92 related articles for article (PubMed ID: 4753048)
1. Inhibition of glycine oxidation in cultured fibroblasts by isoleucine.
Hillman RE; Sowers LH; Cohen JL
Pediatr Res; 1973 Dec; 7(12):945-7. PubMed ID: 4753048
[No Abstract] [Full Text] [Related]
2. Hyperglycinemia with ketosis due to a defect in isoleucine metabolism: a preliminary report.
Keating JP; Feigin RD; Tenenbaum SM; Hillman RE
Pediatrics; 1972 Dec; 50(6):890-5. PubMed ID: 4636454
[No Abstract] [Full Text] [Related]
3. Inhibition of glycine-serine interconversion in cultured human fibroblasts by products of isoleucine catabolism.
Hillman RE; Otto EF
Pediatr Res; 1974 Dec; 8(12):941-5. PubMed ID: 4444863
[No Abstract] [Full Text] [Related]
4. Beta-ketothiolase deficiency as a cause of the "ketotic hyperglycinemia syndrome".
Hillman RE; Keating JP
Pediatrics; 1974 Feb; 53(2):221-5. PubMed ID: 4812006
[No Abstract] [Full Text] [Related]
5. An inherited disorder of isoleucine catabolism causing accumulation of alpha-methylacetoacetate and alpha-methyl-beta -hydroxybutyrate, and intermittent metabolic acidosis.
Daum RS; Scriver CR; Mamer OA; Delvin E; Lamm P; Goldman H
Pediatr Res; 1973 Mar; 7(3):149-60. PubMed ID: 4690360
[No Abstract] [Full Text] [Related]
6. Glycine metabolism and spinal cord disorders.
Bank WJ; Pizer L; Pfendner W
Adv Neurol; 1978; 21():267-78. PubMed ID: 216244
[No Abstract] [Full Text] [Related]
7. Metabolism of [1-(14)C] and [2-(14)C] leucine in cultured skin fibroblasts from patients with isovaleric acidemia. Characterization of metabolic defects.
Tanaka K; Mandell R; Shih VE
J Clin Invest; 1976 Jul; 58(1):164-72. PubMed ID: 932204
[TBL] [Abstract][Full Text] [Related]
8. Physiological significance of glycine cleavage system in human liver as revealed by the study of a case of hyperglycinemia.
Yoshida T; Kikuchi G
Biochem Biophys Res Commun; 1969 May; 35(4):577-83. PubMed ID: 5788511
[No Abstract] [Full Text] [Related]
9. Metabolism of glycine in the nonketotic form of hyperglycinemia.
Ando T; Nyhan WL; Gerritsen T; Gong L; Heiner DC; Bray PF
Pediatr Res; 1968 Jul; 2(4):254-63. PubMed ID: 5669662
[No Abstract] [Full Text] [Related]
10. Diagnosis of inborn errors of phytanic acid oxidation using tritiated phytanic acid.
Zenger-Hain J; Craft DA; Rizzo WB
Prog Clin Biol Res; 1992; 375():399-407. PubMed ID: 1438384
[No Abstract] [Full Text] [Related]
11. Hyperglycinemia with ketoacidosis and leukopenia. Metabolic studies on the nature of the defect.
Soriano JR; Taitz LS; Finberg L; Edelmann CM
Pediatrics; 1967 Jun; 39(6):818-28. PubMed ID: 6026548
[No Abstract] [Full Text] [Related]
12. Isoleucine transport by cultured human fibroblasts. II. Selection of a cell line with reduced isoleucine uptake.
Hillman RE; Otto EF
Biochim Biophys Acta; 1974 Oct; 367(1):81-7. PubMed ID: 4420387
[No Abstract] [Full Text] [Related]
13. Evidence for a short-chain carnitine-acylcarnitine translocase in mitochondria specifically related to the metabolism of branched-chain amino acids.
Roe DS; Roe CR; Brivet M; Sweetman L
Mol Genet Metab; 2000 Jan; 69(1):69-75. PubMed ID: 10655160
[TBL] [Abstract][Full Text] [Related]
14. Valine-sensitive nonketotic hyperglycinemia. Case report.
Krieger I; Hart ZH
J Pediatr; 1974 Jul; 85(1):43-8. PubMed ID: 4855367
[No Abstract] [Full Text] [Related]
15. Screening for inborn errors of fatty acid oxidation in cultured fibroblasts: an overview.
Rhead WJ
Prog Clin Biol Res; 1990; 321():365-82. PubMed ID: 2183237
[No Abstract] [Full Text] [Related]
16. [Human fibroblast bank for studying amino acid disorders and organic acidemias].
del Valle JA; Merinero B; Pérez-Cerdá C; Ugarte M
Rev Esp Fisiol; 1982; 38 Suppl():207-10. PubMed ID: 7146578
[TBL] [Abstract][Full Text] [Related]
17. Multiple acyl-coenzyme A dehydrogenation disorders (MAD) responsive to riboflavin: biochemical studies in fibroblasts.
Roettger V; Marshall T; Amendt B; Rhead WJ
Prog Clin Biol Res; 1992; 375():317-26. PubMed ID: 1438377
[No Abstract] [Full Text] [Related]
18. The conversion of [1-13C]glycine and [2-13C]glycine to [13C]oxalate in primary hyperoxaluria: evidence for the existence of more than one metabolic pathway from glycine to oxalate in man.
Dean BM; Watts RW; Westwick WJ
Clin Sci; 1968 Oct; 35(2):325-35. PubMed ID: 5721235
[No Abstract] [Full Text] [Related]
19. Glycine transport by cultured skin fibroblasts from a patient with isolated hyperglycinuria.
Fénéant M; Moatti N; Lemonnier F; Maccario J; Gautier M; Charpentier C; Lemonnier A
J Inherit Metab Dis; 1980; 3(3):97-8. PubMed ID: 6775149
[TBL] [Abstract][Full Text] [Related]
20. Transport of L-isoleucine by cultured human fibroblasts. Uptake by normal cell lines and isolation of a cell line lacking sodium-dependent uptake.
Hillman RE; Otto EF
J Biol Chem; 1974 Jun; 249(11):3430-5. PubMed ID: 4831221
[No Abstract] [Full Text] [Related]
[Next] [New Search]
