TARGETED DISRUPTION OF THE MOUSE HOMOLOGUE OF GENES RESPONSIBLE FOR HUMAN NEUROLOGICAL DISEASES
- 2 Anni 1995/1997
- 72.304€ Totale Fondi
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Pubblicazioni Scientifiche
- 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
- 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
- 1997 HUMAN MOLECULAR GENETICS
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome