Indoleamine 2,3-dioxygenase (Vietnamese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Indoleamine 2,3-dioxygenase" in Vietnamese language version.

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Global rank Vietnamese rank

26nih.gov

4^th place

7^th place

21doi.org

2^nd place

4acs.org

1,248^th place

822^nd place

1issuu.com

537^th place

2,037^th place

1jleukbio.org

low place

1researchgate.net

120^th place

240^th place

1jbc.org

4,455^th place

2,415^th place

acs.org

pubs.acs.org

Chauhan N, Thackray SJ, Rafice SA, Eaton G, Lee M, Efimov I, Basran J, Jenkins PR, Mowat CG, Chapman SK, Raven EL (tháng 4 năm 2009). “Reassessment of the reaction mechanism in the heme dioxygenases”. Journal of the American Chemical Society. 131 (12): 4186–7. doi:10.1021/ja808326g. PMID 19275153.
Efimov I, Basran J, Thackray SJ, Handa S, Mowat CG, Raven EL (tháng 4 năm 2011). “Structure and reaction mechanism in the heme dioxygenases”. Biochemistry. 50 (14): 2717–24. doi:10.1021/bi101732n. PMID 21361337.
Peng YH, Ueng SH, Tseng CT, Hung MS, Song JS, Wu JS, Liao FY, Fan YS, Wu MH, Hsiao WC, Hsueh CC, Lin SY, Cheng CY, Tu CH, Lee LC, Cheng MF, Shia KS, Shih C, Wu SY (tháng 1 năm 2016). “Important Hydrogen Bond Networks in Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitor Design Revealed by Crystal Structures of Imidazoleisoindole Derivatives with IDO1”. Journal of Medicinal Chemistry. 59 (1): 282–93. doi:10.1021/acs.jmedchem.5b01390. PMID 26642377.
Tojo S, Kohno T, Tanaka T, Kamioka S, Ota Y, Ishii T, Kamimoto K, Asano S, Isobe Y (tháng 10 năm 2014). “Crystal Structures and Structure-Activity Relationships of Imidazothiazole Derivatives as IDO1 Inhibitors”. ACS Medicinal Chemistry Letters. 5 (10): 1119–23. doi:10.1021/acs.jmedchem.5b01390. PMID 25313323.

