Search Results - "Snyder, Floyd F"
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Mutation in Folate Metabolism Causes Epigenetic Instability and Transgenerational Effects on Development
Published in Cell (26-09-2013)“…The importance of maternal folate consumption for normal development is well established, yet the molecular mechanism linking folate metabolism to development…”
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2
Carnitine Profile Changes in Pediatric Hematopoietic Stem Cell Transplant: New Role for Carnitine?
Published in Journal of pediatric hematology/oncology (01-07-2020)“…Carnitine is an essential cofactor for mitochondrial import and oxidation of fatty acids. High-dose chemotherapy and radiation, often required for…”
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3
Synthesis and activity of nucleoside-based antiprotozoan compounds
Published in Bioorganic & medicinal chemistry (01-04-2017)“…[Display omitted] Parasitic protozoa employ a salvage pathway to synthesize purines and generate essential active nucleotides, whereas mammals are capable of…”
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4
Novel nucleoside-based antimalarial compounds
Published in Bioorganic & medicinal chemistry letters (15-06-2016)“…P. falciparum IC50 as low as 110nM with cytotoxicity toward L6 rat myoblast cell line of 111μM and a selectivity index >1000. [Display omitted] The…”
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Identification of ABC transporters acting in vitamin B12 metabolism in Caenorhabditis elegans
Published in Molecular genetics and metabolism (01-12-2017)“…Vitamin B12 (cobalamin, Cbl) is a micronutrient essential to human health. Cbl is not utilized as is but must go through complex subcellular and metabolic…”
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Identification of ABC transporters acting in vitamin B 12 metabolism in Caenorhabditis elegans
Published in Molecular genetics and metabolism (01-12-2017)“…Vitamin B (cobalamin, Cbl) is a micronutrient essential to human health. Cbl is not utilized as is but must go through complex subcellular and metabolic…”
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7
Identification, Expression, and Characterization of Escherichia coli Guanine Deaminase
Published in Journal of Bacteriology (01-08-2000)“…Article Usage Stats Services JB Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley…”
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8
Neurodegeneration in D-bifunctional protein deficiency: diagnostic clues and natural history using serial magnetic resonance imaging
Published in Neuroradiology (01-12-2010)“…We report serial neurodegenerative changes on neuroimaging in a rare peroxisomal disease called D-bifunctional protein deficiency. The pattern of posterior to…”
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Point Mutations at the Purine Nucleoside Phosphorylase Locus Impair Thymocyte Differentiation in the Mouse
Published in Proceedings of the National Academy of Sciences - PNAS (18-03-1997)“…Three point mutations on the Npballele of the purine nucleoside phosphorylase locus in the mouse have been recovered by male germ cell mutagenesis. The mutants…”
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10
Application of Metabolomic Principles to Disorders of Nucleotide Metabolism Reveals New Metabolic Perturbations
Published in Nucleosides, nucleotides & nucleic acids (01-06-2008)“…A metabolomic analysis of plasma amino acids and acylcarnitines was applied to four disorders of nucleotide metabolism. Multivariate analysis gave score plots…”
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11
Vitamin B12 decreases, but does not normalize, homocysteine and methylmalonic acid in end-stage renal disease: A link with glycine metabolism and possible explanation of hyperhomocysteinemia in end-stage renal disease
Published in Metabolism, clinical and experimental (01-02-2003)“…The genetic and environmental factors influencing catabolism of homocysteine in end-stage renal disease (ESRD) patients remain poorly understood. This study…”
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12
Polyethylene glycol-conjugated adenosine phosphorylase: development of alternative enzyme therapy for adenosine deaminase deficiency
Published in Biochimica et biophysica acta (20-03-2003)“…Purine nucleoside phosphorylase had previously been engineered to accept 6-amino substituted purine nucleosides by two active site substitutions, Asn243Asp;…”
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Mitochondrial Function Dependent Proliferation Assay for the Diagnosis of Mitochondrial Disorders in Human Fibroblasts
Published in Nucleosides, nucleotides & nucleic acids (01-10-2004)“…A media has been developed which enables the assessment of mitochondrial function in fibroblasts by measuring proliferation as an end point…”
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14
cDNA sequence of five mouse guanine deaminase (Gda) alleles and mapping to mouse chromosome 19
Published in Genome (01-04-2002)“…Guanine deaminase catalyses the conversion of guanine to xanthine and ammonia, thereby irreversibly removing the guanine base from the pool of…”
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15
Cloning and Characterization of Human Guanine Deaminase
Published in The Journal of biological chemistry (01-03-1999)“…Mouse erythrocyte guanine deaminase has been purified to homogeneity. The native enzyme was dimeric, being comprised of two identical subunits of approximately…”
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Modelling of purine nucleoside metabolism during mouse embryonic development: relative routes of adenosine, deoxyadenosine, and deoxyguanosine metabolism
Published in Biochemistry and cell biology (01-01-1996)“…The individual activities for adenosine kinase, deoxyadenosine kinase, adenosine deaminase, deoxyguanosine kinase, and purine nucleoside phosphorylase were…”
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Effects of medium-chain triglyceride feeding on energy balance in adult humans
Published in Metabolism, clinical and experimental (01-09-1990)“…In recent years, the metabolism of triglycerides has attracted much attention. Oxidation of fatty acids is an essential energy supply, especially when glucose…”
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Assignment of a gene that determines erythrocytic guanosine-5'-triphosphate concentration (Gtpc) to mouse chromosome 9
Published in Genome (01-06-1994)“…Nine inbred mouse strains surveyed for erythrocytic guanosine-5'-triphosphate (GTP) concentration were found to segregate into two discrete groups. Strains…”
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T lymphocytes with a normal ADA gene accumulate after transplantation of transduced autologous umbilical cord blood CD34 + cells in ADA-deficient SCID neonates
Published in Nature medicine (01-07-1998)“…Adenosine deaminase-deficient severe combined immunodeficiency was the first disease investigated for gene therapy because of a postulated production or…”
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Genetic deficiency of purine nucleoside phosphorylase in the mouse. Characterization of partially and severely enzyme deficient mutants
Published in Genome (01-12-1989)“…Two independent mutations of purine nucleoside phosphorylase were identified in the first-generation progeny of male mice that had been treated with the…”
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