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Items: 1 to 20 of 62

1.
Two-stage association study to identify the genetic susceptibility of a novel common variant of rs2075290 in ZPR1 to type 2 diabetes
Fanglin Guan, Yu Niu, Tianxiao Zhang, Songfang Liu, Lei Ma, Ting Qi, Jia Feng, Hong Zuo, Guohong Li, Xufeng Liu, Shujin Wang
Sci Rep. 2016; 6: 29586. Published online 2016 Jul 14. doi: 10.1038/srep29586
PMCID:
PMC4944165
AbstractArticlePDF–807K
2.
Sex-specific Association of the Zinc Finger Protein 259 rs2075290 Polymorphism and Serum Lipid Levels
Lynn Htet Htet Aung, Rui-Xing Yin, Dong-Feng Wu, Wei Wang, Jin-Zhen Wu, Cheng-Wu Liu
Int J Med Sci. 2014; 11(5): 471–478. Published online 2014 Mar 16. doi: 10.7150/ijms.8489
PMCID:
PMC3970100
AbstractArticlePDF–526K
3.
Implication between Genetic Variants from APOA5 and ZPR1 and NAFLD Severity in Patients with Hypertriglyceridemia
Virginia Esteve-Luque, Ariadna Padró-Miquel, Marta Fanlo-Maresma, Emili Corbella, Xavier Corbella, Xavier Pintó, Beatriz Candás-Estébanez
Nutrients. 2021 Feb; 13(2): 552. Published online 2021 Feb 8. doi: 10.3390/nu13020552
PMCID:
PMC7914661
AbstractArticlePDF–305K
4.
Association of the variants in the BUD13-ZNF259 genes and the risk of hyperlipidaemia
Lynn Htet Htet Aung, Rui-Xing Yin, Dong-Feng Wu, Wei Wang, Cheng-Wu Liu, Shang-Ling Pan
J Cell Mol Med. 2014 Jul; 18(7): 1417–1428. Published online 2014 Apr 30. doi: 10.1111/jcmm.12291
PMCID:
PMC4124025
AbstractArticlePDF–955K
5.
Effects of apolipoprotein A5 haplotypes on the ratio of triglyceride to high-density lipoprotein cholesterol and the risk for metabolic syndrome in Koreans
Seongwon Cha, Hyunjoo Yu, Ah Yeon Park, Kwang Hoon Song
Lipids Health Dis. 2014; 13: 45. Published online 2014 Mar 12. doi: 10.1186/1476-511X-13-45
PMCID:
PMC4008339
AbstractArticlePDF–440K
6.
A Replication Study of GWAS-Derived Lipid Genes in Asian Indians: The Chromosomal Region 11q23.3 Harbors Loci Contributing to Triglycerides
Timothy R. Braun, Latonya F. Been, Akhil Singhal, Jacob Worsham, Sarju Ralhan, Gurpreet S. Wander, John C. Chambers, Jaspal S. Kooner, Christopher E. Aston, Dharambir K. Sanghera
PLoS One. 2012; 7(5): e37056. Published online 2012 May 18. doi: 10.1371/journal.pone.0037056
PMCID:
PMC3356398
AbstractArticlePDF–2.4M
7.
Kernel machine SNP set analysis finds the association of BUD13, ZPR1, and APOA5 variants with metabolic syndrome in Tehran Cardio-metabolic Genetics Study
Sajedeh Masjoudi, Bahareh Sedaghati-khayat, Niloufar Javanrouh Givi, Leila Najd Hassan Bonab, Fereidoun Azizi, Maryam S. Daneshpour
Sci Rep. 2021; 11: 10305. Published online 2021 May 13. doi: 10.1038/s41598-021-89509-5
PMCID:
PMC8119714
AbstractArticlePDF–1.6M
8.
Association between the MLX Interacting Protein-Like, BUD13 Homolog and Zinc Finger Protein 259 Gene Polymorphisms and Serum Lipid Levels
Lynn-Htet-Htet Aung, Rui-Xing Yin, Jin-Zhen Wu, Dong-Feng Wu, Wei Wang, Hui Li
Sci Rep. 2014; 4: 5565. Published online 2014 Jul 3. doi: 10.1038/srep05565
PMCID:
PMC5381541
AbstractArticlePDF–4.4M
9.