doi.org

Dai W, Gupta SL (tháng 4 năm 1990). “Molecular cloning, sequencing and expression of human interferon-gamma-inducible indoleamine 2,3-dioxygenase cDNA”. Biochemical and Biophysical Research Communications. 168 (1): 1–8. doi:10.1016/0006-291X(90)91666-G. PMID 2109605.
Najfeld V, Menninger J, Muhleman D, Comings DE, Gupta SL (1993). “Localization of indoleamine 2,3-dioxygenase gene (INDO) to chromosome 8p12-->p11 by fluorescent in situ hybridization”. Cytogenetics and Cell Genetics. 64 (3–4): 231–2. doi:10.1159/000133584. PMID 8404046.
Munn DH, Mellor AL (tháng 3 năm 2013). “Indoleamine 2,3 dioxygenase and metabolic control of immune responses”. Trends in Immunology. 34 (3): 137–43. doi:10.1016/j.it.2012.10.001. PMID 23103127.
Prendergast GC, Smith C, Thomas S, Mandik-Nayak L, Laury-Kleintop L, Metz R, Muller AJ (tháng 7 năm 2014). “Indoleamine 2,3-dioxygenase pathways of pathogenic inflammation and immune escape in cancer”. Cancer Immunology, Immunotherapy. 63 (7): 721–35. doi:10.1007/s00262-014-1549-4. PMID 24711084.
Munn DH, Mellor AL (tháng 3 năm 2016). “IDO in the Tumor Microenvironment: Inflammation, Counter-Regulation, and Tolerance”. Trends in Immunology. 37 (3): 193–207. doi:10.1016/j.it.2016.01.002. PMID 26839260.
Muller AJ, DuHadaway JB, Donover PS, Sutanto-Ward E, Prendergast GC (tháng 3 năm 2005). “Inhibition of indoleamine 2,3-dioxygenase, an immunoregulatory target of the cancer suppression gene Bin1, potentiates cancer chemotherapy”. Nature Medicine. 11 (3): 312–9. doi:10.1038/nm1196. PMID 15711557.
Munn DH, Shafizadeh E, Attwood JT, Bondarev I, Pashine A, Mellor AL (tháng 5 năm 1999). “Inhibition of T cell proliferation by macrophage tryptophan catabolism”. The Journal of Experimental Medicine. 189 (9): 1363–72. doi:10.1084/jem.189.9.1363. PMC 2193062. PMID 10224276.
Wang J, Yu L, Jiang C, Fu X, Liu X, Wang M, Ou C, Cui X, Zhou C, Wang J (tháng 1 năm 2015). “Cerebral ischemia increases bone marrow CD4+CD25+FoxP3+ regulatory T cells in mice via signals from sympathetic nervous system”. Brain, Behavior, and Immunity. 43: 172–83. doi:10.1016/j.bbi.2014.07.022. PMC 4258426. PMID 25110149.
Uyttenhove C, Pilotte L, Théate I, Stroobant V, Colau D, Parmentier N, Boon T, Van den Eynde BJ (tháng 10 năm 2003). “Evidence for a tumoral immune resistance mechanism based on tryptophan degradation by indoleamine 2,3-dioxygenase”. Nature Medicine. 9 (10): 1269–74. doi:10.1038/nm934. PMID 14502282.
Jiang T, Sun Y, Yin Z, Feng S, Sun L, Li Z (2015). “Research progress of indoleamine 2,3-dioxygenase inhibitors”. Future Medicinal Chemistry. 7 (2): 185–201. doi:10.4155/fmc.14.151. PMID 25686005.
Lee HJ, Jeong YI, Lee TH, Jung ID, Lee JS, Lee CM, Kim JI, Joo H, Lee JD, Park YM (tháng 5 năm 2007). “Rosmarinic acid inhibits indoleamine 2,3-dioxygenase expression in murine dendritic cells”. Biochemical Pharmacology. 73 (9): 1412–21. doi:10.1016/j.bcp.2006.12.018. PMID 17229401.
Cesario A, Rocca B, Rutella S (2011). “The interplay between indoleamine 2,3-dioxygenase 1 (IDO1) and cyclooxygenase (COX)-2 in chronic inflammation and cancer”. Current Medicinal Chemistry. 18 (15): 2263–71. doi:10.2174/092986711795656063. PMID 21517752.
Hou DY, Muller AJ, Sharma MD, DuHadaway J, Banerjee T, Johnson M, Mellor AL, Prendergast GC, Munn DH (tháng 1 năm 2007). “Inhibition of indoleamine 2,3-dioxygenase in dendritic cells by stereoisomers of 1-methyl-tryptophan correlates with antitumor responses”. Cancer Research. 67 (2): 792–801. doi:10.1158/0008-5472.CAN-06-2925. PMID 17234791.
Chauhan N, Thackray SJ, Rafice SA, Eaton G, Lee M, Efimov I, Basran J, Jenkins PR, Mowat CG, Chapman SK, Raven EL (tháng 4 năm 2009). “Reassessment of the reaction mechanism in the heme dioxygenases”. Journal of the American Chemical Society. 131 (12): 4186–7. doi:10.1021/ja808326g. PMID 19275153.
Jochems C, Fantini M, Fernando RI, Kwilas AR, Donahue RN, Lepone LM, Grenga I, Kim YS, Brechbiel MW, Gulley JL, Madan RA, Heery CR, Hodge JW, Newton R, Schlom J, Tsang KY (tháng 6 năm 2016). “The IDO1 selective inhibitor epacadostat enhances dendritic cell immunogenicity and lytic ability of tumor antigen-specific T cells”. Oncotarget. 7 (25): 37762–37772. doi:10.18632/oncotarget.9326. PMID 27192116.
Efimov I, Basran J, Thackray SJ, Handa S, Mowat CG, Raven EL (tháng 4 năm 2011). “Structure and reaction mechanism in the heme dioxygenases”. Biochemistry. 50 (14): 2717–24. doi:10.1021/bi101732n. PMID 21361337.
Yanagisawa S, Yotsuya K, Hashiwaki Y, Horitani M, Sugimoto H, Shiro Y, Appelman EH, Ogura T. “Identification of the Fe-O₂ and the Fe=O heme species for indoleamine 2,3-dioxygenase during catalytic turnover”. Chem Lett. 39: 36–37. doi:10.1246/cl.2010.36.
Booth ES, Basran J, Lee M, Handa S, Raven EL (tháng 12 năm 2015). “Substrate Oxidation by Indoleamine 2,3-Dioxygenase: EVIDENCE FOR A COMMON REACTION MECHANISM” (PDF). The Journal of Biological Chemistry. 290 (52): 30924–30. doi:10.1074/jbc.M115.695684. PMC 4692220. PMID 26511316.
Sugimoto H, Oda S, Otsuki T, Hino T, Yoshida T, Shiro Y (tháng 2 năm 2006). “Crystal structure of human indoleamine 2,3-dioxygenase: catalytic mechanism of O2 incorporation by a heme-containing dioxygenase” (PDF). Proceedings of the National Academy of Sciences of the United States of America. 103 (8): 2611–6. doi:10.1073/pnas.0508996103. PMID 16477023.
Peng YH, Ueng SH, Tseng CT, Hung MS, Song JS, Wu JS, Liao FY, Fan YS, Wu MH, Hsiao WC, Hsueh CC, Lin SY, Cheng CY, Tu CH, Lee LC, Cheng MF, Shia KS, Shih C, Wu SY (tháng 1 năm 2016). “Important Hydrogen Bond Networks in Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitor Design Revealed by Crystal Structures of Imidazoleisoindole Derivatives with IDO1”. Journal of Medicinal Chemistry. 59 (1): 282–93. doi:10.1021/acs.jmedchem.5b01390. PMID 26642377.
Tojo S, Kohno T, Tanaka T, Kamioka S, Ota Y, Ishii T, Kamimoto K, Asano S, Isobe Y (tháng 10 năm 2014). “Crystal Structures and Structure-Activity Relationships of Imidazothiazole Derivatives as IDO1 Inhibitors”. ACS Medicinal Chemistry Letters. 5 (10): 1119–23. doi:10.1021/acs.jmedchem.5b01390. PMID 25313323.

