PMC Links for Nucleotide (Select 1519244876) - PMC

Select item 66941321.

HENA, heterogeneous network-based data set for Alzheimer’s disease

Elena Sügis, Jerome Dauvillier, Anna Leontjeva, Priit Adler, Valerie Hindie, Thomas Moncion, Vincent Collura, Rachel Daudin, Yann Loe-Mie, Yann Herault, Jean-Charles Lambert, Henning Hermjakob, Tal Pupko, Jean-Christophe Rain, Ioannis Xenarios, Jaak Vilo, Michel Simonneau, Hedi Peterson

Sci Data. 2019; 6: 151. Published online 2019 Aug 14. doi: 10.1038/s41597-019-0152-0

PMCID:: PMC6694132

Abstract Article PDF–2.8M

Select item 65895772.

Intersectin-1 interacts with the golgin GCC88 to couple the actin network and Golgi architecture

Christian Makhoul, Prajakta Gosavi, Regina Duffield, Bronwen Delbridge, Nicholas A. Williamson, Paul A. Gleeson

Mol Biol Cell. 2019 Feb 1; 30(3): 370–386. doi: 10.1091/mbc.E18-05-0313

PMCID:: PMC6589577

Abstract Article PDF–3.3M

Select item 60572693.

A Flat BAR Protein Promotes Actin Polymerization at the Base of Clathrin-Coated Pits

Leonardo Almeida-Souza, Rene A.W. Frank, Javier García-Nafría, Adeline Colussi, Nushan Gunawardana, Christopher M. Johnson, Minmin Yu, Gillian Howard, Byron Andrews, Yvonne Vallis, Harvey T. McMahon

Cell. 2018 Jul 12; 174(2): 325–337.e14. doi: 10.1016/j.cell.2018.05.020

PMCID:: PMC6057269

Abstract Article

Select item 11712074.

The EH and SH3 domain Ese proteins regulate endocytosis by linking to dynamin and Eps15.

A S Sengar, W Wang, J Bishay, S Cohen, S E Egan

EMBO J. 1999 Mar 1; 18(5): 1159–1171. doi: 10.1093/emboj/18.5.1159

PMCID:: PMC1171207

Summary PDF–1.1M

Select item 59204065.

Uncovering the heterogeneous genetic variations in two insulin-expressing tumors in a patient with MEN1

Zai Wang, Liguo Liu, Jie Luo, Jing Guo, Min Zhai, Wenjian Zhang, Zhiying Yang

Oncol Lett. 2018 May; 15(5): 7123–7131. Published online 2018 Mar 6. doi: 10.3892/ol.2018.8184

PMCID:: PMC5920406

Abstract Article PDF–1.5M

Select item 43138476.

Integrative analysis of sequencing and array genotype data for discovering disease associations with rare mutations

Yi-Juan Hu, Yun Li, Paul L. Auer, Dan-Yu Lin

Proc Natl Acad Sci U S A. 2015 Jan 27; 112(4): 1019–1024. Published online 2015 Jan 12. doi: 10.1073/pnas.1406143112

PMCID:: PMC4313847

Abstract Article PDF–938K

Select item 34286537.

A systematic comparison and evaluation of high density exon arrays and RNA-seq technology used to unravel the peripheral blood transcriptome of sickle cell disease

Nalini Raghavachari, Jennifer Barb, Yanqin Yang, Poching Liu, Kimberly Woodhouse, Daniel Levy, Christopher J O‘Donnell, Peter J Munson, Gregory J Kato

BMC Med Genomics. 2012; 5: 28. Published online 2012 Jun 29. doi: 10.1186/1755-8794-5-28

PMCID:: PMC3428653

Abstract Article PDF–3.4M

Select item 32793678.

Auditory Function in the Tc1 Mouse Model of Down Syndrome Suggests a Limited Region of Human Chromosome 21 Involved in Otitis Media

Stephanie Kuhn, Neil Ingham, Selina Pearson, Susan M. Gribble, Stephen Clayton, Karen P. Steel, Walter Marcotti

PLoS One. 2012; 7(2): e31433. Published online 2012 Feb 14. doi: 10.1371/journal.pone.0031433

PMCID:: PMC3279367

Abstract Article PDF–661K

Select item 15022979.

Computational prediction of methylation status in human genomic sequences

Rajdeep Das, Nevenka Dimitrova, Zhenyu Xuan, Robert A. Rollins, Fatemah Haghighi, John R. Edwards, Jingyue Ju, Timothy H. Bestor, Michael Q. Zhang

Proc Natl Acad Sci U S A. 2006 Jul 11; 103(28): 10713–10716. Published online 2006 Jul 3. doi: 10.1073/pnas.0602949103

PMCID:: PMC1502297

Abstract Article PDF–757K

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