histidine has been researched along with Hyperthyroxinemia in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 4 (80.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Angkeow, P; Hayashi, Y; Refetoff, S; Sunthornthepvarakul, T; Weiss, RE | 1 |
Bhagavan, NV; Cody, LR; Mandel, M; Petersen, CE; Reimer, N; Scottolini, AG | 1 |
Bhagavan, NV; Ha, CE; Harohalli, K; Park, D; Petersen, CE | 1 |
Braverman, LE; Choo, KB; Fang, SL; Lin, HD; Tang, KT; Yang, HJ | 1 |
Bhagavan, NV; Ha, CE; Harohalli, K; Park, DS; Petersen, CE | 1 |
5 other study(ies) available for histidine and Hyperthyroxinemia
Article | Year |
---|---|
An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families.
Topics: Arginine; Codon; DNA, Complementary; Histidine; Humans; Hyperthyroxinemia; Mutation; Pedigree; Phenotype; Serum Albumin; Thyroxine; Triiodothyronine, Reverse | 1994 |
A point mutation in the human serum albumin gene results in familial dysalbuminaemic hyperthyroxinaemia.
Topics: Amino Acid Sequence; Arginine; Base Sequence; Deoxyribonucleases, Type II Site-Specific; DNA Primers; Histidine; Humans; Hyperthyroxinemia; Molecular Sequence Data; Point Mutation; Polymerase Chain Reaction; Protein Binding; Restriction Mapping; Serum Albumin; Trypsin | 1994 |
Mutagenesis studies of thyroxine binding to human serum albumin define an important structural characteristic of subdomain 2A.
Topics: Arginine; Binding Sites; Histidine; Humans; Hyperthyroxinemia; Kinetics; Mutagenesis, Site-Directed; Protein Binding; Serum Albumin; Spectrometry, Fluorescence; Structure-Activity Relationship; Thyroxine | 1997 |
A point mutation in the albumin gene in a Chinese patient with familial dysalbuminemic hyperthyroxinemia.
Topics: Aged; Amino Acid Substitution; Arginine; Asian People; Codon; Genes, Dominant; Histidine; Humans; Hyperthyroxinemia; Male; Point Mutation; Serum Albumin; Taiwan | 1999 |
Familial dysalbuminemic byperthyroxinemia may result in altered warfarin pharmacokinetics.
Topics: Amino Acid Substitution; Arginine; Dialysis; Histidine; Humans; Hyperthyroxinemia; Kinetics; Mutagenesis, Insertional; Mutation; Protein Binding; Serum Albumin; Spectrometry, Fluorescence; Warfarin | 2000 |