issuu.com

Abdollahi, Mostafa: Case Study Oshtoran Syndrome [1] Retrieved ngày 3 tháng 6 năm 2016

jbc.org

Booth ES, Basran J, Lee M, Handa S, Raven EL (tháng 12 năm 2015). “Substrate Oxidation by Indoleamine 2,3-Dioxygenase: EVIDENCE FOR A COMMON REACTION MECHANISM” (PDF). The Journal of Biological Chemistry. 290 (52): 30924–30. doi:10.1074/jbc.M115.695684. PMC 4692220. PMID 26511316.

jleukbio.org

Chiarugi A, Dello Sbarba P, Paccagnini A, Donnini S, Filippi S, Moroni F (tháng 8 năm 2000). “Combined inhibition of indoleamine 2,3-dioxygenase and nitric oxide synthase modulates neurotoxin release by interferon-gamma-activated macrophages”. Journal of Leukocyte Biology. 68 (2): 260–6. PMID 10947071.^{[liên kết hỏng]}

nih.gov

pubmed.ncbi.nlm.nih.gov

Dai W, Gupta SL (tháng 4 năm 1990). “Molecular cloning, sequencing and expression of human interferon-gamma-inducible indoleamine 2,3-dioxygenase cDNA”. Biochemical and Biophysical Research Communications. 168 (1): 1–8. doi:10.1016/0006-291X(90)91666-G. PMID 2109605.
Najfeld V, Menninger J, Muhleman D, Comings DE, Gupta SL (1993). “Localization of indoleamine 2,3-dioxygenase gene (INDO) to chromosome 8p12-->p11 by fluorescent in situ hybridization”. Cytogenetics and Cell Genetics. 64 (3–4): 231–2. doi:10.1159/000133584. PMID 8404046.
Munn DH, Mellor AL (tháng 3 năm 2013). “Indoleamine 2,3 dioxygenase and metabolic control of immune responses”. Trends in Immunology. 34 (3): 137–43. doi:10.1016/j.it.2012.10.001. PMID 23103127.
Prendergast GC, Smith C, Thomas S, Mandik-Nayak L, Laury-Kleintop L, Metz R, Muller AJ (tháng 7 năm 2014). “Indoleamine 2,3-dioxygenase pathways of pathogenic inflammation and immune escape in cancer”. Cancer Immunology, Immunotherapy. 63 (7): 721–35. doi:10.1007/s00262-014-1549-4. PMID 24711084.
Munn DH, Mellor AL (tháng 3 năm 2016). “IDO in the Tumor Microenvironment: Inflammation, Counter-Regulation, and Tolerance”. Trends in Immunology. 37 (3): 193–207. doi:10.1016/j.it.2016.01.002. PMID 26839260.
Muller AJ, DuHadaway JB, Donover PS, Sutanto-Ward E, Prendergast GC (tháng 3 năm 2005). “Inhibition of indoleamine 2,3-dioxygenase, an immunoregulatory target of the cancer suppression gene Bin1, potentiates cancer chemotherapy”. Nature Medicine. 11 (3): 312–9. doi:10.1038/nm1196. PMID 15711557.
Munn DH, Shafizadeh E, Attwood JT, Bondarev I, Pashine A, Mellor AL (tháng 5 năm 1999). “Inhibition of T cell proliferation by macrophage tryptophan catabolism”. The Journal of Experimental Medicine. 189 (9): 1363–72. doi:10.1084/jem.189.9.1363. PMC 2193062. PMID 10224276.
Wang J, Yu L, Jiang C, Fu X, Liu X, Wang M, Ou C, Cui X, Zhou C, Wang J (tháng 1 năm 2015). “Cerebral ischemia increases bone marrow CD4+CD25+FoxP3+ regulatory T cells in mice via signals from sympathetic nervous system”. Brain, Behavior, and Immunity. 43: 172–83. doi:10.1016/j.bbi.2014.07.022. PMC 4258426. PMID 25110149.
Uyttenhove C, Pilotte L, Théate I, Stroobant V, Colau D, Parmentier N, Boon T, Van den Eynde BJ (tháng 10 năm 2003). “Evidence for a tumoral immune resistance mechanism based on tryptophan degradation by indoleamine 2,3-dioxygenase”. Nature Medicine. 9 (10): 1269–74. doi:10.1038/nm934. PMID 14502282.
Jiang T, Sun Y, Yin Z, Feng S, Sun L, Li Z (2015). “Research progress of indoleamine 2,3-dioxygenase inhibitors”. Future Medicinal Chemistry. 7 (2): 185–201. doi:10.4155/fmc.14.151. PMID 25686005.
