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MeSH Review

Endoplasmic Reticulum

 
 
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Disease relevance of Endoplasmic Reticulum

 

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Chemical compound and disease context of Endoplasmic Reticulum

 

Biological context of Endoplasmic Reticulum

 

Anatomical context of Endoplasmic Reticulum

 

Associations of Endoplasmic Reticulum with chemical compounds

 

Gene context of Endoplasmic Reticulum

 

Analytical, diagnostic and therapeutic context of Endoplasmic Reticulum

References

  1. Degradation of CFTR by the ubiquitin-proteasome pathway. Ward, C.L., Omura, S., Kopito, R.R. Cell (1995) [Pubmed]
  2. The human cytomegalovirus US11 gene product dislocates MHC class I heavy chains from the endoplasmic reticulum to the cytosol. Wiertz, E.J., Jones, T.R., Sun, L., Bogyo, M., Geuze, H.J., Ploegh, H.L. Cell (1996) [Pubmed]
  3. Vesicular stomatitis virus glycoprotein is sorted and concentrated during export from the endoplasmic reticulum. Balch, W.E., McCaffery, J.M., Plutner, H., Farquhar, M.G. Cell (1994) [Pubmed]
  4. Transporter-independent processing of HIV-1 envelope protein for recognition by CD8+ T cells. Hammond, S.A., Bollinger, R.C., Tobery, T.W., Silliciano, R.F. Nature (1993) [Pubmed]
  5. Age-dependent diarrhea induced by a rotaviral nonstructural glycoprotein. Ball, J.M., Tian, P., Zeng, C.Q., Morris, A.P., Estes, M.K. Science (1996) [Pubmed]
  6. Latent S49P neuroserpin forms polymers in the dementia familial encephalopathy with neuroserpin inclusion bodies. Onda, M., Belorgey, D., Sharp, L.K., Lomas, D.A. J. Biol. Chem. (2005) [Pubmed]
  7. alpha-keto-beta-methyl-n-valeric acid diminishes reactive oxygen species and alters endoplasmic reticulum Ca(2+) stores. Huang, H.M., Zhang, H., Ou, H.C., Chen, H.L., Gibson, G.E. Free Radic. Biol. Med. (2004) [Pubmed]
  8. Effects of ethanol on lipid metabolism. Baraona, E., Lieber, C.S. J. Lipid Res. (1979) [Pubmed]
  9. Congenital disorder of glycosylation type Id: clinical phenotype, molecular analysis, prenatal diagnosis, and glycosylation of fetal proteins. Denecke, J., Kranz, C., von Kleist-Retzow, J.C.h., Bosse, K., Herkenrath, P., Debus, O., Harms, E., Marquardt, T. Pediatr. Res. (2005) [Pubmed]
  10. X-box binding protein 1 (XBP1) C--116G polymorphisms in bipolar disorders and age of onset. Hou, S.J., Yen, F.C., Cheng, C.Y., Tsai, S.J., Hong, C.J. Neurosci. Lett. (2004) [Pubmed]
  11. Antigen processing and presentation by the class I major histocompatibility complex. York, I.A., Rock, K.L. Annu. Rev. Immunol. (1996) [Pubmed]
  12. Assembly, transport, and function of MHC class II molecules. Cresswell, P. Annu. Rev. Immunol. (1994) [Pubmed]
  13. Transporters of nucleotide sugars, ATP, and nucleotide sulfate in the endoplasmic reticulum and Golgi apparatus. Hirschberg, C.B., Robbins, P.W., Abeijon, C. Annu. Rev. Biochem. (1998) [Pubmed]
  14. Acyl-coenzyme A:cholesterol acyltransferase. Chang, T.Y., Chang, C.C., Cheng, D. Annu. Rev. Biochem. (1997) [Pubmed]
  15. Role of alternative splicing in generating isoform diversity among plasma membrane calcium pumps. Strehler, E.E., Zacharias, D.A. Physiol. Rev. (2001) [Pubmed]
