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Select item 85793041.

Integrated Analysis of Expression and Prognostic Values of Acyl-CoA Dehydrogenase short-chain in Colorectal Cancer

Qi Wu, Tao Yan, Yijiao Chen, Jiang Chang, Yudong Jiang, Dexiang Zhu, Ye Wei

Int J Med Sci. 2021; 18(16): 3631–3643. Published online 2021 Sep 7. doi: 10.7150/ijms.63953

PMCID:: PMC8579304

Article PDF–2.5M

Select item 77933212.

The minor C-allele of the rs2014355 variant in ACADS gene is associated with exercise-induced increase in HDL cholesterol levels in Taiwanese adults

Tzi-Peng Yang, Fen-Fen Shih, Ming-Yi Hsu, Meng-Hsiun Tsai, Oswald Ndi Nfor, Pei-Hsing Chen, Chien-Chang Ho, Chuan-Chao Lin, Yung-Po Liaw

Medicine (Baltimore) 2021 Jan 8; 100(1): e23838. Published online 2021 Jan 8. doi: 10.1097/MD.0000000000023838

PMCID:: PMC7793321

Article PDF–200K

Select item 68344143.

ACADS acts as a potential methylation biomarker associated with the proliferation and metastasis of hepatocellular carcinomas

Diyu Chen, Xiaode Feng, Zhen Lv, Xiaofeng Xu, Yuejie Lu, Wenxuan Wu, Hao Wu, Hua Liu, Linping Cao, Sunyi Ye, Jianzhong Chen, Jian Wu

Aging (Albany NY) 2019 Oct 31; 11(20): 8825–8844. Published online 2019 Oct 25. doi: 10.18632/aging.102292

PMCID:: PMC6834414

Article PDF–3.9M

Select item 59105524.

An unusually high frequency of SCAD deficiency caused by two pathogenic variants in the ACADS gene and its relationship to the ethnic structure in Slovakia

Jana Lisyová, Ján Chandoga, Petra Jungová, Marcel Repiský, Mária Knapková, Martina Machková, Svetozár Dluholucký, Darina Behúlová, Jana Šaligová, Ľudmila Potočňáková, Miroslava Lysinová, Daniel Böhmer

BMC Med Genet. 2018; 19: 64. Published online 2018 Apr 20. doi: 10.1186/s12881-018-0566-0

PMCID:: PMC5910552

Article PDF–810K

Select item 30228005.

The minor C-allele of rs2014355 in ACADS is associated with reduced insulin release following an oral glucose load

Malene Hornbak, Karina Banasik, Johanne M Justesen, Nikolaj T Krarup, Camilla H Sandholt, Åsa Andersson, Annelli Sandbæk, Torsten Lauritzen, Charlotta Pisinger, Daniel R Witte, Thorkild IA Sørensen, Oluf Pedersen, Torben Hansen

BMC Med Genet. 2011; 12: 4. Published online 2011 Jan 6. doi: 10.1186/1471-2350-12-4

PMCID:: PMC3022800

Article PDF–176K

Select item 27205456.

Mini-Review: Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Reena Jethva, Michael J. Bennett, Jerry Vockley

Mol Genet Metab. Author manuscript; available in PMC 2009 Dec 1.

Published in final edited form as: Mol Genet Metab. 2008 Dec; 95(4): 195–200. Published online 2008 Nov 5. doi: 10.1016/j.ymgme.2008.09.007

PMCID:: PMC2720545

Article PDF–61K

Select item 11342637.

Mitochondrial short-chain acyl-CoA dehydrogenase of human liver and kidney can function as an oxidase.

G Vanhove, P P Van Veldhoven, H J Eyssen, G P Mannaerts

Biochem J. 1993 May 15; 292(Pt 1): 23–30. doi: 10.1042/bj2920023

PMCID:: PMC1134263

Summary Page Browse PDF–1.5M

Select item 3038678.

Molecular cloning and nucleotide sequence of complementary DNAs encoding human short chain acyl-coenzyme A dehydrogenase and the study of the molecular basis of human short chain acyl-coenzyme A dehydrogenase deficiency.

