Published in J Clin Endocrinol Metab on September 01, 2000
Association of genetic polymorphism of PPARγ-2, ACE, MTHFR, FABP-2 and FTO genes in risk prediction of type 2 diabetes mellitus. J Biomed Sci (2013) 0.92
Enterocyte fatty acid-binding proteins (FABPs): different functions of liver and intestinal FABPs in the intestine. Prostaglandins Leukot Essent Fatty Acids (2014) 0.91
Functional polymorphisms to modulate luminal lipid exposure and risk of colorectal cancer. Cancer Epidemiol (2010) 0.86
Variation in the FABP2 promoter alters transcriptional activity and is associated with body composition and plasma lipid levels. Hum Genet (2003) 0.83
Polymorphism of FABP2 and PPARG2 genes in risk prediction of cataract among North Indian population. Meta Gene (2014) 0.76
APOE and FABP2 Polymorphisms and History of Myocardial Infarction, Stroke, Diabetes, and Gallbladder Disease. Cholesterol (2011) 0.75
Polymorphism of the FABP2 gene: a population frequency analysis and an association study with cardiovascular risk markers in Argentina. BMC Med Genet (2007) 0.75
Prospective study of coronary heart disease incidence in relation to fasting total homocysteine, related genetic polymorphisms, and B vitamins: the Atherosclerosis Risk in Communities (ARIC) study. Circulation (1998) 2.88
Cystathionine beta-synthase mutations in homocystinuria. Hum Mutat (1999) 1.96
ABO blood group, other risk factors and incidence of venous thromboembolism: the Longitudinal Investigation of Thromboembolism Etiology (LITE). J Thromb Haemost (2007) 1.59
Long-term outcome of Hurler syndrome following bone marrow transplantation. Am J Med Genet (1993) 1.38
In vivo chloroquine-induced inhibition of insulin degradation in a diabetic patient with severe insulin resistance. Diabetes (1984) 1.30
Isozymes of rabbit phosphofructokinase. Electrophoretic and immunochemical studies. J Biol Chem (1973) 1.20
Treatment of late infantile metachromatic leukodystrophy by bone marrow transplantation. N Engl J Med (1990) 1.19
A prospective study of coronary heart disease and the hemochromatosis gene (HFE) C282Y mutation: the Atherosclerosis Risk in Communities (ARIC) study. Atherosclerosis (2001) 1.15
Functional modeling of vitamin responsiveness in yeast: a common pyridoxine-responsive cystathionine beta-synthase mutation in homocystinuria. Hum Mol Genet (1997) 1.13
Six new mutations in the ornithine transcarbamylase gene detected by single-strand conformational polymorphism. Pediatr Res (1992) 1.12
Relationship of the human cumulus-free oocyte maturational profile with in vitro outcome parameters after intracytoplasmic sperm injection. J Assist Reprod Genet (1999) 1.02
Ethnicity, plasma phospholipid fatty acid composition and inflammatory/endothelial activation biomarkers in the Multi-Ethnic Study of Atherosclerosis (MESA). Eur J Clin Nutr (2012) 1.02
Rabbit brain phosphofructokinase. Comparison of regulatory properties with those of other phosphofructokinase isozymes. J Biol Chem (1974) 1.01
Delayed pulmonary phosphatidylglycerol synthesis and reversal by prenatal dexamethasone in fetal rats of streptozotocin-diabetic mothers. Exp Lung Res (1983) 0.98
Studies of phenylketonurics with dermatitis. J Am Acad Dermatol (1981) 0.96
Short-term and long-term variability of plasma homocysteine measurement. Clin Chem (1997) 0.96
Distribution of phosphofructokinase isozymes in rabbit, mouse, guinea pig and rat. Comp Biochem Physiol B (1975) 0.93
Phosphatidylglycerol in 261 samples of amniotic fluid from normal and diabetic pregnancies, as measured by one-dimensional thin-layer chromatography. Clin Chem (1979) 0.92
Detection of azoospermic factor genes in Chinese men with azoospermia or severe oligozoospermia. J Assist Reprod Genet (1999) 0.91
