1997
DOI: 10.1007/978-3-662-03493-4_8
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Clinical and Biomedical Applications of Proteomics

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Cited by 38 publications
(5 citation statements)
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“…Because the number of proteins can strongly exceed the number of genes, the task of assigning functional roles to all of these proteins is a formidable task. Although some simplification is offered by the fact that a typical eukaryotic cell may express only 5000–10,000 genes (Hochstrasser, 1997), there is still clearly a need for systematic ways of identifying smaller groups of genes/proteins that are related by function. One of the premises of functional proteomics is that this goal can be achieved via functional stimulation or perturbation of the complex cellular networks.…”
Section: Why Functional Proteomics?mentioning
confidence: 99%
“…Because the number of proteins can strongly exceed the number of genes, the task of assigning functional roles to all of these proteins is a formidable task. Although some simplification is offered by the fact that a typical eukaryotic cell may express only 5000–10,000 genes (Hochstrasser, 1997), there is still clearly a need for systematic ways of identifying smaller groups of genes/proteins that are related by function. One of the premises of functional proteomics is that this goal can be achieved via functional stimulation or perturbation of the complex cellular networks.…”
Section: Why Functional Proteomics?mentioning
confidence: 99%
“…There is already a vast body of literature applying proteomics in many different areas of clinical and biochemical interest and in the study of the pathogenesis, development, prevention, and treatment of a wide range of diseases [1]. …”
Section: Introductionmentioning
confidence: 99%
“…Proteomics is a relatively new but rapidly maturing discipline within life science research for understanding the biology of an organism via the large-scale study of the proteins expressed by the organism. There is already a vast body of literature applying proteomics in many different areas of clinical and biochemical interest and in the study of the pathogenesis, development, prevention, and treatment of a wide range of diseases [ 1 ].…”
Section: Introductionmentioning
confidence: 99%
“…11). Furthermore, the broad range of protein solubility makes it nearly impossible to detect a complete proteome in a 2-DE gel, since poorly soluble and low abundant proteins are lost [21]. Despite the use of tedious protocols for fractionated detergent extractions, it is still impossible to detect 10-15% of total proteins; vice versa, major abundant and easily soluble proteins like albumin and immunoglobulin G (IgG) are too dominant in a gel, thereby abrogating a sensitive analysis.…”
Section: -De and Protein Identificationmentioning
confidence: 99%