نتایج جستجو برای: methylene tetrahydrofolate dehydrogenase mthfd1

تعداد نتایج: 88908  

Journal: :Molecular genetics and metabolism 2000
M A Medina M I Amores-Sánchez

Homocysteine is a sulfur-containing, nonproteinogenic amino acid biosynthesized from methionine which has a key place in common between the folate cycle and the activated methyl cycle. Homocysteine export into the extracellular medium reflects an imbalance between homocysteine production and metabolism (1). Hyperhomocysteinemia has been associated with folate or cobalamine deficiencies, and als...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2012
Eric M Koehn Laura L Perissinotti Salah Moghram Arjun Prabhakar Scott A Lesley Irimpan I Mathews Amnon Kohen

The DNA nucleotide thymidylate is synthesized by the enzyme thymidylate synthase, which catalyzes the reductive methylation of deoxyuridylate using the cofactor methylene-tetrahydrofolate (CH(2)H(4)folate). Most organisms, including humans, rely on the thyA- or TYMS-encoded classic thymidylate synthase, whereas, certain microorganisms, including all Rickettsia and other pathogens, use an altern...

2018
Kana Asano Takeo Suzuki Ayaka Saito Fan-Yan Wei Yoshiho Ikeuchi Tomoyuki Numata Ryou Tanaka Yoshihisa Yamane Takeshi Yamamoto Takanobu Goto Yoshihito Kishita Kei Murayama Akira Ohtake Yasushi Okazaki Kazuhito Tomizawa Yuriko Sakaguchi Tsutomu Suzuki

Modified uridine containing taurine, 5-taurinomethyluridine (τm5U), is found at the anticodon first position of mitochondrial (mt-)transfer RNAs (tRNAs). Previously, we reported that τm5U is absent in mt-tRNAs with pathogenic mutations associated with mitochondrial diseases. However, biogenesis and physiological role of τm5U remained elusive. Here, we elucidated τm5U biogenesis by confirming th...

Journal: :Clinical and Developmental Immunology 2006
Alice D. Chang Raffi Tachdjian Kerry Gallagher Deborah K. McCurdy Charles Lassman E. Richard Stiehm Ora Yadin

We studied a 14 year-old boy with partial DiGeorge syndrome (DGS), status post complete repair of Tetralogy of Fallot, who developed antiphospholipid syndrome (APS) and type III mixed cryoglobulinemia. He presented with recurrent fever and dyspnea upon exertion secondary to right pulmonary embolus on chest computed tomography (CT). Coagulation studies revealed homozygous methylene tetrahydrofol...

Journal: :Clinical science 2002
Joey M Kaye Kim G Stanton Vincent J McCann Samuel D Vasikaran Valerie Burke Roger R Taylor Frank M van Bockxmeer

In the present study, the determinants of fasting plasma homocysteine in diabetic subjects were examined; whether plasma homocysteine and vascular disease are related and the influence of the C677T polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene on serum and erythrocyte folate, plasma homocysteine and vascular disease. Diabetic clinic subjects (Type I, n=354; Type II, n=392...

Journal: :Molecular Vision 2008
Bao Jian Fan Teresa Chen Cynthia Grosskreutz Louis Pasquale Douglas Rhee Elizabeth DelBono Jonathan L. Haines Janey L. Wiggs

PURPOSE To evaluate genes involved in homocysteine metabolism as secondary risk factors for pseudoexfoliation syndrome (PXFS) and the associated glaucoma (PXFG). METHODS One hundred eighty-six unrelated patients with PXFS, including 140 patients with PXFG and 127 unrelated control subjects were recruited from the Massachusetts Eye and Ear Infirmary. All the patients and controls were Caucasia...

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