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KA Rack

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Yeast Artificial Chromosomes

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Helena Urbankova; Peter Van Loo; Peter Vandenberghe; Johan Verschuere; Mathijs Baens; Wim de Kelver; Chris de Wolf-Peeters; André Delannoy; Hilde Demuynck; Daan Dierickx; Julio Finalet Ferreiro; Marie Jarošová; Beata Katrincsakova; Lucienne Michaux; KA Rack; Thomas Tousseyn; Iwona Wlodarska
Recurrent breakpoints in 14q32.13/TCL1A region in mature B-cell neoplasms with villous lymphocytes.
Fiona M Ross; Pieter Sonneveld; Adele M Testi; Zuzana Zemanova; Geneviève Ameye; Hervé Avet-Loiseau; Paolo Bernasconi; Laura Chiecchio; Anna Collin; Klara Dalva; Sonia Fabris; Norma C Gutiérrez; N. Emil U. Hermansen; Clare Hodkinson; Marie Jarosova; Hans E Johnsen; Gitte Kerndrup; Petr Kuglik; Dariusz Ladon; Peter Liebisch; Brigitte Maes; Kyra Michalova; Lucienne Michau; Kai Neben; Mette Nyegaard; Sheila O'Connor; Hélène A Poirel; Rebecca Protheroe; KA Rack; Alberto Rocci
Report from the European Myeloma Network on interphase FISH in multiple myeloma and related disorders.
Natalie Put; Benoît Quilichini; KA Rack; Isabelle Radford-Weiss; Stéphanie Struski; Katrien Van Roosbroeck; Peter Vandenberghe; Iwona Wlodarska; Carole Barin; Caroline Brusselmans; Elise Chapiro; Nicole Dastugue; Virginie Eclache; Sandra Fert-Ferrer; Nathalie Gachard; Carine Gervais; Anne Hagemeijer; Peter Konings; Sophy Laibe; Christine Lefebvre; Peter Meeus; Lucienne Michaux; Yves Moreau; Marie-Joëlle Mozziconacci; Florence Nguyen Khac; Hélène A Poirel
Chronic lymphocytic leukemia and prolymphocytic leukemia with MYC translocations: a subgroup with an aggressive disease course.

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All Publications

2012: Helena Urbankova; Peter Van Loo; Peter Vandenberghe; Johan Verschuere; Mathijs Baens; Wim de Kelver; Chris de Wolf-Peeters; André Delannoy; Hilde Demuynck; Daan Dierickx; Julio Finalet Ferreiro; Marie Jarošová; Beata Katrincsakova; Lucienne Michaux; KA Rack; Thomas Tousseyn; Iwona Wlodarska
Recurrent breakpoints in 14q32.13/TCL1A region in mature B-cell neoplasms with villous lymphocytes.
Leukemia & lymphoma 2012;53(12):2449-55.
2012: Fiona M Ross; Pieter Sonneveld; Adele M Testi; Zuzana Zemanova; Geneviève Ameye; Hervé Avet-Loiseau; Paolo Bernasconi; Laura Chiecchio; Anna Collin; Klara Dalva; Sonia Fabris; Norma C Gutiérrez; N. Emil U. Hermansen; Clare Hodkinson; Marie Jarosova; Hans E Johnsen; Gitte Kerndrup; Petr Kuglik; Dariusz Ladon; Peter Liebisch; Brigitte Maes; Kyra Michalova; Lucienne Michau; Kai Neben; Mette Nyegaard; Sheila O'Connor; Hélène A Poirel; Rebecca Protheroe; KA Rack; Alberto Rocci
Report from the European Myeloma Network on interphase FISH in multiple myeloma and related disorders.
Haematologica 2012;97(8):1272-7.
2012: Natalie Put; Benoît Quilichini; KA Rack; Isabelle Radford-Weiss; Stéphanie Struski; Katrien Van Roosbroeck; Peter Vandenberghe; Iwona Wlodarska; Carole Barin; Caroline Brusselmans; Elise Chapiro; Nicole Dastugue; Virginie Eclache; Sandra Fert-Ferrer; Nathalie Gachard; Carine Gervais; Anne Hagemeijer; Peter Konings; Sophy Laibe; Christine Lefebvre; Peter Meeus; Lucienne Michaux; Yves Moreau; Marie-Joëlle Mozziconacci; Florence Nguyen Khac; Hélène A Poirel
Chronic lymphocytic leukemia and prolymphocytic leukemia with MYC translocations: a subgroup with an aggressive disease course.