Chiarugi A, Dello Sbarba P, Paccagnini A, Donnini S, Filippi S, Moroni F (tháng 8 năm 2000). “Combined inhibition of indoleamine 2,3-dioxygenase and nitric oxide synthase modulates neurotoxin release by interferon-gamma-activated macrophages”. Journal of Leukocyte Biology. 68 (2): 260–6. PMID 10947071.^{[liên kết hỏng]}
Lee HJ, Jeong YI, Lee TH, Jung ID, Lee JS, Lee CM, Kim JI, Joo H, Lee JD, Park YM (tháng 5 năm 2007). “Rosmarinic acid inhibits indoleamine 2,3-dioxygenase expression in murine dendritic cells”. Biochemical Pharmacology. 73 (9): 1412–21. doi:10.1016/j.bcp.2006.12.018. PMID 17229401.
Cesario A, Rocca B, Rutella S (2011). “The interplay between indoleamine 2,3-dioxygenase 1 (IDO1) and cyclooxygenase (COX)-2 in chronic inflammation and cancer”. Current Medicinal Chemistry. 18 (15): 2263–71. doi:10.2174/092986711795656063. PMID 21517752.
Hou DY, Muller AJ, Sharma MD, DuHadaway J, Banerjee T, Johnson M, Mellor AL, Prendergast GC, Munn DH (tháng 1 năm 2007). “Inhibition of indoleamine 2,3-dioxygenase in dendritic cells by stereoisomers of 1-methyl-tryptophan correlates with antitumor responses”. Cancer Research. 67 (2): 792–801. doi:10.1158/0008-5472.CAN-06-2925. PMID 17234791.
Chauhan N, Thackray SJ, Rafice SA, Eaton G, Lee M, Efimov I, Basran J, Jenkins PR, Mowat CG, Chapman SK, Raven EL (tháng 4 năm 2009). “Reassessment of the reaction mechanism in the heme dioxygenases”. Journal of the American Chemical Society. 131 (12): 4186–7. doi:10.1021/ja808326g. PMID 19275153.
Jochems C, Fantini M, Fernando RI, Kwilas AR, Donahue RN, Lepone LM, Grenga I, Kim YS, Brechbiel MW, Gulley JL, Madan RA, Heery CR, Hodge JW, Newton R, Schlom J, Tsang KY (tháng 6 năm 2016). “The IDO1 selective inhibitor epacadostat enhances dendritic cell immunogenicity and lytic ability of tumor antigen-specific T cells”. Oncotarget. 7 (25): 37762–37772. doi:10.18632/oncotarget.9326. PMID 27192116.
Efimov I, Basran J, Thackray SJ, Handa S, Mowat CG, Raven EL (tháng 4 năm 2011). “Structure and reaction mechanism in the heme dioxygenases”. Biochemistry. 50 (14): 2717–24. doi:10.1021/bi101732n. PMID 21361337.
Booth ES, Basran J, Lee M, Handa S, Raven EL (tháng 12 năm 2015). “Substrate Oxidation by Indoleamine 2,3-Dioxygenase: EVIDENCE FOR A COMMON REACTION MECHANISM” (PDF). The Journal of Biological Chemistry. 290 (52): 30924–30. doi:10.1074/jbc.M115.695684. PMC 4692220. PMID 26511316.
Sugimoto H, Oda S, Otsuki T, Hino T, Yoshida T, Shiro Y (tháng 2 năm 2006). “Crystal structure of human indoleamine 2,3-dioxygenase: catalytic mechanism of O2 incorporation by a heme-containing dioxygenase” (PDF). Proceedings of the National Academy of Sciences of the United States of America. 103 (8): 2611–6. doi:10.1073/pnas.0508996103. PMID 16477023.
Peng YH, Ueng SH, Tseng CT, Hung MS, Song JS, Wu JS, Liao FY, Fan YS, Wu MH, Hsiao WC, Hsueh CC, Lin SY, Cheng CY, Tu CH, Lee LC, Cheng MF, Shia KS, Shih C, Wu SY (tháng 1 năm 2016). “Important Hydrogen Bond Networks in Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitor Design Revealed by Crystal Structures of Imidazoleisoindole Derivatives with IDO1”. Journal of Medicinal Chemistry. 59 (1): 282–93. doi:10.1021/acs.jmedchem.5b01390. PMID 26642377.
Tojo S, Kohno T, Tanaka T, Kamioka S, Ota Y, Ishii T, Kamimoto K, Asano S, Isobe Y (tháng 10 năm 2014). “Crystal Structures and Structure-Activity Relationships of Imidazothiazole Derivatives as IDO1 Inhibitors”. ACS Medicinal Chemistry Letters. 5 (10): 1119–23. doi:10.1021/acs.jmedchem.5b01390. PMID 25313323.

