-
3
-
-
0036730624
-
Methods for measuring sulfur amino acid metabolism
-
Hoffer L.J. Methods for measuring sulfur amino acid metabolism. Curr Opin Clin Nutr Metab Care. 5:2002;511-517
-
(2002)
Curr Opin Clin Nutr Metab Care
, vol.5
, pp. 511-517
-
-
Hoffer, L.J.1
-
4
-
-
0000167774
-
Disorders of transsulfuration
-
C.R. Scriver, A. Beaudet, Sly W.S. et al. New York, NY: McGraw-Hill
-
Mudd S.H., Levy H.L., Kraus J.P. Disorders of transsulfuration. Scriver C.R., Beaudet A., Sly W.S.,, et al. The Metabolic and Molecular Bases of Inherited Disease. vol 8:2001;2007-2056 McGraw-Hill, New York, NY
-
(2001)
The Metabolic and Molecular Bases of Inherited Disease
, vol.8
, pp. 2007-2056
-
-
Mudd, S.H.1
Levy, H.L.2
Kraus, J.P.3
-
6
-
-
0033880861
-
Methionine transamination in patients with homocystinuria due to cystathionine beta-synthase deficiency
-
Tangerman A., Wilcken B., Levy H.L., et al. Methionine transamination in patients with homocystinuria due to cystathionine beta-synthase deficiency. Metabolism. 49:2000;1071-1077
-
(2000)
Metabolism
, vol.49
, pp. 1071-1077
-
-
Tangerman, A.1
Wilcken, B.2
Levy, H.L.3
-
7
-
-
0018934312
-
Labile methyl group balances in the human: The role of sarcosine
-
Mudd S.H., Ebert M.H., Scriver C.R. Labile methyl group balances in the human The role of sarcosine. Metabolism. 29:1980;707-720
-
(1980)
Metabolism
, vol.29
, pp. 707-720
-
-
Mudd, S.H.1
Ebert, M.H.2
Scriver, C.R.3
-
8
-
-
0026533906
-
The pathogenesis of homocysteinemia: Interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine
-
Selhub J., Miller J.W. The pathogenesis of homocysteinemia Interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine. Am J Clin Nutr. 55:1992;131-138
-
(1992)
Am J Clin Nutr
, vol.55
, pp. 131-138
-
-
Selhub, J.1
Miller, J.W.2
-
9
-
-
0032771346
-
Homocysteine metabolism
-
Selhub J. Homocysteine metabolism. Ann Rev Nutr. 19:1999;217-246
-
(1999)
Ann Rev Nutr
, vol.19
, pp. 217-246
-
-
Selhub, J.1
-
10
-
-
0023854335
-
Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency
-
Gahl W.A., Bernardini I., Finkelstein J.D., et al. Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency. J Clin Invest. 81:1988;390-397
-
(1988)
J Clin Invest
, vol.81
, pp. 390-397
-
-
Gahl, W.A.1
Bernardini, I.2
Finkelstein, J.D.3
-
11
-
-
0033818441
-
Pathways and regulation of homocysteine metabolism in mammals
-
Finkelstein J.D. Pathways and regulation of homocysteine metabolism in mammals. Semin Thromb Hemost. 26:2000;219-225
-
(2000)
Semin Thromb Hemost
, vol.26
, pp. 219-225
-
-
Finkelstein, J.D.1
-
12
-
-
0030046153
-
The importance of transmethylation reactions to methionine metabolism in sheep: Effects of supplementation with creatine and choline
-
Lobley G.E., Connell A., Revell D. The importance of transmethylation reactions to methionine metabolism in sheep effects of supplementation with creatine and choline. Br J Nutr. 75:1996;47-56
-
(1996)
Br J Nutr
, vol.75
, pp. 47-56
-
-
Lobley, G.E.1
Connell, A.2
Revell, D.3
-
13
-
-
0035195248
-
Methylation demand and homocysteine metabolism: Effects of dietary provision of creatine and guanidinoacetate
-
Stead L.M., Au K.P., Jacobs R.L., et al. Methylation demand and homocysteine metabolism Effects of dietary provision of creatine and guanidinoacetate. Am J Physiol. 281:2001;E1095-E1100
-
(2001)
Am J Physiol
, vol.281
-
-
Stead, L.M.1
Au, K.P.2
Jacobs, R.L.3
-
15
-
-
0036461162
-
Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolism
-
Luka Z., Cerone R., Phillips J.A., et al. Mutations in human glycine N-methyltransferase give insights into its role in methionine metabolism. Hum Genet. 110:2002;68-74
-
(2002)
Hum Genet
, vol.110
, pp. 68-74
-
-
Luka, Z.1
Cerone, R.2
Phillips, J.A.3
-
16
-
-
0034827802
-
Glycine N-methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia
-
Mudd S.H., Cerone R., Schiaffino M.C., et al. Glycine N-methyltransferase deficiency A novel inborn error causing persistent isolated hypermethioninaemia. J Inherit Metab Dis. 24:2001;448-464
-
(2001)
J Inherit Metab Dis
, vol.24
, pp. 448-464
-
-
Mudd, S.H.1
Cerone, R.2
Schiaffino, M.C.3
-
17
-
-
0942298956
-
Glycine N-methyltransferase deficiency: A new patient with a novel mutation
-
Augoustides-Savvopoulou P., Luka Z., Karyda S., et al. Glycine N-methyltransferase deficiency A new patient with a novel mutation. J Inherit Metab Dis. 26:2003;745-759
-
(2003)
J Inherit Metab Dis
, vol.26
, pp. 745-759
-
-
Augoustides-Savvopoulou, P.1
Luka, Z.2
Karyda, S.3
-
18
-
-
0037369901
-
Regulation of sulfur amino acid metabolism in men in response to changes in sulfur amino acid intakes
-
Di Buono M., Wykes L.J., Cole D.E., et al. Regulation of sulfur amino acid metabolism in men in response to changes in sulfur amino acid intakes. J Nutr. 133:2003;733-739
-
(2003)
J Nutr
, vol.133
, pp. 733-739
-
-
Di Buono, M.1
Wykes, L.J.2
Cole, D.E.3
-
20
-
-
0032825230
-
Homocysteine and methionine metabolism in ESRD: A stable isotope study
-
van Guldener C., Kulik W., Berger R., et al. Homocysteine and methionine metabolism in ESRD A stable isotope study. Kidney Int. 56:1999;1064-1071
-
(1999)
Kidney Int
, vol.56
, pp. 1064-1071
-
-
Van Guldener, C.1
Kulik, W.2
Berger, R.3
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