Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis
暂无分享,去创建一个
Pak Chung Sham | Chao Xing | Dingjun Hao | Shulan Yang | Yubin Deng | Hang Zhou | Chong Chen | Caixia Xu | P. Sham | C. Khor | Quanzhen Li | Xiaoming Yang | Wenjie Gao | Hang Zhou | Peiqiang Su | Caixia Xu | K. Cheung | D. Chan | Silong Sun | D. Hao | Quan-Zhen Li | Dongsheng Huang | Youqiang Song | K. Luk | Xianjian Qiu | Zizhao Wu | Bo Gao | Dongsheng Huang | Gabriel Liu | Silong Sun | Danny Chan | Chiea Chuen Khor | Jun-lin Yang | Peiqiang Su | Wenjie Gao | Taifeng Zhou | Bo Gao | Chengjie Lian | Zizhao Wu | Xianjian Qiu | Xiaoming Yang | Esam Alattar | Wentao Liu | Deying Su | Yulan Chen | Kenneth M C Cheung | Keith K D Luk | Gabriel Liu | Junlin Yang | Youqiang Song | Yu-bin Deng | Chong Chen | Chengjie Lian | Yulan Chen | Shulan Yang | Deying Su | Taifeng Zhou | Wentao Liu | Chao Xing | E. Alattar | D. Huang | X. Qiu
[1] Yan Peng,et al. Melatonin reversed tumor necrosis factor‐alpha‐inhibited osteogenesis of human mesenchymal stem cells by stabilizing SMAD1 protein , 2016, Journal of pineal research.
[2] R. Henkelman,et al. Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature , 2016, Science.
[3] Wei Li,et al. AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis , 2016, Journal of Medical Genetics.
[4] Y. Kamatani,et al. A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis. , 2015, American journal of human genetics.
[5] 田原 康玄,et al. 生活習慣病とgenome-wide association study , 2015 .
[6] F. Clerget-Darpoux,et al. Functional variants of POC5 identified in patients with idiopathic scoliosis. , 2015, The Journal of clinical investigation.
[7] P. King,et al. Induction of SHP2 Deficiency in Chondrocytes Causes Severe Scoliosis and Kyphosis in Mice , 2013, Spine.
[8] Susan R. Wente,et al. Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease system , 2013, Proceedings of the National Academy of Sciences.
[9] Todd A. Johnson,et al. Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis , 2013, Nature Genetics.
[10] F. Altaf,et al. Adolescent idiopathic scoliosis , 2013, BMJ : British Medical Journal.
[11] M Timothy Hresko,et al. Clinical practice. Idiopathic scoliosis in adolescents. , 2013, The New England journal of medicine.
[12] Yan Peng,et al. Association between Common Variants near LBX1 and Adolescent Idiopathic Scoliosis Replicated in the Chinese Han Population , 2013, PloS one.
[13] Todd A. Johnson,et al. A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis , 2011, Nature Genetics.
[14] D. Stevenson,et al. The musculoskeletal phenotype of the RASopathies , 2011, American journal of medical genetics. Part C, Seminars in medical genetics.
[15] F. Clerget-Darpoux,et al. New disease gene location and high genetic heterogeneity in idiopathic scoliosis , 2011, European Journal of Human Genetics.
[16] C. Heldin,et al. Erk 5 is necessary for sustained PDGF-induced Akt phosphorylation and inhibition of apoptosis. , 2010, Cellular signalling.
[17] R. Chettier,et al. Polygenic inheritance of adolescent idiopathic scoliosis: A study of extended families in Utah , 2010, American journal of medical genetics. Part A.
[18] A. Bowcock,et al. Genetic Linkage Localizes an Adolescent Idiopathic Scoliosis and Pectus Excavatum Gene to Chromosome 18 q , 2009, Spine.
[19] J. Weber,et al. Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel , 2007, Journal of Medical Genetics.
[20] N. Tang,et al. Genetic association of complex traits: using idiopathic scoliosis as an example. , 2007, Clinical orthopaedics and related research.
[21] A. Esparís-Ogando,et al. Erk5 nuclear location is independent on dual phosphorylation, and favours resistance to TRAIL-induced apoptosis. , 2007, Cellular signalling.
[22] Alexander F. Wilson,et al. Identification of Candidate Regions for Familial Idiopathic Scoliosis , 2005, Spine.
[23] M. Mangino,et al. Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11 , 2002, Human Genetics.
[24] B V Reamy,et al. Adolescent idiopathic scoliosis: review and current concepts. , 2001, American family physician.
[25] R. Strausberg,et al. High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[26] M. White,et al. Contribution of the ERK5/MEK5 Pathway to Ras/Raf Signaling and Growth Control* , 1999, The Journal of Biological Chemistry.
[27] A. Oestreich,et al. Scoliosis circa 2000: radiologic imaging perspective , 1998, Skeletal Radiology.
[28] K. Reinker,et al. Scoliosis in Twins: A Meta‐analysis of the Literature and Report of Six Cases , 1997, Spine.
[29] R. Winter,et al. Adolescent idiopathic scoliosis , 1991, The Lancet.
[30] E. J. Riseborough,et al. A genetic survey of idiopathic scoliosis in Boston, Massachusetts. , 1973, The Journal of bone and joint surgery. American volume.
[31] R. Wynne‐Davies. Familial (idiopathic) scoliosis. A family survey. , 1968, The Journal of bone and joint surgery. British volume.
[32] 三宅 敦. Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3 , 2014 .
[33] A. Oestreich,et al. Scoliosis circa 2000: radiologic imaging perspective. I. Diagnosis and pretreatment evaluation. , 1998, Skeletal radiology.
[34] B. Wang,et al. Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls , 2022 .
[35] Y. Kamatani,et al. A Functional SNP in BNC 2 Is Associated with Adolescent Idiopathic Scoliosis , 2022 .