Ants Kurg

Ants Kurg

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Ants Kurg

Ants Kurg

Publications by authors named "Ants Kurg"

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A dual colour FISH method for routine validation of sexed Bos taurus semen.

BMC Vet Res 2019 Apr 3;15(1):104. Epub 2019 Apr 3.

Institute of Molecular and Cell Biology, University of Tartu, Riia 23, 51010, Tartu, Estonia.

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http://dx.doi.org/10.1186/s12917-019-1839-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6446427PMC
April 2019

A speculative outlook on embryonic aneuploidy: Can molecular pathways be involved?

Dev Biol 2019 03 31;447(1):3-13. Epub 2018 Jan 31.

Department of Biomedicine, Institute of Bio- and Translational Medicine, University of Tartu, Tartu 50411, Estonia; Competence Centre on Health Technologies, Tartu 50410, Estonia; Department of Obstetrics and Gynecology, Institute of Clinical Medicine, University of Tartu, Tartu 51014, Estonia; Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki 00029, Finland.

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http://dx.doi.org/10.1016/j.ydbio.2018.01.014DOI Listing
March 2019

Karyotype of the blastocoel fluid demonstrates low concordance with both trophectoderm and inner cell mass.

Fertil Steril 2018 06;109(6):1127-1134.e1

Cytogenetics Laboratory, Research Institute of Medical Genetics, Tomsk National Research Medical Center of Russian Academy of Sciences, Tomsk, Russian Federation; Department of Medical Genetics, Siberian State Medical University, Tomsk, Russian Federation.

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http://dx.doi.org/10.1016/j.fertnstert.2018.02.008DOI Listing
June 2018

Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome.

BMC Genomics 2015 Sep 16;16:703. Epub 2015 Sep 16.

Competence Centre on Health Technologies, Tiigi 61b, 50410, Tartu, Estonia.

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http://dx.doi.org/10.1186/s12864-015-1916-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573927PMC
September 2015

Syndromic intellectual disability: a new phenotype caused by an aromatic amino acid decarboxylase gene (DDC) variant.

Gene 2015 Apr 14;559(2):144-8. Epub 2015 Jan 14.

Unit of Medical Genetics, Department of Medical and Surgical Sciences, Policlinico St. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.

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http://dx.doi.org/10.1016/j.gene.2015.01.026DOI Listing
April 2015

Monozygotic twins with 17q21.31 microdeletion syndrome.

Twin Res Hum Genet 2014 Oct 9;17(5):405-10. Epub 2014 Jun 9.

Department of Biology and Medical Genetics,Charles University 2nd Faculty of Medicine and University Hospital Motol,Prague,Czech Republic.

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http://dx.doi.org/10.1017/thg.2014.29DOI Listing
October 2014

The human WBSCR22 protein is involved in the biogenesis of the 40S ribosomal subunits in mammalian cells.

PLoS One 2013 23;8(9):e75686. Epub 2013 Sep 23.

Center of Biomedical Technology, Institute of Technology, University of Tartu, Tartu, Estonia.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0075686PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781059PMC
July 2014

Nucleic acid detection technologies and marker molecules in bacterial diagnostics.

Expert Rev Mol Diagn 2014 May 11;14(4):489-500. Epub 2014 Apr 11.

Department of Biotechnology, IMCB, University of Tartu, Riia 23, Tartu 51010, Estonia.

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http://www.tandfonline.com/doi/full/10.1586/14737159.2014.90
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http://dx.doi.org/10.1586/14737159.2014.908710DOI Listing
May 2014

Chromosomal microarray analysis as a first-tier clinical diagnostic test: Estonian experience.

Mol Genet Genomic Med 2014 Mar 9;2(2):166-75. Epub 2014 Jan 9.

Department of Genetics, United Laboratories, Tartu University Hospital Tartu, Estonia ; Department of Pediatrics, University of Tartu Tartu, Estonia.

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http://dx.doi.org/10.1002/mgg3.57DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3960059PMC
March 2014

Patient with dup(5)(q35.2-q35.3) reciprocal to the common Sotos syndrome deletion and review of the literature.

Eur J Med Genet 2013 Apr 28;56(4):202-6. Epub 2013 Jan 28.

Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, 23 Riia Street, 51010 Tartu, Estonia.

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http://linkinghub.elsevier.com/retrieve/pii/S176972121300026
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http://dx.doi.org/10.1016/j.ejmg.2013.01.008DOI Listing
April 2013

A patient with de novo 0.45 Mb deletion of 2p16.1: the role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome.

Am J Med Genet A 2013 Apr 12;161A(4):865-70. Epub 2013 Mar 12.

