Cloning and characterization of the gene encoding human NPL4, a protein interacting with the ubiquitin fusion-degradation protein (UFD1L)

This publication has 24 references indexed in Scilit:

• DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1
  Nature Genetics, 2001
• Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome
  European Journal of Human Genetics, 1999
• The DNA sequence of human chromosome 22
  Nature, 1999
• Gapped BLAST and PSI-BLAST: a new generation of protein database search programs
  Nucleic Acids Research, 1997
• The Uba2 and Ufd1 proteins of Saccharomyces cerevisiae interact with poly(A) polymerase and affect the polyadenylation activity of cell extracts
  Molecular Genetics and Genomics, 1997
• Nuclear transport defects and nuclear envelope alterations are associated with mutation of the Saccharomyces cerevisiae NPL4 gene.
  Molecular Biology of the Cell, 1996
• A Proteolytic Pathway That Recognizes Ubiquitin as a Degradation Signal
  Journal of Biological Chemistry, 1995
• Chromosome Mapping of the Human Arrestin (SAG), β-Arrestin 2 (ARRB2), and β-Adrenergic Receptor Kinase 2 (ADRBK2) Genes
  Genomics, 1994
• DiGeorge syndrome: an historical review of clinical and cytogenetic features.
  Journal of Medical Genetics, 1993
• A novel genetic system to detect protein–protein interactions
  Nature, 1989