Compounds > arginine

arginine and Hyperthyroxinemia

arginine has been researched along with Hyperthyroxinemia in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's4 (66.67)18.2507
2000's2 (33.33)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hoshikawa, S; Ito, S; Kaise, N; Mori, K; Nakagawa, Y; Yoshida, K1
Angkeow, P; Hayashi, Y; Refetoff, S; Sunthornthepvarakul, T; Weiss, RE1
Bhagavan, NV; Cody, LR; Mandel, M; Petersen, CE; Reimer, N; Scottolini, AG1
Bhagavan, NV; Ha, CE; Harohalli, K; Park, D; Petersen, CE1
Braverman, LE; Choo, KB; Fang, SL; Lin, HD; Tang, KT; Yang, HJ1
Bhagavan, NV; Ha, CE; Harohalli, K; Park, DS; Petersen, CE1

Other Studies

6 other study(ies) available for arginine and Hyperthyroxinemia

ArticleYear
Artifactually elevated serum-free thyroxine levels measured by equilibrium dialysis in a pregnant woman with familial dysalbuminemic hyperthyroxinemia.
    Thyroid : official journal of the American Thyroid Association, 2004, Volume: 14, Issue:2

    Topics: Adult; Amino Acid Substitution; Arginine; Artifacts; Cytosine; Dialysis; Female; Genes, Dominant; Guanine; Hemofiltration; Humans; Hyperthyroxinemia; Metabolism, Inborn Errors; Mutation; Pregnancy; Pregnancy Complications; Proline; Radioimmunoassay; Serum Albumin; Thyroxine; Thyroxine-Binding Proteins

2004
An identical missense mutation in the albumin gene results in familial dysalbuminemic hyperthyroxinemia in 8 unrelated families.
    Biochemical and biophysical research communications, 1994, Jul-29, Volume: 202, Issue:2

    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.
    Journal of medical genetics, 1994, Volume: 31, Issue:5

    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.
    Biochemistry, 1997, Jun-10, Volume: 36, Issue:23

    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.
    European journal of endocrinology, 1999, Volume: 141, Issue:4

    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.
    Chemico-biological interactions, 2000, Feb-01, Volume: 124, Issue:3

    Topics: Amino Acid Substitution; Arginine; Dialysis; Histidine; Humans; Hyperthyroxinemia; Kinetics; Mutagenesis, Insertional; Mutation; Protein Binding; Serum Albumin; Spectrometry, Fluorescence; Warfarin

2000