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Molecular Genetics and Metabolism|April 20, 2011
Indications for a genetic association of a VCP polymorphism with the pathogenesis of sporadic Paget's disease of bone, but not for TNFSF11 (RANKL) and IL-6 polymorphismsPui Yan Jenny Chung, Greet Beyens, Fenna de Freitas, et al.American Journal of Human Genetics|August 16, 2006
A new autosomal recessive form of Stickler syndrome is caused by a mutation in the COL9A1 geneGuy Van Camp, Rikkert L Snoeckx, Nele Hilgert, et al.Pathology, Research and Practice|January 25, 2022
Malignant pleural mesothelioma with an EML4-ALK fusion: Expect the unexpected!Fleur Cordier, Joni Van der Meulen, Nadine van Roy, et al.Human Genetics|September 15, 2010
The majority of the genetic risk for Paget's disease of bone is explained by genetic variants close to the CSF1, OPTN, TM7SF4, and TNFRSF11A genesPui Yan Jenny Chung, Greet Beyens, Steven Boonen, et al.Seminars in Musculoskeletal Radiology|December 24, 2015
Soft Tissue Tumors in Adults: ESSR-Approved Guidelines for Diagnostic ImagingIris M Noebauer-Huhmann, Marc-André Weber, Radhesh K Lalam, et al.Brain, Behavior, and Immunity|December 4, 2018
State-associated changes in longitudinal [18F]-PBR111 TSPO PET imaging of psychosis patients: Evidence for the accelerated ageing hypothesis?Livia De Picker, Julie Ottoy, Jeroen Verhaeghe, et al.The Journal of Clinical Investigation|April 4, 2007
Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humansLiesbeth Van Wesenbeeck, Paul R Odgren, Fraser P Coxon, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 22, 2010
Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bonePui Yan Jenny Chung, Greet Beyens, Philip L Riches, et al.Nature Genetics|October 19, 2004
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosisJan Hellemans, Olena Preobrazhenska, Andy Willaert, et al.Pageof 10