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American Journal of Human Genetics|April 16, 2019
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of MicrogliaNynke Oosterhof, Irene J Chang, Ehsan Ghayoor Karimiani, et al.Molecular & Cellular Proteomics : MCP|June 29, 2026
Platelet proteome links metabolism to reactivity in Essential ThrombocythemiaXiomara Guerrero-Carreño, Sanne Smits, Alfonso Esteban Lasso, et al.Nature Cell Biology|May 18, 2010
Jarid2 is a PRC2 component in embryonic stem cells required for multi-lineage differentiation and recruitment of PRC1 and RNA Polymerase II to developmental regulatorsDavid Landeira, Stephan Sauer, Raymond Poot, et al.Acta Neuropathologica|June 17, 2022
Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophyWoutje M Berdowski, Herma C van der Linde, Marjolein Breur, et al.Nature Cell Biology|July 6, 2023
Dynamic de novo heterochromatin assembly and disassembly at replication forks ensures fork stabilityVincent Gaggioli, Calvin S Y Lo, Nazaret Reverón-Gómez, et al.Science Advances|May 6, 2021
SMARCAD1-mediated active replication fork stability maintains genome integrityCalvin Shun Yu Lo, Marvin van Toorn, Vincent Gaggioli, et al.Developmental Cell|October 15, 2013
CFEOM1-associated kinesin KIF21A is a cortical microtubule growth inhibitorBabet van der Vaart, Wilhelmina E van Riel, Harinath Doodhi, et al.EMBO Reports|April 23, 2021
Loss of enteric neuronal Ndrg4 promotes colorectal cancer via increased release of Nid1 and Fbln2Nathalie Vaes, Simone L Schonkeren, Glenn Rademakers, et al.American Journal of Human Genetics|September 10, 2019
Loss of SMPD4 Causes a Developmental Disorder Characterized by Microcephaly and Congenital ArthrogryposisPamela Magini, Daphne J Smits, Laura Vandervore, et al.Pageof 9