Multiple susceptibility loci at chromosome 11q23.3 are associated with plasma triglyceride in East Asians
Bayasgalan Gombojav, Soo Ji Lee, Minjung Kho, Yun-Mi Song, Kayoung Lee, Joohon Sung
J Lipid Res. 2016 Feb; 57(2): 318–324. doi: 10.1194/jlr.P063461
PMCID:
PMC4727427
AbstractArticlePDF–651K
10.
ZPR1 prevents R-loop accumulation, upregulates SMN2 expression and rescues spinal muscular atrophy
Annapoorna Kannan, Xiaoting Jiang, Lan He, Saif Ahmad, Laxman Gangwani
Brain. 2020 Jan; 143(1): 69–93. Published online 2019 Dec 12. doi: 10.1093/brain/awz373
Correction in:
Brain. 2020 Mar; 143(3): e24.
PMCID:
PMC6935747
AbstractArticlePDF–3.4M
11.
Effects of Polymorphisms in APOA4-APOA5-ZNF259-BUD13 Gene Cluster on Plasma Levels of Triglycerides and Risk of Coronary Heart Disease in a Chinese Han Population
Qianxi Fu, Xiaojun Tang, Juan Chen, Li Su, Mingjun Zhang, Long Wang, Jinjin Jing, Li Zhou
PLoS One. 2015; 10(9): e0138652. Published online 2015 Sep 23. doi: 10.1371/journal.pone.0138652
PMCID:
PMC4580433
AbstractArticlePDF–993K
12.
Meta-analysis of genome-wide association studies for circulating phylloquinone concentrations
Hassan S Dashti, M Kyla Shea, Caren E Smith, Toshiko Tanaka, Adela Hruby, Kris Richardson, Thomas J Wang, Mike A Nalls, Xiuqing Guo, Yongmei Liu, Jie Yao, Dalin Li, W Craig Johnson, Emelia J Benjamin, Stephen B Kritchevsky, David S Siscovick, José M Ordovás, Sarah L Booth
Am J Clin Nutr. 2014 Dec; 100(6): 1462–1469. Published online 2014 Oct 8. doi: 10.3945/ajcn.114.093146
PMCID:
PMC4232014
AbstractArticlePDF–304K
13.
ZPR1 Is Essential for Survival and Is Required for Localization of the Survival Motor Neurons (SMN) Protein to Cajal Bodies
Laxman Gangwani, Richard A. Flavell, Roger J. Davis
Mol Cell Biol. 2005 Apr; 25(7): 2744–2756. doi: 10.1128/MCB.25.7.2744-2756.2005
PMCID:
PMC1061650
AbstractArticlePDF–1.4M
14.
The Cytoplasmic Zinc Finger Protein ZPR1 Accumulates in the Nucleolus of Proliferating Cells
Zoya Galcheva-Gargova, Laxman Gangwani, Konstantin N. Konstantinov, Monique Mikrut, Steven J. Theroux, Tamar Enoch, Roger J. Davis
Mol Biol Cell. 1998 Oct; 9(10): 2963–2971. doi: 10.1091/mbc.9.10.2963
PMCID:
PMC25573
AbstractArticlePDF–489K
15.
Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip
Tom R Gaunt, Delilah Zabaneh, Sonia Shah, Anna Guyatt, Christophe Ladroue, Meena Kumari, Fotios Drenos, Tina Shah, Philippa J Talmud, Juan Pablo Casas, Gordon Lowe, Ann Rumley, Debbie A Lawlor, Mika Kivimaki, John Whittaker, Aroon D Hingorani, Steve E Humphries, Ian N Day
Thromb Haemost. Author manuscript; available in PMC 2014 Jun 24.
Published in final edited form as: Thromb Haemost. 2013 Oct 31; 110(5): 995–1003. Published online 2013 Aug 29. doi: 10.1160/TH13-02-0087
PMCID:
PMC4067543
AbstractArticlePDF–1.0M
16.
