Proteins are specifically altered in disease - Really?

Expert Review of Proteomics

Volumn 3, Issue 5, 2006, Pages 469-470

  Zabel, Claus ^a  

^a CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

PEROXIREDOXIN;

DEGENERATIVE DISEASE; DISEASE COURSE; EDITORIAL; GEL ELECTROPHORESIS; HISTOPATHOLOGY; HUNTINGTON CHOREA; IMMUNOHISTOCHEMISTRY; MASS SPECTROMETRY; NERVE CELL DEGENERATION; NONHUMAN; PARKINSON DISEASE; PROTEIN ANALYSIS; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN INTERACTION; PROTEIN SYNTHESIS; WESTERN BLOTTING;

ANIMALS; DISEASE; GENE EXPRESSION PROFILING; HUMANS; NEURODEGENERATIVE DISEASES; POLYMORPHISM, GENETIC; PROTEINS; RESEARCH;

EID: 33750628942     PISSN: 14789450     EISSN: 17448387     Source Type: Journal    
DOI: 10.1586/14789450.3.5.469     Document Type: Editorial

References (3)

1. Zabel C, Sagi D, Kaindl AM et al. Comparative proteomics in neurodegenerative and non-neurodegenerative diseases suggest nodal point proteins in regulatory networking. J. Proteome Res. 5 (8), 1948-1958 (2006).
2. Haynes C, Oldfield CJ, Ji F et al. Intrinsic disorder is a common feature of hub proteins from four eukaryotic interactomes. PLoS Comput. Biol. 2,(8), E100 (2006).
3. Human Protein Reference Database www.hprd.org