Annals of hematology 2012;91(6):863-73.
2012: Francois P Duhoux; Christian Herens; Marina Lafage; Sophy Laibe; Dominique Latinne; Jeanne-Marie Libouton; Eric Lippert; Lucienne Michaux; Carmen P Montano-Almendras; Marie-Joëlle Mozziconacci; Francine Mugneret; N Nadal; Hélène A Poirel; KA Rack; Sophie Raynaud; Steven Richebourg; Catherine Roche-Lestienne; Frank Speleman; Stéphanie Struski; Pascaline Talmant; Sylvie Taviaux; Isabelle Tigaud; Iwona Wlodarska; Geneviève Ameye; Nathalie Auger; Khadija Bahloula; Jean-Baptiste Demoulin
PRDM16 (1p36) translocations define a distinct entity of myeloid malignancies with poor prognosis but may also occur in lymphoid malignancies.
British journal of haematology 2012;156(1):76-88.
2006: Serge Romana; Isabelle Radford-Weiss; Raouf Ben-Abdelali; C Schluth; A Petit; Nicole Dastugue; Pascaline Talmant; Chrystèle Bilhou-Nabera; Francine Mugneret; Marina Lafage-Pochitaloff; Marie-Joëlle Mozziconacci; J Andrieu; Jean-Luc Lai; Christine Terre; KA Rack; Pascale Cornillet-Lefebvre; Isabelle Luquet; N Nadal; Florence Nguyen Khac; Christine Perot; Jacqueline van den Akker; Sandra Fert-Ferrer; Christine Cabrol; Christiane Charrin; Isabelle Tigaud; Hélène A Poirel; Michel Vekemans; Olivier A Bernard; Roland Berger
NUP98 rearrangements in hematopoietic malignancies: a study of the Groupe Francophone de Cytogénétique Hématologique.
Leukemia 2006;20(4):696-706.
1999: C J Harrison; Isabelle Radford-Weiss; F Ross; KA Rack; Gwenaël Le Guyader; Michel Vekemans; Elizabeth Macintyre
Fluorescence in situ hybridization analysis of masked (8;21)(q22;q22) translocations.
Cancer genetics and cytogenetics 1999;112(1):15-20.
1998: KA Rack; F Salomon-Nguyen; Isabelle Radford-Weiss; M O Gil; C Schmitt; Coralie Belanger; Sylvie Nusbaum; Michel Vekemans; Françoise Valensi; Elizabeth Macintyre
FISH detection of chromosome 14q32/IgH translocations: evaluation in follicular lymphoma.
British journal of haematology 1998;103(2):495-504.
1998: KA Rack; Eric Delabesse; Isabelle Radford-Weiss; P Bourquelot; Gwenaël Le Guyader; Michel Vekemans; Elizabeth Macintyre
Simultaneous detection of MYC, BVR1, and PVT1 translocations in lymphoid malignancies by fluorescence in situ hybridization.
Genes, chromosomes & cancer 1998;23(3):220-6.
1998: Xavier Troussard; Laurent Mauvieux; Isabelle Radford-Weiss; KA Rack; Françoise Valensi; Richard Garand; Michel Vekemans; Georges Flandrin; Elizabeth Macintyre
Genetic analysis of splenic lymphoma with villous lymphocytes: a Groupe Français d'Hématologie Cellulaire (GFHC) study.
British journal of haematology 1998;101(4):712-21.
1997: KA Rack; F Cornélis; Isabelle Radford-Weiss; Alain BERNHEIM; C J Harrison; Olivier Hermine; Marguerite Prieur; Michel Vekemans; Elizabeth Macintyre
A chromosome 14q11/TCR alpha/delta specific yeast artificial chromosome improves the detection rate and characterization of chromosome abnormalities in T-lymphoproliferative disorders.
Blood 1997;90(3):1233-40.