Influence of 699C-->T and 1080C-->T polymorphisms of the cystathionine beta-synthase gene on plasma homocysteine levels. Clin Genet (2000) 0.91
Screening urine of 3-week-old newborns: transient methylmalonic and hydroxyphenyllactic aciduria. Biochem Med Metab Biol (1992) 0.90
Aspartyl residue 10 is essential for ATPase activity of rat hsc70. J Biol Chem (1993) 0.90
Relation between plasma homocysteine concentration, the 844ins68 variant of the cystathionine beta-synthase gene, and pyridoxal-5'-phosphate concentration. Mol Genet Metab (1999) 0.90
Perilipin polymorphism interacts with saturated fat and carbohydrates to modulate insulin resistance. Nutr Metab Cardiovasc Dis (2010) 0.89
Factor VII coagulant activity, factor VII -670A/C and -402G/A polymorphisms, and risk of venous thromboembolism. J Thromb Haemost (2007) 0.88
Relation of C-reactive protein and other cardiovascular risk factors to penile vascular disease in men with erectile dysfunction. Int J Impot Res (2003) 0.88
Effect of retinoic acid on implantation and post-implantation development of mouse embryos in vitro. Hum Reprod (2001) 0.88
Prospective study of the A455V polymorphism in the thrombomodulin gene, plasma thrombomodulin, and incidence of venous thromboembolism: the LITE Study. J Thromb Haemost (2003) 0.88
Clinical implications of intracytoplasmic sperm injection using cryopreserved testicular spermatozoa from men with azoospermia. J Reprod Med (2000) 0.87
The shift of an increase in phosphofructokinase activity from protein synthesis-dependent to -independent mode during concanavalin A induced lymphocyte proliferation. Biochem Biophys Res Commun (1980) 0.85
Relation between the insertion/deletion polymorphism of the angiotensin I converting enzyme gene and restenosis after coronary stenting. J Cardiovasc Risk (2000) 0.85
Preliminary evidence of genetic determinants of adiponectin response to fenofibrate in the Genetics of Lipid Lowering Drugs and Diet Network. Nutr Metab Cardiovasc Dis (2012) 0.85
Effects of fluvastatin (XU 62-320), an HMG-CoA reductase inhibitor, on the distribution and composition of low density lipoprotein subspecies in humans. Atherosclerosis (1991) 0.84
Improved thin-layer chromatography of disaturated phosphatidylcholine in amniotic fluid. Clin Chem (1981) 0.84
Determination of the efficiency of controlled ovarian hyperstimulation in the gonadotropin-releasing hormone agonist-suppression cycle using the initial follicle count during gonadotropin stimulation. J Assist Reprod Genet (2001) 0.84
Obesity modifies the association between plasma phospholipid polyunsaturated fatty acids and markers of inflammation: the Multi-Ethnic Study of Atherosclerosis. Int J Obes (Lond) (2011) 0.84
Simple and rapid method for extraction of DNA from fresh and cryopreserved clotted human blood. Clin Chem (1996) 0.84
Approaches to study interactions between kinesin motors and membranes. Methods Mol Biol (2001) 0.83
Carbamyl phosphate synthetase and ornithine transcarbamylase activities in enzyme-deficient human liver measured by radiochromatography and correlated with outcome. Pediatr Res (1989) 0.83
Variable number tandem repeat in exon/intron border of the cystathionine beta-synthase gene: a single nucleotide substitution in the second repeat prevents multiple alternate splicing. Am J Med Genet (2000) 0.83
NK cell imaging by in vitro and in vivo labelling approaches. Q J Nucl Med Mol Imaging (2014) 0.83
A common mutation in the methylenetetrahydrofolate reductase gene (C677T) increases the risk for deep-vein thrombosis in patients with mutant factor V (factor V:Q506). Arterioscler Thromb Vasc Biol (1997) 0.83
Functional size of photosynthetic electron transport chain determined by radiation inactivation. Plant Physiol (1987) 0.83
Identification and characterization of androgen receptor associated coregulators in prostate cancer cells. J Biol Regul Homeost Agents (2001) 0.83
Deletion polymorphism at the angiotensin-converting enzyme gene in Turkish patients with coronary artery disease. Scand J Clin Lab Invest (1998) 0.83
Functional and molecular imaging: applications for diagnosis and staging of localised prostate cancer. Clin Oncol (R Coll Radiol) (2013) 0.82
Cloning and nucleotide sequencing of the second internal transcribed spacer of ribosomal DNA for three species of Eimeria from chickens in Taiwan. Vet J (2005) 0.82
Endothelial nitric oxide gene polymorphism (Glu298Asp) is not associated with coronary artery disease in Turkish population. Thromb Haemost (2002) 0.82
Absence of mutations in the regulatory domain of the gap junction protein connexin 43 in patients with visceroatrial heterotaxy. Heart (1997) 0.82
ADAM17_i33708A>G polymorphism interacts with dietary n-6 polyunsaturated fatty acids to modulate obesity risk in the Genetics of Lipid Lowering Drugs and Diet Network study. Nutr Metab Cardiovasc Dis (2009) 0.81
Phenylketonuric patients decades after diet. J Inherit Metab Dis (1995) 0.81
Amino acid abnormalities in infants with extrahepatic biliary atresia and cirrhosis. J Pediatr Gastroenterol Nutr (1988) 0.81
Orthodontic correction of a mandibular first molar deeply impacted by an odontoma: a case report. Quintessence Int (1997) 0.81
Effect of hypothermic pulmonary artery flushing on capillary filtration coefficient. Transplantation (2000) 0.80
Hybridization of rabbit muscle and liver phosphofructokinases. Arch Biochem Biophys (1972) 0.80
Changes in composition and distribution of LDL subspecies in hypertriglyceridemic and hypercholesterolemic patients during gemfibrozil therapy. Atherosclerosis (1994) 0.80
Comparison of enzymatic activity with evidence of engraftment in patients with inborn errors of metabolism receiving allogeneic marrow transplantation. Birth Defects Orig Artic Ser (1986) 0.80
Clinical manifestations of mannosidosis--a longitudinal study. Am J Med (1976) 0.80
Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction. Clin Cardiol (2001) 0.80
Optimization of intrabone delivery of hematopoietic progenitor cells in a swine model using cell radiolabeling with [89]zirconium. Am J Transplant (2015) 0.80
Effects of induction anesthetic agents on outcome of assisted reproductive technology: a comparison of propofol and thiopental sodium. Chang Gung Med J (2000) 0.80
Tensile bond strength of reused orthodontic metal brackets. Zhonghua Ya Yi Xue Hui Za Zhi (1991) 0.80
Tyrosinase inhibition due to interaction of homocyst(e)ine with copper: the mechanism for reversible hypopigmentation in homocystinuria due to cystathionine beta-synthase deficiency. Am J Hum Genet (1995) 0.80
Lipoprotein receptor-related protein 1 variants and dietary fatty acids: meta-analysis of European origin and African American studies. Int J Obes (Lond) (2013) 0.79
Semen studies on phenylketonurics. Biochem Med (1981) 0.79
Fetal rat lung phosphatidylcholine synthesis in diabetic and normal pregnancies: a comparison of prenatal dexamethasone treatments. Biochim Biophys Acta (1981) 0.79
The effect of a novel intergenic polymorphism (rs11774572) on HDL-cholesterol concentrations depends on TaqIB polymorphism in the cholesterol ester transfer protein gene. Nutr Metab Cardiovasc Dis (2009) 0.79
Psychiatric diagnosis and behavioral characteristics of phenylketonuric children. J Nerv Ment Dis (1986) 0.78
Single-strand conformational polymorphisms (SSCP): studies of the genetic polymorphisms of exon 4 of apolipoprotein C III. Clin Biochem (1995) 0.78
