PMC Links for Nucleotide (Select 1519311975) - PMC

Select item 55316111.

Architecture of the human interactome defines protein communities and disease networks

Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper

Nature. Author manuscript; available in PMC 2017 Nov 17.

Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366

PMCID:: PMC5531611

Abstract Article PDF–2.7M

Select item 49924562.

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

Abstract Article PDF–1.7M

Select item 49382013.

NDUFAF5 Hydroxylates NDUFS7 at an Early Stage in the Assembly of Human Complex I

Virginie F. Rhein, Joe Carroll, Shujing Ding, Ian M. Fearnley, John E. Walker

J Biol Chem. 2016 Jul 8; 291(28): 14851–14860. Published online 2016 May 18. doi: 10.1074/jbc.M116.734970

PMCID:: PMC4938201

Abstract Article PDF–2.7M

Select item 29212754.

Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome

M Gerards, W Sluiter, B J C van den Bosch, L E A de Wit, C M H Calis, M Frentzen, H Akbari, K Schoonderwoerd, H R Scholte, R J Jongbloed, A T M Hendrickx, I F M de Coo, H J M Smeets

J Med Genet. 2010 Aug; 47(8): 507–512. Published online 2009 Jun 18. doi: 10.1136/jmg.2009.067553

PMCID:: PMC2921275

Abstract Article PDF–519K

Select item 25619345.

Mutation of C20orf7 Disrupts Complex I Assembly and Causes Lethal Neonatal Mitochondrial Disease

Canny Sugiana, David J. Pagliarini, Matthew McKenzie, Denise M. Kirby, Renato Salemi, Khaled K. Abu-Amero, Hans-Henrik M. Dahl, Wendy M. Hutchison, Katherine A. Vascotto, Stacey M. Smith, Robert F. Newbold, John Christodoulou, Sarah Calvo, Vamsi K. Mootha, Michael T. Ryan, David R. Thorburn

Am J Hum Genet. 2008 Oct 10; 83(4): 468–478. Published online 2008 Oct 3. doi: 10.1016/j.ajhg.2008.09.009

PMCID:: PMC2561934

Abstract Article PDF–1.1M

Select item 66053626.

Changes in Methionine Metabolism and Histone H3 Trimethylation Are Linked to Mitochondrial Defects in Multiple Sclerosis

Naveen Kumar Singhal, Shuo Li, Erland Arning, Kholoud Alkhayer, Robert Clements, Zachary Sarcyk, Rohan S. Dassanayake, Nicola E. Brasch, Ernest J. Freeman, Teodoro Bottiglieri, Jennifer McDonough

J Neurosci. 2015 Nov 11; 35(45): 15170–15186. doi: 10.1523/JNEUROSCI.4349-14.2015

PMCID:: PMC6605362

Abstract Article PDF–5.4M

Select item 61629517.

Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder

Elizabeth A. Normand, Alicia Braxton, Salma Nassef, Patricia A. Ward, Francesco Vetrini, Weimin He, Vipulkumar Patel, Chunjing Qu, Lauren E. Westerfield, Samantha Stover, Avinash V. Dharmadhikari, Donna M. Muzny, Richard A. Gibbs, Hongzheng Dai, Linyan Meng, Xia Wang, Rui Xiao, Pengfei Liu, Weimin Bi, Fan Xia, Magdalena Walkiewicz, Ignatia B. Van den Veyver, Christine M. Eng, Yaping Yang

Genome Med. 2018; 10: 74. Published online 2018 Sep 28. doi: 10.1186/s13073-018-0582-x

PMCID:: PMC6162951

Abstract Article PDF–844K

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