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Human Molecular Genetics|June 23, 2018
Biallelic B3GALT6 mutations cause spondylodysplastic Ehlers-Danlos syndromeTim Van Damme, Xiaomeng Pang, Brecht Guillemyn, et al.Nature Chemical Biology|April 24, 2019
Disruption of endocytosis through chemical inhibition of clathrin heavy chain functionWim Dejonghe, Isha Sharma, Bram Denoo, et al.The Plant Cell|August 18, 2018
A Spatiotemporal DNA Endoploidy Map of the Arabidopsis Root Reveals Roles for the Endocycle in Root Development and Stress AdaptationRahul Bhosale, Veronique Boudolf, Fabiola Cuevas, et al.Autophagy|February 28, 2023
HSPB8 frameshift mutant aggregates weaken chaperone-assisted selective autophagy in neuromyopathiesBarbara Tedesco, Leen Vendredy, Elias Adriaenssens, et al.EMBO Molecular Medicine|September 11, 2020
Zinc inhibits lethal inflammatory shock by preventing microbe-induced interferon signature in intestinal epitheliumJolien Souffriau, Steven Timmermans, Tineke Vanderhaeghen, et al.Cell Reports|December 29, 2021
Macrophages are metabolically heterogeneous within the tumor microenvironmentXenia Geeraerts, Juan Fernández-Garcia, Felix J Hartmann, et al.The Plant Cell|November 21, 2007
Downregulation of cinnamoyl-coenzyme A reductase in poplar: multiple-level phenotyping reveals effects on cell wall polymer metabolism and structureJean-Charles Leplé, Rebecca Dauwe, Kris Morreel, et al.The Plant Cell|July 19, 2018
Nonselective Chemical Inhibition of Sec7 Domain-Containing ARF GTPase Exchange FactorsKiril Mishev, Qing Lu, Bram Denoo, et al.Human Mutation|January 31, 2020
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertilityGiulia Ascari, Frank Peelman, Pietro Farinelli, et al.American Journal of Human Genetics|May 15, 2021
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndromeLore Pottie, Christin S Adamo, Aude Beyens, et al.Pageof 16