Literature DB >> 28629900

Multiple analyses indicate the specific association of NR1I3, C6 and TNN with low hip BMD risk.

Ying-Ying Han1, Lan-Juan Zhao2, Yong Lin1, Hao He2, Qing Tian2, Wei Zhu3, Hui Shen2, Xiang-Ding Chen2, Hong-Wen Deng4.   

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Year:  2017        PMID： 28629900      PMCID： PMC5822710          DOI： 10.1016/j.jgg.2017.05.004

Source DB:  PubMed          Journal:  J Genet Genomics        ISSN： 1673-8527            Impact factor:   4.275


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  18 in total

1.  Comparing methods for performing trans-ethnic meta-analysis of genome-wide association studies.

Authors:  Xu Wang; Hui-Xiang Chua; Peng Chen; Rick Twee-Hee Ong; Xueling Sim; Weihua Zhang; Fumihiko Takeuchi; Xuanyao Liu; Chiea-Chuen Khor; Wan-Ting Tay; Ching-Yu Cheng; Chen Suo; Jianjun Liu; Tin Aung; Kee-Seng Chia; Jaspal S Kooner; John C Chambers; Tien-Yin Wong; E-Shyong Tai; Norihiro Kato; Yik-Ying Teo
Journal:  Hum Mol Genet       Date:  2013-02-12       Impact factor: 6.150

2.  Active ERK1/2 protein interacts with the phosphorylated nuclear constitutive active/androstane receptor (CAR; NR1I3), repressing dephosphorylation and sequestering CAR in the cytoplasm.

Authors:  Makoto Osabe; Masahiko Negishi
Journal:  J Biol Chem       Date:  2011-08-26       Impact factor: 5.157

Review 3.  Fc receptors and their role in immune regulation and autoimmunity.

Authors:  Toshiyuki Takai
Journal:  J Clin Immunol       Date:  2005-01       Impact factor: 8.317

4.  ADAMTS1 and MMP1 proteolytically engage EGF-like ligands in an osteolytic signaling cascade for bone metastasis.

Authors:  Xin Lu; Qiongqing Wang; Guohong Hu; Catherine Van Poznak; Martin Fleisher; Michael Reiss; Joan Massagué; Yibin Kang
Journal:  Genes Dev       Date:  2009-07-16       Impact factor: 11.361

5.  Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders.

Authors:  M B Hammer; G Eleuch-Fayache; J R Gibbs; S K Arepalli; S B Chong; C Sassi; Y Bouhlal; F Hentati; R Amouri; A B Singleton
Journal:  Eur J Neurol       Date:  2012-10-09       Impact factor: 6.089

6.  Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.

Authors:  Unnur Styrkarsdottir; Gudmar Thorleifsson; Patrick Sulem; Daniel F Gudbjartsson; Asgeir Sigurdsson; Aslaug Jonasdottir; Adalbjorg Jonasdottir; Asmundur Oddsson; Agnar Helgason; Olafur T Magnusson; G Bragi Walters; Michael L Frigge; Hafdis T Helgadottir; Hrefna Johannsdottir; Kristin Bergsteinsdottir; Margret H Ogmundsdottir; Jacqueline R Center; Tuan V Nguyen; John A Eisman; Claus Christiansen; Erikur Steingrimsson; Jon G Jonasson; Laufey Tryggvadottir; Gudmundur I Eyjolfsson; Asgeir Theodors; Thorvaldur Jonsson; Thorvaldur Ingvarsson; Isleifur Olafsson; Thorunn Rafnar; Augustine Kong; Gunnar Sigurdsson; Gisli Masson; Unnur Thorsteinsdottir; Kari Stefansson
Journal:  Nature       Date:  2013-05-05       Impact factor: 49.962

7.  Variation in the Kozak sequence of WNT16 results in an increased translation and is associated with osteoporosis related parameters.

Authors:  Gretl Hendrickx; Eveline Boudin; Igor Fijałkowski; Torben Leo Nielsen; Marianne Andersen; Kim Brixen; Wim Van Hul
Journal:  Bone       Date:  2013-11-01       Impact factor: 4.398

8.  Polymorphisms in predicted miRNA binding sites and osteoporosis.

Authors:  Shu-Feng Lei; Christopher J Papasian; Hong-Wen Deng
Journal:  J Bone Miner Res       Date:  2011-01       Impact factor: 6.741

9.  Multistage genome-wide association meta-analyses identified two new loci for bone mineral density.

Authors:  Lei Zhang; Hyung Jin Choi; Karol Estrada; Paul J Leo; Jian Li; Yu-Fang Pei; Yinping Zhang; Yong Lin; Hui Shen; Yao-Zhong Liu; Yongjun Liu; Yingchun Zhao; Ji-Gang Zhang; Qing Tian; Yu-ping Wang; Yingying Han; Shu Ran; Rong Hai; Xue-Zhen Zhu; Shuyan Wu; Han Yan; Xiaogang Liu; Tie-Lin Yang; Yan Guo; Feng Zhang; Yan-fang Guo; Yuan Chen; Xiangding Chen; Lijun Tan; Lishu Zhang; Fei-Yan Deng; Hongyi Deng; Fernando Rivadeneira; Emma L Duncan; Jong Young Lee; Bok Ghee Han; Nam H Cho; Geoffrey C Nicholson; Eugene McCloskey; Richard Eastell; Richard L Prince; John A Eisman; Graeme Jones; Ian R Reid; Philip N Sambrook; Elaine M Dennison; Patrick Danoy; Laura M Yerges-Armstrong; Elizabeth A Streeten; Tian Hu; Shuanglin Xiang; Christopher J Papasian; Matthew A Brown; Chan Soo Shin; André G Uitterlinden; Hong-Wen Deng
Journal:  Hum Mol Genet       Date:  2013-11-17       Impact factor: 6.150

Review 10.  Exome sequencing and complex disease: practical aspects of rare variant association studies.

Authors:  Ron Do; Sekar Kathiresan; Gonçalo R Abecasis
Journal:  Hum Mol Genet       Date:  2012-09-13       Impact factor: 6.150
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  1 in total

1.  Stable transmission of complex chromosomal rearrangements involving chromosome 1q derived from constitutional chromoanagenesis.

Authors:  Mary A Gudipati; Elizabeth Waters; Carol Greene; Nidhi Goel; Nicole L Hoppman; Beth A Pitel; Matthew R Webley; Ying Zou
Journal:  Mol Cytogenet       Date:  2019-10-31       Impact factor: 2.009
  1 in total

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