Showing results (21-30 of 75) with videos related to
Sort By:
Pageof 8
BMC Medical Genetics|July 12, 2011
Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotypeTracy L McGregor, Christina A Gurnett, Matthew B Dobbs, et al.Human Genetics|April 17, 2004
SNTG1, the gene encoding gamma1-syntrophin: a candidate gene for idiopathic scoliosisStavros Bashiardes, Rose Veile, Missy Allen, et al.Scientific Reports|June 14, 2016
Whole Exome Screening Identifies Novel and Recurrent WISP3 Mutations Causing Progressive Pseudorheumatoid Dysplasia in Jammu and Kashmir-IndiaEkta Rai, Ankit Mahajan, Parvinder Kumar, et al.Current Genomics|May 3, 2011
Clinical, Molecular, and Genetic Characteristics of PAPA Syndrome: A ReviewElisabeth J Smith, Florence Allantaz, Lynda Bennett, et al.American Journal of Medical Genetics. Part A|November 26, 2009
Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfootAudrey R Ester, Katelyn S Weymouth, Amber Burt, et al.NPJ Digital Medicine|March 26, 2026
Deep learning-based precision phenotyping of spine curvature identifies novel genetic risk loci for scoliosis in the UK BiobankMichael Zeosky, Eucharist Kun, Siddharth Reddy, et al.Human Molecular Genetics|November 12, 2020
Genomic characterization of the adolescent idiopathic scoliosis-associated transcriptome and regulomeNadja Makki, Jingjing Zhao, Zhaoyang Liu, et al.Bone Research|March 21, 2020
The cartilage matrisome in adolescent idiopathic scoliosisCarol A Wise, Diane Sepich, Aki Ushiki, et al.Disease Models & Mechanisms|June 18, 2021
Saturation mutagenesis defines novel mouse models of severe spine deformityJonathan J Rios, Kristin Denton, Hao Yu, et al.Bioengineering (Basel, Switzerland)|July 27, 2024
Deep Learning-Based Automated Measurement of Murine Bone Length in RadiographsRuichen Rong, Kristin Denton, Kevin W Jin, et al.Pageof 8