| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/HUMU.23296 |
| P698 | PubMed publication ID | 28714182 |
| P50 | author | Chao Xing | Q41503549 |
| Kenneth M Cheung | Q56894872 | ||
| You-Qiang Song | Q64878533 | ||
| Ding Jun Hao | Q88910955 | ||
| P2093 | author name string | Danny Chan | |
| Xiaoming Yang | |||
| Quan-Zhen Li | |||
| Dongsheng Huang | |||
| Chong Chen | |||
| Bo Gao | |||
| Wentao Liu | |||
| Junlin Yang | |||
| Hang Zhou | |||
| Shulan Yang | |||
| Peiqiang Su | |||
| Gabriel Liu | |||
| Chiea Chuen Khor | |||
| Pak Chung Sham | |||
| Caixia Xu | |||
| Yubin Deng | |||
| Wenjie Gao | |||
| Yulan Chen | |||
| Chengjie Lian | |||
| Xianjian Qiu | |||
| Zizhao Wu | |||
| Silong Sun | |||
| Taifeng Zhou | |||
| Deying Su | |||
| Esam Alattar | |||
| Keith K D Luk | |||
| P2860 | cites work | Contribution of the ERK5/MEK5 pathway to Ras/Raf signaling and growth control | Q28146025 |
| Assignment of a locus for autosomal dominant idiopathic scoliosis (IS) to human chromosome 17p11 | Q28208125 | ||
| Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis | Q28290491 | ||
| Functional variants of POC5 identified in patients with idiopathic scoliosis | Q30628365 | ||
| Clinical practice. Idiopathic scoliosis in adolescents | Q34035816 | ||
| New disease gene location and high genetic heterogeneity in idiopathic scoliosis. | Q34170982 | ||
| Association between common variants near LBX1 and adolescent idiopathic scoliosis replicated in the Chinese Han population | Q34544798 | ||
| Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3. | Q34984067 | ||
| A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis | Q36068737 | ||
| Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls | Q36128818 | ||
| Genetic association of complex traits: using idiopathic scoliosis as an example | Q36833934 | ||
| AKAP2 identified as a novel gene mutated in a Chinese family with adolescent idiopathic scoliosis | Q37085614 | ||
| Genetic linkage localizes an adolescent idiopathic scoliosis and pectus excavatum gene to chromosome 18 q. | Q37089296 | ||
| Efficient multiplex biallelic zebrafish genome editing using a CRISPR nuclease system | Q37117695 | ||
| Induction of SHP2 deficiency in chondrocytes causes severe scoliosis and kyphosis in mice | Q37394616 | ||
| The musculoskeletal phenotype of the RASopathies | Q37865455 | ||
| Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature | Q41542474 | ||
| Erk 5 is necessary for sustained PDGF-induced Akt phosphorylation and inhibition of apoptosis | Q43170136 | ||
| A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis. | Q50998791 | ||
| Melatonin reversed tumor necrosis factor-alpha-inhibited osteogenesis of human mesenchymal stem cells by stabilizing SMAD1 protein. | Q51718842 | ||
| Scoliosis circa 2000: radiologic imaging perspective | Q54191376 | ||
| Scoliosis in twins. A meta-analysis of the literature and report of six cases | Q73719623 | ||
| Erk5 nuclear location is independent on dual phosphorylation, and favours resistance to TRAIL-induced apoptosis | Q79816809 | ||
| Adolescent idiopathic scoliosis | Q81213364 | ||
| Assignment of two loci for autosomal dominant adolescent idiopathic scoliosis to chromosomes 9q31.2-q34.2 and 17q25.3-qtel | Q81431632 | ||
| Identification of candidate regions for familial idiopathic scoliosis | Q81753467 | ||
| Polygenic inheritance of adolescent idiopathic scoliosis: a study of extended families in Utah | Q84122799 | ||
| Adolescent idiopathic scoliosis | Q86695493 | ||
| Adolescent idiopathic scoliosis | Q89216494 | ||
| P433 | issue | 11 | |
| P921 | main subject | scoliosis | Q174857 |
| teenager | Q1492760 | ||
| adolescent idiopathic scoliosis | Q55950311 | ||
| P304 | page(s) | 1500-1510 | |
| P577 | publication date | 2017-07-17 | |
| P1433 | published in | Human Mutation | Q5937269 |
| P1476 | title | Rare coding variants in MAPK7 predispose to adolescent idiopathic scoliosis | |
| P478 | volume | 38 |
| Q89976612 | Clinical Observations and Treatment Approaches for Scoliosis in Prader-Willi Syndrome |
| Q99565703 | Conditional ablation of MAPK7 expression in chondrocytes impairs endochondral bone formation in limbs and adaptation of chondrocytes to hypoxia |
| Q92932114 | Dstyk mutation leads to congenital scoliosis-like vertebral malformations in zebrafish via dysregulated mTORC1/TFEB pathway |
| Q92879431 | Research progress on the etiology and pathogenesis of adolescent idiopathic scoliosis |
| Q92277791 | The Progress of CRISPR/Cas9-Mediated Gene Editing in Generating Mouse/Zebrafish Models of Human Skeletal Diseases |
| Q57729296 | The potential of CRISPR/Cas9 genome editing for the study and treatment of intervertebral disc pathologies |
| Q94476031 | The publication trends and hot spots of scoliosis research from 2009 to 2018: a 10-year bibliometric analysis |
| Q92542662 | Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis |
| Q64240809 | mutation causes muscular dysplasia and arthrogryposis |
Search more.