Literature DB >> 15004461

Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method.

A Weise1, A Heller, H Starke, K Mrasek, A Kuechler, B L Pool-Zobel, U Claussen, T Liehr.   

Abstract

Multicolor chromosome banding (MCB) using one single chromosome-specific MCB probe set per experiment was previously reported as powerful tool in molecular cytogenetics for the characterization of all kinds of human marker chromosomes. However, a quick analysis of karyotypes with highly complex chromosomal changes was hampered by the problem that up to 24 MCB experiments were necessary for a comprehensive karyotype description. To overcome that limitation the 138 available region-specific microdissection-derived libraries for all human chromosomes were combined to one single probe set, called multitude MCB (mMCB). A typical fluorescence banding pattern along the human karyotype is produced, which can be evaluated either by transforming these profiles into chromosome region-specific pseudo-colors or more reliably by studying the fluorescence profiles. The mMCB probe set has been applied on chromosomes of normal male and female probands, two primary myelodysplastic syndromes and two solid tumor cell lines. Additionally, a cell line of Gorilla gorilla (GGO) studied previously by single chromosome-specific MCB was reevaluated by the mMCB method. All results were in concordance with those obtained in parallel or by other cytogenetic and molecular cytogenetic approaches indicating that mMCB is a powerful multicolor FISH banding tool for fast characterization of complex karyotypes. Copyright 2003 S. Karger AG, Basel

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Year:  2003        PMID: 15004461     DOI: 10.1159/000076286

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  10 in total

1.  Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set.

Authors:  Anja Weise; Kristin Mrasek; Ina Fickelscher; Uwe Claussen; Sau Wai Cheung; Wei Wen Cai; Thomas Liehr; Nadezda Kosyakova
Journal:  J Histochem Cytochem       Date:  2008-02-05       Impact factor: 2.479

2.  A novel IGH@ gene rearrangement associated with CDKN2A/B deletion in young adult B-cell acute lymphoblastic leukemia.

Authors:  Moneeb A K Othman; Beata Grygalewicz; Barbara Pienkowska-Grela; Jolanta Rygier; Anna Ejduk; Martina Rincic; Joana B Melo; Isabel M Carreira; Britta Meyer; Thomas Liehr
Journal:  Oncol Lett       Date:  2016-01-29       Impact factor: 2.967

3.  Novel Cryptic Rearrangements in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Involving the MLL Gene.

Authors:  Moneeb A K Othman; Beata Grygalewicz; Barbara Pienkowska-Grela; Martina Rincic; Katharina Rittscher; Joana B Melo; Isabel M Carreira; Britta Meyer; Watek Marzena; Thomas Liehr
Journal:  J Histochem Cytochem       Date:  2015-02-19       Impact factor: 2.479

4.  Painting the chromosomes of Brachypodium: current status and future prospects.

Authors:  Dominika Idziak; Alexander Betekhtin; Elzbieta Wolny; Karolina Lesniewska; Jonathan Wright; Melanie Febrer; Michael W Bevan; Glyn Jenkins; Robert Hasterok
Journal:  Chromosoma       Date:  2011-06-11       Impact factor: 4.316

5.  High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia.

Authors:  Moneeb A K Othman; Joana B Melo; Isabel M Carreira; Martina Rincic; Anita Glaser; Beata Grygalewicz; Bernd Gruhn; Kathleen Wilhelm; Katharina Rittscher; Britta Meyer; Maria Luiza Macedo Silva; Terezinha de Jesus Marques Salles; Thomas Liehr
Journal:  Mol Cytogenet       Date:  2015-06-30       Impact factor: 2.009

6.  A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia.

Authors:  Moneeb A K Othman; Martina Rincic; Joana B Melo; Isabel M Carreira; Eyad Alhourani; Friederike Hunstig; Anita Glaser; Thomas Liehr
Journal:  Leuk Res Treatment       Date:  2014-10-08

7.  Microdissection of lampbrush chromosomes as an approach for generation of locus-specific FISH-probes and samples for high-throughput sequencing.

Authors:  Anna Zlotina; Tatiana Kulikova; Nadezda Kosyakova; Thomas Liehr; Alla Krasikova
Journal:  BMC Genomics       Date:  2016-02-20       Impact factor: 3.969

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

Authors:  Maria Luiza Macedo Silva; Maria do Socorro Pombo-de-Oliveira; Susana C Raimondi; Hasmik Mkrtchyan; Eliana Abdelhay; Amanda Faria de Figueiredo; Mariana Tavares de Souza; Daniela Ribeiro Ney Garcia; Eliane Maria Soares de Ventura; Adriana Martins de Sousa; Thomas Liehr
Journal:  Mol Cytogenet       Date:  2009-02-19       Impact factor: 2.009

9.  Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon.

Authors:  Marina Manvelyan; Friederike Hunstig; Kristin Mrasek; Samarth Bhatt; Franck Pellestor; Anja Weise; Thomas Liehr
Journal:  Mol Cytogenet       Date:  2008-04-29       Impact factor: 2.009

10.  First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae).

Authors:  Fan Xiaobo; Krit Pinthong; Hasmik Mkrtchyan; Pornnarong Siripiyasing; Nadezda Kosyakova; Weerayuth Supiwong; Alongkoad Tanomtong; Arunrat Chaveerach; Thomas Liehr; Marcelo de Bello Cioffi; Anja Weise
Journal:  Mol Cytogenet       Date:  2013-12-17       Impact factor: 2.009

  10 in total

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