Indications for a tumor suppressor gene at 22q11 involved in the pathogenesis of ependymal tumors and distinct from hSNF5/INI1

Acta Neuropathologica

Volumn 102, Issue 1, 2001, Pages 69-74

  Kraus, Jürgen A ^a   De Millas, Walter ^a   Sörensen, Nils ^b   Herbold, Christian ^b   Schichor, Christian ^b   Tonn, Jörg C ^b   Wiestler, Otmar D ^a   Von Deimling, Andreas ^c   Pietsch, Torsten ^a  

^a UNIVERSITY HOSPITAL BONN   (Germany)

^b UNIVERSITY OF WÜRZBURG   (Germany)

^c HUMBOLDT UNIVERSITY   (Germany)

Author keywords

Brain neoplasms; Ependymoma; hSNF5 INI1; Tumor suppressor gene

Indexed keywords

BIOLOGICAL MARKER; GENE PRODUCT; MICROSATELLITE DNA; PROTEIN HSNF5; PROTEIN INI1; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ALLELE; ARTICLE; CHILD; CHROMOSOME 22Q; CHROMOSOME ARM; CHROMOSOME LOSS; CHROMOSOME STRUCTURE; CLINICAL ARTICLE; CONTROLLED STUDY; DNA FLANKING REGION; EPENDYMA CELL; EPENDYMOMA; FEMALE; GENE DELETION; GENE LOCATION; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC CODE; GENETIC DISORDER; GENETIC PREDISPOSITION; HUMAN; HUMAN TISSUE; KIDNEY TUMOR; MALE; MOLECULAR GENETICS; NEUROEPITHELIOMA; NEUROFIBROMATOSIS; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; RHABDOID TUMOR; SPINAL CORD TUMOR; TUMOR CLASSIFICATION; TUMOR SUPPRESSOR GENE;

EID: 0034902932     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004010000353     Document Type: Article

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