Concepedia

General Mitochondrial Trifunctional Protein (TFP) Deficiency as a Result of Either α- or β-Subunit Mutations Exhibits Similar Phenotypes Because Mutations in Either Subunit Alter TFP Complex Expression and Subunit Turnover

Ute Spiekerkoetter, Zaza Khuchua, Yue Zou, Arnold W. Strauss

Pediatric Research · 2003 · 102 citations · 22 references

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22

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

Ulrich K. Laemmli · Nature · 1970 · 251.6K citations

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A Fetal Fatty-Acid Oxidation Disorder as a Cause of Liver Disease in Pregnant Women

Jamal A. Ibdah, Michael J. Bennett, Piero Rinaldo et al. · New England Journal of Medicine · 1999 · 500 citations · Full text

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Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency: Clinical Presentation and Follow-Up of 50 Patients

M. E. J. den Boer, Ronald J. A. Wanders, Andrew A. M. Morris et al. · PEDIATRICS · 2002 · 194 citations

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Combined enzyme defect of mitochondrial fatty acid oxidation.

Sandra L. Jackson, Rajinder Singh Kler, K. Bartlett et al. · Journal of Clinical Investigation · 1992 · 128 citations · Full text

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Molecular and phenotypic heterogeneity in mitochondrial trifunctional protein deficiency due to ?-subunit mutations

Ute Spiekerkoetter, Bin Sun, Zaza Khuchua et al. · Human Mutation · 2003 · 118 citations

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