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Cancer Nursing|June 21, 2022
Development of Training in Problem Solving for Caregivers of Childhood Brain Tumor SurvivorsJanet A Deatrick, Kathleen A Knafl, George J Knafl, et al.Pathology, Research and Practice|December 9, 2019
Ten patients with high-grade transformation of acinic cell carcinomas: Expression profiling of β-catenin and cyclin D1 is usefulLauren E Yue, Shabnam Samankan, Xulei Liu, et al.Inorganic Chemistry|February 4, 2021
Expanding the Nonaqueous Chemistry of Neptunium: Synthesis and Structural Characterization of [Np(NR2)3Cl], [Np(NR2)3Cl]-, and [Np{N(R)(SiMe2CH2)}2(NR2)]- (R = SiMe3)Selena L Staun, Lauren M Stevens, Danil E Smiles, et al.Journal of Hematology & Oncology|August 17, 2022
Triple MAPK inhibition salvaged a relapsed post-BCMA CAR-T cell therapy multiple myeloma patient with a BRAF V600E subclonal mutationMuhammad Elnaggar, Sarita Agte, Paula Restrepo, et al.Nature Nanotechnology|August 4, 2022
Nanozyme-catalysed CRISPR assay for preamplification-free detection of non-coding RNAsMarta Broto, Michael M Kaminski, Christopher Adrianus, et al.American Journal of Medical Genetics. Part A|May 15, 2012
Characterization of six novel patients with MECP2 duplications due to unbalanced rearrangements of the X chromosomeJennifer N Sanmann, Danielle L Bishay, Lois J Starr, et al.Tissue Antigens|February 17, 2005
Chromosome 5q candidate genes in coeliac disease: genetic variation at IL4, IL5, IL9, IL13, IL17B and NR3C1A W Ryan, J M Thornton, K Brophy, et al.Genes and Immunity|October 21, 2005
Haplotypes in the CTLA4 region are associated with coeliac disease in the Irish populationK Brophy, A W Ryan, J M Thornton, et al.Brain : a Journal of Neurology|April 25, 2000
Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological studyJ C Janssen, M Hall, N C Fox, et al.Annals of Neurology|May 6, 2003
Polymicrogyria and absence of pineal gland due to PAX6 mutationTejal N Mitchell, Samantha L Free, Kathleen A Williamson, et al.Pageof 248