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The Journal of Biological Chemistry|March 30, 2001
Divergent N-terminal sequences of a deubiquitinating enzyme modulate substrate specificityH Lin, L Yin, J Reid, et al.
The Journal of Pathology|June 1, 1990
Ubiquitin carboxyl-terminal hydrolase (PGP 9.5) is selectively present in ubiquitinated inclusion bodies characteristic of human neurodegenerative diseasesJ Lowe, H McDermott, M Landon, et al.
Current Eye Research|August 1, 1984
Gentamicin diffusion across hydrogel bandage lenses and its kinetic distribution on the eyeB E McCarey, F H Schmidt, K D Wilkinson, et al.
The EMBO Journal|August 15, 1997
In vivo disassembly of free polyubiquitin chains by yeast Ubp14 modulates rates of protein degradation by the proteasomeAmerik AYu, S Swaminathan, B A Krantz, et al.
The Journal of Biological Chemistry|May 16, 2000
Functional consequence of substitutions at residue 171 in human galactose-1-phosphate uridylyltransferaseC Crews, K D Wilkinson, L Wells, et al.
Nucleic Acids Research|May 29, 2001
The fragile X mental retardation protein inhibits translation via interacting with mRNAZ Li, Y Zhang, L Ku, et al.
The Journal of Biological Chemistry|September 20, 1997
Inhibition of the 26 S proteasome by polyubiquitin chains synthesized to have defined lengthsJ Piotrowski, R Beal, L Hoffman, et al.
The EMBO Journal|July 1, 1997
Crystal structure of a deubiquitinating enzyme (human UCH-L3) at 1.8 A resolutionS C Johnston, C N Larsen, W J Cook, et al.
The EMBO Journal|September 22, 2001
A novel active site-directed probe specific for deubiquitylating enzymes reveals proteasome association of USP14A Borodovsky, B M Kessler, R Casagrande, et al.
The Journal of Biological Chemistry|June 23, 1998
Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation proteinV Brown, K Small, L Lakkis, et al.
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