Results 241 to 250 of about 23,011 (262)
Some of the next articles are maybe not open access.

The auto‐oxidation of tetrahydrobiopterin

European Journal of Biochemistry, 1988
The product of the aerobic oxidation of tetrahydrobiopterin, quinonoid dihydrobiopterin, is unstable and rapidly rearranges to form a 7,8‐dihydropteridine. Kaufman [Kaufman, S. (1967) J. Biol. Chem. 242, 3934–3943] identified the stable product produced in 0.1 M phosphate pH 6.8, as 7,8‐dihydrobiopterin. However, Armarego et al. [Armarego, W. L.
M D, Davis, S, Kaufman, S, Milstien
openaire   +2 more sources

International database of tetrahydrobiopterin deficiencies

Journal of Inherited Metabolic Disease, 1995
SummaryApproximately 2% of newborns with hyperphenylalaninaemia are deficient in tetrahydrobiopterin. Selective screening must be performed in all instances where hyperphenylalaninaemia is detected by neonatal screening. In the last 20 years, 308 patients with tetrahydrobiopterin deficiencies have been recognized as a result of screening carried out ...
N, Blau, I, Barnes, J L, Dhondt
openaire   +2 more sources

Maternal Phenylketonuria and Tetrahydrobiopterin

Pediatrics, 2008
Untreated maternal phenylketonuria (PKU) results in a significant occurrence of microcephaly and congenital heart disease in the offspring. Before the documentation of this fact by Lenke and Levy1 in 1980, there was confusion as to the occurrence of these abnormalities.
openaire   +2 more sources

Tetrahydrobiopterin Metabolism

1988
Tetrahydrobiopterin is the cofactor for the hydroxylation of phenylalanine, tyrosine and tryptophan and is therefore essential for the production of monoamine neurotransmitters. Neopterin, a biosynthetic precusor of tetrahydrobiopterin, and biopterin appear in urine. In normal subjects the urinary neopterin to biopterin ratio has been found to be about
openaire   +1 more source

Tetrahydrobiopterin-(BH4-)Mangelkrankheiten

2014
Die Krankheitsgruppe umfasst 6 angeborene Stoffwechselstorungen, die mit einem Tetrahydrobiopterinmangel (BH4-Mangel) entweder aufgrund einer gestorten BH4-Biosynthese oder eines gestorten BH4-Recyclings einhergehen. Tetrahydrobiopterin (BH4) ist ein essenzieller Kofaktor bei der Biosynthese der Neurotransmitter Dopamin und Serotonin und bei der ...
T. Opladen, N. Blau
openaire   +1 more source

Tetrahydrobiopterin and phenylketonuria

The Journal of Pediatrics, 2011
PORTA, FRANCESCO   +4 more
openaire   +1 more source

Tetrahydrobiopterin

2000
Steven S. Gross   +3 more
openaire   +1 more source

Tetrahydrobiopterin

Trends in Cardiovascular Medicine, 2004
openaire   +1 more source

Tetrahydrobiopterin

2010
Christina E. Higgins, Steven S. Gross
openaire   +1 more source

Home - About - Disclaimer - Privacy