Literature DB >> 11354630

A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).

A Nietzel1, M Rocchi, H Starke, A Heller, W Fiedler, I Wlodarska, I F Loncarevic, V Beensen, U Claussen, T Liehr.   

Abstract

Centromere-specific multi-color FISH (cenM-FISH) is a new multicolor FISH technique that allows the simultaneous characterization of all human centromeres by using labeled centromeric satellite DNA as probes. This approach allows the rapid identification of all human centromeres by their individual pseudo-coloring in one single step and is therefore a powerful tool in molecular cytogenetics. CenM-FISH fills a gap in multicolor karyotyping using WCP probes and distinguishes all centromeric regions apart from the evolutionary highly conserved regions on the chromosomes 13 and 21. The usefulness of the cenM-FISH technique for the characterization of small supernumerary marker chromosomes with no (or nearly no) euchromatin and restricted amounts of available sample material is demonstrated in prenatal, postnatal, and tumor cytogenetic cases. In addition, rarely described markers with the involvement of heterochromatic material inserted into homogeneously staining regions could be identified and characterized by using the cenM-FISH technique.

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Year:  2001        PMID: 11354630     DOI: 10.1007/s004390100459

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  27 in total

1.  Higher-order organization and compartmentalization of satellite DNA PIM357 in species of the coleopteran genus Pimelia.

Authors:  Joan Pon; Carlos Juan; Eduard Petitpierre
Journal:  Chromosome Res       Date:  2002       Impact factor: 5.239

2.  Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs).

Authors:  T Liehr; G Hickmann; P Kozlowski; U Claussen; H Starke
Journal:  Chromosome Res       Date:  2004       Impact factor: 5.239

3.  How to narrow down chromosomal breakpoints in small and large derivative chromosomes--a new probe set.

Authors:  Ahmed B Hamid; Katharina Kreskowski; Anja Weise; Nadezda Kosayakova; Kristin Mrasek; Martin Voigt; Roberta Santos Guilherme; Rebecca Wagner; David Hardekopf; Sona Pekova; Tatyana Karamysheva; Thomas Liehr; Elisabeth Klein
Journal:  J Appl Genet       Date:  2012-04-29       Impact factor: 3.240

4.  A new multicolor fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH.

Authors:  Maria Bucksch; Monika Ziegler; Nadezda Kosayakova; Milene V Mulatinho; Milene V Mulhatino; Juan C Llerena; Susanne Morlot; Wolfgang Fischer; Anna D Polityko; Anna I Kulpanovich; Michael B Petersen; Britta Belitz; Vladimir Trifonov; Anja Weise; Thomas Liehr; Ahmed B Hamid
Journal:  J Histochem Cytochem       Date:  2012-04-17       Impact factor: 2.479

5.  Twenty-four chromosome FISH in human IVF embryos reveals patterns of post-zygotic chromosome segregation and nuclear organisation.

Authors:  D Ioannou; K G L Fonseka; E J Meershoek; A R Thornhill; A Abogrein; M Ellis; D K Griffin
Journal:  Chromosome Res       Date:  2012-06-29       Impact factor: 5.239

6.  Human interphase chromosomes: a review of available molecular cytogenetic technologies.

Authors:  Svetlana G Vorsanova; Yuri B Yurov; Ivan Y Iourov
Journal:  Mol Cytogenet       Date:  2010-01-11       Impact factor: 2.009

7.  Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis.

Authors:  Diane Van Opstal; Marjan Boter; Petra Noomen; Malgorzata Srebniak; Guus Hamers; Robert-Jan H Galjaard
Journal:  Mol Cytogenet       Date:  2011-01-14       Impact factor: 2.009

8.  Human male recombination maps for individual chromosomes.

Authors:  Fei Sun; Maria Oliver-Bonet; Thomas Liehr; Heike Starke; Evelyn Ko; Alfred Rademaker; Joaquima Navarro; Jordi Benet; Renée H Martin
Journal:  Am J Hum Genet       Date:  2004-02-18       Impact factor: 11.025

9.  Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report.

Authors:  Joaquín Fernández-Toral; Laura Rodríguez; Ana Plasencia; María Luisa Martínez-Frías; Elisabeth Ewers; Ahmed B Hamid; Monika Ziegler; Thomas Liehr
Journal:  J Med Case Rep       Date:  2010-08-03

10.  Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.

Authors:  Joanna Pietrzak; Kristin Mrasek; Ewa Obersztyn; Pawel Stankiewicz; Nadezda Kosyakova; Anja Weise; Sau Wai Cheung; Wei Wen Cai; Ferdinand von Eggeling; Tadeusz Mazurczak; Ewa Bocian; Thomas Liehr
Journal:  J Appl Genet       Date:  2007       Impact factor: 3.240

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