Compounds > phenylalanine

phenylalanine and Crigler Najjar Syndrome

phenylalanine has been researched along with Crigler Najjar Syndrome in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aboura, A; Capel, L; Gajdos, V; Labrune, P; Lachaux, A; Parisot, F; Petit, FM; Poüs, C; Tachdjian, G1
Gridelli, B; Kaiser, C; Owens, IS; Ritter, JK; Yeatman, MT1

Other Studies

2 other study(ies) available for phenylalanine and Crigler Najjar Syndrome

ArticleYear
Paternal isodisomy for chromosome 2 as the cause of Crigler-Najjar type I syndrome.
    European journal of human genetics : EJHG, 2005, Volume: 13, Issue:3

    Topics: Base Sequence; Bilirubin; Chromosome Mapping; Chromosomes, Human, Pair 2; Crigler-Najjar Syndrome; DNA; Fatal Outcome; Fathers; Glucuronosyltransferase; Humans; Infant; Infant, Newborn; Male; Microsatellite Repeats; Mothers; Phenylalanine; Sequence Deletion; Uniparental Disomy

2005
A phenylalanine codon deletion at the UGT1 gene complex locus of a Crigler-Najjar type I patient generates a pH-sensitive bilirubin UDP-glucuronosyltransferase.
    The Journal of biological chemistry, 1993, Nov-05, Volume: 268, Issue:31

    Topics: Alleles; Amino Acid Sequence; Animals; Base Sequence; Codon; Crigler-Najjar Syndrome; DNA Primers; Female; Glucuronosyltransferase; Humans; Hydrogen-Ion Concentration; Male; Microsomes, Liver; Molecular Sequence Data; Phenylalanine; Rats; Sequence Alignment; Sequence Deletion; Sequence Homology, Amino Acid

1993