PMC Links for Nucleotide (Select 1677500858) - PMC - NCBI

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Items: 4

Select item 67426461.

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations

Robert Fragoza, Jishnu Das, Shayne D. Wierbowski, Jin Liang, Tina N. Tran, Siqi Liang, Juan F. Beltran, Christen A. Rivera-Erick, Kaixiong Ye, Ting-Yi Wang, Li Yao, Matthew Mort, Peter D. Stenson, David N. Cooper, Xiaomu Wei, Alon Keinan, John C. Schimenti, Andrew G. Clark, Haiyuan Yu

Nat Commun. 2019; 10: 4141. Published online 2019 Sep 12. doi: 10.1038/s41467-019-11959-3

PMCID:: PMC6742646

Abstract Article PDF–1.2M

Select item 28440852.

2.6 Å X-ray Crystal Structure of Human p53R2, a p53 Inducible Ribonucleotide Reductase

Peter Smith, Bingsen Zhou, Nam Ho, Yate-Ching Yuan, Leila Su, Shiou-Chuan Tsai, Yun Yen

Biochemistry. Author manuscript; available in PMC 2010 Nov 24.

Published in final edited form as: Biochemistry. 2009 Nov 24; 48(46): 11134–11141. doi: 10.1021/bi9001425

PMCID:: PMC2844085

Abstract Article PDF–3.5M

Select item 27476473.

Mitochondrial Neurogastrointestinal Encephalopathy Due to Mutations in RRM2B

Aziz Shaibani, Oleg A. Shchelochkov, Shulin Zhang, Panagiotis Katsonis, Olivier Lichtarge, Lee-Jun Wong, Marwan Shinawi

Arch Neurol. Author manuscript; available in PMC 2009 Nov 1.

Published in final edited form as: Arch Neurol. 2009 Aug; 66(8): 1028–1032. doi: 10.1001/archneurol.2009.139

PMCID:: PMC2747647

Abstract Article PDF–963K

Select item 27252684.

A Heterozygous Truncating Mutation in RRM2B Causes Autosomal-Dominant Progressive External Ophthalmoplegia with Multiple mtDNA Deletions

Henna Tyynismaa, Emil Ylikallio, Mehul Patel, Maria J. Molnar, Ronald G. Haller, Anu Suomalainen

Am J Hum Genet. 2009 Aug 14; 85(2): 290–295. doi: 10.1016/j.ajhg.2009.07.009

PMCID:: PMC2725268

Abstract Article PDF–472K

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