  16. Expression of the endoplasmic reticulum molecular chaperone (ORP150) rescues hippocampal neurons from glutamate toxicity. Kitao, Y., Ozawa, K., Miyazaki, M., Tamatani, M., Kobayashi, T., Yanagi, H., Okabe, M., Ikawa, M., Yamashima, T., Stern, D.M., Hori, O., Ogawa, S. J. Clin. Invest. (2001) [Pubmed]
  17. Betaine decreases hyperhomocysteinemia, endoplasmic reticulum stress, and liver injury in alcohol-fed mice. Ji, C., Kaplowitz, N. Gastroenterology (2003) [Pubmed]
  18. Integration of a small integral membrane protein, M2, of influenza virus into the endoplasmic reticulum: analysis of the internal signal-anchor domain of a protein with an ectoplasmic NH2 terminus. Hull, J.D., Gilmore, R., Lamb, R.A. J. Cell Biol. (1988) [Pubmed]
  19. A gene on chromosome 11q23 coding for a putative glucose- 6-phosphate translocase is mutated in glycogen-storage disease types Ib and Ic. Veiga-da-Cunha, M., Gerin, I., Chen, Y.T., de Barsy, T., de Lonlay, P., Dionisi-Vici, C., Fenske, C.D., Lee, P.J., Leonard, J.V., Maire, I., McConkie-Rosell, A., Schweitzer, S., Vikkula, M., Van Schaftingen, E. Am. J. Hum. Genet. (1998) [Pubmed]
  20. Dissecting the role of the golgi complex and lipid rafts in biosynthetic transport of cholesterol to the cell surface. Heino, S., Lusa, S., Somerharju, P., Ehnholm, C., Olkkonen, V.M., Ikonen, E. Proc. Natl. Acad. Sci. U.S.A. (2000) [Pubmed]
  21. A mammalian homolog of SEC61p and SECYp is associated with ribosomes and nascent polypeptides during translocation. Görlich, D., Prehn, S., Hartmann, E., Kalies, K.U., Rapoport, T.A. Cell (1992) [Pubmed]
  22. An internal signal sequence: the asialoglycoprotein receptor membrane anchor. Spiess, M., Lodish, H.F. Cell (1986) [Pubmed]
  23. Involvement of the esterase active site of egasyn in compartmentalization of beta-glucuronidase within the endoplasmic reticulum. Medda, S., Stevens, A.M., Swank, R.T. Cell (1987) [Pubmed]
  24. A functionally defective allele of TAP1 results in loss of MHC class I antigen presentation in a human lung cancer. Chen, H.L., Gabrilovich, D., Tampé, R., Girgis, K.R., Nadaf, S., Carbone, D.P. Nat. Genet. (1996) [Pubmed]
  25. Endoplasmic reticulum stress activates cleavage of CREBH to induce a systemic inflammatory response. Zhang, K., Shen, X., Wu, J., Sakaki, K., Saunders, T., Rutkowski, D.T., Back, S.H., Kaufman, R.J. Cell (2006) [Pubmed]
  26. Intracellular CFTR: localization and function. Bradbury, N.A. Physiol. Rev. (1999) [Pubmed]
  27. Ryanodine receptors of striated muscles: a complex channel capable of multiple interactions. Franzini-Armstrong, C., Protasi, F. Physiol. Rev. (1997) [Pubmed]
  28. Multisubunit assembly of an integral plasma membrane channel protein, gap junction connexin43, occurs after exit from the ER. Musil, L.S., Goodenough, D.A. Cell (1993) [Pubmed]
  29. Regulated intracellular ligand transport and proteolysis control EGF signal activation in Drosophila. Lee, J.R., Urban, S., Garvey, C.F., Freeman, M. Cell (2001) [Pubmed]
  30. SREBP-1, a membrane-bound transcription factor released by sterol-regulated proteolysis. Wang, X., Sato, R., Brown, M.S., Hua, X., Goldstein, J.L. Cell (1994) [Pubmed]
