Page last updated: 2024-08-17

lysine and Lipid Metabolism, Inborn Error

lysine has been researched along with Lipid Metabolism, Inborn Error in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (33.33)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (66.67)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
de Boer, VC; Houten, SM; Pougovkina, O; Te Brinke, H; Wanders, RJ	1
Bonito, CA; Guedes, RC; Leandro, J; Leandro, P; Louro, F; Nunes, J; Ventura, FV	1
Gardner, LI	1

Reviews

1 review(s) available for lysine and Lipid Metabolism, Inborn Error

Article	Year
Genetically expressed abnormalities in the fetus. Clinical obstetrics and gynecology, 1974, Volume: 17, Issue:3 Topics: Adrenal Insufficiency; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Ammonia; Anemia, Sickle Cell; Anencephaly; Carbohydrate Metabolism, Inborn Errors; Fabry Disease; Female; Fetal Diseases; Fetus; Gangliosides; Gaucher Disease; Humans; Karyotyping; Lipid Metabolism, Inborn Errors; Lipidoses; Lysine; Metabolism, Inborn Errors; Mucopolysaccharidoses; Polyploidy; Pregnancy; Propionates; Sphingolipidoses; Turner Syndrome; Vitamin B 12	1974

Article

Year

Genetically expressed abnormalities in the fetus.

Clinical obstetrics and gynecology, 1974, Volume: 17, Issue:3

Topics: Adrenal Insufficiency; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Ammonia; Anemia, Sickle Cell; Anencephaly; Carbohydrate Metabolism, Inborn Errors; Fabry Disease; Female; Fetal Diseases; Fetus; Gangliosides; Gaucher Disease; Humans; Karyotyping; Lipid Metabolism, Inborn Errors; Lipidoses; Lysine; Metabolism, Inborn Errors; Mucopolysaccharidoses; Polyploidy; Pregnancy; Propionates; Sphingolipidoses; Turner Syndrome; Vitamin B 12

1974

Other Studies

2 other study(ies) available for lysine and Lipid Metabolism, Inborn Error

Article	Year
Aberrant protein acylation is a common observation in inborn errors of acyl-CoA metabolism. Journal of inherited metabolic disease, 2014, Volume: 37, Issue:5 Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; Acylation; Animals; Cell Line; Fatty Acids; Humans; Lipid Metabolism, Inborn Errors; Lysine; Mice; Mice, Inbred BALB C; Mitochondria, Liver; Proteins	2014
Unveiling the Pathogenic Molecular Mechanisms of the Most Common Variant (p.K329E) in Medium-Chain Acyl-CoA Dehydrogenase Deficiency by in Vitro and in Silico Approaches. Biochemistry, 2016, Dec-27, Volume: 55, Issue:51 Topics: Acyl-CoA Dehydrogenase; Biocatalysis; Computer Simulation; Enzyme Stability; Glutamic Acid; Humans; Kinetics; Lipid Metabolism, Inborn Errors; Lysine; Models, Molecular; Motion; Mutation, Missense; Principal Component Analysis; Protein Binding; Protein Domains; Protein Multimerization; Temperature	2016

Article

Year

Aberrant protein acylation is a common observation in inborn errors of acyl-CoA metabolism.

Journal of inherited metabolic disease, 2014, Volume: 37, Issue:5

Topics: Acyl Coenzyme A; Acyl-CoA Dehydrogenase; Acylation; Animals; Cell Line; Fatty Acids; Humans; Lipid Metabolism, Inborn Errors; Lysine; Mice; Mice, Inbred BALB C; Mitochondria, Liver; Proteins

2014

Unveiling the Pathogenic Molecular Mechanisms of the Most Common Variant (p.K329E) in Medium-Chain Acyl-CoA Dehydrogenase Deficiency by in Vitro and in Silico Approaches.

Biochemistry, 2016, Dec-27, Volume: 55, Issue:51

Topics: Acyl-CoA Dehydrogenase; Biocatalysis; Computer Simulation; Enzyme Stability; Glutamic Acid; Humans; Kinetics; Lipid Metabolism, Inborn Errors; Lysine; Models, Molecular; Motion; Mutation, Missense; Principal Component Analysis; Protein Binding; Protein Domains; Protein Multimerization; Temperature

2016