PEX2 抗体

Steinberg, Chen, Wei, Moser, Moser, Cutting, Braverman: "The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum." in: Molecular genetics and metabolism, Vol. 83, Issue 3, pp. 252-63, (2004) (PubMed).

Kim, Lowenson, MacLaren, Clarke, Young: "Deficiency of a protein-repair enzyme results in the accumulation of altered proteins, retardation of growth, and fatal seizures in mice." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 94, Issue 12, pp. 6132-7, (1997) (PubMed).

MacLaren, Clarke: "Expression and purification of a human recombinant methyltransferase that repairs damaged proteins." in: Protein expression and purification, Vol. 6, Issue 1, pp. 99-108, (1995) (PubMed).

Galus, Lagos, Romanik, OConnor: "Structural analysis of transcripts for the protein L-isoaspartyl methyltransferase reveals multiple transcription initiation sites and a distinct pattern of expression in mouse testis: identification of a 5'-flanking sequence with promoter activity." in: Archives of biochemistry and biophysics, Vol. 312, Issue 2, pp. 524-33, (1994) (PubMed).

MacLaren, Kagan, Clarke: "Alternative splicing of the human isoaspartyl protein carboxyl methyltransferase RNA leads to the generation of a C-terminal -RDEL sequence in isozyme II." in: Biochemical and biophysical research communications, Vol. 185, Issue 1, pp. 277-83, (1992) (PubMed).

Romanik, Ladino, Killoy, DArdenne, OConnor: "Genomic organization and tissue expression of the murine gene encoding the protein beta-aspartate methyltransferase." in: Gene, Vol. 118, Issue 2, pp. 217-22, (1992) (PubMed).