Free amino acid analysis of untimed and 24-h urine samples compared. Clin Chem (1980) 0.78
Screening for urinary oligosaccharides and simple sugars by thin-layer chromatography. Med Lab Sci (1979) 0.78
Comparable clinical outcomes of tubal embryo transfer for oligoastheno-teratozoospermia treated with intracytoplasmic sperm injection and for female infertility treated with in vitro fertilization. Chang Gung Med J (2000) 0.78
Intensive pulmonary care after liver surgery: a retrospective survey from a single center. Transplant Proc (2013) 0.78
Identification of human DNA sequences complementary to chromosomal RNA with an improved RNA/DNA gradient hybridization technique. Biochim Biophys Acta (1977) 0.77
Assay of disaturated phosphatidylcholine in amniotic fluid as a test of fetal lung maturity: experience with 2000 analyses. Clin Chem (1987) 0.77
Timed intercourse after intrauterine insemination for treatment of infertility. Eur J Obstet Gynecol Reprod Biol (1998) 0.77
Disturbance of pulmonary prostaglandin metabolism in fetuses of alloxan-diabetic rabbits. Biochim Biophys Acta (1982) 0.77
Screening for gene deletions and known mutations in 13 patients with ornithine transcarbamylase deficiency. Biochem Med Metab Biol (1992) 0.77
Deletion polymorphism of the angiotensin I converting enzyme gene is a potent risk factor for coronary artery ectasia. Heart (2003) 0.77
Nonadditive interactions in protein folding: the zipper model of cytochrome C. J Biol Phys (2008) 0.77
Characterization of mutations in the cystathionine beta-synthase gene in Irish patients with homocystinuria. Mol Genet Metab (1998) 0.76
Trichothiodystrophy and associated anomalies: a variant of SIBIDS or new symptom complex? Pediatr Dermatol (1993) 0.76
Relationship between morphologic malocclusion and temporomandibular disorders in orthodontic patients prior to treatment. Funct Orthod (1998) 0.76
Carotid intima-media thickness and ACE-gene polymorphism in hemodialysis patients. J Nephrol (1999) 0.76
The effect of prenatal dexamethasone on fetal rat lung prostaglandin synthesis. Prostaglandins Leukot Med (1983) 0.76
A kinetic model for phosphofructokinase based on the paradoxical action of effectors. Biochem Biophys Res Commun (1976) 0.76
Identification of chicken liver glucose transporter. Arch Biochem Biophys (1994) 0.76
3-Hydroxy-3-methylglutaryl-CoA lyase deficiency as detected by radiochemical assay in cell extracts by thin-layer chromatography, and identification of three new cases. Clin Chem (1990) 0.75
Two different timings of intrauterine insemination for non-male infertility. J Assist Reprod Genet (2000) 0.75
Mapping of polysomal messenger RNA and heterogeneous nuclear RNA to the lightly staining G-bands of human chromosomes. Cytogenet Cell Genet (1978) 0.75
Laboratory assessment of mild hyperhomocysteinemia as an independent risk factor for occlusive vascular diseases. Clin Chem (1996) 0.75
Amiodarone phenocopy of Fabry's keratopathy. JAMA (1983) 0.75
Amniotic fluid phosphatidylglycerol in diabetic and control pregnant patients at different gestational lengths. Am J Obstet Gynecol (1984) 0.75
Absorbance of amniotic fluid at 650 nm as a fetal lung maturity test: a comparison with the lecithin/sphingomyelin ratio and tests for disaturated phosphatidylcholine and phosphatidylglycerol. Am J Obstet Gynecol (1983) 0.75
Reduced plasma haptoglobin and urinary taurine in familial seizures identified through the multisib strategy. Am J Med Genet (1986) 0.75
The prevalence of TMD in orthodontic patients prior to treatment at NCKUH in southern Taiwan. National Cheng Kung University Hospital. Funct Orthod (1998) 0.75