Published in J Lipid Res on March 01, 1987
A novel mouse model of lipotoxic cardiomyopathy. J Clin Invest (2001) 4.35
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Novel auxin transport inhibitors phenocopy the auxin influx carrier mutation aux1. Plant J (2001) 1.67
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Maternal serum-alpha-fetoprotein and low birth-weight. Lancet (1977) 1.64
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts. J Pediatr (1994) 1.59
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Synergistic heterozygosity: disease resulting from multiple partial defects in one or more metabolic pathways. Mol Genet Metab (2000) 1.44
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Defects of metabolism of fatty acids in the sudden infant death syndrome. Br Med J (Clin Res Ed) (1985) 1.34
Potentially hazardous compound in a herbal slimming remedy. Lancet (1992) 1.26
Trials with the auditory response cradle. 1--Neonatal responses to auditory stimuli. Br J Audiol (1979) 1.25
Acylcarnitines in fibroblasts of patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and other fatty acid oxidation disorders. J Inherit Metab Dis (2000) 1.22
Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome. Br Med J (Clin Res Ed) (1984) 1.19
Mitochondrial respiratory chain complex I deficiency with clinical and biochemical features of long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency. J Pediatr (2000) 1.18
Transfer and expression of foreign genes in mammalian cells. Biotechniques (2000) 1.18
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The Arabidopsis AUX1 gene: a model system to study mRNA processing in plants. Plant Mol Biol (1998) 1.11
Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency. J Clin Invest (1995) 1.11
Chinese herbs for eczema, the active compound? Lancet (1991) 1.10
The metabolic autopsy comes of age. Clin Chem (2001) 1.10
Evidence for fatty acid oxidation in human placenta, and the relationship of fatty acid oxidation enzyme activities with gestational age. Placenta (2002) 1.09
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Detection of intrauterine growth retardation by ultrasound: preliminary communication. J R Soc Med (1981) 1.08
Maternal acute fatty liver of pregnancy associated with fetal trifunctional protein deficiency: molecular characterization of a novel maternal mutant allele. Pediatr Res (1996) 1.07
3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children. J Pediatr (1998) 1.07
Molecular characterization of L-CPT I deficiency in six patients: insights into function of the native enzyme. J Lipid Res (2001) 1.07
Some problems of alpha-fetoprotein screening. Lancet (1978) 1.06
Clinical and biochemical characterization of short-chain acyl-coenzyme A dehydrogenase deficiency. J Pediatr (1995) 1.05
Trials with the Auditory Response Cradle. II--The neonatal respiratory response to an auditory stimulus. Br J Audiol (1980) 1.05
3-Methylglutaconic aciduria associated with Pearson syndrome and respiratory chain defects. J Pediatr (1992) 1.04
The cyanide poisoning necropsy: an appraisal of risk factors. J Clin Pathol (1992) 1.04
Cell marking in Arabidopsis thaliana and its application to patch-clamp studies. Plant J (1998) 1.04
Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatally. J Inherit Metab Dis (1984) 1.03
The effects of dietary omega-3 polyunsaturated fatty acids on erythrocyte membrane phospholipids, erythrocyte deformability and blood viscosity in healthy volunteers. Atherosclerosis (1985) 1.01
Batten disease: evaluation of CLN3 mutations on protein localization and function. Hum Mol Genet (2000) 1.00
Trials with the auditory response cradle III: head turns and startles as auditory responses in the neonate. Br J Audiol (1980) 1.00
Late-onset holocarboxylase synthetase deficiency. J Inherit Metab Dis (1996) 1.00
The Arabidopsis thaliana/Myzus persicae model system demonstrates that a single gene can influence the interaction between a plant and a sap-feeding insect. Mol Ecol (2006) 0.99
Taccalonolide binding to tubulin imparts microtubule stability and potent in vivo activity. Cancer Res (2013) 0.98
Inherited long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and a fetal-maternal interaction cause maternal liver disease and other pregnancy complications. Semin Perinatol (1999) 0.98