ncbi.nlm.nih.gov

“Entrez Gene: INDO indoleamine-pyrrole 2,3 dioxygenase”.
Munn DH, Shafizadeh E, Attwood JT, Bondarev I, Pashine A, Mellor AL (tháng 5 năm 1999). “Inhibition of T cell proliferation by macrophage tryptophan catabolism”. The Journal of Experimental Medicine. 189 (9): 1363–72. doi:10.1084/jem.189.9.1363. PMC 2193062. PMID 10224276.
Wang J, Yu L, Jiang C, Fu X, Liu X, Wang M, Ou C, Cui X, Zhou C, Wang J (tháng 1 năm 2015). “Cerebral ischemia increases bone marrow CD4+CD25+FoxP3+ regulatory T cells in mice via signals from sympathetic nervous system”. Brain, Behavior, and Immunity. 43: 172–83. doi:10.1016/j.bbi.2014.07.022. PMC 4258426. PMID 25110149.
Booth ES, Basran J, Lee M, Handa S, Raven EL (tháng 12 năm 2015). “Substrate Oxidation by Indoleamine 2,3-Dioxygenase: EVIDENCE FOR A COMMON REACTION MECHANISM” (PDF). The Journal of Biological Chemistry. 290 (52): 30924–30. doi:10.1074/jbc.M115.695684. PMC 4692220. PMID 26511316.
Sugimoto H, Oda S, Otsuki T, Hino T, Yoshida T, Shiro Y (tháng 2 năm 2006). “Crystal structure of human indoleamine 2,3-dioxygenase: catalytic mechanism of O2 incorporation by a heme-containing dioxygenase” (PDF). Proceedings of the National Academy of Sciences of the United States of America. 103 (8): 2611–6. doi:10.1073/pnas.0508996103. PMID 16477023.

researchgate.net

Yanagisawa S, Yotsuya K, Hashiwaki Y, Horitani M, Sugimoto H, Shiro Y, Appelman EH, Ogura T. “Identification of the Fe-O₂ and the Fe=O heme species for indoleamine 2,3-dioxygenase during catalytic turnover”. Chem Lett. 39: 36–37. doi:10.1246/cl.2010.36.