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homocysteine metabolic process
Known as:
Hcy metabolic process
, Hcy metabolism
, homocysteine metabolism
The chemical reactions and pathways involving homocysteine, the amino acid alpha-amino-gamma-mercaptobutanoic acid. Homocysteine is an important…
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National Institutes of Health
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Related topics
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2 relations
negative regulation of homocysteine metabolic process
regulation of homocysteine metabolic process
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2003
Highly Cited
2003
Homocysteine accumulates in supernatants of stimulated human peripheral blood mononuclear cells
K. Schroecksnadel
,
B. Frick
,
B. Wirleitner
,
H. Schennach
,
D. Fuchs
Clinical and Experimental Immunology
2003
Corpus ID: 39073410
Moderate hyperhomocysteinaemia is associated with atherosclerosis, thrombosis and also with stroke and dementia. Elevated…
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Highly Cited
2003
Highly Cited
2003
Candidate gene studies in focal dystonia
D. Sibbing
,
Friedrich Asmus
,
+8 authors
Oliver Bandmann
Neurology
2003
Corpus ID: 22632202
Background: Genetic susceptibility factors for focal idiopathic torsion dystonia (F-ITD) are not established. Mutations in the…
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Review
2003
Review
2003
Hyperhomocysteinemia and Immune Activation
K. Schroecksnadel
,
B. Frick
,
C. Winkler
,
F. Leblhuber
,
B. Wirleitner
,
D. Fuchs
Clinical Chemistry and Laboratory Medicine
2003
Corpus ID: 29188141
Abstract Hyperhomocysteinemia is an established risk factor for atherosclerosis, thrombosis and other vascular diseases…
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Highly Cited
2002
Highly Cited
2002
Progressive cerebral edema associated with high methionine levels and betaine therapy in a patient with cystathionine beta-synthase (CBS) deficiency.
R. Yaghmai
,
A. Kashani
,
+8 authors
N. Braverman
American journal of medical genetics
2002
Corpus ID: 1741035
Cystathionine beta-synthase (CBS) deficiency, the most common form of homocystinuria, is an autosomal recessive inborn error of…
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2002
2002
The effect of troglitazone on plasma homocysteine, hepatic and red blood cell S-adenosyl methionine, and S-adenosyl homocysteine and enzymes in homocysteine metabolism in Zucker rats.
V. Fonseca
,
M. Keebler
,
+4 authors
D. B. McNamara
Metabolism: Clinical and Experimental
2002
Corpus ID: 26280022
We studied the effect of troglitazone on the plasma concentrations of homocysteine (tHcy), the erythrocyte and hepatic…
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Highly Cited
2001
Highly Cited
2001
Genetic Defects as Important Factors for Moderate Hyperhomocysteinemia
J. Geisel
,
Ilona Zimbelmann
,
+4 authors
W. Herrmann
Clinical Chemistry and Laboratory Medicine
2001
Corpus ID: 19852651
Abstract The genes for the enzymes methylenetetrahydrofolate reductase (MTHFR), methionine synthase (MS), methionine synthase…
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Highly Cited
2001
Highly Cited
2001
Rapid Diagnosis of Methylmalonic and Propionic Aci- Demias: Quantitative Tandem Mass Spectrometric Anal- Ysis of Propionylcarnitine in Filter-paper Blood Speci- Mens Obtained from Newborns
D. Chace
,
J. DiPerna
,
Theodore A. Kalas
,
Ronald W. Johnson
,
E. Naylor
2001
Corpus ID: 2229508
homocysteine metabolism or whether increased tHcy may be attributable to impaired renal function or higher prevalence of other…
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2001
2001
Plasma total homocysteine concentration in nephrotic patients with idiopathic membranous nephropathy.
M. Árnadóttir
,
B. Hultberg
,
A. Berg
Nephrology, Dialysis and Transplantation
2001
Corpus ID: 43097191
BACKGROUND The atherothrombotic risk pattern of the nephrotic syndrome resembles that of hyperhomocysteinemia. However, the…
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2000
2000
Role of amniotic fluid homocysteine level and of fetal 5, 10-methylenetetrahydrafolate reductase genotype in the etiology of neural tube defects.
K. Wenstrom
,
G. Johanning
,
J. Owen
,
K. Johnston
,
Shannon Acton
,
T. Tamura
American journal of medical genetics
2000
Corpus ID: 12226534
A mutation in the gene 5,10-methylenetetrahydrofolate reductase (MTHFR), leading to altered homocysteine metabolism, has been…
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Highly Cited
1974
Highly Cited
1974
Mental retardation, megaloblastic anaemia, methylmalonic aciduria and abnormal homocysteine metabolism due to an error in vitamin B12 metabolism.
M. J. Dillon
,
J. M. England
,
+10 authors
I. Wise
Clinical science and molecular medicine
1974
Corpus ID: 38733057
SUMMARY 1. The case is described of a child with retarded physical and mental development, recurrent megaloblastic anaemia…
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