Showing results (81-90 of 262) with videos related to
Sort By:
Pageof 27
The American Journal of Pathology|October 29, 2004
Loss of p53 sensitizes mice with a mutation in Ccm1 (KRIT1) to development of cerebral vascular malformationsNicholas W Plummer, Carol J Gallione, Sudha Srinivasan, et al.BMC Research Notes|August 5, 2018
Genetic and genomic stability across lymphoblastoid cell line expansionsLaura B Scheinfeldt, Kelly Hodges, Jonathan Pevsner, et al.Journal of Computational Biology : a Journal of Computational Molecular Cell Biology|August 19, 2008
Estimating genome-wide copy number using allele-specific mixture modelsWenyi Wang, Benilton Carvalho, Nathaniel D Miller, et al.The Journal of Experimental Medicine|December 18, 2013
EndoU is a novel regulator of AICD during peripheral B cell selectionJonathan C Poe, Evgueni I Kountikov, Jacquelyn M Lykken, et al.Journal of Magnetic Resonance Imaging : JMRI|June 21, 2006
Dynamic MR perfusion and proton MR spectroscopic imaging in Sturge-Weber syndrome: correlation with neurological symptomsDoris D M Lin, Peter B Barker, Laura A Hatfield, et al.Journal of Child Neurology|January 19, 2006
Quantitative analysis of cerebral cortical atrophy and correlation with clinical severity in unilateral Sturge-Weber syndromeThomas M Kelley, Laura A Hatfield, Doris D M Lin, et al.Neurosurgery|June 7, 2005
Giant infiltrative cavernous malformation: clinical presentation, intervention, and genetic analysis: case reportMichael T Lawton, G Edward Vates, Alfredo Quinones-Hinojosa, et al.Developmental Medicine and Child Neurology|December 24, 2011
Updates and future horizons on the understanding, diagnosis, and treatment of Sturge-Weber syndrome brain involvementWarren Lo, Douglas A Marchuk, Karen L Ball, et al.Psychiatric Genetics|February 28, 2003
Associations among the NEO Personality Inventory, Revised and the serotonin transporter gene-linked polymorphic region in elders: effects of depression and genderBeverly H Brummett, Ilene C Siegler, Douglas R McQuoid, et al.American Journal of Human Genetics|October 22, 2019
Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1Daniel A Snellings, Carol J Gallione, Dewi S Clark, et al.Pageof 27