Concepedia

Molecular basis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of the major disease-causing mutation in the α-subunit of the mitochondrial trifunctional protein

Lodewijk IJlst, R. J. A. Wanders, S. Ushikubo, Takehiko Kamijo, Takashi Hashimoto

Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism · 1994 · 159 citations · 19 references

DOI

Concepts

References

19

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

Analytical Biochemistry · 1987 · 63.3K citations

, , +12

Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. II. Purification and properties of enoyl-coenzyme A (CoA) hydratase/3-hydroxyacyl-CoA dehydrogenase/3-ketoacyl-CoA thiolase trifunctional protein.

Yasushi Uchida, Kaoru Izai, T Orii et al. · Journal of Biological Chemistry · 1992 · 345 citations · Full text

, , +17

Novel fatty acid beta-oxidation enzymes in rat liver mitochondria. I. Purification and properties of very-long-chain acyl-coenzyme A dehydrogenase.

Kaoru Izai, Yasushi Uchida, T Orii et al. · Journal of Biological Chemistry · 1992 · 246 citations · Full text

, , +16

Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation

Ronald J. A. Wanders, Lodewijk IJlst, F Poggi et al. · Biochemical and Biophysical Research Communications · 1992 · 154 citations

, , +16

Human liver long-chain 3-hydroxyacyl-coenzyme a dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria

K. Carpenter, R. J. Pollitt, Bruce Middleton · Biochemical and Biophysical Research Communications · 1992 · 147 citations

, , +11