  31. Cytochrome P-4502E1: its physiological and pathological role. Lieber, C.S. Physiol. Rev. (1997) [Pubmed]
  32. Short cytoplasmic sequences serve as retention signals for transmembrane proteins in the endoplasmic reticulum. Nilsson, T., Jackson, M., Peterson, P.A. Cell (1989) [Pubmed]
  33. NAADP mobilizes Ca(2+) from reserve granules, lysosome-related organelles, in sea urchin eggs. Churchill, G.C., Okada, Y., Thomas, J.M., Genazzani, A.A., Patel, S., Galione, A. Cell (2002) [Pubmed]
  34. Microtubule-dependent retrograde transport of proteins into the ER in the presence of brefeldin A suggests an ER recycling pathway. Lippincott-Schwartz, J., Donaldson, J.G., Schweizer, A., Berger, E.G., Hauri, H.P., Yuan, L.C., Klausner, R.D. Cell (1990) [Pubmed]
  35. Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease. Sakuntabhai, A., Ruiz-Perez, V., Carter, S., Jacobsen, N., Burge, S., Monk, S., Smith, M., Munro, C.S., O'Donovan, M., Craddock, N., Kucherlapati, R., Rees, J.L., Owen, M., Lathrop, G.M., Monaco, A.P., Strachan, T., Hovnanian, A. Nat. Genet. (1999) [Pubmed]
  36. Sterol resistance in CHO cells traced to point mutation in SREBP cleavage-activating protein. Hua, X., Nohturfft, A., Goldstein, J.L., Brown, M.S. Cell (1996) [Pubmed]
  37. Bos1p, an integral membrane protein of the endoplasmic reticulum to Golgi transport vesicles, is required for their fusion competence. Lian, J.P., Ferro-Novick, S. Cell (1993) [Pubmed]
  38. Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy. Senderek, J., Krieger, M., Stendel, C., Bergmann, C., Moser, M., Breitbach-Faller, N., Rudnik-Schöneborn, S., Blaschek, A., Wolf, N.I., Harting, I., North, K., Smith, J., Muntoni, F., Brockington, M., Quijano-Roy, S., Renault, F., Herrmann, R., Hendershot, L.M., Schröder, J.M., Lochmüller, H., Topaloglu, H., Voit, T., Weis, J., Ebinger, F., Zerres, K. Nat. Genet. (2005) [Pubmed]
  39. Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease. Drenth, J.P., te Morsche, R.H., Smink, R., Bonifacino, J.S., Jansen, J.B. Nat. Genet. (2003) [Pubmed]
  40. The nontransmembrane tyrosine phosphatase PTP-1B localizes to the endoplasmic reticulum via its 35 amino acid C-terminal sequence. Frangioni, J.V., Beahm, P.H., Shifrin, V., Jost, C.A., Neel, B.G. Cell (1992) [Pubmed]
  41. Molecular basis of autosomal dominant neurohypophyseal diabetes insipidus. Cellular toxicity caused by the accumulation of mutant vasopressin precursors within the endoplasmic reticulum. Ito, M., Jameson, J.L., Ito, M. J. Clin. Invest. (1997) [Pubmed]
  42. TNF-alpha induced c-IAP1/TRAF2 complex translocation to a Ubc6-containing compartment and TRAF2 ubiquitination. Wu, C.J., Conze, D.B., Li, X., Ying, S.X., Hanover, J.A., Ashwell, J.D. EMBO J. (2005) [Pubmed]
  43. A novel dynamin-like protein associates with cytoplasmic vesicles and tubules of the endoplasmic reticulum in mammalian cells. Yoon, Y., Pitts, K.R., Dahan, S., McNiven, M.A. J. Cell Biol. (1998) [Pubmed]
  44. Biosynthesis of high density lipoprotein by chicken liver: conjugation of nascent lipids with apoprotein A1. Banerjee, D., Redman, C.M. J. Cell Biol. (1984) [Pubmed]
 
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