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Disorder of fatty acid metabolism
Known as:
Fatty Acid Metabolism Disorder
A group of genetic disorders that result from the inability to produce or use an enzyme required to oxidize fatty acids, resulting in an inability to…
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National Institutes of Health
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Related topics
Related topics
3 relations
Adrenal cortical hypofunction
Broader (2)
Disease
Lipid Metabolism Disorders
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Sirtuin 3‐mediated deacetylation of acyl‐CoA synthetase family member 3 by protocatechuic acid attenuates non‐alcoholic fatty liver disease
Ruimin Sun
,
Xiao-nan Kang
,
+10 authors
Jihong Yao
British Journal of Pharmacology
2020
Corpus ID: 219562772
Hepatic fatty acid metabolism disorder, a key pathogenic mechanism underlying non‐alcoholic fatty liver disease (NAFLD), is…
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Highly Cited
2019
Highly Cited
2019
Maternal exposure to different sizes of polystyrene microplastics during gestation causes metabolic disorders in their offspring.
Ting Luo
,
Yi Zhang
,
+6 authors
Yuanxiang Jin
Environmental Pollution
2019
Corpus ID: 202573280
2018
2018
Cardiomyocyte-Restricted Low Density Lipoprotein Receptor-Related Protein 6 (LRP6) Deletion Leads to Lethal Dilated Cardiomyopathy Partly Through Drp1 Signaling
Zhidan Chen
,
Yang Li
,
+20 authors
Y. Zou
Theranostics
2018
Corpus ID: 44016349
Low density lipoprotein receptor-related protein 6 (LRP6), a wnt co-receptor, regulates multiple functions in various organs…
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2018
2018
ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin‐Responsive Multiple Acyl–Coenzyme A Dehydrogenation Deficiency
Jingwen Xu
,
Duo-ling Li
,
+12 authors
Chuanzhu Yan
Annals of Neurology
2018
Corpus ID: 52300986
Riboflavin‐responsive multiple acyl–coenzyme A dehydrogenation deficiency (RR‐MADD) is an inherited fatty acid metabolism…
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2016
2016
NF-E2-related factor 2 deletion facilitates hepatic fatty acids metabolism disorder induced by high-fat diet via regulating related genes in mice.
Xinghe Wang
,
Chunyan Li
,
Shang-Rong Xu
,
M. Ishfaq
,
Xiuying Zhang
Food and Chemical Toxicology
2016
Corpus ID: 32268508
Review
2014
Review
2014
Anesthetic agents in patients with very long‐chain acyl‐coenzyme A dehydrogenase deficiency: a literature review
C. Redshaw
,
Catherine Stewart
Paediatric anaesthesia
2014
Corpus ID: 19583098
Very long‐chain acyl‐coenzyme A dehydrongenase deficiency (VLCADD) is a rare disorder of fatty acid metabolism that renders…
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2012
2012
Long‐term strategies for the treatment of Refsum's disease using therapeutic apheresis
D. Zolotov
,
S. Wagner
,
K. Kalb
,
J. Bunia
,
A. Heibges
,
R. Klingel
Journal of clinical apheresis
2012
Corpus ID: 6929912
Refsum's disease is a rare autosomal recessive disorder of fatty acid metabolism. Poorly metabolized phytanic acid accumulates in…
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2007
2007
NMR-spectroscopy-based metabonomic approach to the analysis of Bay41-4109, a novel anti-HBV compound, induced hepatotoxicity in rats.
Chang Shi
,
Chun-qi Wu
,
An-min Cao
,
H. Sheng
,
Xianxia Yan
,
Ming-yang Liao
Toxicology Letters
2007
Corpus ID: 40660140
Highly Cited
2004
Highly Cited
2004
Is autism a disorder of fatty acid metabolism? Possible dysfunction of mitochondrial beta-oxidation by long chain acyl-CoA dehydrogenase.
Tonya Clark-Taylor
,
Benjamin E Clark-Taylor
Medical Hypotheses
2004
Corpus ID: 26143348
Highly Cited
1995
Highly Cited
1995
Interactions of a very long chain fatty acid with model membranes and serum albumin. Implications for the pathogenesis of adrenoleukodystrophy.
J. Ho
,
H. Moser
,
Y. Kishimoto
,
J. Hamilton
Journal of Clinical Investigation
1995
Corpus ID: 26080399
Adrenoleukodystrophy (ALD) is an inherited disorder of fatty acid metabolism marked by accumulation of very long chain saturated…
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