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Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2013
Attitudes of Canadian researchers toward the return to participants of incidental and targeted genomic findings obtained in a pediatric research settingConrad V Fernandez, Caron Strahlendorf, Denise Avard, et al.Journal of Neuro-Oncology|November 27, 2019
Correction to: Efficacy of Dabrafenib for three children with brainstem BRAF<sup>V600E</sup> positive gangliogliomaPhilippe Laflamme, Maria Kondyli, Tariq Aljared, et al.Eneuro|April 9, 2022
<i>Drosophila</i> Tet Is Required for Maintaining Glial Homeostasis in Developing and Adult Fly BrainsFelice Frey, Jawdat Sandakly, Mirna Ghannam, et al.Oncotarget|February 10, 2018
Reduced recruitment of 53BP1 during interstrand crosslink repair is associated with genetically inherited attenuation of mitomycin C sensitivity in a family with Fanconi anemiaEmilie Lesport, Alina Ferster, Armand Biver, et al.Cancer Research|February 3, 2006
Isolation of a natural inhibitor of human malignant glial cell invasion: inter alpha-trypsin inhibitor heavy chain 2Tamra E Werbowetski-Ogilvie, Nathalie Y R Agar, Roberta M Waldkircher de Oliveira, et al.Free Neuropathology|June 7, 2023
Medulloblastoma and Cowden syndrome: Further evidence of an associationSteffen Albrecht, Barbara Miedzybrodzki, Laura Palma, et al.Neuro-Oncology|February 5, 2019
Identification of genes functionally involved in the detrimental effects of mutant histone H3.3-K27M in Drosophila melanogasterJohannes Berlandi, Amel Chaouch, Nicolas De Jay, et al.Clinical Immunology (Orlando, Fla.)|February 28, 2009
Relative CD4 lymphopenia and a skewed memory phenotype are the main immunologic abnormalities in a child with Omenn syndrome due to homozygous RAG1-C2633T hypomorphic mutationChristine McCusker, Simon Hotte, Francoise Le Deist, et al.The Journal of Clinical Investigation|November 17, 2004
Severe combined immunodeficiency caused by deficiency in either the delta or the epsilon subunit of CD3Geneviève de Saint Basile, Frédéric Geissmann, Elisabeth Flori, et al.Pediatric Blood & Cancer|May 17, 2017
H3.1 K36M mutation in a congenital-onset soft tissue neoplasmKristin D Kernohan, David Grynspan, Raveena Ramphal, et al.Pageof 25