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Nature Genetics
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May 26, 2015
Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome
Alicia Guemez-Gamboa, Long N Nguyen, Hongbo Yang, et al.
Journal of Inherited Metabolic Disease
|
April 2, 2020
Responsiveness of sphingosine phosphate lyase insufficiency syndrome to vitamin B6 cofactor supplementation
Piming Zhao, Isaac D Liu, Jeffrey B Hodgin, et al.
Cell Research
|
February 1, 2024
MFSD7c functions as a transporter of choline at the blood-brain barrier
Xuan Thi Anh Nguyen, Thanh Nha Uyen Le, Toan Q Nguyen, et al.
BMC Medicine
|
April 13, 2025
Sexual dimorphism in the association of umbilical cord blood lipidome with abdominal fat in early childhood
Kothandaraman Narasimhan, Mya Thway Tint, Li Chen, et al.
Brain : a Journal of Neurology
|
January 6, 2017
A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis
Mustafa Y Ahmed, Aisha Al-Khayat, Fathiya Al-Murshedi, et al.
BMC Medicine
|
July 24, 2022
Population-based plasma lipidomics reveals developmental changes in metabolism and signatures of obesity risk: a mother-offspring cohort study
Sartaj Ahmad Mir, Li Chen, Satvika Burugupalli, et al.
Nature Communications
|
May 28, 2026
A lipidomics roadmap: from basic research to societal challenges
Maria Fedorova, Anne K Bendt, Justine Bertrand-Michel, et al.
Plos Pathogens
|
May 3, 2013
A mechanistic paradigm for broad-spectrum antivirals that target virus-cell fusion
Frederic Vigant, Jihye Lee, Axel Hollmann, et al.
Diabetologia
|
December 2, 2024
Metabolomics profiling in multi-ancestral individuals with type 2 diabetes in Singapore identified metabolites associated with renal function decline
Yuqing Chen, Federico Torta, Hiromi W L Koh, et al.
Nature
|
February 11, 2026
Targeting excessive cholesterol deposition alleviates secondary lymphoedema
Hwee Ying Lim, Yuning Zhang, Syaza Hazwany Mohammad Azhar, et al.
Page
of 33
Search research articles
Search
Showing results (311-320 of 328) with videos related to
Sort By:
Page
of 33
Nature Genetics
|
May 26, 2015
Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome
Alicia Guemez-Gamboa, Long N Nguyen, Hongbo Yang, et al.
Journal of Inherited Metabolic Disease
|
April 2, 2020
Responsiveness of sphingosine phosphate lyase insufficiency syndrome to vitamin B6 cofactor supplementation
Piming Zhao, Isaac D Liu, Jeffrey B Hodgin, et al.
Cell Research
|
February 1, 2024
MFSD7c functions as a transporter of choline at the blood-brain barrier
Xuan Thi Anh Nguyen, Thanh Nha Uyen Le, Toan Q Nguyen, et al.
BMC Medicine
|
April 13, 2025
Sexual dimorphism in the association of umbilical cord blood lipidome with abdominal fat in early childhood
Kothandaraman Narasimhan, Mya Thway Tint, Li Chen, et al.
Brain : a Journal of Neurology
|
January 6, 2017
A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis
Mustafa Y Ahmed, Aisha Al-Khayat, Fathiya Al-Murshedi, et al.
BMC Medicine
|
July 24, 2022
Population-based plasma lipidomics reveals developmental changes in metabolism and signatures of obesity risk: a mother-offspring cohort study
Sartaj Ahmad Mir, Li Chen, Satvika Burugupalli, et al.
Nature Communications
|
May 28, 2026
A lipidomics roadmap: from basic research to societal challenges
Maria Fedorova, Anne K Bendt, Justine Bertrand-Michel, et al.
Plos Pathogens
|
May 3, 2013
A mechanistic paradigm for broad-spectrum antivirals that target virus-cell fusion
Frederic Vigant, Jihye Lee, Axel Hollmann, et al.
Diabetologia
|
December 2, 2024
Metabolomics profiling in multi-ancestral individuals with type 2 diabetes in Singapore identified metabolites associated with renal function decline
Yuqing Chen, Federico Torta, Hiromi W L Koh, et al.
Nature
|
February 11, 2026
Targeting excessive cholesterol deposition alleviates secondary lymphoedema
Hwee Ying Lim, Yuning Zhang, Syaza Hazwany Mohammad Azhar, et al.
Page
of 33