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Acquired resistance to IDH inhibition through trans or cis dimer-interface mutations
Author / Creator:Intlekofer, Andrew M. ; Shih, Alan H. ; Wang, Bo ; Nazir, Abbas ; Rustenburg, Ariën S. ; Albanese, Steven K. ; Patel, Minal ; Famulare, Christopher ; Correa, Fabian M. ; Takemoto, Naofumi ; Durani, Vidushi ; Liu, Hui ; Taylor, Justin ; Farnoud, Noushin ; Papaemmanuil, Elli ; Cross, Justin R. ; Tallman, Martin S. ; Arcila, Maria E. ; Roshal, Mikhail ; Petsko, Gregory A. ; Wu, Bin ; Choe, Sung ; Konteatis, Zenon D. ; Biller, Scott A. ; Chodera, John D. ; Thompson, Craig B. ; Levine, Ross L. ; Stein, Eytan M.
Publisher:London: Nature Publishing Group UK
Journal title:Nature (London), 2018-07, Vol.559 (7712), p.125-129
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Clinical pharmacokinetics and pharmacodynamics of ivosidenib, an oral, targeted inhibitor of mutant IDH1, in patients with advanced solid tumors
Author / Creator:Fan, Bin ; Mellinghoff, Ingo K. ; Wen, Patrick Y. ; Lowery, Maeve A. ; Goyal, Lipika ; Tap, William D. ; Pandya, Shuchi S. ; Manyak, Erika ; Jiang, Liewen ; Liu, Guowen ; Nimkar, Tara ; Gliser, Camelia ; Prahl Judge, Molly ; Agresta, Sam ; Yang, Hua ; Dai, David
Publisher:New York: Springer US
Journal title:Investigational new drugs, 2020-04, Vol.38 (2), p.433-444
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Prognostic significance of 2-hydroxyglutarate levels in acute myeloid leukemia in China
Author / Creator:Wang, Jiang-Han ; Chen, Wen-Lian ; Li, Jun-Min ; Wu, Song-Fang ; Chen, Tian-Lu ; Zhu, Yong-Mei ; Zhang, Wei-Na ; Li, Yang ; Qiu, Yun-Ping ; Zhao, Ai-Hua ; Mi, Jian-Qing ; Jin, Jie ; Wang, Yun-Gui ; Ma, Qiu-Ling ; Huang, He ; Wu, De-Pei ; Wang, Qin-Rong ; Li, Yan ; Yan, Xiao-Jing ; Yan, Jin-Song ; Li, Jian-Yong ; Wang, Shuai ; Huang, Xiao-Jun ; Wang, Bing-Shun ; Jia, Wei ; Shen, Yang ; Chen, Zhu ; Chen, Sai-Juan
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2013-10, Vol.110 (42), p.17017-17022
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2-Hydroxyglutarate is not a metabolite; d-2-hydroxyglutarate and l-2-hydroxyglutarate are
Author / Creator:Struys, Eduard A
Publisher:United States: National Acad Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2013-12, Vol.110 (51), p.E4939-E4939
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New targets for monitoring and therapy in Barth syndrome
Author / Creator:Thompson, W. Reid ; DeCroes, Brittany ; McClellan, Rebecca ; Rubens, Jessica ; Vaz, Frédéric M. ; Kristaponis, Kara ; Avramopoulos, Dimitrios ; Vernon, Hilary J.
Publisher:New York: Nature Publishing Group US
Journal title:Genetics in medicine, 2016-10, Vol.18 (10), p.1001-1010
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Isocitrate dehydrogenase 2 mutations correlate with leukemic transformation and are predicted by 2-hydroxyglutarate in myelodysplastic syndromes
Author / Creator:Lin, Peipei ; Luo, Yingwan ; Zhu, Shuanghong ; Maggio, Dominic ; Yang, Haiyang ; Hu, Chao ; Wang, Jinghan ; Zhang, Hua ; Ren, Yanling ; Zhou, Xinping ; Mei, Chen ; Ma, Liya ; Xu, Weilai ; Ye, Li ; Zhuang, Zhengping ; Jin, Jie ; Tong, Hongyan
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of cancer research and clinical oncology, 2018-06, Vol.144 (6), p.1037-1047
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Pretreatment d-2-hydroxyglutarate serum levels negatively impact on outcome in IDH1-mutated acute myeloid leukemia
Author / Creator:Balss, J ; Thiede, C ; Bochtler, T ; Okun, J G ; Saadati, M ; Benner, A ; Pusch, S ; Ehninger, G ; Schaich, M ; Ho, A D ; von Deimling, A ; Krämer, A ; Heilig, C E
Publisher:London: Nature Publishing Group UK
Journal title:Leukemia, 2016-04, Vol.30 (4), p.782-788
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Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease—different clinical entities and comparable perinatal renal abnormalities
Author / Creator:Hackl, Agnes ; Mehler, Katrin ; Gottschalk, Ingo ; Vierzig, Anne ; Eydam, Marcus ; Hauke, Jan ; Beck, Bodo B. ; Liebau, Max C. ; Ensenauer, Regina ; Weber, Lutz T. ; Habbig, Sandra
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Pediatric nephrology (Berlin, West), 2017-05, Vol.32 (5), p.791-800
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Metabolitic profiling of amino acids in paraquat-induced acute kidney injury
Author / Creator:Wan, Xiuxian ; Li, XinHua ; Wang, Qiang ; Zheng, Bin ; Zhou, Chunyu ; Kang, Xin ; Hu, Dayong ; Bao, Hui ; Peng, Ai
Publisher:Singapore: Springer Singapore
Journal title:Clinical and experimental nephrology, 2019-04, Vol.23 (4), p.474-483
