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Brain & Development|January 23, 2023
Neurological insights on two siblings with GM3 synthase deficiency due to novel compound heterozygous ST3GAL5 variantsShiena Watanabe, Ming Lei, Eiji Nakagawa, et al.
Cancer Science|August 23, 2007
GM3 synthase gene is a novel biomarker for histological classification and drug sensitivity against epidermal growth factor receptor tyrosine kinase inhibitors in non-small cell lung cancerMariko Noguchi, Tomoko Suzuki, Kazuya Kabayama, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 28, 2009
Mice lacking ganglioside GM3 synthase exhibit complete hearing loss due to selective degeneration of the organ of CortiMisato Yoshikawa, Shinji Go, Kotaro Takasaki, et al.
American Journal of Medical Genetics. Part A|July 1, 2022
Functional validation of novel variants in B4GALNT1 associated with early-onset complex hereditary spastic paraplegia with impaired ganglioside synthesisJulian Emanuel Alecu, Yuhsuke Ohmi, Robiul H Bhuiyan, et al.
Cellular and Molecular Life Sciences : CMLS|May 30, 2023
Cell density-dependent membrane distribution of ganglioside GM3 in melanoma cellsMotohide Murate, Noriko Yokoyama, Nario Tomishige, et al.
The EMBO Journal|September 13, 2021
GRASP55 regulates intra-Golgi localization of glycosylation enzymes to control glycosphingolipid biosynthesisPrathyush Pothukuchi, Ilenia Agliarulo, Marinella Pirozzi, et al.
The Journal of Clinical Investigation|December 10, 2015
Targeting ceramide synthase 6-dependent metastasis-prone phenotype in lung cancer cellsMotoshi Suzuki, Ke Cao, Seiichi Kato, et al.
Frontiers in Neuroscience|August 15, 2024
Functional evaluation of novel variants of <i>B4GALNT1</i> in a patient with hereditary spastic paraplegia and the general populationKei-Ichiro Inamori, Katsuya Nakamura, Fumi Shishido, et al.
The EMBO Journal|May 8, 2020
Homeostatic and pathogenic roles of GM3 ganglioside molecular species in TLR4 signaling in obesityHirotaka Kanoh, Takahiro Nitta, Shinji Go, et al.
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