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Biomaterials|April 7, 2007
The performance of poly-epsilon-caprolactone scaffolds in a rabbit femur model with and without autologous stromal cells and BMP4L Savarino, N Baldini, M Greco, et al.Human Molecular Genetics|February 3, 2000
Differentially regulated and evolved genes in the fully sequenced Xq/Yq pseudoautosomal regionA Ciccodicola, M D'Esposito, T Esposito, et al.American Journal of Human Genetics|October 24, 2001
Survival of male patients with incontinentia pigmenti carrying a lethal mutation can be explained by somatic mosaicism or Klinefelter syndromeS Kenwrick, H Woffendin, T Jakins, et al.Nature|June 6, 2000
Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) ConsortiumA Smahi, G Courtois, P Vabres, et al.Nature|September 4, 2020
The innate immunity protein IFITM3 modulates γ-secretase in Alzheimer's diseaseJi-Yeun Hur, Georgia R Frost, Xianzhong Wu, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 23, 2023
Genetic associations with age at dementia onset in the PSEN1 E280A Colombian kindredJesse Nicholas Cochran, Juliana Acosta-Uribe, Bianca T Esposito, et al.The Lancet. Neurology|January 22, 2022
Variant-dependent heterogeneity in amyloid β burden in autosomal dominant Alzheimer's disease: cross-sectional and longitudinal analyses of an observational studyJasmeer P Chhatwal, Stephanie A Schultz, Eric McDade, et al.Pageof 5