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Links from Nucleotide

Items: 7

1.
Mitochondrial protein interaction mapping identifies new regulators of respiratory chain function
Brendan J. Floyd, Emily M. Wilkerson, Mike T. Veling, Catie E. Minogue, Chuanwu Xia, Emily T. Beebe, Russell L. Wrobel, Holly Cho, Laura S. Kremer, Charlotte L. Alston, Katarzyna A. Gromek, Brendan K. Dolan, Arne Ulbrich, Jonathan A. Stefely, Sarah L. Bohl, Kelly M. Werner, Adam Jochem, Michael S. Westphall, Jarred W. Rensvold, Robert W. Taylor, Holger Prokisch, Jung-Ja P. Kim, Joshua J. Coon, David J. Pagliarini
Mol Cell. Author manuscript; available in PMC 2017 Aug 18.
Published in final edited form as: Mol Cell. 2016 Aug 18; 63(4): 621–632. Published online 2016 Aug 4. doi: 10.1016/j.molcel.2016.06.033
PMCID:
PMC4992456
AbstractArticlePDF–1.7M
2.
Kinetic and Spectral Properties of Isovaleryl-CoA Dehydrogenase and Interaction with Ligands
Al-Walid A. Mohsen, Jerry Vockley
Biochimie. Author manuscript; available in PMC 2016 Jan 1.
Published in final edited form as: Biochimie. 2015 Jan; 108: 108–119. Published online 2014 Nov 18. doi: 10.1016/j.biochi.2014.11.007
PMCID:
PMC4280362
AbstractArticlePDF–2.7M
3.
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
AbstractArticlePDF–2.4M
4.
Molecular characterization of four different classes of mutations in the isovaleryl-CoA dehydrogenase gene responsible for isovaleric acidemia.
J Vockley, B Parimoo, K Tanaka
Am J Hum Genet. 1991 Jul; 49(1): 147–157.
PMCID:
PMC1683224
SummaryPage BrowsePDF–1.8M
5.
Nucleotide sequence of messenger RNA encoding human isovaleryl-coenzyme A dehydrogenase and its expression in isovaleric acidemia fibroblasts.
Y Matsubara, M Ito, R Glassberg, S Satyabhama, Y Ikeda, K Tanaka
J Clin Invest. 1990 Apr; 85(4): 1058–1064. doi: 10.1172/JCI114536
PMCID:
PMC296535
SummaryPage BrowsePDF–1.6M
6.
3‐Hydroxyisobutyryl‐CoA hydrolase deficiency in an Iranian child with novel HIBCH compound heterozygous mutations
Parvaneh Karimzadeh, Mohammad Saberi, Kobra Sheidaee, Mitra Nourbakhsh, Mohammad Keramatipour
Clin Case Rep. 2019 Feb; 7(2): 375–380. Published online 2019 Jan 15. doi: 10.1002/ccr3.1998
PMCID:
PMC6389474
AbstractArticlePDF–322K
7.
Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemia
Yong-Wha Lee, Dong Hwan Lee, Jerry Vockley, Nam-Doo Kim, You Kyoung Lee, Chang-Seok Ki
Mol Genet Metab. Author manuscript; available in PMC 2014 Aug 18.
Published in final edited form as: Mol Genet Metab. 2007 Sep-Oct; 92(0): 71–77. Published online 2007 Jun 18. doi: 10.1016/j.ymgme.2007.05.003
PMCID:
PMC4136440
AbstractArticlePDF–1.7M

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