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Direct comparison of quantitative digital PCR and 2-hydroxyglutarate enantiomeric ratio for IDH mutant allele frequency assessment in myeloid malignancy
Author / Creator:Wiseman, D H ; Struys, E A ; Wilks, D P ; Clark, C I ; Dennis, M W ; Jansen, E E W ; Salomons, G S ; Somervaille, T C P
Publisher:London: Nature Publishing Group UK
Journal title:Leukemia, 2015-12, Vol.29 (12), p.2421-2423
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Reply to Struys: Role of biomarker of 2-hydroxyglutarate in acute myeloid leukemia
Author / Creator:Shen, Yang ; Wang, Jing-Han ; Chen, Wen-Lian ; Jia, Wei ; Chen, Sai-Juan ; Chen, Zhu
Publisher:United States: National Acad Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2013-12, Vol.110 (51), p.E4940-E4940
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Iron-induced epigenetic abnormalities of mouse bone marrow through aberrant activation of aconitase and isocitrate dehydrogenase
Author / Creator:Yamamoto, Masayo ; Tanaka, Hiroki ; Toki, Yasumichi ; Hatayama, Mayumi ; Ito, Satoshi ; Addo, Lynda ; Shindo, Motohiro ; Sasaki, Katsunori ; Ikuta, Katsuya ; Ohtake, Takaaki ; Fujiya, Mikihiro ; Torimoto, Yoshihiro ; Kohgo, Yutaka
Publisher:Tokyo: Springer Japan
Journal title:International journal of hematology, 2016-10, Vol.104 (4), p.491-501
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Dyskinesia in a Child: A Concern for a Rare Neuro-Metabolic Disorder
Author / Creator:Hafeez, Ayesha ; Fatima, Safia ; Chaudhry, Nayyar ; Khadim, Muhammad Tahir
Publisher:Pakistan: College of Physicians and Surgeons Pakistan
Journal title:Journal of the College of Physicians and Surgeons--Pakistan, 2019-01, Vol.29 (1), p.84-86
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A novel compound heterozygous mutation in a Chinese boy with L-2-hydroxyglutaric aciduria: a case study
Author / Creator:Tai, Hongfei ; Zhang, Zaiqiang
Publisher:England: BioMed Central Ltd
Journal title:BMC neurology, 2015-07, Vol.15 (1), p.117-117, Article 117
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The sodium-dependent di- and tricarboxylate transporter, NaCT, is not responsible for the uptake of D-, L-2-hydroxyglutarate and 3-hydroxyglutarate into neurons
Author / Creator:Brauburger, Katja ; Burckhardt, Gerhard ; Burckhardt, Birgitta C.
Publisher:Dordrecht: Springer Netherlands
Journal title:Journal of inherited metabolic disease, 2011-04, Vol.34 (2), p.477-482
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Sensitivity and specificity of free and total glutaric acid and 3‐hydroxyglutaric acid measurements by stable‐isotope dilution assays for the diagnosis of glutaric aciduria type I
Author / Creator:Baric, I. ; Wagner, L. ; Feyh, P. ; Liesert, M. ; Buckel, W. ; Hoffmann, G. F.
Publisher:Dordrecht: Kluwer Academic Publishers
Journal title:Journal of inherited metabolic disease, 1999-12, Vol.22 (8), p.867-882
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Glutaric Acidemia, Type I, Missed by Newborn Screening in an Infant With Dystonia Following Promethazine Administration
Author / Creator:Smith, Wendy E ; Millington, David S ; Koeberl, Dwight D ; Lesser, Philip S
Publisher:Elk Grove Village, IL: Am Acad Pediatrics
Journal title:Pediatrics (Evanston), 2001-05, Vol.107 (5), p.1184-1187
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Recurrent and novel mutations of GCDH gene in Chinese glutaric acidemia type I families
Author / Creator:Tang, Nelson L.S. ; Hui, Joannie ; Law, L.K. ; Lam, Y.Y. ; Chan, K.Y. ; Yeung, W.L. ; Chan, Albert Y.W. ; Cheung, K.L. ; Fok, T.F.
Publisher:New York: John Wiley & Sons, Inc
Journal title:Human mutation, 2000-11, Vol.16 (5), p.446-446
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OPA3 mutation screening in patients with unexplained 3‐methylglutaconic aciduria
Author / Creator:Neas, K. ; Bennetts, B. ; Carpenter, K. ; White, R. ; Kirk, E. P. ; Wilson, M. ; Kelley, R. ; Baric, I. ; Christodoulou, J.
Publisher:Dordrecht: Kluwer Academic Publishers
Journal title:Journal of inherited metabolic disease, 2005-08, Vol.28 (4), p.525-532
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Development of pathogenic concepts in glutaryl‐CoA dehydrogenase deficiency: The challenge
Author / Creator:Goodman, S. I.
Publisher:Dordrecht: Kluwer Academic Publishers
Journal title:Journal of inherited metabolic disease, 2004, Vol.27 (6), p.801-803
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Acquired resistance to IDH inhibition through trans or cis dimer-interface mutations

