GeneChip analyses point to novel pathogenetic mechanisms in mantle cell lymphoma

British Journal of Haematology

Volumn 144, Issue 3, 2009, Pages 317-331

  Vater, Inga ^a   Wagner, Florian ^b,h   Kreuz, Markus ^c   Berger, Hilmar ^c   Martín Subero, José I ^a   Pott, Christiane ^a   Martinez Climent, Jose A ^d   Klapper, Wolfram ^a   Krause, Kristina ^a   Dyer, Martin J S ^e   Gesk, Stefan ^a   Harder, Lana ^a   Zamo, Alberto ^f   Dreyling, Martin ^g   Hasenclever, Dirk ^c   Arnold, Norbert ^a   Siebert, Reiner ^a  

^a UNIVERSITY OF KIEL   (Germany)

^b German Genome Resource Center RZPD   (Germany)

^c UNIVERSITY OF LEIPZIG   (Germany)

^d UNIVERSITY OF NAVARRA   (Spain)

^e UNIVERSITY OF LEICESTER   (United Kingdom)

^f UNIVERSITY OF VERONA   (Italy)

^g LUDWIG MAXIMILIANS UNIVERSITY   (Germany)

^h ATLAS BIOLABS GMBH   (Germany)

Author keywords

Mantle cell lymphoma; Microarray; Microtubule associated proteins; Partial uniparental disomy; Single nucleotide polymorphisms

Indexed keywords

MICROTUBULE ASSOCIATED PROTEIN; MICROTUBULE ASSOCIATED PROTEIN 2; MICROTUBULE ASSOCIATED PROTEIN 6; PROTEIN P53; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME LOSS; CLINICAL ARTICLE; CONTROLLED STUDY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MAPPING; GENETIC GAIN; HUMAN; HUMAN CELL; HUMAN TISSUE; MANTLE CELL LYMPHOMA; MUTATIONAL ANALYSIS; PATHOGENESIS; PRIORITY JOURNAL; UNIPARENTAL DISOMY;

CELL LINE, TUMOR; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 14; GENE AMPLIFICATION; GENE DELETION; GENE EXPRESSION PROFILING; GENOMICS; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LOSS OF HETEROZYGOSITY; LYMPHOMA, MANTLE-CELL; MICROTUBULE-ASSOCIATED PROTEINS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; TRANSLOCATION, GENETIC; UNIPARENTAL DISOMY;

EID: 58449094041     PISSN: 00071048     EISSN: 13652141     Source Type: Journal    
DOI: 10.1111/j.1365-2141.2008.07443.x     Document Type: Article

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