Search Results - "O'Leary, V B"
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Innocuous full-length botulinum neurotoxin targets and promotes the expression of lentiviral vectors in central and autonomic neurons
Published in Gene therapy (01-07-2011)“…Fragments of botulinum neurotoxin (BoNT) have been explored as potential targeting moieties and carriers of biomolecules into neurons, although with lower…”
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2
A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects: Report of the Birth Defects Research Group
Published in American journal of human genetics (01-11-2002)“…Women who take folic acid periconceptionally reduce their risk of having a child with a neural tube defect (NTD) by >50%. A variant form of…”
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3
Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association
Published in Molecular genetics and metabolism (01-07-2005)“…Methionine synthase reductase (MTRR) regenerates methylated cobalamin levels from the oxidised cob(II)alamin form and in so doing plays a crucial role in…”
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4
Exercise-induced reversal of insulin resistance in obese elderly is associated with reduced visceral fat
Published in Journal of applied physiology (1985) (01-05-2006)“…1 Schwartz Center for Metabolism and Nutrition, and Departments of 2 Medicine, 3 Physiology, 4 Nutrition, and 5 Reproductive Biology, Case Western Reserve…”
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5
Analysis of the human folate receptor β gene for an association with neural tube defects
Published in Molecular genetics and metabolism (01-06-2003)“…The folate receptor β (FRβ) gene encodes a receptor that binds and transports 5-methyltetrahydrofolate. FRβ polymorphisms may potentially alter folate delivery…”
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6
Reduced folate carrier polymorphisms and neural tube defect risk
Published in Molecular genetics and metabolism (01-04-2006)“…The reduced folate carrier ( RFCI) is essential for folate transport into cells. Low folate is an important cause of neural tube defects (NTDs), and a…”
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7
MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae
Published in American journal of medical genetics. Part A (01-02-2005)“…This study examined the relationship between folate/homocysteine‐related genetic polymorphisms: MTHFD1 1958G → A (R653Q), MTHFR 677C → T (A222V), MTHFR 1298A →…”
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8
Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population
Published in Birth defects research. A Clinical and molecular teratology (01-04-2005)“…BACKGROUND Decreased maternal folate levels are associated with having a child with a neural tube defect (NTD), and periconceptual folic acid supplementation…”
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9
Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects
Published in Journal of human genetics (01-04-2003)“…The thermolabile variant (677TT) of methylenetetrahydrofolate reductase (MTHFR) is a known risk factor for neural tube defects (NTDs). The relationship between…”
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10
Screening for new MTHFR polymorphisms and NTD risk
Published in American journal of medical genetics. Part A (01-10-2005)“…The enzyme, 5,10‐methylenetetrahydrofolate reductase (MTHFR) plays a key role in cellular folate metabolism. The A222V (677C‐>T) polymorphism is a confirmed…”
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Alleviation of Trigeminal Nociception Using p75 Neurotrophin Receptor Targeted Lentiviral Interference Therapy
Published in Neurotherapeutics (01-04-2018)“…Acute and chronic trigeminal (TG) neuropathies are the cause of considerable distress, with limited treatments available at present. Nociceptive neurons…”
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12
Polymorphisms within the vitamin B 12 dependent methylmalonyl-coA mutase are not risk factors for neural tube defects
Published in Molecular genetics and metabolism (01-12-2003)“…Methionine synthase and methylmalonyl-CoA mutase (mutase) are the only two known vitamin B 12 (B 12) dependent enzymes in humans. A lower level of B 12 has…”
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13
MTRR and MTHFR polymorphism: Link to Down syndrome?
Published in American journal of medical genetics (15-01-2002)“…Polymorphisms in genes encoding the folate metabolizing enzymes methylenetetrahydrofolate reductase (MTHFR C677T) and methionine synthase reductase (MTRR A66G)…”
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