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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|October 24, 2008
Pediatric glioblastoma cell line shows different patterns of expression of transmembrane ABC transporters after in vitro exposure to vinblastineElvis Terci Valera, Maria Angélica Abdalla de Freitas Cortez, Rosane Gomes de Paula Queiroz, et al.
Human Molecular Genetics|April 18, 2013
Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instabilityTangui Le Guen, Laurent Jullien, Fabien Touzot, et al.
Molecular Cell|October 13, 2020
H3 K27M and EZHIP Impede H3K27-Methylation Spreading by Inhibiting Allosterically Stimulated PRC2Siddhant U Jain, Andrew Q Rashoff, Samuel D Krabbenhoft, et al.
Nature|May 30, 2014
CTP synthase 1 deficiency in humans reveals its central role in lymphocyte proliferationEmmanuel Martin, Noé Palmic, Sylvia Sanquer, et al.
The Journal of Allergy and Clinical Immunology|October 15, 2014
An inherited immunoglobulin class-switch recombination deficiency associated with a defect in the INO80 chromatin remodeling complexSven Kracker, Michela Di Virgilio, Jeremy Schwartzentruber, et al.
The Journal of Allergy and Clinical Immunology|March 26, 2013
Whole-exome sequencing identifies Coronin-1A deficiency in 3 siblings with immunodeficiency and EBV-associated B-cell lymphoproliferationDespina Moshous, Emmanuel Martin, Wassila Carpentier, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|November 23, 2023
Comprehensive Genomic Analysis of Cemento-Ossifying FibromaRicardo Santiago Gomez, Ahmed El Mouatani, Filipe Fideles Duarte-Andrade, et al.
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