Department of Biology and Medical Genetics, Charles University 2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.

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http://dx.doi.org/10.1002/ajmg.a.35783DOI Listing
April 2013

Label-free, multiplexed detection of bacterial tmRNA using silicon photonic microring resonators.

Biosens Bioelectron 2012 Jun-Jul;36(1):56-61. Epub 2012 Apr 6.

Department of Biotechnology, Institute of Molecular and Cellular Biology, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1016/j.bios.2012.03.037DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3367093PMC
October 2012

Balanced reciprocal translocation t(5;13)(q33;q12) and 9q31.1 microduplication in a man suffering from infertility and pollinosis.

J Appl Genet 2012 Feb 29;53(1):93-7. Epub 2011 Nov 29.

Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Ravila 19, Tartu, Estonia.

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http://dx.doi.org/10.1007/s13353-011-0078-5DOI Listing
February 2012

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.

Authors:
Sébastien Jacquemont Alexandre Reymond Flore Zufferey Louise Harewood Robin G Walters Zoltán Kutalik Danielle Martinet Yiping Shen Armand Valsesia Noam D Beckmann Gudmar Thorleifsson Marco Belfiore Sonia Bouquillon Dominique Campion Nicole de Leeuw Bert B A de Vries Tõnu Esko Bridget A Fernandez Fernando Fernández-Aranda José Manuel Fernández-Real Mònica Gratacòs Audrey Guilmatre Juliane Hoyer Marjo-Riitta Jarvelin R Frank Kooy Ants Kurg Cédric Le Caignec Katrin Männik Orah S Platt Damien Sanlaville Mieke M Van Haelst Sergi Villatoro Gomez Faida Walha Bai-Lin Wu Yongguo Yu Azzedine Aboura Marie-Claude Addor Yves Alembik Stylianos E Antonarakis Benoît Arveiler Magalie Barth Nathalie Bednarek Frédérique Béna Sven Bergmann Mylène Beri Laura Bernardini Bettina Blaumeiser Dominique Bonneau Armand Bottani Odile Boute Han G Brunner Dorothée Cailley Patrick Callier Jean Chiesa Jacqueline Chrast Lachlan Coin Charles Coutton Jean-Marie Cuisset Jean-Christophe Cuvellier Albert David Bénédicte de Freminville Bruno Delobel Marie-Ange Delrue Bénédicte Demeer Dominique Descamps Gérard Didelot Klaus Dieterich Vittoria Disciglio Martine Doco-Fenzy Séverine Drunat Bénédicte Duban-Bedu Christèle Dubourg Julia S El-Sayed Moustafa Paul Elliott Brigitte H W Faas Laurence Faivre Anne Faudet Florence Fellmann Alessandra Ferrarini Richard Fisher Elisabeth Flori Lukas Forer Dominique Gaillard Marion Gerard Christian Gieger Stefania Gimelli Giorgio Gimelli Hans J Grabe Agnès Guichet Olivier Guillin Anna-Liisa Hartikainen Délphine Heron Loyse Hippolyte Muriel Holder Georg Homuth Bertrand Isidor Sylvie Jaillard Zdenek Jaros Susana Jiménez-Murcia Géraldine Joly Helas Philippe Jonveaux Satu Kaksonen Boris Keren Anita Kloss-Brandstätter Nine V A M Knoers David A Koolen Peter M Kroisel Florian Kronenberg Audrey Labalme Emilie Landais Elisabetta Lapi Valérie Layet Solenn Legallic Bruno Leheup Barbara Leube Suzanne Lewis Josette Lucas Kay D MacDermot Pall Magnusson Christian Marshall Michèle Mathieu-Dramard Mark I McCarthy Thomas Meitinger Maria Antonietta Mencarelli Giuseppe Merla Alexandre Moerman Vincent Mooser Fanny Morice-Picard Mafalda Mucciolo Matthias Nauck Ndeye Coumba Ndiaye Ann Nordgren Laurent Pasquier Florence Petit Rolph Pfundt Ghislaine Plessis Evica Rajcan-Separovic Gian Paolo Ramelli Anita Rauch Roberto Ravazzolo Andre Reis Alessandra Renieri Cristobal Richart Janina S Ried Claudine Rieubland Wendy Roberts Katharina M Roetzer Caroline Rooryck Massimiliano Rossi Evald Saemundsen Véronique Satre Claudia Schurmann Engilbert Sigurdsson Dimitri J Stavropoulos Hreinn Stefansson Carola Tengström Unnur Thorsteinsdóttir Francisco J Tinahones Renaud Touraine Louis Vallée Ellen van Binsbergen Nathalie Van der Aa Catherine Vincent-Delorme Sophie Visvikis-Siest Peter Vollenweider Henry Völzke Anneke T Vulto-van Silfhout Gérard Waeber Carina Wallgren-Pettersson Robert M Witwicki Simon Zwolinksi Joris Andrieux Xavier Estivill James F Gusella Omar Gustafsson Andres Metspalu Stephen W Scherer Kari Stefansson Alexandra I F Blakemore Jacques S Beckmann Philippe Froguel

Nature 2011 Aug 31;478(7367):97-102. Epub 2011 Aug 31.

