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Nature Genetics|August 28, 2012
A low-frequency variant at 8q24.21 is strongly associated with risk of oligodendroglial tumors and astrocytomas with IDH1 or IDH2 mutationRobert B Jenkins, Yuanyuan Xiao, Hugues Sicotte, et al.Scientific Reports|May 11, 2018
Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21Quinn T Ostrom, Ben Kinnersley, Margaret R Wrensch, et al.The New England Journal of Medicine|June 11, 2015
Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in TumorsJeanette E Eckel-Passow, Daniel H Lachance, Annette M Molinaro, et al.Neuro-Oncology|August 21, 2018
Sex-specific gene and pathway modeling of inherited glioma riskQuinn T Ostrom, Warren Coleman, William Huang, et al.Seminars in Arthritis and Rheumatism|February 4, 2024
The Sjögren's Working Group: The 2023 OMERACT meeting and provisional domain generationRachael A Gordon, Yann Nguyen, Nathan Foulquier, et al.Nature Reviews. Rheumatology|June 10, 2025
2023 International Rome consensus for the nomenclature of Sjögren diseaseManuel Ramos-Casals, Alan N Baer, María Del Pilar Brito-Zerón, et al.Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.Perspectives on Psychological Science : a Journal of the Association for Psychological Science|July 18, 2015
Registered Replication Report: Schooler and Engstler-Schooler (1990)V K Alogna, M K Attaya, P Aucoin, et al.Pageof 67