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Arthritis and Rheumatism|February 14, 2012
β-glucan triggers spondylarthritis and Crohn's disease-like ileitis in SKG miceMerja Ruutu, Gethin Thomas, Roland Steck, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 14, 2011
Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and backscattered electron imagingAngelo Karunaratne, Christopher R Esapa, Jennifer Hiller, et al.BMC Medicine|August 29, 2013
A novel serogenetic approach determines the community prevalence of celiac disease and informs improved diagnostic pathwaysRobert P Anderson, Margaret J Henry, Roberta Taylor, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 24, 2023
Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate MetabolismNeelam Hassan, Celia L Gregson, Haotian Tang, et al.Bonekey Reports|February 7, 2014
Whole exome sequencing is an efficient, sensitive and specific method of mutation detection in osteogenesis imperfecta and Marfan syndromeAideen M McInerney-Leo, Mhairi S Marshall, Brooke Gardiner, et al.Pediatric Diabetes|September 8, 2018
Comprehensive genetic screening: The prevalence of maturity-onset diabetes of the young gene variants in a population-based childhood diabetes cohortStephanie R Johnson, Jonathan J Ellis, Paul J Leo, et al.Molecular Genetics & Genomic Medicine|November 30, 2016
Rare variants in optic disc area gene <i>CARD10</i> enriched in primary open-angle glaucomaTiger Zhou, Emmanuelle Souzeau, Shiwani Sharma, et al.Clinical and Experimental Rheumatology|October 18, 2016
Genetic diagnostic profiling in axial spondyloarthritis: a real world studyGothic P Thomas, Dana Willner, Philip C Robinson, et al.American Journal of Human Genetics|August 6, 2013
Short-rib polydactyly and Jeune syndromes are caused by mutations in WDR60Aideen M McInerney-Leo, Miriam Schmidts, Claudio R Cortés, et al.Endocrinology|December 5, 2013
An N-ethyl-N-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excessLiz Bentley, Christopher T Esapa, M Andrew Nesbit, et al.Pageof 38