threonine and Bilirubinemia

threonine has been researched along with Bilirubinemia in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Forget, BG; Gallagher, PG; Morrow, JS; Zhang, Z	1
Berge, T; Borgfors, N; Brun, A; von Studnitz, W	1

Other Studies

2 other study(ies) available for threonine and Bilirubinemia

Article	Year
Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site. Laboratory investigation; a journal of technical methods and pathology, 2004, Volume: 84, Issue:2 Topics: Binding Sites; DNA Primers; Elliptocytosis, Hereditary; Erythrocyte Membrane; Female; Heterozygote; Humans; Hydrophobic and Hydrophilic Interactions; Hyperbilirubinemia; Infant, Newborn; Isoleucine; Male; Models, Molecular; Pedigree; Point Mutation; Protein Conformation; Sequence Analysis, DNA; Spectrin; Threonine	2004
Encephalopathy in combination with a new pattern of aminoaciduria. Acta paediatrica Scandinavica, 1969, Volume: 58, Issue:1 Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Central Nervous System; Chromatography; Cyanosis; Dyspnea, Paroxysmal; Electroencephalography; Exchange Transfusion, Whole Blood; Humans; Hyperbilirubinemia; Infant; Infant, Newborn; Infant, Premature, Diseases; Male; Serine; Spectrophotometry; Threonine	1969

Article

Year

Mutation of a highly conserved isoleucine disrupts hydrophobic interactions in the alpha beta spectrin self-association binding site.

Laboratory investigation; a journal of technical methods and pathology, 2004, Volume: 84, Issue:2

Topics: Binding Sites; DNA Primers; Elliptocytosis, Hereditary; Erythrocyte Membrane; Female; Heterozygote; Humans; Hydrophobic and Hydrophilic Interactions; Hyperbilirubinemia; Infant, Newborn; Isoleucine; Male; Models, Molecular; Pedigree; Point Mutation; Protein Conformation; Sequence Analysis, DNA; Spectrin; Threonine

2004

Encephalopathy in combination with a new pattern of aminoaciduria.

Acta paediatrica Scandinavica, 1969, Volume: 58, Issue:1

Topics: Alanine; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Central Nervous System; Chromatography; Cyanosis; Dyspnea, Paroxysmal; Electroencephalography; Exchange Transfusion, Whole Blood; Humans; Hyperbilirubinemia; Infant; Infant, Newborn; Infant, Premature, Diseases; Male; Serine; Spectrophotometry; Threonine

1969