1996: H Poirel; KA Rack; Eric Delabesse; Isabelle Radford-Weiss; Xavier Troussard; C Debert; Daniel Leboeuf; Christian Bastard; Françoise Picard; A Veil-Buzyn; Georges Flandrin; O Bernard; Elizabeth Macintyre
Incidence and characterization of MLL gene (11q23) rearrangements in acute myeloid leukemia M1 and M5.
Blood 1996;87(6):2496-505.
1995: S Lewis; D Oscier; Jacqueline Boultwood; F Ross; M Fitchett; KA Rack; G Abrahamson; V Buckle; james wainscoat
Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion.
American journal of hematology 1995;49(3):194-200.
1995: H Poirel; Isabelle Radford-Weiss; KA Rack; Xavier Troussard; A Veil; Françoise Valensi; Françoise Picard; Martine Guesnu; Daniel Leboeuf; Josiane Melle
Detection of the chromosome 16 CBF beta-MYH11 fusion transcript in myelomonocytic leukemias.
Blood 1995;85(5):1313-22.
1994: KA Rack; J Chelly; Richard J Gibbons; S Rider; D Benjamin; R G Lafreniére; D Oscier; R W Hendriks; IW Craig; H F Willard
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia.
Human molecular genetics 1994;3(7):1053-9.
1993: N S Thomas; J Chelly; Jonathan (Jon) Zonana; K J Davies; S Morgan; J Gault; KA Rack; V J Buckle; Neil Brockdorff; A Clarke
Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA).
Human molecular genetics 1993;2(10):1679-85.
1993: KA Rack; Peter C Harris; A B MacCarthy; R Boone; H Raynham; M McKinley; M Fitchett; C M Towe; P Rudd; J A Armour
Characterization of three de novo derivative chromosomes 16 by "reverse chromosome painting" and molecular analysis.
American journal of human genetics 1993;52(5):987-97.
1993: G M Abrahamson; KA Rack; David Oscier; M Fitchett; V J Buckle; james wainscoat
Comparison of cytogenetic and restriction fragment length polymorphism analyses for the detection of loss of chromosome material in clonal hemopoietic disorders.
American journal of hematology 1993;42(2):171-6.
1992: C N Robson; D Hochhauser; R Craig; KA Rack; V J Buckle; I D Hickson
Structure of the human DNA repair gene HAP1 and its localisation to chromosome 14q 11.2-12.
Nucleic acids research 1992;20(17):4417-21.
1991: G Abrahamson; Jacqueline Boultwood; J Madden; S Kelly; David Oscier; KA Rack; V J Buckle; james wainscoat
Clonality of cell populations in refractory anaemia using combined approach of gene loss and X-linked restriction fragment length polymorphism-methylation analyses.
British journal of haematology 1991;79(4):550-5.
1991: Jacqueline Boultwood; KA Rack; S Kelly; J Madden; A Y Sakaguchi; L M Wang; David Oscier; V J Buckle; james wainscoat
Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(14):6176-80.
1991: Mark Hirst; KA Rack; Y Nakahori; A Roche; M V Bell; G Flynn; Z Christadoulou; R N MacKinnon; M Francis; A J Littler
A YAC contig across the fragile X site defines the region of fragility.
Nucleic acids research 1991;19(12):3283-8.
1991: G M Abrahamson; KA Rack; V J Buckle; David Oscier; S Kelly; james wainscoat
Translocation 1;7 in hematologic disorders--a report of three further cases. Absence of amplification of the gene for the epidermal growth factor receptor.
Cancer genetics and cytogenetics 1991;53(1):91-5.
1991: Andrew O M Wilkie; Douglas R Higgs; KA Rack; V J Buckle; N K Spurr; N Fischel-Ghodsian; Isabella Ceccherini; W R Brown; Peter C Harris
Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16.
Cell 1991;64(3):595-606.
1990: Jacqueline Boultwood; KA Rack; V J Buckle; S Kelly; J Madden; David Oscier; james wainscoat
Homozygous deletion of FMS in a patient with the 5q- syndrome.
British journal of haematology 1990;76(2):310-1.
1990: Jacqueline Boultwood; G Abrahamson; V J Buckle; KA Rack; David Oscier; james wainscoat
Structure of the granulocyte macrophage colony-stimulating factor gene in patients with the myelodysplastic syndromes.
American journal of hematology 1990;34(2):157-8.