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10.1016/S0074-7696(06)52005-4

http://scihub22266oqcxt.onion/10.1016/S0074-7696(06)52005-4
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16984815!7112332!16984815
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suck abstract from ncbi

pmid16984815      Int+Rev+Cytol 2006 ; 252 (ä): 1-69
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  • Cell biology of membrane trafficking in human disease #MMPMID16984815
  • Howell GJ; Holloway ZG; Cobbold C; Monaco AP; Ponnambalam S
  • Int Rev Cytol 2006[]; 252 (ä): 1-69 PMID16984815show ga
  • Understanding the molecular and cellular mechanisms underlying membrane traffic pathways is crucial to the treatment and cure of human disease. Various human diseases caused by changes in cellular homeostasis arise through a single gene mutation(s) resulting in compromised membrane trafficking. Many pathogenic agents such as viruses, bacteria, or parasites have evolved mechanisms to subvert the host cell response to infection, or have hijacked cellular mechanisms to proliferate and ensure pathogen survival. Understanding the consequence of genetic mutations or pathogenic infection on membrane traffic has also enabled greater understanding of the interactions between organisms and the surrounding environment. This review focuses on human genetic defects and molecular mechanisms that underlie eukaryote exocytosis and endocytosis and current and future prospects for alleviation of a variety of human diseases.
  • |*Cell Physiological Phenomena[MESH]
  • |*Genetic Diseases, Inborn/metabolism/physiopathology/therapy[MESH]
  • |*Membrane Proteins/genetics/metabolism[MESH]
  • |Animals[MESH]
  • |Biological Transport[MESH]
  • |Cell Membrane/*physiology[MESH]
  • |Cytoskeleton/metabolism[MESH]
  • |Endocytosis/*physiology[MESH]
  • |Endoplasmic Reticulum/metabolism[MESH]
  • |Exocytosis/*physiology[MESH]
  • |Genetic Therapy[MESH]
  • |Golgi Apparatus/metabolism[MESH]
  • |Humans[MESH]
  • |Lysosomes/metabolism[MESH]
  • |Signal Transduction/physiology[MESH]


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