E Naito, H Ozasa, Y Ikeda, K Tanaka

J Clin Invest. 1989 May; 83(5): 1605–1613. doi: 10.1172/JCI114058

PMCID:: PMC303867

Summary Page Browse PDF–1.8M

Select item 2966089.

Identification of two variant short chain acyl-coenzyme A dehydrogenase alleles, each containing a different point mutation in a patient with short chain acyl-coenzyme A dehydrogenase deficiency.

E Naito, Y Indo, K Tanaka

J Clin Invest. 1990 May; 85(5): 1575–1582. doi: 10.1172/JCI114607

PMCID:: PMC296608

Summary Page Browse PDF–1.9M

Select item 410262910.

Metabolic Heritability at Birth: Implications for Chronic Disease Research

Kelli K. Ryckman, Caitlin J. Smith, Laura L Jelliffe-Pawlowski, Allison M. Momany, Stanton L. Berberich, Jeffrey C. Murray

Hum Genet. Author manuscript; available in PMC 2015 Aug 1.

Published in final edited form as: Hum Genet. 2014 Aug; 133(8): 1049–1057. Published online 2014 May 22. doi: 10.1007/s00439-014-1450-4

PMCID:: PMC4102629

Article PDF–193K

Select item 871448211.

山东省济宁地区新生儿脂肪酸氧化代谢病筛查及随访分析

Chiju YANG, Caihong SHI, Cheng ZHOU, Qiuhua WAN, Yanbin ZHOU, Xigui CHEN, Xianlian JIN, Chenggang HUANG, Peng XU

Zhejiang Da Xue Xue Bao Yi Xue Ban. 2021 Aug; 50(4): 472–480. Chinese. doi: 10.3724/zdxbyxb-2021-0259

PMCID:: PMC8714482

Article PDF–2.2M

Select item 377390412.

A genomewide perspective of genetic variation in human metabolism

Thomas Illig, Christian Gieger, Guangju Zhai, Werner Römisch-Margl, Rui Wang-Sattler, Cornelia Prehn, Elisabeth Altmaier, Gabi Kastenmüller, Bernet S. Kato, Hans-Werner Mewes, Thomas Meitinger, Martin Hrabé de Angelis, Florian Kronenberg, Nicole Soranzo, H.-Erich Wichmann, Tim D. Spector, Jerzy Adamski, Karsten Suhre

Nat Genet. Author manuscript; available in PMC 2013 Sep 16.

Published in final edited form as: Nat Genet. 2010 Feb; 42(2): 137–141. Published online 2009 Dec 27. doi: 10.1038/ng.507

PMCID:: PMC3773904

Article PDF–482K

Select item 393051013.

Genome-Wide Association Study of Metabolic Traits Reveals Novel Gene-Metabolite-Disease Links

Rico Rueedi, Mirko Ledda, Andrew W. Nicholls, Reza M. Salek, Pedro Marques-Vidal, Edgard Morya, Koichi Sameshima, Ivan Montoliu, Laeticia Da Silva, Sebastiano Collino, François-Pierre Martin, Serge Rezzi, Christoph Steinbeck, Dawn M. Waterworth, Gérard Waeber, Peter Vollenweider, Jacques S. Beckmann, Johannes Le Coutre, Vincent Mooser, Sven Bergmann, Ulrich K. Genick, Zoltán Kutalik

PLoS Genet. 2014 Feb; 10(2): e1004132. Published online 2014 Feb 20. doi: 10.1371/journal.pgen.1004132

PMCID:: PMC3930510

Article PDF–491K

Select item 285410614.

Louise K Sjöholm, Leena Kovanen, Sirkku T Saarikoski, Martin Schalling, Catharina Lavebratt, Timo Partonen

J Circadian Rhythms. 2010; 8: 1. Published online 2010 Jan 21. doi: 10.1186/1740-3391-8-1

PMCID:: PMC2854106

Article PDF–288K

Select item 269714115.

NPAS2 and PER2 are linked to risk factors of the metabolic syndrome

Ani Englund, Leena Kovanen, Sirkku T Saarikoski, Jari Haukka, Antti Reunanen, Arpo Aromaa, Jouko Lönnqvist, Timo Partonen

J Circadian Rhythms. 2009; 7: 5. Published online 2009 May 26. doi: 10.1186/1740-3391-7-5

PMCID:: PMC2697141

Article PDF–679K

Select item 301760216.

Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing

Wenyi Wang, Peidong Shen, Sreedevi Thiyagarajan, Shengrong Lin, Curtis Palm, Rita Horvath, Thomas Klopstock, David Cutler, Lynn Pique, Iris Schrijver, Ronald W. Davis, Michael Mindrinos, Terence P. Speed, Curt Scharfe

Nucleic Acids Res. 2011 Jan; 39(1): 44–58. Published online 2010 Sep 15. doi: 10.1093/nar/gkq750

PMCID:: PMC3017602

Article PDF–1.4M

Select item 383283817.

Human metabolic individuality in biomedical and pharmaceutical research

Karsten Suhre, So-Youn Shin, Ann-Kristin Petersen, Robert P. Mohney, David Meredith, Brigitte Wägele, Elisabeth Altmaier, CARDIoGRAM, Panos Deloukas, Jeanette Erdmann, Elin Grundberg, Christopher J. Hammond, Martin Hrabé de Angelis, Gabi Kastenmüller, Anna Köttgen, Florian Kronenberg, Massimo Mangino, Christa Meisinger, Thomas Meitinger, Hans-Werner Mewes, Michael V. Milburn, Cornelia Prehn, Johannes Raffler, Janina S. Ried, Werner Römisch-Margl, Nilesh J. Samani, Kerrin S. Small, H.-Erich Wichmann, Guangju Zhai, Thomas Illig, Tim D. Spector, Jerzy Adamski, Nicole Soranzo, Christian Gieger

Nature. Author manuscript; available in PMC 2013 Nov 19.

Published in final edited form as: Nature. 2011 Aug 31; 477(7362): 10.1038/nature10354. Published online 2011 Aug 31. doi: 10.1038/nature10354

PMCID:: PMC3832838

Article PDF–839K

Select item 406425418.

An atlas of genetic influences on human blood metabolites

So-Youn Shin, Eric B. Fauman, Ann-Kristin Petersen, Jan Krumsiek, Rita Santos, Jie Huang, Matthias Arnold, Idil Erte, Vincenzo Forgetta, Tsun-Po Yang, Klaudia Walter, Cristina Menni, Lu Chen, Louella Vasquez, Ana M. Valdes, Craig L. Hyde, Vicky Wang, Daniel Ziemek, Phoebe Roberts, Li Xi, Elin Grundberg, The Multiple Tissue Human Expression Resource (MuTHER) Consortium, Melanie Waldenberger, J. Brent Richards, Robert P. Mohney, Michael V. Milburn, Sally L. John, Jeff Trimmer, Fabian J. Theis, John P. Overington, Karsten Suhre, M. Julia Brosnan, Christian Gieger, Gabi Kastenmüller, Tim D Spector, Nicole Soranzo

Nat Genet. Author manuscript; available in PMC 2014 Dec 1.

Published in final edited form as: Nat Genet. 2014 Jun; 46(6): 543–550. Published online 2014 May 11. doi: 10.1038/ng.2982

PMCID:: PMC4064254

Article PDF–2.4M

Select item 294347619.

Genetic Variants in Nuclear-Encoded Mitochondrial Genes Influence AIDS Progression

Sher L. Hendrickson, James A. Lautenberger, Leslie Wei Chinn, Michael Malasky, Efe Sezgin, Lawrence A. Kingsley, James J. Goedert, Gregory D. Kirk, Edward D. Gomperts, Susan P. Buchbinder, Jennifer L. Troyer, Stephen J. O'Brien

PLoS One. 2010; 5(9): e12862. Published online 2010 Sep 21. doi: 10.1371/journal.pone.0012862

PMCID:: PMC2943476

Article PDF–461K

Select item 294516820.

Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study

Swneke D. Bailey, Changchun Xie, Ron Do, Alexandre Montpetit, Rafael Diaz, Viswanathan Mohan, Bernard Keavney, Salim Yusuf, Hertzel C. Gerstein, James C. Engert, Sonia Anand, on behalf of the DREAM investigators

Diabetes Care. 2010 Oct; 33(10): 2250–2253. Published online 2010 Jul 13. doi: 10.2337/dc10-0452

PMCID:: PMC2945168

Article PDF–153K

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