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Scientific Reports|December 3, 2016
Loss of EGFR-ASAP1 signaling in metastatic and unresectable hepatoblastomaSarangarajan Ranganathan, Mylarappa Ningappa, Chethan Ashokkumar, et al.Frontiers in Genetics|April 12, 2019
Identification of Target Genes at Juvenile Idiopathic Arthritis GWAS Loci in Human NeutrophilsJunyi Li, Xiucheng Yuan, Michael E March, et al.The Journal of Clinical Endocrinology and Metabolism|August 24, 2018
Heterozygous Mutations in TBX1 as a Cause of Isolated HypoparathyroidismDong Li, Christopher T Gordon, Myriam Oufadem, et al.American Journal of Medical Genetics. Part A|March 7, 2022
Exome and RNA-Seq analyses of an incomplete penetrance variant in USP9X in female-specific syndromic intellectual disabilityDong Li, Michael E March, Tiancheng Wang, et al.Human Molecular Genetics|August 21, 2014
Genome-wide association study of maternal and inherited effects on left-sided cardiac malformationsLaura E Mitchell, A J Agopian, Angela Bhalla, et al.Birth Defects Research|April 12, 2017
Rare copy number variants in patients with congenital conotruncal heart defectsHongbo M Xie, Petra Werner, Dwight Stambolian, et al.Cell Biochemistry and Biophysics|April 5, 2007
Functional polymorphism and differential regulation of CYSLTR1 transcription in human airway smooth muscle and monocytesNathalie P Duroudier, Ian Sayers, Charlotte Carabott Castagna, et al.Neuroimage|January 12, 2012
Impact of in-scanner head motion on multiple measures of functional connectivity: relevance for studies of neurodevelopment in youthTheodore D Satterthwaite, Daniel H Wolf, James Loughead, et al.Obesity (Silver Spring, Md.)|February 7, 2012
Association of type 2 diabetes susceptibility loci with one-year weight loss in the look AHEAD clinical trialInga Peter, Jeanne M McCaffery, Alyson Kelley-Hedgepeth, et al.Journal of Immunology (Baltimore, Md. : 1950)|January 23, 2023
Elevated Levels of the Cytokine LIGHT in Pediatric Crohn's DiseaseChristopher J Cardinale, Debra J Abrams, Frank D Mentch, et al.Pageof 91