(Q28235198)

8

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Simon Olpin

object named as

Simon E Olpin

13

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author name string

Cheryl R Greenberg

1

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Louise A Dilling

2

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G Robert Thompson

3

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Lorne E Seargeant

4

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James C Haworth

5

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Susan Phillips

6

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Alicia Chan

7

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Paula J Waters

9

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Yolanda Lillquist

11

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Ronald J A Wanders

Molecular Genetics and Metabolism

12

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language of work or name

English

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publication date

April 2009

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published in

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volume

96

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page(s)

201-7

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issue

4

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cites work

A novel brain-expressed protein related to carnitine palmitoyltransferase I

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Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency.

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Rate-dependent distal renal tubular acidosis and carnitine palmitoyltransferase I deficiency

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Hepatic and Muscular Presentations of Carnitine Palmitoyl Transferase Deficiency: Two Distinct Entities

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Brief report: renal tubular acidosis in carnitine palmitoyltransferase type 1 deficiency

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Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite family

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Molecular basis of hepatic carnitine palmitoyltransferase I deficiency

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Features of carnitine palmitoyltransferase type I deficiency

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Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

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Hepatic carnitine palmitoyltransferase I deficiency presenting as maternal illness in pregnancy

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The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy

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Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele

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A simple screening test for fatty acid oxidation defects using whole-blood palmitate oxidation

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Complementation analysis of fatty acid oxidation disorders

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Evidence for intermediate channeling in mitochondrial beta-oxidation

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Quantitative acylcarnitine profiling in fibroblasts using [U-13C] palmitic acid: an improved tool for the diagnosis of fatty acid oxidation defects

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Analysis of carnitine esters by radio-high performance liquid chromatography in cultured skin fibroblasts from patients with mitochondrial fatty acid oxidation disorders

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A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts

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cDNA cloning, sequence analysis, and chromosomal localization of the gene for human carnitine palmitoyltransferase

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Mortality in the Kivalliq Region of Nunavut, 1987-1996.

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Identification of conserved amino acid residues in rat liver carnitine palmitoyltransferase I critical for malonyl-CoA inhibition. Mutation of methionine 593 abolishes malonyl-CoA inhibition

7 January 2021

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Structural model of a malonyl-CoA-binding site of carnitine octanoyltransferase and carnitine palmitoyltransferase I: mutational analysis of a malonyl-CoA affinity domain

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Structural model of carnitine palmitoyltransferase I based on the carnitine acetyltransferase crystal

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Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency.

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Control of mitochondrial beta-oxidation flux

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Ketogenic diets and physical performance

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The effects of fish oil supplementation in pregnancy on breast milk fatty acid composition over the course of lactation: a randomized controlled trial.

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