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Clinical pharmacokinetics and pharmacodynamics of ivosidenib, an oral, targeted inhibitor of mutant IDH1, in patients with advanced solid tumors

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Prognostic significance of 2-hydroxyglutarate levels in acute myeloid leukemia in China

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2-Hydroxyglutarate is not a metabolite; d-2-hydroxyglutarate and l-2-hydroxyglutarate are

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New targets for monitoring and therapy in Barth syndrome

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Isocitrate dehydrogenase 2 mutations correlate with leukemic transformation and are predicted by 2-hydroxyglutarate in myelodysplastic syndromes

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Pretreatment d-2-hydroxyglutarate serum levels negatively impact on outcome in IDH1-mutated acute myeloid leukemia

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Disorders of fatty acid oxidation and autosomal recessive polycystic kidney disease—different clinical entities and comparable perinatal renal abnormalities

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Metabolitic profiling of amino acids in paraquat-induced acute kidney injury

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Direct comparison of quantitative digital PCR and 2-hydroxyglutarate enantiomeric ratio for IDH mutant allele frequency assessment in myeloid malignancy

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Reply to Struys: Role of biomarker of 2-hydroxyglutarate in acute myeloid leukemia

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Iron-induced epigenetic abnormalities of mouse bone marrow through aberrant activation of aconitase and isocitrate dehydrogenase

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Dyskinesia in a Child: A Concern for a Rare Neuro-Metabolic Disorder

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A novel compound heterozygous mutation in a Chinese boy with L-2-hydroxyglutaric aciduria: a case study

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The sodium-dependent di- and tricarboxylate transporter, NaCT, is not responsible for the uptake of D-, L-2-hydroxyglutarate and 3-hydroxyglutarate into neurons

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Sensitivity and specificity of free and total glutaric acid and 3‐hydroxyglutaric acid measurements by stable‐isotope dilution assays for the diagnosis of glutaric aciduria type I

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Glutaric Acidemia, Type I, Missed by Newborn Screening in an Infant With Dystonia Following Promethazine Administration

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Recurrent and novel mutations of GCDH gene in Chinese glutaric acidemia type I families

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OPA3 mutation screening in patients with unexplained 3‐methylglutaconic aciduria

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Development of pathogenic concepts in glutaryl‐CoA dehydrogenase deficiency: The challenge

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