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Items: 16

1.
A novel p53 regulator, C16ORF72/TAPR1, buffers against telomerase inhibition
Yahya Benslimane, María Sánchez‐Osuna, Jasmin Coulombe‐Huntington, Thierry Bertomeu, Danielle Henry, Caroline Huard, Éric Bonneil, Pierre Thibault, Mike Tyers, Lea Harrington
Aging Cell. 2021 Apr; 20(4): e13331. Published online 2021 Mar 4. doi: 10.1111/acel.13331
PMCID:
PMC8045932
AbstractArticlePDF–1.9M
2.
Structure of the human sodium leak channel NALCN in complex with FAM155A
Jiongfang Xie, Meng Ke, Lizhen Xu, Shiyi Lin, Jin Huang, Jiabei Zhang, Fan Yang, Jianping Wu, Zhen Yan
Nat Commun. 2020; 11: 5831. Published online 2020 Nov 17. doi: 10.1038/s41467-020-19667-z
PMCID:
PMC7672056
AbstractArticlePDF–3.4M
3.
The NALCN channel complex is voltage sensitive and directly modulated by extracellular calcium
H. C. Chua, M. Wulf, C. Weidling, L. P. Rasmussen, S. A. Pless
Sci Adv. 2020 Apr; 6(17): eaaz3154. Published online 2020 Apr 24. doi: 10.1126/sciadv.aaz3154
PMCID:
PMC7182417
AbstractArticlePDF–12M
4.
Common variation in FAM155A is associated with diverticulitis but not diverticulosis
Matthias C. Reichert, Juozas Kupcinskas, Antje Schulz, Christoph Schramm, Susanne N. Weber, Marcin Krawczyk, Christoph Jüngst, Markus Casper, Frank Grünhage, Beate Appenrodt, Vincent Zimmer, Algimantas Tamelis, Jaune I. Lukosiene, Neringa Pauziene, Gediminas Kiudelis, Laimas Jonaitis, Tobias Goeser, Maciej Malinowski, Matthias Glanemann, Limas Kupcinskas, Frank Lammert
Sci Rep. 2020; 10: 1658. Published online 2020 Feb 3. doi: 10.1038/s41598-020-58437-1
PMCID:
PMC6997170
AbstractArticlePDF–1.2M
5.
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis
Snaevar Sigurdsson, Kristjan F. Alexandersson, Patrick Sulem, Bjarke Feenstra, Steinunn Gudmundsdottir, Gisli H. Halldorsson, Sigurgeir Olafsson, Asgeir Sigurdsson, Thorunn Rafnar, Thorgeir Thorgeirsson, Erik Sørensen, Andreas Nordholm-Carstensen, Jakob Burcharth, Jens Andersen, Henrik Stig Jørgensen, Emma Possfelt-Møller, Henrik Ullum, Gudmar Thorleifsson, Gisli Masson, Unnur Thorsteinsdottir, Mads Melbye, Daniel F. Gudbjartsson, Tryggvi Stefansson, Ingileif Jonsdottir, Kari Stefansson
Nat Commun. 2017; 8: 15789. Published online 2017 Jun 6. doi: 10.1038/ncomms15789
PMCID:
PMC5467205
AbstractArticlePDF–822K
6.
Genome-Wide Association Study of a Heart Failure-Related Metabolomic Profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) Study
Bing Yu, Yan Zheng, Danny Alexander, Teri A. Manolio, Alvaro Alonso, Jennifer A. Nettleton, Eric Boerwinkle
Genet Epidemiol. Author manuscript; available in PMC 2014 Jul 2.
Published in final edited form as: Genet Epidemiol. 2013 Dec; 37(8): 840–845. Published online 2013 Aug 11. doi: 10.1002/gepi.21752
PMCID:
PMC4079107
AbstractArticlePDF–269K
7.
Ancient association between cation leak channels and Mid1 proteins is conserved in fungi and animals
Alfredo Ghezzi, Benjamin J. Liebeskind, Ammon Thompson, Nigel S. Atkinson, Harold H. Zakon
Front Mol Neurosci. 2014; 7: 15. Published online 2014 Mar 7. doi: 10.3389/fnmol.2014.00015
PMCID:
PMC3945613
AbstractArticlePDF–1.6M
8.
