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Cheen Fei Chin

Showing results (11-20 of 15) with videos related to

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The Journal of Clinical Investigation|July 3, 2025
SPNS1 variants cause multiorgan disease and implicate lysophospholipid transport as critical for mTOR-regulated lipid homeostasisMenglan He, Mei Ding, Michaela Chocholouskova, et al.
The Journal of Clinical Investigation|July 18, 2023
Blood-derived lysophospholipid sustains hepatic phospholipids and fat storage necessary for hepatoprotection in overnutritionCheen Fei Chin, Dwight LA Galam, Liang Gao, et al.
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.
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.
European Journal of Human Genetics : EJHG|June 24, 2020
Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging featuresMarcello Scala, Geok Lin Chua, Cheen Fei Chin, et al.
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Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
The Journal of Clinical Investigation|July 3, 2025
SPNS1 variants cause multiorgan disease and implicate lysophospholipid transport as critical for mTOR-regulated lipid homeostasisMenglan He, Mei Ding, Michaela Chocholouskova, et al.
The Journal of Clinical Investigation|July 18, 2023
Blood-derived lysophospholipid sustains hepatic phospholipids and fat storage necessary for hepatoprotection in overnutritionCheen Fei Chin, Dwight LA Galam, Liang Gao, et al.
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.
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.
European Journal of Human Genetics : EJHG|June 24, 2020
Biallelic MFSD2A variants associated with congenital microcephaly, developmental delay, and recognizable neuroimaging featuresMarcello Scala, Geok Lin Chua, Cheen Fei Chin, et al.
Pageof 2