The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defect. J Inherit Metab Dis (1985) 0.96
Mathematical modelling of the Aux/IAA negative feedback loop. Bull Math Biol (2010) 0.96
Mellituria and postprandial blood sugar curves in dogs after the ingestion of various carbohydrates with the diet. J Nutr (1966) 0.94
Structural and functional analysis of cationic transfection lipids: the hydrophobic domain. Gene Ther (1996) 0.93
Fibroblast studies documenting a case of peroxisomal 2-methylacyl-CoA racemase deficiency: possible link between racemase deficiency and malabsorption and vitamin K deficiency. Eur J Clin Invest (2001) 0.93
beta-Ketothiolase (2-methylacetoacetyl-coenzyme A thiolase) deficiency: identification of two patients in Israel. J Inherit Metab Dis (1996) 0.93
Mucocele of the cystic duct remnant in eight liver transplant recipients: findings at cholangiography, CT, and US. Radiology (1990) 0.93
Riboflavin-responsive ethylmalonic-adipic aciduria. J Inherit Metab Dis (1985) 0.92
Cyclosporin concentrations in whole blood and plasma. Clin Chem (1984) 0.92
Anaphylactic reaction during anaesthesia associated with positive intradermal skin test to fentanyl. Can Anaesth Soc J (1986) 0.92
Crystallization of diphtheria toxin. J Mol Biol (1991) 0.91
Pregnancies associated with low maternal serum alpha-fetoprotein concentrations. Am J Obstet Gynecol (1979) 0.91
Osmotic blood-brain barrier modification: clinical documentation by enhanced CT scanning and/or radionuclide brain scanning. AJR Am J Roentgenol (1983) 0.91
N-acetylaspartylglutamate in Canavan disease: an adverse effector? Eur J Pediatr (1999) 0.90
Acylcoenzyme A dehydrogenase deficiency in heart tissue from infants who died unexpectedly with fatty change in the liver. Br Med J (Clin Res Ed) (1988) 0.90
Structure and function of 3 alpha-hydroxysteroid dehydrogenase. Steroids (1997) 0.90
Clinical and biochemical features of fatty acid oxidation disorders. Curr Opin Pediatr (1998) 0.90
Mild trifunctional protein deficiency is associated with progressive neuropathy and myopathy and suggests a novel genotype-phenotype correlation. J Clin Invest (1998) 0.89
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathy. Neurology (1999) 0.89
Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death. Lancet (1987) 0.89
Inborn errors of metabolism diagnosed in sudden death cases by acylcarnitine analysis of postmortem bile. Clin Chem (1995) 0.88
The influence of fetal sex upon liquor cytology as a means of estimating gestational age. J Obstet Gynaecol Br Commonw (1972) 0.88
Combined malonic, methylmalonic and ethylmalonic acid semialdehyde dehydrogenase deficiencies: an inborn error of beta-alanine, L-valine and L-alloisoleucine metabolism? J Inherit Metab Dis (1993) 0.87
The camptomelic syndrome in two female siblings. Clin Genet (1980) 0.87
Effects of dietary fish oil supplementation on the fatty acid composition of the human platelet membrane: demonstration of selectivity in the incorporation of eicosapentaenoic acid into membrane phospholipid pools. Clin Sci (Lond) (1985) 0.87
Liver disease in pregnancy and fetal fatty acid oxidation defects. Mol Genet Metab (2000) 0.87
Auxin transport: providing a sense of direction during plant development. Biochem Soc Trans (2000) 0.87
A simple HPLC method for the determination of urate in serum and urine using 8-chlorotheophylline as internal standard. Med Lab Sci (1984) 0.87
Removal of intra-abdominal intrauterine contraceptive devices. Br J Obstet Gynaecol (1978) 0.87
Regulation of biologically active dimeric inhibin A and B from infancy to adulthood in the male. J Clin Endocrinol Metab (1998) 0.87
Tissue expression and subcellular localization of CLN3, the Batten disease protein. Mol Genet Metab (1999) 0.86
Glutaric aciduria type 1: biochemical investigations and postmortem findings. Eur J Pediatr (1986) 0.86
Newborn acoustic reflexes to noise and pure-tone signals. J Speech Hear Res (1982) 0.86
Sudden cardiac arrest during percutaneous ultrasonic nephrostolithotomy. Anesthesiology (1984) 0.86
The counterion influence on cationic lipid-mediated transfection of plasmid DNA. Biochim Biophys Acta (1996) 0.85