TARGETED DISRUPTION OF THE MOUSE HOMOLOGUE OF GENES RESPONSIBLE FOR HUMAN NEUROLOGICAL DISEASES

Scientific Publications

• 1999 MOLECULAR GENETICS AND METABOLISM

  Isolation and characterization of a novel transcript embedded within HIRA, a gene deleted in DiGeorge syndrome

• 1996 HUMAN MOLECULAR GENETICS

  cDNA characterization and chromosomal mapping of two human homologues of the Drosophila dishevelled polarity gene

• 1997 HUMAN MOLECULAR GENETICS

  UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome

• 2000 DEVELOPMENT

  Sox2 regulatory sequences direct expression of a beta-geo transgene to telencephalic neural stem cells and precursors of the mouse embryo, revealing regionalization of gene expression in CNS stem cells

• 1996 AMERICAN JOURNAL OF HUMAN GENETICS

  Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome

• 2001 CYTOGENETICS AND CELL GENETICS

  Cloning and molecular characterization of three Ubiquitin Fusion Degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster