P. A. Wood

发表

Deficiency in short-chain fatty acid β-oxidation affects theta oscillations during sleep

E. Neidhart, M. Tafti, P. Franken, 2003, Nature Genetics.

P. A. Wood, 1994 .

Differential induction of genes in liver and brown adipose tissue regulated by peroxisome proliferator-activated receptor-alpha during fasting and cold exposure in acyl-CoA dehydrogenase-deficient mice.

P. A. Wood, E. Goetzman, L. Tian, 2005, Molecular genetics and metabolism.

A Rostrocaudal Muscular Dystrophy Caused by a Defect in Choline Kinase Beta, the First Enzyme in Phosphatidylcholine Biosynthesis*

W. Frankel, D. Vance, P. A. Wood, 2006, Journal of Biological Chemistry.

Evaluation of liver fatty acid oxidation in the leptin-deficient obese mouse.

B. Gower, P. A. Wood, T. Nagy, 2002, Molecular genetics and metabolism.

Homozygous carnitine palmitoyltransferase 1a (liver isoform) deficiency is lethal in the mouse.

P. A. Wood, T. Schoeb, C. Hoppel, 2005, Molecular genetics and metabolism.

Carnitine Palmitoyltransferase-1b Deficiency Aggravates Pressure Overload–Induced Cardiac Hypertrophy Caused by Lipotoxicity

P. A. Wood, Teayoun Kim, J. Prasain, 2012, Circulation.

Carnitine Palmitoyltransferase-1 b ( CPT 1 b ) Deficiency Aggravates Pressure-Overload-Induced Cardiac Hypertrophy due to Lipotoxicity

P. A. Wood, Teayoun Kim, J. Prasain, 2012 .

Mouse Models for Disorders of Mitochondrial Fatty Acid β-Oxidation

P. A. Wood, A. M. Schuier, 2002 .

Long-term effects of high-fat or high-carbohydrate diets on glucose tolerance in mice with heterozygous carnitine palmitoyltransferase-1a deficiency

B. Gower, P. A. Wood, T. Schoeb, 2011, Nutrition & Diabetes.

Chromosomal locations of the mouse fatty acid oxidation genes Cpt1a, Cpt1b, Cpt2, Acadvl, and metabolically related Crat gene

P. A. Wood, K. Johnson, K. B. Cox, 1998, Mammalian Genome.

Transgenic expression of n‐3 fatty acid desaturase (fat‐1) in C57/BL6 mice: Effects on glucose homeostasis and body weight

P. A. Wood, S. Ji, R. Hardy, 2009, Journal of cellular biochemistry.

Lipoprotein Secretion and Triglyceride Stores in the Heart*

J. Björkegren, S. Young, P. A. Wood, 2001, The Journal of Biological Chemistry.

Elevation rate of glycosylated hemoglobins in dogs after induction of experimental diabetes mellitus.

P. A. Wood, J. Smith, 1982, Metabolism: clinical and experimental.

Mouse models for disorders of mitochondrial fatty acid beta-oxidation.

P. A. Wood, A. Schuler, 2002, ILAR journal.

Characterization of carnitine and fatty acid metabolism in the long-chain acyl-CoA dehydrogenase-deficient mouse.

R. Wanders, P. A. Wood, F. Vaz, 2005, The Biochemical journal.

Mitochondrial fatty acid oxidation disorders: pathophysiological studies in mouse models

P. A. Wood, U. Spiekerkoetter, 2010, Journal of Inherited Metabolic Disease.

Cardiac Hypertrophy in Mice with Long-Chain Acyl-CoA Dehydrogenase (LCAD) or Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency

P. A. Wood, S. Barnes, L. Tian, 2009, Laboratory Investigation.

Dietary phytoestrogens increase metabolic resistance (cold tolerance) in long-chain acyl-CoA dehydrogenase-deficient mice.

B. Gower, P. A. Wood, S. Barnes, 2004, The Journal of nutrition.

Carnitine Palmitoyltransferase 1b Deficiency Protects Mice from Diet-Induced Insulin Resistance

P. A. Wood, T. Nagy, M. Young, 2014, Journal of diabetes & metabolism.

Studies of arginine metabolism and salt sensitivity in the Dahl/Rapp rat models of hypertension.

P. A. Wood, P. Sanders, D. A. Hamm, 1998, Molecular genetics and metabolism.

Fluorescence Polarization Analysis, Lipid Composition, and Na+, K+‐ATPase Kinetics of Synaptosomal Membranes in Feline GM1 and GM2 Gangliosidosis

H. J. Baker, P. A. Wood, M. McBride, 1985, Journal of neurochemistry.

Connecting the dots: obesity, fatty acids and cancer

P. A. Wood, 2009, Laboratory Investigation.

Expression of human argininosuccinate synthetase after retroviral-mediated gene transfer

A. Beaudet, W. O'Brien, P. A. Wood, 1986, Somatic cell and molecular genetics.

Phenotype assessment: are you missing something?

P. A. Wood, 2000, Comparative medicine.

A Thyroid Hormone Response Unit Formed between the Promoter and First Intron of the Carnitine Palmitoyltransferase-Iα Gene Mediates the Liver-specific Induction by Thyroid Hormone*

P. A. Wood, E. Park, L. Jackson‐Hayes, 2003, The Journal of Biological Chemistry.

Functional correction of short-chain acyl-CoA dehydrogenase deficiency in transgenic mice: implications for gene therapy of human mitochondrial enzyme deficiencies.

P. A. Wood, C. Pinkert, A. Brix, 1997, Human molecular genetics.

Influence of dietary fatty acid chain-length on metabolic tolerance in mouse models of inherited defects in mitochondrial fatty acid beta-oxidation.

B. Gower, P. A. Wood, P. Rinaldo, 2004, Molecular genetics and metabolism.

Biochemical Basis of Type AB GM2 Gangliosidosis in a Japanese Spaniel

P. A. Wood, Yu-Teh Li, Y. Ishikawa, 1987, Journal of neurochemistry.

Cobalamin deficiency associated with methylmalonic acidemia in a cat.

R. T. Miller, P. A. Wood, F. Ledley, 1992, Journal of the American Veterinary Medical Association.

Disrupted blastocoele formation reveals a critical developmental role for long-chain acyl-CoA dehydrogenase.

P. A. Wood, Paul S Berger, Philip A Wood, 2004, Molecular Genetics and Metabolism.

Effects of short-chain acyl-CoA dehydrogenase deficiency on development expression of metabolic enzyme genes in the mouse.

P. A. Wood, M. Hinsdale, D. A. Hamm, 1996, Biochemical and molecular medicine.

Pathologic characterization of short‐chain acyl‐CoA dehydrogenase deficiency in BALB/cByJ mice

P. A. Wood, D. Armstrong, M. L. Masiowski, 1993, American journal of medical genetics.

Structural characterization of the mouse long-chain acyl-CoA dehydrogenase gene and 5′ regulatory region

D. Kurtz, P. A. Wood, R. Tolwani, 1998, Mammalian Genome.

Medium-Chain Acyl-CoA Dehydrogenase Deficiency in Gene-Targeted Mice

P. A. Wood, T. Schoeb, J. Vockley, 2005, PLoS genetics.

Targeted disruption of mouse long-chain acyl-CoA dehydrogenase gene reveals crucial roles for fatty acid oxidation.

D. Kurtz, W. O'Brien, P. A. Wood, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Mitochondrial dysfunction due to long-chain Acyl-CoA dehydrogenase deficiency causes hepatic steatosis and hepatic insulin resistance

G. Shulman, G. Cline, P. A. Wood, 2007, Proceedings of the National Academy of Sciences.

Genomic structure and genetic drift in C57BL/6 congenic metabolic mutant mice.

P. A. Wood, A. Almodovar, R. Luther, 2013, Molecular genetics and metabolism.

Potential of nutrigenetics in the treatment of metabolic disorders

P. A. Wood, 2008, Expert review of endocrinology & metabolism.

Abnormal nonshivering thermogenesis in mice with inherited defects of fatty acid oxidation.

D. Kurtz, P. A. Wood, K. Walsh, 1998, The Journal of clinical investigation.

Expression of human argininosuccinate synthetase in murine hematopoietic cells in vivo

A. Beaudet, W. O'Brien, P. A. Wood, 1989, Somatic Cell Genetics.

Homozygous carnitine palmitoyltransferase 1b (muscle isoform) deficiency is lethal in the mouse.

P. A. Wood, T. Schoeb, C. Hoppel, 2005, Molecular genetics and metabolism.

Structural and Functional Genomics of the CPT1B Gene for Muscle-type Carnitine Palmitoyltransferase I in Mammals*

P. Terpstra, P. A. Wood, N. Huijkman, 2002, The Journal of Biological Chemistry.

Retrovirus-mediated gene transfer of argininosuccinate synthetase into cultured rodent cells and human citrullinemic fibroblasts.

A. Beaudet, W. O'Brien, P. A. Wood, 1986, Cold Spring Harbor symposia on quantitative biology.

Carnitine Palmitoyltransferase 1b Deficient Mice Develop Severe Insulin Resistance After Prolonged High Fat Diet Feeding

P. A. Wood, Teayoun Kim, Qinglin Yang, 2014, Journal of diabetes & metabolism.

Structure and chromosomal location of the mouse medium-chain acyl-CoA dehydrogenase-encoding gene and its promoter.