A genome-wide association study for reading and language abilities in two population cohorts
M Luciano, D M Evans, N K Hansell, S E Medland, G W Montgomery, N G Martin, M J Wright, T C Bates
Genes Brain Behav. 2013 Aug; 12(6): 645–652. Published online 2013 Jun 20. doi: 10.1111/gbb.12053
PMCID:
PMC3908370
AbstractArticlePDF–513K
9.
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis
Cross-Disorder Group of the Psychiatric Genomics Consortium
Lancet. Author manuscript; available in PMC 2014 Apr 20.
Published in final edited form as: Lancet. 2013 Apr 20; 381(9875): 1371–1379. Published online 2013 Feb 28. doi: 10.1016/S0140-6736(12)62129-1
PMCID:
PMC3714010
AbstractArticlePDF–878K
10.
A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis
Nicolas Greliche, Marine Germain, Jean-Charles Lambert, William Cohen, Marion Bertrand, Anne-Marie Dupuis, Luc Letenneur, Mark Lathrop, Philippe Amouyel, Pierre-Emmanuel Morange, David-Alexandre Trégouët
BMC Med Genet. 2013; 14: 36. Published online 2013 Mar 20. doi: 10.1186/1471-2350-14-36
PMCID:
PMC3607886
AbstractArticlePDF–191K
11.
Novel Genetic Loci Identified for the Pathophysiology of Childhood Obesity in the Hispanic Population
Anthony G. Comuzzie, Shelley A. Cole, Sandra L. Laston, V. Saroja Voruganti, Karin Haack, Richard A. Gibbs, Nancy F. Butte
PLoS One. 2012; 7(12): e51954. Published online 2012 Dec 14. doi: 10.1371/journal.pone.0051954
PMCID:
PMC3522587
AbstractArticlePDF–130K
12.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
13.
Genome-wide association scan of trait depression
Antonio Terracciano, Toshiko Tanaka, Angelina R. Sutin, Serena Sanna, Barbara Deiana, Sandra Lai, Manuela Uda, David Schlessinger, Gonçalo R. Abecasis, Luigi Ferrucci, Paul T. Costa, Jr.
Biol Psychiatry. Author manuscript; available in PMC 2011 Nov 1.
Published in final edited form as: Biol Psychiatry. 2010 Nov 1; 68(9): 811–817. Published online 2010 Aug 25. doi: 10.1016/j.biopsych.2010.06.030
PMCID:
PMC2955852
AbstractArticlePDF–233K
14.
Personalized Smoking Cessation: Interactions between Nicotine Dose, Dependence and Quit-Success Genotype Score
Jed E Rose, Frédérique M Behm, Tomas Drgon, Catherine Johnson, George R Uhl
Mol Med. 2010 Jul-Aug; 16(7-8): 247–253. Published online 2010 Mar 17. doi: 10.2119/molmed.2009.00159
Correction in:
Mol Med. 2012; 18(1): 729.
PMCID:
PMC2896464
AbstractArticlePDF–2.4M
15.
Diversification of transcriptional modulation: Large-scale identification and characterization of putative alternative promoters of human genes
Kouichi Kimura, Ai Wakamatsu, Yutaka Suzuki, Toshio Ota, Tetsuo Nishikawa, Riu Yamashita, Jun-ichi Yamamoto, Mitsuo Sekine, Katsuki Tsuritani, Hiroyuki Wakaguri, Shizuko Ishii, Tomoyasu Sugiyama, Kaoru Saito, Yuko Isono, Ryotaro Irie, Norihiro Kushida, Takahiro Yoneyama, Rie Otsuka, Katsuhiro Kanda, Takahide Yokoi, Hiroshi Kondo, Masako Wagatsuma, Katsuji Murakawa, Shinichi Ishida, Tadashi Ishibashi, Asako Takahashi-Fujii, Tomoo Tanase, Keiichi Nagai, Hisashi Kikuchi, Kenta Nakai, Takao Isogai, Sumio Sugano
Genome Res. 2006 Jan; 16(1): 55–65. doi: 10.1101/gr.4039406
PMCID:
PMC1356129
AbstractArticlePDF–438K
16.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K

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