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Brigitte Schlegelberger

Researcher at University of Kiel

Publications -  94
Citations -  4159

Brigitte Schlegelberger is an academic researcher from University of Kiel. The author has contributed to research in topics: Fluorescence in situ hybridization & Chromosomal translocation. The author has an hindex of 30, co-authored 94 publications receiving 4079 citations. Previous affiliations of Brigitte Schlegelberger include Hannover Medical School.

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Journal ArticleDOI

A physical map of the human genome.

John Douglas Mcpherson, +119 more
- 15 Feb 2001 - 
TL;DR: The construction of the whole-genome bacterial artificial chromosome (BAC) map and its integration with previous landmark maps and information from mapping efforts focused on specific chromosomal regions are reported.
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Inactivating mutations and overexpression of BCL10, a caspase recruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32).

TL;DR: Mucosa-associated lymphoid tissue (MALT) lymphomas most frequently involve the gastrointestinal tract and are the most common subset of extranodal non-Hodgkin lymphoma (NHL), and overexpression of BCL10, a novel apoptotic signalling gene that encodes an amino-terminal caspase recruitment domain (CARD), in MALT lymphomas might have a twofold lymphomagenic effect.
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Patients with de novo acute myeloid leukaemia and complex karyotype aberrations show a poor prognosis despite intensive treatment: a study of 90 patients

TL;DR: In conclusion, complex chromosome aberrations in de novo AML predicted a dismal outcome, even when patients were treated with intensive chemotherapy, and patients under the age of 60’years with complex aberrant karyotypes may benefit from HAM treatment during induction.
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Simultaneous fluorescence immunophenotyping and interphase cytogenetics: a contribution to the characterization of tumor cells.

TL;DR: Using this method, numerically aberrant tumor cells can be identified by interphase cytogenetics and subsequently analyzed immunophenotypically, and since all interphase cellsCan be analyzed, the results are not limited by the number and banding quality of analyzable mitoses.
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Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 11q22.3-923.1 in lymphoproliferative disorders.

TL;DR: A single critical region of 2-3 Mb in size is identified in which 11q14-923 aberrations in LPD cluster are identified, providing the basis for the identification of the gene(s) at 11q22.3- 923.1 that are involved in the pathogenesis of LPD.