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alanine and Hyperoxaluria

alanine has been researched along with Hyperoxaluria in 8 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Hyperoxaluria: Excretion of an excessive amount of OXALATES in the urine.

Research Excerpts

ExcerptRelevanceReference
"We have studied the characteristics of human liver alanine-glyoxylate aminotransferase, which is deficient in hyperoxaluria type I, an inherited disorder of glyoxylate metabolism."7.68Human liver L-alanine-glyoxylate aminotransferase: characteristics and activity in controls and hyperoxaluria type I patients using a simple spectrophotometric method. ( Jurriaans, S; Ofman, R; Ruiter, J; Schutgens, RB; Tager, JM; van Roermund, CW; Wanders, RJ, 1990)
"A case of primary hyperoxaluria type 1 with complete deficiency of alanine:glyoxalate aminotransferase that first manifested at the age of 59 with irreversible acute on chronic renal failure is reported."3.68Late presentation and development of nephrocalcinosis in primary hyperoxaluria. ( Doust, B; Irish, AB, 1992)
"We examined the effect of vitamin B6 deficiency on glyoxylate metabolism and hepatic alanine: glyoxylate aminotransferase (AGT) activity in rats with normal or high glyoxylate intake."1.33Effect of vitamin B6 deficiency on glyoxylate metabolism in rats with or without glyoxylate overload. ( Hokama, S; Morozumi, M; Nishijima, S; Ogawa, Y; Oshiro, Y; Sugaya, K; Uchida, A, 2006)
"We found that AGT activity in two hyperoxaluria type 1 patients was reduced as compared with controls."1.28High-performance liquid chromatographic microassay for L-alanine:glyoxylate aminotransferase activity in human liver. ( Cosseddu, D; Linari, F; Marangella, M; Pellegrino, S; Petrarulo, M, 1992)

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19902 (25.00)18.7374
1990's4 (50.00)18.2507
2000's1 (12.50)29.6817
2010's1 (12.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Assimos, DG1
GABURRO, D1
VOLPATO, S1
SCARPA, P1
Nishijima, S1
Sugaya, K1
Hokama, S1
Oshiro, Y1
Uchida, A1
Morozumi, M1
Ogawa, Y1
Pirulli, D1
Puzzer, D1
Ferri, L1
Crovella, S1
Amoroso, A1
Ferrettini, C1
Marangella, M2
Mazzola, G1
Florian, F1
Petrarulo, M1
Pellegrino, S1
Cosseddu, D1
Linari, F1
Irish, AB1
Doust, B1
Wanders, RJ1
Ruiter, J1
van Roermund, CW1
Schutgens, RB1
Ofman, R1
Jurriaans, S1
Tager, JM1
Danpure, CJ1
Jennings, PR1
Watts, RW1

Other Studies

8 other studies available for alanine and Hyperoxaluria

ArticleYear
Re: Pyridoxamine and Pyridoxal are More Effective than Pyridoxine in Rescuing Folding-Defective Variants of Human Alanine:Glyoxylate Aminotransferase Causing Primary Hyperoxaluria Type I.
    The Journal of urology, 2016, Volume: 195, Issue:4 Pt 1

    Topics: Alanine; Humans; Hyperoxaluria; Hyperoxaluria, Primary; Pyridoxal; Pyridoxamine; Pyridoxine

2016
[CONGENITAL DYSMETABOLIC CEREBROPATHY WITH HYPERGLYCEMIA, HYPERALANINURIA AND HYPEROXALURIA].
    Les Cahiers du College de medecine des hopitaux de Paris, 1963, Oct-15, Volume: 4

    Topics: Alanine; Brain Diseases; Child; Humans; Hyperglycemia; Hyperoxaluria; Infant; Intellectual Disabilit

1963
Effect of vitamin B6 deficiency on glyoxylate metabolism in rats with or without glyoxylate overload.
    Biomedical research (Tokyo, Japan), 2006, Volume: 27, Issue:3

    Topics: Alanine; Alanine Transaminase; Animals; Glyoxylates; Hyperoxaluria; Liver; Male; Rats; Rats, Wistar;

2006
Molecular analysis of hyperoxaluria type 1 in Italian patients reveals eight new mutations in the alanine: glyoxylate aminotransferase gene.
    Human genetics, 1999, Volume: 104, Issue:6

    Topics: Alanine; Base Sequence; Exons; Gene Deletion; Humans; Hyperoxaluria; Italy; Molecular Sequence Data;

1999
High-performance liquid chromatographic microassay for L-alanine:glyoxylate aminotransferase activity in human liver.
    Clinica chimica acta; international journal of clinical chemistry, 1992, Jun-30, Volume: 208, Issue:3

    Topics: Alanine; Alanine Transaminase; Chromatography, High Pressure Liquid; Colorimetry; Glyoxylates; Human

1992
Late presentation and development of nephrocalcinosis in primary hyperoxaluria.
    Australian and New Zealand journal of medicine, 1992, Volume: 22, Issue:1

    Topics: Alanine; Female; Humans; Hyperoxaluria; Middle Aged; Nephrocalcinosis; Radionuclide Imaging

1992
Human liver L-alanine-glyoxylate aminotransferase: characteristics and activity in controls and hyperoxaluria type I patients using a simple spectrophotometric method.
    Clinica chimica acta; international journal of clinical chemistry, 1990, Aug-15, Volume: 189, Issue:2

    Topics: Alanine; Alanine Transaminase; Biopsy; Glyoxylates; Humans; Hydrogen-Ion Concentration; Hyperoxaluri

1990
Enzymological diagnosis of primary hyperoxaluria type 1 by measurement of hepatic alanine: glyoxylate aminotransferase activity.
    Lancet (London, England), 1987, Feb-07, Volume: 1, Issue:8528

    Topics: Adolescent; Alanine; Child; Child, Preschool; Female; Humans; Hyperoxaluria; Liver; Male; Prognosis;

1987