v:
Haematologica, Vol 95, Iss 4 (2010)
Background Additional chromosomal aberrations in Philadelphia chromosome-positive chronic myeloid leukemia are non-random and strongly associated with disease progression, but their prognostic impact and effect on treatment response is not clear. Poi
Externí odkaz:
https://doaj.org/article/c4a7292cc6db4fdebaad6db8e99ebaa6
Autor:
Jörg Westermann, Seval Türkmen, Renate Arnold, Michaela Schwarz, Bernd Dörken, Philipp Hemmati, Philipp le Coutre, Thomas Burmeister, Christiane Bommer, Nina Rosa Neuendorff
Publikováno v:
Acta Haematologica. 133:237-241
The presence of a Philadelphia chromosome with a corresponding BCR-ABL1 rearrangement is the hallmark of chronic myeloid leukemia, but is considered a very rare event in de novo acute myeloid leukemia (AML). Here, we report the first case in which a
Autor:
Heidemarie Neitzel, Reham Moftah, Dalal El-Kaffash, Mohsen Karbasiyan, Christiane Bommer, Raymonda Varon, Salah Marzouk
Publikováno v:
Advances in Reproductive Sciences. :21-28
Objectives: The currently available methods for rapid prenatal diagnosis of common chromosomal aneuploidies are either Interphase-Fluorescence in Situ Hybridisation (I-FISH) or Quanti- tative Fluorescent Polymerase Chain Reaction (QF-PCR). QF-PCR rep
Autor:
Manfred Grabherr, Richard Reinhardt, Stefan Mundlos, Patricia Heyn, Heidemarie Neitzel, Anja Weise, Martin Werber, Bernd Timmermann, Thomas Liehr, Kateryna Konrat, Carola Dietrich, Katrin Hoffmann, Nadezdaa Kosyakova, Tom H. Lindner, Christiane Bommer, Anna Rajab
Publikováno v:
European Journal of Human Genetics. 18:457-462
The linkage of disease gene mapping with DNA sequencing is an essential strategy for defining the genetic basis of a disease. New massively parallel sequencing procedures will greatly facilitate this process, although enrichment for the target region
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 20:546-552
Objective Congenital heart defects (CHD), particularly conotruncal anomalies, may be associated with deletion of chromosome 22q11.2. Thymic aplasia or hypoplasia is known to be a typical feature in this condition. We aimed to establish (i) the preval
Autor:
Rolf Becker, R. D. Wegner, Gundula Thiel, Rainer Bollmann, Ines Schulzke, H. Körner, C. Tennstedt, Christiane Bommer, Katarina Lehmann, Maik Urban
Publikováno v:
American Journal of Medical Genetics. 108:97-104
Prenatal and postnatal findings in three fetuses with a ring chromosome 6 are presented, and the literature of this rare cytogenetic disorder is reviewed. The described fetuses illustrate the broad spectrum of the clinical manifestation of ring chrom
Autor:
Nina Rosa, Neuendorff, Michaela, Schwarz, Philipp, Hemmati, Seval, Türkmen, Christiane, Bommer, Thomas, Burmeister, Bernd, Dörken, Philipp, le Coutre, Renate, Arnold, Jörg, Westermann
Publikováno v:
Acta haematologica. 133(2)
The presence of a Philadelphia chromosome with a corresponding BCR-ABL1 rearrangement is the hallmark of chronic myeloid leukemia, but is considered a very rare event in de novo acute myeloid leukemia (AML). Here, we report the first case in which a
Autor:
Una Janke, Michaela Endres, Christian Kaps, Lars Morawietz, Christiane Bommer, Marc Trimborn, Peter C. Kreuz, Jan-Philipp Krüger
Publikováno v:
Acta biomaterialia. 8(4)
Scaffold-assisted autologous chondrocyte implantation (ACI) is an effective clinical procedure for cartilage repair. The aim of our study was to evaluate the chromosomal stability of human chondrocytes subjected to typical cell culture procedures nee
Autor:
Theo D. Kim, Gökben Koca, Michaela Schwarz, Peter T. Daniel, Hendrik Nogai, Bernd Dörken, Seval Türkmen, Philipp le Coutre, Christiane Bommer
Publikováno v:
Haematologica. 95(4)
Background Additional chromosomal aberrations in Philadelphia chromosome-positive chronic myeloid leukemia are non-random and strongly associated with disease progression, but their prognostic impact and effect on treatment response is not clear. Poi
Autor:
Gundula Thiel, Seval Türkmen, Christiane Bommer, Heidemarie Neitzel, Andrea Stroux, Martin Schmidt-Hieber, Gregor Richter, Lutz Uharek, Igor Wolfgang Blau, Olga Blau, Eckhard Thiel
Publikováno v:
Cancer genetics and cytogenetics. 198(2)
We analyzed karyotype stability in 22 patients with acute leukemia at relapse or disease progression after allogeneic stem cell transplantation (allo-SCT). Karyotypes before and at relapse after allo-SCT were different in 15 patients (68%), the most