Citations to this article

Transport and metabolism of sarcosine in hypersarcosinemic and normal phenotypes
Francis H. Glorieux, … , Edgard Delvin, Fazl Mohyuddin
Francis H. Glorieux, … , Edgard Delvin, Fazl Mohyuddin
Published November 1, 1971
Citation Information: J Clin Invest. 1971;50(11):2313-2322. https://doi.org/10.1172/JCI106729.
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Transport and metabolism of sarcosine in hypersarcosinemic and normal phenotypes

Abstract

An adolescent male proband with hypersarcosinemia was discovered incidentally in a French-Canadian family; no specific disease was associated with the trait. The hypersarcosinemia is not diminished by dietary folic acid even in pharmacologic doses (30 mg/day). The normal absence of sarcosine dehydrogenase in cultured human skin fibroblasts and in leukocytes was confirmed, thus eliminating these tissues as useful sources for further investigation of mutant sarcosinemic phenotypes and genotypes.

Authors

Francis H. Glorieux, Charles R. Scriver, Edgard Delvin, Fazl Mohyuddin

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Year: 2024 2016 2009 2006 2000 1992 1986 1984 1983 1981 1980 1979 1976 1975 Total
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Citations to this article (17)

Title and authors Publication Year
Changes in Plasma Concentration of Free Proteinogenic and Non-Proteinogenic Amino Acids in High-Performance Sprinters over a 6-Month Training Cycle
Kusy K, Matysiak J, Zarębska EA, Klupczyńska-Gabryszak A, Ciekot-Sołtysiak M, Plewa S, Kokot ZJ, Dereziński P, Zieliński J 		Journal of Clinical Medicine 2024
High-Yielding Automated Convergent Synthesis of No-Carrier-Added [11C-Carbonyl]-Labeled Amino Acids Using the Strecker Reaction
J Xing, A Brooks, D Fink, H Zhang, M Piert, P Scott, X Shao 		Synlett : accounts and rapid communications in synthetic organic chemistry 2016
Prospective Associations of Systemic and Urinary Choline Metabolites with Incident Type 2 Diabetes
GF Svingen, H Schartum-Hansen, ER Pedersen, PM Ueland, GS Tell, G Mellgren, PR Njølstad, R Seifert, E Strand, T Karlsson, O Nygård 		Clinical chemistry 2016
A randomized, double-blind, placebo-controlled comparison study of sarcosine ( N-methylglycine) and d-serine add-on treatment for schizophrenia
HY Lane, CH Lin, YJ Huang, CH Liao, YC Chang, GE Tsai 		The International Journal of Neuropsychopharmacology 2009
Transporters as Targets for Drugs
S Napier, M Bingham 		2009
Characterization of canine mitochondrial protein expression in natural and induced forms of idiopathic dilated cardiomyopathy
R Lopes, PF Solter, DD Sisson, MA Oyama, R Prosek 		American Journal of Veterinary Research 2006
The dendritic architecture of the cholinergic plexus in the rabbit retina: Selective labeling by glycine accumulation in the presence of sarcosine
DI Vaney, DV Pow 		The Journal of Comparative Neurology 2000
sar: a genetic mouse model for human sarcosinemia generated by ethylnitrosourea mutagenesis
CO Harding, P Williams, DM Pflanzer, RE Colwell, PW Lyne, JA Wolff 		Proceedings of the National Academy of Sciences 1992
Sarcosinaemia in a retarded, amaurotic child.
Sewell AC, Krille M, Wilhelm I 		European Journal of Pediatrics 1986
Fluorometric evaluation of sarcosine in urine and serum
G Bellon, AM Lundy, A Malgras, JP Borel 		Journal of Chromatography B: Biomedical Sciences and Applications 1984
Variability in the phenotypic expression of abnormal sarcosine metabolism in a family
ES Kang, J Seyer, TA Todd, C Herrera 		Human Genetics 1983
Kidney and Body Fluids
E Kinne-Saffran, R Beauwens, R Kinne, H Murer 		Kidney and Body Fluids 1981
Labile methyl group balances in the human: The role of sarcosine
SH Mudd, MH Ebert, CR Scriver 		Metabolism 1980
Folic acid dependent hypersarcosinaemia
W Blom, J Fernandes 		Clinica Chimica Acta 1979
Genetic aspects of renal tubular transport: Diversity and topology of carriers
CR Scriver, RW Chesney, RR McInnes 		Kidney International 1976
Role of epithelial architecture and intracellular metabolism in proline uptake and transtubular reclamation in PRO/re mouse kidney
CR Scriver, RR McInnes, F Mohyuddin 		Proceedings of the National Academy of Sciences 1975
Hypersarcosinemia with craniostenosis-syndactylism syndrome
R Minami, K Olek, P Wardenbach 		Human Genetics 1975

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