Bennett MJ - Search Results

1

Intact alpha-subunit is required for membrane-binding of human mitochondrial trifunctional beta-oxidation protein, but is not necessary for conferring 3-ketoacyl-CoA thiolase activity to the beta-subunit.

Weinberger MJ, Rinaldo P, Strauss AW, Bennett MJ. Weinberger MJ, et al. Among authors: bennett mj. Biochem Biophys Res Commun. 1995 Apr 6;209(1):47-52. doi: 10.1006/bbrc.1995.1468. Biochem Biophys Res Commun. 1995. PMID: 7726862 Free article.

2

Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: a new defect of fatty acid oxidation.

Bennett MJ, Weinberger MJ, Kobori JA, Rinaldo P, Burlina AB. Bennett MJ, et al. Pediatr Res. 1996 Jan;39(1):185-8. doi: 10.1203/00006450-199601000-00031. Pediatr Res. 1996. PMID: 8825408

3

Inborn errors of mitochondrial fatty acid oxidation.

Bennett MJ, Rinaldo P, Strauss AW. Bennett MJ, et al. Crit Rev Clin Lab Sci. 2000 Feb;37(1):1-44. doi: 10.1080/10408360091174169. Crit Rev Clin Lab Sci. 2000. PMID: 10737439 Review.

4

General mitochondrial trifunctional protein (TFP) deficiency as a result of either alpha- or beta-subunit mutations exhibits similar phenotypes because mutations in either subunit alter TFP complex expression and subunit turnover.

Spiekerkoetter U, Khuchua Z, Yue Z, Bennett MJ, Strauss AW. Spiekerkoetter U, et al. Among authors: bennett mj. Pediatr Res. 2004 Feb;55(2):190-6. doi: 10.1203/01.PDR.0000103931.80055.06. Epub 2003 Nov 19. Pediatr Res. 2004. PMID: 14630990

5

Mutations in long-chain 3-hydroxyacyl coenzyme a dehydrogenase are associated with placental maternal floor infarction/massive perivillous fibrin deposition.

Griffin AC, Strauss AW, Bennett MJ, Ernst LM. Griffin AC, et al. Among authors: bennett mj. Pediatr Dev Pathol. 2012 Sep-Oct;15(5):368-74. doi: 10.2350/12-05-1198-OA.1. Epub 2012 Jul 2. Pediatr Dev Pathol. 2012. PMID: 22746996

6

Fatty acid oxidation disorders.

Rinaldo P, Matern D, Bennett MJ. Rinaldo P, et al. Among authors: bennett mj. Annu Rev Physiol. 2002;64:477-502. doi: 10.1146/annurev.physiol.64.082201.154705. Annu Rev Physiol. 2002. PMID: 11826276 Review.

7

Fetal genotypes and pregnancy outcomes in 35 families with mitochondrial trifunctional protein mutations.

Yang Z, Zhao Y, Bennett MJ, Strauss AW, Ibdah JA. Yang Z, et al. Among authors: bennett mj. Am J Obstet Gynecol. 2002 Sep;187(3):715-20. doi: 10.1067/mob.2002.125893. Am J Obstet Gynecol. 2002. PMID: 12237653

8

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

Spiekerkoetter U, Sun B, Khuchua Z, Bennett MJ, Strauss AW. Spiekerkoetter U, et al. Among authors: bennett mj. Hum Mutat. 2003 Jun;21(6):598-607. doi: 10.1002/humu.10211. Hum Mutat. 2003. PMID: 12754706

9

Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency.

Brackett JC, Sims HF, Rinaldo P, Shapiro S, Powell CK, Bennett MJ, Strauss AW. Brackett JC, et al. Among authors: bennett mj. J Clin Invest. 1995 May;95(5):2076-82. doi: 10.1172/JCI117894. J Clin Invest. 1995. PMID: 7738175 Free PMC article.

10

Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Bennett MJ, Weinberger MJ, Sherwood WG, Burlina AB. Bennett MJ, et al. J Inherit Metab Dis. 1994;17(3):283-6. doi: 10.1007/BF00711808. J Inherit Metab Dis. 1994. PMID: 7807934 No abstract available.

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