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Cell Reports|March 20, 2024
Synaptic homeostasis transiently leverages Hebbian mechanisms for a multiphasic response to inactivitySimón E D Sun, Daniel Levenstein, Boxing Li, et al.Human Molecular Genetics|February 4, 2017
Infantile neurodegenerative disorder associated with mutations in TBCD, an essential gene in the tubulin heterodimer assembly pathwayShimon Edvardson, Guoling Tian, Hayley Cullen, et al.Journal of Medical Genetics|June 9, 2016
Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryosRuizhi Feng, Zheng Yan, Bin Li, et al.Cell|June 4, 2020
Neuronal Inactivity Co-opts LTP Machinery to Drive Potassium Channel Splicing and Homeostatic Spike WideningBoxing Li, Benjamin S Suutari, Simón(e) D. Sun, et al.Human Molecular Genetics|December 26, 2016
Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stabilityMartin W Breuss, Thai Nguyen, Anjana Srivatsan, et al.Cell|January 16, 2007
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humansDavid A Keays, Guoling Tian, Karine Poirier, et al.American Journal of Human Genetics|December 5, 2017
Mutations in TUBB4B Cause a Distinctive Sensorineural DiseaseRomain Luscan, Sabrina Mechaussier, Antoine Paul, et al.Cell Reports|December 19, 2012
Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalitiesMartin Breuss, Julian Ik-Tsen Heng, Karine Poirier, et al.Nature Genetics|May 26, 2009
Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyriaXavier Hubert Jaglin, Karine Poirier, Yoann Saillour, et al.American Journal of Human Genetics|December 7, 2015
Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze TypeMala Isrie, Martin Breuss, Guoling Tian, et al.Pageof 3