Search Results - "Gulati, Sumedha"

Defects in Auxiliary Redox Proteins Lead to Functional Methionine Synthase Deficiency by Gulati, Sumedha, Chen, Zhiqiang, Brody, Lawrence C., Rosenblatt, David S., Banerjee, Ruma

“…Methionine synthase catalyzes a methyl transfer reaction from methyltetrahydrofolate to homocysteine to form methionine and tetrahydrofolate and is dependent…”
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Disruption of a Regulatory System Involving Cobalamin Distribution and Function in a Methionine-dependent Human Glioma Cell Line by Fiskerstrand, Torunn, Riedel, Bettina, Ueland, Per M., Seetharam, Bellur, Pezacka, Ewa H., Gulati, Sumedha, Bose, Santanu, Banerjee, Ruma, Berge, Rolf K., Refsum, Helga

“…Cobalamin metabolism and function were investigated at the levels from transcobalamin II (TCII) receptor to the cobalamin-dependent enzymes, methionine…”
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Transforming growth factor-β activation of phosphatidylinositol 3-kinase is independent of Smad2 and Smad3 and regulates fibroblast responses via p21-activated kinase-2 by WILKES, Mark C, MITCHELL, Hugh, PENHEITER, Sumedha Gulati, DORE, Jules J, SUZUKI, Kaori, EDENS, Maryanne, SHARMA, Deepak K, PAGANO, Richard E, LEOF, Edward B

“…Transforming growth factor-beta (TGF-beta) stimulates cellular proliferation and transformation to a myofibroblast phenotype in vivo and in a subset of…”
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Posttranscriptional Regulation of Mammalian Methionine Synthase by B12 by Gulati, Sumedha, Brody, Lawrence C., Banerjee, Ruma

“…Methionine synthase is one of two key enzymes involved in the removal of the metabolite, homocysteine. Elevated homocysteine levels constitute a risk factor…”
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Transforming Growth Factor-{szligbeta} Activation of Phosphatidylinositol 3-Kinase Is Independent of Smad2 and Smad3 and Regulates Fibroblast Responses via p21-Activated Kinase-2 by Wilkes, Mark C, Mitchell, Hugh, Penheiter, Sumedha Gulati, Dore, Jules J, Suzuki, Kaori, Edens, Maryanne, Sharma, Deepak K, Pagano, Richard E, Leof, Edward B

“…Transforming growth factor-{szligbeta} (TGF-{szligbeta}) stimulates cellular proliferation and transformation to a myofibroblast phenotype in vivo and in a…”
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Defects in Human Methionine Synthase in cblG Patients by Gulati, Sumedha, Baker, Priscilla, Li, Yunan N., Fowler, Brian, Kruger, Warren, Brody, Lawrence C., Banerjee, Ruma

“…Inborn errors resulting in isolated functional methionine synthase deficiency fall into two complementation groups, cblG and cblE. Using biochemical approaches…”
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Purification and kinetic mechanism of a mammalian methionine synthase from pig liver by Chen, Z, Crippen, K, Gulati, S, Banerjee, R

“…Porcine hepatic methionine synthase has been purified to near homogeneity. The enzyme is isolated in two forms which were purified approximately 9,000- and…”
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Methionine synthase from pig liver by Banerjee, R, Chen, Z, Gulati, S

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Cloning, Mapping and RNA Analysis of the Human Methionine Synthase Gene by Li, Yunan N., Gulati, Sumedha, Baker, Priscilla J., Brody, Lawrence C., Banerjee, Ruma, Kruger, Warren D.

“…Elevated levels of plasma homocysteine is a risk factor in both birth defects and vascular disease. Methionine synthase (MS) is a cobalamin dependent enzyme…”
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Biochemical and genetic characterization of mammalian methionine synthase by Gulati, Sumedha

“…Mammalian methionine synthase (5-methyl-homocysteine methyltransferase; EC 2.1.1.13) is a cobalamin dependent enzyme that catalyzes the transfer of a methyl…”
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