Results 61 to 70 of about 291,374 (170)
Inborn defects in vitamin B12 (cobalamin) metabolism including CblG pathology caused by mutations in the MTR gene encoding the methionine synthase (MS) enzyme are responsible for the development of persistent symptoms upon treatment, particularly neurological, neurocognitive, and ophthalmological symptoms.
openaire +2 more sources
Cobamide metabolism, regulation, and adaptation in Mycobacterium tuberculosis
Cobamides play a paradoxical but critical role in the biology of Mycobacterium tuberculosis (Mtb), the causative agent of tuberculosis. Although Mtb retains nearly all cobalamin (Cbl) biosynthetic genes and encodes multiple cobamide-requiring enzymes ...
Terry Kipkorir +4 more
doaj +1 more source
Background Classical homocystinuria is an autosomal recessive disorder caused by profound cystathionine β‐synthase deficiency. Its biochemical hallmarks are high concentrations of plasma homocyst(e)ine and methionine. Clinical manifestations include lens
John Allen +5 more
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Purification, characterisation and inhibition of methionine synthase from rat liver [PDF]
Cobalamin-dependent methionine synthase catalyses the transfer of a methyl group from methyltetrahydrofolate to homocysteine, generating tetrahydrofolate and methionine.
Ast, Tamara
core +1 more source
Soybean (Glycine max (L.) Merr.) is a major crop that provides plant-origin protein and oil for humans and livestock. Although the soybean vegetative tissues and seeds provide a major source of high-quality protein, they suffer from low concentration of ...
Yang YU +8 more
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Polymorphisms in genes MTHFR, MTR and MTRR are not risk factors for cleft lip/palate in South Brazil
Non-syndromic cleft lip and palate (CL/P) occurs due to interaction between genetic and environmental factors. Abnormalities in homocysteine metabolism may play a role in its etiology due to polymorphisms in genes involved in this pathway. Because of the
A.P.C. Brandalize +5 more
doaj
Systems genetics identifies methionine as a high risk factor for Alzheimer's disease
As a dietary strategy, methionine restriction has been reported to promote longevity and regulate metabolic disorders. However, the role and possible regulatory mechanisms underlying methionine in neurodegenerative diseases such as Alzheimer's disease ...
Congmin Wang +10 more
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INHIBITION OF FETAL METHIONINE SYNTHASE BY NITROUS OXIDE
The activity of the enzyme methionine synthase in fetal and maternal liver was investigated before and after exposure to nitrous oxide. Timed-pregnant rats on day 19 of gestation were exposed to either 10% or 50% nitrous oxide for various times up to 240 min.
J M, Baden, M, Serra, R I, Mazze
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Staple crops in human and livestock diets suffer from deficiencies in certain “essential” amino acids including methionine. With the goal of increasing methionine in rice seed, we generated a pair of “Push × Pull” double transgenic lines, each containing
Sarah J. Whitcomb +8 more
doaj +1 more source
CBS domains form energy-sensing modules whose binding of adenosine ligands is disrupted by disease mutations [PDF]
CBS domains are defined as sequence motifs that occur in several different proteins in all kingdoms of life. Although thought to be regulatory, their exact functions have been unknown.
John W. Scott +20 more
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