Service of Medical Genetics, Centre Hospitalier Universitaire Vaudois, 1011 Lausanne, Switzerland.

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http://dx.doi.org/10.1038/nature10406DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637175PMC
August 2011

Fluoride-cleavable, fluorescently labelled reversible terminators: synthesis and use in primer extension.

Chemistry 2011 Mar 3;17(10):2903-15. Epub 2011 Feb 3.

Institut für Organische Chemie und Chemische Biologie, J.W. Goethe Universität Frankfurt am Main, Max-von-Laue Strasse 7, 60438 Frankfurt am Main, Germany.

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http://dx.doi.org/10.1002/chem.201001952DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3110862PMC
March 2011

Detection of NASBA amplified bacterial tmRNA molecules on SLICSel designed microarray probes.

BMC Biotechnol 2011 Feb 28;11:17. Epub 2011 Feb 28.

Dept, of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1186/1472-6750-11-17DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051898PMC
February 2011

Synthesis of four colors fluorescently labelled 3'-O-blocked nucleotides with fluoride cleavable blocking group and linker for array based Sequencing-by-Synthesis applications.

Nucleic Acids Symp Ser (Oxf) 2008 (52):345-6

Institut für Organische Chemie und Chemische Biologie, J. W. Goethe Universität Frankfurt am Main, Max-von-Laue Str. 7, D-60438 Frankfurt am Main, Germany.

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http://dx.doi.org/10.1093/nass/nrn174DOI Listing
November 2010

Detection of tmRNA molecules on microarrays at low temperatures using helper oligonucleotides.

BMC Biotechnol 2010 Apr 28;10:34. Epub 2010 Apr 28.

Department of Bioinformatics, Institute of Molecular and Cell Biology, University of Tartu, Riia 23, Tartu, 51010, Estonia.

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http://dx.doi.org/10.1186/1472-6750-10-34DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2873282PMC
April 2010

Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications.

BMC Biotechnol 2009 May 15;9:45. Epub 2009 May 15.

Department of Biotechnology, Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.

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http://dx.doi.org/10.1186/1472-6750-9-45DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685129PMC
May 2009

Array-MAPH: a methodology for the detection of locus copy-number changes in complex genomes.

Nat Protoc 2008 ;3(5):849-65

Department of Cytogenetics, The Cyprus Institute of Neurology & Genetics, Nicosia, Cyprus.

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http://dx.doi.org/10.1038/nprot.2008.49DOI Listing
August 2008

Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization.

Eur J Hum Genet 2007 Feb 22;15(2):162-72. Epub 2006 Nov 22.

Department of Cytogenetics, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.

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http://dx.doi.org/10.1038/sj.ejhg.5201738DOI Listing
February 2007

Association study of sporadic Parkinson's disease genetic risk factors in patients from Russia by APEX technology.

Neurosci Lett 2006 Sep 28;405(3):212-6. Epub 2006 Jul 28.

Institute of Molecular Genetics, Russian Academy of Sciences, Kurchatov sq. 2, Moscow 123 182, Russia.

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http://dx.doi.org/10.1016/j.neulet.2006.06.066DOI Listing
September 2006

Analysis of SNP profiles in patients with major depressive disorder.

Int J Neuropsychopharmacol 2006 Apr 1;9(2):167-74. Epub 2005 Jun 1.

Department of Physiology, University of Tartu, Tartu, EstoniaVisgenyx Ltd, Tartu, Estonia.

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http://dx.doi.org/10.1017/S1461145705005468DOI Listing
April 2006

MAPH: from gels to microarrays.

Eur J Med Genet 2005 Jul-Sep;48(3):241-9

Department of Cytogenetics, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.

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http://dx.doi.org/10.1016/j.ejmg.2005.04.011DOI Listing
November 2005

Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray.

Clin Chem 2002 Nov;48(11):2051-4

IARC, International Agency for Research on Cancer, 150, Cours Albert Thomas, Lyon 69372, France.

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November 2002