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15. Shechter I, et al, (2003). IDH1 gene transcription is sterol regulated and activated by SREBP-1a and SREBP-2 in human hepatoma HepG2 cells: evidence that IDH1 may regulate lipogenesis in hepatic cells. J Lipid Res 44:2169–2180, PMID 12923220.  
 
15. Shechter I, et al, (2003). IDH1 gene transcription is sterol regulated and activated by SREBP-1a and SREBP-2 in human hepatoma HepG2 cells: evidence that IDH1 may regulate lipogenesis in hepatic cells. J Lipid Res 44:2169–2180, PMID 12923220.  
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16. Joseph, J. W. et al. The Mitochondrial Citrate/Isocitrate Carrier Plays a Regulatory Role in Glucose-stimulated Insulin Secretion. J. Biol. Chem. 281, 35624–35632 (2006). PMID: 17001083
+
16. Joseph JW, et al., (2006). The mitochondrial citrate/isocitrate carrier plays a regulatory role in glucose-stimulated insulin secretion. J Biol Chem 281:35624–35632, PMID 17001083.
   −
17. Koh, H.-J. et al. Cytosolic NADP + -dependent Isocitrate Dehydrogenase Plays a Key Role in Lipid Metabolism. J. Biol. Chem. 279, 39968–39974 (2004). PMID: 15254034  
+
17. Koh H-J, et al., (204). Cytosolic NADP + -dependent isocitrate dehydrogenase plays a key role in lipid metabolism. J Biol Chem 279:39968–39974, PMID 15254034.
   −
18. Ronnebaum, S. M. et al. A Pyruvate Cycling Pathway Involving Cytosolic NADP-dependent Isocitrate Dehydrogenase Regulates Glucose-stimulated Insulin Secretion. J. Biol. Chem. 281, 30593–30602 (2006). PMID: 16912049  
+
18. Ronnebaum SM, et al., (2006). A pyruvate cycling pathway involving cytosolic NADP-dependent isocitrate dehydrogenase regulates glucose-stimulated insulin secretion. J Biol Chem 281:30593–30602, PMID 16912049.
   −
19. Reitman, Z. J. & Yan, H. Isocitrate Dehydrogenase 1 and 2 Mutations in Cancer: Alterations at a Crossroads of Cellular Metabolism. JNCI J. Natl. Cancer Inst. 102, 932–941 (2010). PMID: 20513808  
+
19. Reitman ZJ and Yan H, (2010). Isocitrate dehydrogenase 1 and 2 mutations in cancer: alterations at a crossroads of cellular metabolism. J Natl Cancer Inst 102:932–941, PMID 20513808.
   −
20. Yan, H. et al. IDH1 and IDH2 mutations in gliomas. N. Engl. J. Med. 360, 765–773 (2009). PMID: 23532369
+
20. Yan H, et al., (2009). IDH1 and IDH2 mutations in gliomas. N Engl J Med 360:765–773, PMID 23532369.
   −
21. Sanson, M. et al. Isocitrate Dehydrogenase 1 Codon 132 Mutation Is an Important Prognostic Biomarker in Gliomas. J. Clin. Oncol. 27, 4150–4154 (2009). PMID: 19636000  
+
21. Sanson M, et al., (2009). Isocitrate dehydrogenase 1 Codon 132 mutation is an important prognostic biomarker in gliomas. J Clin Oncol 27:4150–4154, PMID 19636000.
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22. Nobusawa, S., Watanabe, T., Kleihues, P. & Ohgaki, H. IDH1 Mutations as Molecular Signature and Predictive Factor of Secondary Glioblastomas. Clin. Cancer Res. 15, 6002–6007 (2009). PMID: 19755387  
+
22. Nobusawa S, et al., (2009). IDH1 mutations as molecular signature and predictive factor of secondary glioblastomas. Clin Cancer Res 15:6002–6007, PMID 19755387.
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23. Lugowska, I. et al. IDH1/2 Mutations Predict Shorter Survival in Chondrosarcoma. J. Cancer 9, 998–1005 (2018). PMID: 29581779  
+
23. Lugowska I, et al., (2018). IDH1/2 mutations predict shorter survival in chondrosarcoma. J Cancer 9:998–1005, PMID 29581779.
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24. Amary, M. F. et al. IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours. J. Pathol. 224, 334–343 (2011). PMID: 21598255  
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24. Amary MF, et al., (2011). IDH1 and IDH2 mutations are frequent events in central chondrosarcoma and central and periosteal chondromas but not in other mesenchymal tumours. J Pathol 224:334–343, PMID 21598255.
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25. Pansuriya, T. C. et al. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome. Nat. Genet. 43, 1256–1261 (2011). PMID: 22057234  
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25. Pansuriya TC, et al., (2011). Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome. Nat Genet 43:1256–1261, PMID 22057234.
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26. Wang, P. et al. Mutations in isocitrate dehydrogenase 1 and 2 occur frequently in intrahepatic cholangiocarcinomas and share hypermethylation targets with glioblastomas. Oncogene 32, 3091–3100 (2013). PMID: 22824796
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26. Wang P, et al., (2013). Mutations in isocitrate dehydrogenase 1 and 2 occur frequently in intrahepatic cholangiocarcinomas and share hypermethylation targets with glioblastomas. Oncogene 32:3091–3100, PMID 22824796.
   −
27. Borger, D. R. et al. Frequent Mutation of Isocitrate Dehydrogenase (IDH)1 and IDH2 in Cholangiocarcinoma Identified Through Broad-Based Tumor Genotyping. The Oncologist 17, 72–79 (2012). PMID: 22180306  
+
27. Borger DR, et al., (2012). Frequent mutation of isocitrate dehydrogenase (IDH)1 and IDH2 in cholangiocarcinoma identified through broad-based tumor genotyping. The Oncologist 17:72–79, PMID 22180306.
   −
28. Churi, C. R. et al. Mutation Profiling in Cholangiocarcinoma: Prognostic and Therapeutic Implications. PLOS ONE 9, e115383 (2014). PMID: 25536104  
+
28. Churi CR, et al., (2014). Mutation profiling in cholangiocarcinoma: prognostic and therapeutic implications. PLOS ONE 9:e115383, PMID 25536104.
   −
29. Goyal, L. et al. Prognosis and Clinicopathologic Features of Patients With Advanced Stage Isocitrate Dehydrogenase (IDH) Mutant and IDH Wild-Type Intrahepatic Cholangiocarcinoma. The Oncologist 20, 1019–1027 (2015). PMID: 26245674  
+
29. Goyal L, et al., (2015). Prognosis and clinicopathologic features of patients with advanced stage isocitrate dehydrogenase (IDH) mutant and IDH wild-type intrahepatic cholangiocarcinoma. The Oncologist 20:1019–1027, PMID 26245674.
   −
30. Jiao, Y. et al. Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A and PBRM1 in intrahepatic cholangiocarcinomas. Nat. Genet. 45, 1470–1473 (2013). PMID: 24185509  
+
30. Jiao Y, et al., (2013). Exome sequencing identifies frequent inactivating mutations in BAP1, ARID1A and PBRM1 in intrahepatic cholangiocarcinomas. Nat Genet 45:1470–1473, PMID 24185509.
    
31. Mardis, E. R. et al. Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome. N. Engl. J. Med. 361, 1058–1066 (2009). PMID: 19657110  
 
31. Mardis, E. R. et al. Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome. N. Engl. J. Med. 361, 1058–1066 (2009). PMID: 19657110