D. Kurtz, P. A. Wood, M. Davisson, 1996, Gene.

Short-Chain Acyl-Coenzyme A Dehydrogenase Activity, Antigen, and Biosynthesis Are Absent in the BALB/cByJ Mouse

P. A. Wood, B. Amendt, W. Rhead, 1992, Pediatric Research.

Transgenic mouse with human mutant p53 expression in the prostate epithelium

P. A. Wood, I. Eltoum, C. Pinkert, 2004, The Prostate.

Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse.

D Matern, P A Wood, J R Lindsey, 2001, Human molecular genetics.

Resistance to high-fat diet-induced obesity and insulin resistance in mice with very long-chain acyl-CoA dehydrogenase deficiency.

G. Shulman, P. A. Wood, Dongyan Zhang, 2010, Cell metabolism.

Evaluation of a colorimetric method for canine glycosylated hemoglobin.

P. A. Wood, J. Smith, K. Moore, 1982, American journal of veterinary research.

Genetically modified mouse models for disorders of fatty acid metabolism: pursuing the nutrigenomics of insulin resistance and type 2 diabetes.

P. A. Wood, Philip A Wood, 2004, Nutrition.

Null allele at Bcd-1 locus in BALB/cByJ mice is due to a deletion in the short-chain acyl-CoA dehydrogenase gene and results in missplicing of mRNA.

P. A. Wood, M. Hinsdale, C. Kelly, 1993, Genomics.

Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency in Mice

P. A. Wood, B. Amendt, D. Millington, 1989, Pediatric Research.

Transgenic studies of fatty acid oxidation gene expression in nonobese diabetic mice.

B. Gower, D. Kurtz, P. A. Wood, 2000, Journal of lipid research.

Cloning and characterization of the mouse short-chain acyl-CoA dehydrogenase cDNA.

P. A. Wood, M. Hinsdale, C. Kelly, 1993, Genomics.

Cloning and characterization of the mouse short-chain acyl-CoA dehydrogenase gene

P. A. Wood, C. Kelly, 1996, Mammalian Genome.

Defects in mitochondrial beta-oxidation of fatty acids.

P. A. Wood, Philip A. Wood, 1999, Current opinion in lipidology.

Lessons learned from the mouse model of short-chain acyl-CoA dehydrogenase deficiency.

P. A. Wood, W. Rhead, M. Hinsdale, 1999, Advances in experimental medicine and biology.

HIV protease inhibitor ritonavir induces lipoatrophy in male mice.

B. Gower, M. Saag, P. A. Wood, 2003, AIDS research and human retroviruses.

Acadl-SNP based genotyping assay for long-chain acyl-CoA dehydrogenase deficient mice.

P. A. Wood, A. Almodovar, R. Luther, 2012, Molecular genetics and metabolism.

Glycosylated hemoglobin and canine diabetes mellitus.

P. A. Wood, J. Smith, 1980, Journal of the American Veterinary Medical Association.

RNA expression and chromosomal location of the mouse long-chain acyl-CoA dehydrogenase gene.

P. A. Wood, M. Davisson, K. Johnson, 1995, Genomics.

Molecular cloning and characterization of the mouse medium-chain acyl-CoA dehydrogenase cDNA.

P. A. Wood, R. Tolwani, S. Farmer, 1994, Genomics.

Molecular studies of mouse medium and long-chain acyl-CoA dehydrogenase genes for site-directed mutagenesis of embryonic stem cells.

P. A. Wood, J. Mountz, D. Kelly, 1992, Progress in clinical and biological research.

Synergistic heterozygosity in mice with inherited enzyme deficiencies of mitochondrial fatty acid beta-oxidation.

B. Gower, P. A. Wood, J. Vockley, 2005, Molecular genetics and metabolism.

Overview Phenotype Assessment: Are You Missing Something?

P. A. Wood, 2000 .

The clinical and pathologic heterogeneity of feline alpha-mannosidosis.

P. A. Wood, S. Walkley, J. Cummings, 1988, Journal of veterinary internal medicine.

GM1 Gangliosidosis in Portuguese Water Dogs: Pathologic and Biochemical Findings

P. A. Wood, L. Shell, R. Carithers, 1988, Veterinary pathology.

Mitochondrial 2,4-dienoyl-CoA Reductase Deficiency in Mice Results in Severe Hypoglycemia with Stress Intolerance and Unimpaired Ketogenesis

K. Autio, I. Miinalainen, P. A. Wood, 2009, PLoS genetics.

Transcriptional control of a nuclear gene encoding a mitochondrial fatty acid oxidation enzyme in transgenic mice: role for nuclear receptors in cardiac and brown adipose expression

P. A. Wood, Richard Vega, P. Wood, 1996, Molecular and cellular biology.