Literature DB >> 12050860

FISH banding methods: applications in research and diagnostics.

Thomas Liehr1, Anita Heller, Heike Starke, Uwe Claussen.   

Abstract

Recently, several chromosome banding techniques based on fluorescence in situ hybridization (FISH) have been developed for the human and the mouse genome. In contrast to the standard chromosome banding techniques presently used, giving a protein-related banding pattern, those FISH techniques are DNA-specific. Currently the FISH banding methods are still under development and no high resolution banding technique is available that can be used for a whole genome in one hybridization. Nevertheless, FISH banding methods were used successfully for research in evolution- and radiation-biology, as well as for studies on the nuclear architecture. Moreover, their suitability for diagnostic purposes has been proven in prenatal, postnatal and tumor cytogenetics, indicating that they are an important tool with the potential to partly replace the conventional banding techniques in future.

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Year:  2002        PMID: 12050860     DOI: 10.1586/14737159.2.3.217

Source DB:  PubMed          Journal:  Expert Rev Mol Diagn        ISSN: 1473-7159            Impact factor:   5.225


  9 in total

1.  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

2.  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

Review 3.  A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.

Authors:  Jörg Seidel; Anita Heller; Gabriele Senger; Heike Starke; Ilse Chudoba; Christina Kelbova; Holger Tönnies; Heidemarie Neitzel; Claudia Haase; Volkmar Beensen; Felix Zintl; Uwe Claussen; Thomas Liehr
Journal:  Eur J Pediatr       Date:  2003-06-19       Impact factor: 3.183

4.  Elongated mouse chromosomes suitable for enhanced molecular cytogenetics.

Authors:  Sherif Louis; Katalin Benedek; Michael Mowat; George Klein; Sabine Mai
Journal:  Cytotechnology       Date:  2004-03       Impact factor: 2.058

5.  Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes.

Authors:  Chiara Castronovo; Emanuele Valtorta; Milena Crippa; Sara Tedoldi; Lorenza Romitti; Maria Cristina Amione; Silvana Guerneri; Daniela Rusconi; Lucia Ballarati; Donatella Milani; Enrico Grosso; Pietro Cavalli; Daniela Giardino; Maria Teresa Bonati; Lidia Larizza; Palma Finelli
Journal:  Mol Cytogenet       Date:  2013-10-30       Impact factor: 2.009

6.  Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.

Authors:  Saadia Amasdl; Abdelhafid Natiq; Siham Chafai Elalaoui; Aziza Sbiti; Thomas Liehr; Abdelaziz Sefiani
Journal:  J Med Case Rep       Date:  2016-05-13

Review 7.  Exceptional Chromosomal Evolution and Cryptic Speciation of Blind Mole Rats Nannospalax leucodon (Spalacinae, Rodentia) from South-Eastern Europe.

Authors:  Ivo Savić; Duško Ćirović; Vanja Bugarski-Stanojević
Journal:  Genes (Basel)       Date:  2017-10-25       Impact factor: 4.096

8.  X-autosome and X-Y Translocations in Female Carriers: X-chromosome Inactivation Easily Detectable by 5-ethynyl-2-deoxyuridine (EdU).

Authors:  M Donat; A Louis; K Kreskowski; M Ziegler; A Weise; I Schreyer; T Liehr
Journal:  Balkan J Med Genet       Date:  2017-06-30       Impact factor: 0.519

9.  The progress on genetic analysis of nasopharyngeal carcinoma.

Authors:  Xiaofeng Zhou; Jing Cui; Virgilia Macias; André A Kajdacsy-Balla; Hui Ye; Jianguang Wang; P Nagesh Rao
Journal:  Comp Funct Genomics       Date:  2007
  9 in total

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