The zinc finger protein ZPR1 is a potential modifier of spinal muscular atrophy
Saif Ahmad, Yi Wang, Gouse M. Shaik, Arthur H. Burghes, Laxman Gangwani
Hum Mol Genet. 2012 Jun 15; 21(12): 2745–2758. Published online 2012 Mar 14. doi: 10.1093/hmg/dds102
PMCID:
PMC3363332
AbstractArticlePDF–782K
17.
Genome-wide association study identifies common variants associated with circulating vitamin E levels
Jacqueline M. Major, Kai Yu, William Wheeler, Hong Zhang, Marilyn C. Cornelis, Margaret E. Wright, Meredith Yeager, Kirk Snyder, Stephanie J. Weinstein, Alison Mondul, Heather Eliassen, Mark Purdue, Aditi Hazra, Catherine A. McCarty, Sara Hendrickson, Jarmo Virtamo, David Hunter, Stephen Chanock, Peter Kraft, Demetrius Albanes
Hum Mol Genet. 2011 Oct 1; 20(19): 3876–3883. Published online 2011 Jul 5. doi: 10.1093/hmg/ddr296
PMCID:
PMC3168288
AbstractArticlePDF–187K
18.
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies
Harald Grallert, Josée Dupuis, Joshua C. Bis, Abbas Dehghan, Maja Barbalic, Jens Baumert, Chen Lu, Nicholas L. Smith, André G. Uitterlinden, Robert Roberts, Natalie Khuseyinova, Renate B. Schnabel, Kenneth M. Rice, Fernando Rivadeneira, Ron C. Hoogeveen, João Daniel Fontes, Christa Meisinger, John F. Keaney, Jr., Rozenn Lemaitre, Yurii S. Aulchenko, Ramachandran S. Vasan, Stephen Ellis, Stanley L. Hazen, Cornelia M. van Duijn, Jeanenne J. Nelson, Winfried März, Heribert Schunkert, Ruth M. McPherson, Heide A. Stirnadel-Farrant, Bruce M. Psaty, Christian Gieger, David Siscovick, Albert Hofman, Thomas Illig, Mary Cushman, Jennifer F. Yamamoto, Jerome I. Rotter, Martin G. Larson, Alexandre F.R. Stewart, Eric Boerwinkle, Jacqueline C.M. Witteman, Russell P. Tracy, Wolfgang Koenig, Emelia J. Benjamin, Christie M. Ballantyne
Eur Heart J. 2012 Jan; 33(2): 238–251. Published online 2011 Oct 14. doi: 10.1093/eurheartj/ehr372
PMCID:
PMC3258449
AbstractArticlePDF–670K
19.
Mutation skew in genes identified by genome-wide association study of hypertriglyceridemia
Christopher T. Johansen, Jian Wang, Matthew B. Lanktree, Henian Cao, Adam D. McIntyre, Matthew R. Ban, Rebecca A. Martins, Brooke A. Kennedy, Reina G. Hassell, Maartje E. Visser, Stephen M. Schwartz, Benjamin F. Voight, Roberto Elosua, Veikko Salomaa, Christopher J. O'Donnell, Geesje M. Dallinga-Thie, Sonia S. Anand, Salim Yusuf, Murray W. Huff, Sekar Kathiresan, Robert A. Hegele
Nat Genet. Author manuscript; available in PMC 2011 Jan 7.
Published in final edited form as: Nat Genet. 2010 Aug; 42(8): 684–687. Published online 2010 Jul 25. doi: 10.1038/ng.628
PMCID:
PMC3017369
AbstractArticlePDF–62K
20.
SMN, the Spinal Muscular Atrophy Protein, Forms a Pre-Import Snrnp Complex with Snurportin1 and Importin β
Usha Narayanan, Jason K. Ospina, Mark R. Frey, Michael D. Hebert, A. Gregory Matera
Hum Mol Genet. Author manuscript; available in PMC 2006 Nov 1.
Published in final edited form as: Hum Mol Genet. 2002 Jul 15; 11(15): 1785–1795. doi: 10.1093/hmg/11.15.1785
PMCID:
PMC1630493
AbstractArticlePDF–727K

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