Found: 20
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A mutation of EPT1 (SELENOI) underlies a new disorder of Kennedy pathway phospholipid biosynthesis.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Cholesterol binding, efflux, and a PDZ-interacting domain of scavenger receptor-BI mediate HDL-initiated signaling.
- Published in:
- 2005
- By:
- Publication type:
- journal article
A partially inactivating mutation in the sodium-dependent lysophosphatidylcholine transporter MFSD2A causes a non-lethal microcephaly syndrome.
- Published in:
- Nature Genetics, 2015, v. 47, n. 7, p. 814, doi. 10.1038/ng.3313
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- Publication type:
- Article
Inactivating mutations in MFSD2A, required for omega-3 fatty acid transport in brain, cause a lethal microcephaly syndrome.
- Published in:
- Nature Genetics, 2015, v. 47, n. 7, p. 809, doi. 10.1038/ng.3311
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- Publication type:
- Article
The lysolipid transporter Mfsd2a regulates lipogenesis in the developing brain.
- Published in:
- PLoS Biology, 2018, v. 16, n. 8, p. 1, doi. 10.1371/journal.pbio.2006443
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- Publication type:
- Article
SR-BI and Protein-Protein Interactions in Hepatic High Density Lipoprotein Metabolism.
- Published in:
- Reviews in Endocrine & Metabolic Disorders, 2004, v. 5, n. 4, p. 327
- By:
- Publication type:
- Article
A Novel Splice-Site Mutation in ALS2 Establishes the Diagnosis of Juvenile Amyotrophic Lateral Sclerosis in a Family with Early Onset Anarthria and Generalized Dystonias.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0113258
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- Publication type:
- Article
Major Facilitator Superfamily Domain-Containing Protein 2a (MFSD2A) Has Roles in Body Growth, Motor Function, and Lipid Metabolism.
- Published in:
- PLoS ONE, 2012, v. 7, n. 11, p. 1, doi. 10.1371/journal.pone.0050629
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- Publication type:
- Article
Structural Insights into Triglyceride Storage Mediated by Fat Storage-Inducing Transmembrane (FIT) Protein 2.
- Published in:
- PLoS ONE, 2010, v. 5, n. 5, p. 1, doi. 10.1371/journal.pone.0010796
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- Publication type:
- Article
Receptors and Lipid Transfer Proteins in HDL Metabolism.
- Published in:
- Annals of the New York Academy of Sciences, 2000, v. 902, n. 1, p. 103, doi. 10.1111/j.1749-6632.2000.tb06305.x
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- Publication type:
- Article
Cover Feature: Application of Neuron‐Selective Fluorescent Probe, NeuA, To Identify Mouse Retinal Degeneration (ChemBioChem 11/2021).
- Published in:
- ChemBioChem, 2021, v. 22, n. 11, p. 1853, doi. 10.1002/cbic.202100206
- By:
- Publication type:
- Article
Application of Neuron‐Selective Fluorescent Probe, NeuA, To Identify Mouse Retinal Degeneration.
- Published in:
- ChemBioChem, 2021, v. 22, n. 11, p. 1915, doi. 10.1002/cbic.202100011
- By:
- Publication type:
- Article
Fat storage-inducing transmembrane protein 2 (FIT2) is less abundant in type 2 diabetes, and regulates triglyceride accumulation and insulin sensitivity in adipocytes.
- Published in:
- FASEB Journal, 2019, v. 33, n. 1, p. 430, doi. 10.1096/fj.201701321RR
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- Publication type:
- Article
Decreased DHA‐containing phospholipids in the neocortex of dementia with Lewy bodies are associated with soluble Aβ<sub>42</sub>, phosphorylated α‐synuclein, and synaptopathology.
- Published in:
- Brain Pathology, 2023, v. 33, n. 6, p. 1, doi. 10.1111/bpa.13190
- By:
- Publication type:
- Article
Inhibition of Candida parapsilosis Fatty Acid Synthase (Fas2) Induces Mitochondrial Cell Death in Serum.
- Published in:
- PLoS Pathogens, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.ppat.1002879
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- Publication type:
- Article
Mfsd2a is a transporter for the essential omega-3 fatty acid docosahexaenoic acid.
- Published in:
- Nature, 2014, v. 509, n. 7501, p. 503, doi. 10.1038/nature13241
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- Publication type:
- Article
Trypanosoma cruzi Utilizes the Host Low Density Lipoprotein Receptor in Invasion.
- Published in:
- PLoS Neglected Tropical Diseases, 2011, v. 5, n. 2, p. 1, doi. 10.1371/journal.pntd.0000953
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- Publication type:
- Article
SCS3 and YFT2 Link Transcription of Phospholipid Biosynthetic Genes to ER Stress and the UPR.
- Published in:
- PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002890
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- Publication type:
- Article
Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelination.
- Published in:
- Neurogenetics, 2018, v. 19, n. 4, p. 227, doi. 10.1007/s10048-018-0556-6
- By:
- Publication type:
- Article
MicroRNAs Are Required for the Feature Maintenance and Differentiation of Brown Adipocytes.
- Published in:
- Diabetes, 2014, v. 63, n. 12, p. 4045, doi. 10.2337/db14-0466
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- Publication type:
- Article