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Proceedings of the National Academy of Sciences of the United States of America|September 26, 2022
Spns1 is a lysophospholipid transporter mediating lysosomal phospholipid salvageMenglan He, Alvin C Y Kuk, Mei Ding, et al.Cell Reports|December 25, 2024
Self-maintenance of zonal hepatocytes during adult homeostasis and their complex plasticity upon distinct liver injuriesChow Hiang Ang, Philip Arandjelovic, Jinming Cheng, et al.Nature|October 19, 2017
Mfsd2b is essential for the sphingosine-1-phosphate export in erythrocytes and plateletsThiet M Vu, Ayako-Nakamura Ishizu, Juat Chin Foo, et al.Diabetes|July 11, 2014
MicroRNAs are required for the feature maintenance and differentiation of brown adipocytesHye-Jin Kim, Hyunjii Cho, Ryan Alexander, et al.Journal of Immunology (Baltimore, Md. : 1950)|May 26, 2019
The Lysophosphatidylcholine Transporter MFSD2A Is Essential for CD8+ Memory T Cell Maintenance and Secondary Response to InfectionAnn R Piccirillo, Eric J Hyzny, Lisa Y Beppu, et al.Nature Genetics|May 26, 2015
A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndromeVafa Alakbarzade, Abdul Hameed, Debra Q Y Quek, et al.Circulation Research|December 30, 2020
Single-Cell Analysis of Blood-Brain Barrier Response to Pericyte LossMaarja A Mäe, Liqun He, Sofia Nordling, et al.Nature|June 17, 2021
Structural basis of omega-3 fatty acid transport across the blood-brain barrierRosemary J Cater, Geok Lin Chua, Satchal K Erramilli, et al.Proceedings of the National Academy of Sciences of the United States of America|March 7, 2022
Destabilization of β Cell FIT2 by saturated fatty acids alter lipid droplet numbers and contribute to ER stress and diabetesXiaofeng Zheng, Qing Wei Calvin Ho, Minni Chua, et al.Nature Genetics|May 26, 2015
Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndromeAlicia Guemez-Gamboa, Long N Nguyen, Hongbo Yang, et al.Pageof 7