Compounds > arginine

arginine and Goiter

arginine has been researched along with Goiter in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (28.57)18.2507
2000's5 (71.43)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ishinaga, H; Majima, Y; Shimizu, T; Tsukamoto, K; Usami, S; Yuta, A1
Domené, S; Gutnisky, VJ; Medeiros-Neto, G; Moya, CM; Rivolta, CM; Targovnik, HM; Toniolo, JV; Varela, V1
Arvan, P; Bae, JH; Hossain, SA; Jongsamak, P; Kim, PS; Lee, J; Li, B; Menon, S; Panijpan, B1
Colin, IM; Denef, JF; Jameson, JL; Ketelslegers, JM; Lüscher, TF; Maiter, DM; Nava, E; Toussaint, D; vanDenhove, MF1
Mendive, FM; Rossetti, LC; Targovnik, HM; Vassart, G1
Abe, S; Hoshino, T; Isoda, H; Iwasaki, S; Usami , S; Watanabe, T1
Furuhashi, A; Miura, Y; Mori, N; Murakami, H; Naganawa, S; Nakashima, T; Nakayama, A; Sato, E; Tadokoro, M1

Other Studies

7 other study(ies) available for arginine and Goiter

ArticleYear
Pendred's syndrome with goiter and enlarged vestibular aqueducts diagnosed by PDS gene mutation.
    Head & neck, 2002, Volume: 24, Issue:7

    Topics: Aged; Arginine; Biological Transport; Carrier Proteins; DNA Mutational Analysis; Female; Goiter; Hearing Loss, Sensorineural; Histidine; Humans; Membrane Transport Proteins; Mutation, Missense; Pedigree; Sulfate Transporters

2002
Two distinct compound heterozygous constellations (R277X/IVS34-1G>C and R277X/R1511X) in the thyroglobulin (TG) gene in affected individuals of a Brazilian kindred with congenital goiter and defective TG synthesis.
    The Journal of clinical endocrinology and metabolism, 2004, Volume: 89, Issue:2

    Topics: Amino Acid Sequence; Amino Acid Substitution; Arginine; Base Sequence; Brazil; Chromosome Segregation; Codon, Terminator; Cytosine; Founder Effect; Genetic Markers; Goiter; Heterozygote; Humans; Male; Molecular Sequence Data; Pedigree; Polymorphism, Single Nucleotide; Thymine; Thyroglobulin

2004
Defective protein folding and intracellular retention of thyroglobulin-R19K mutant as a cause of human congenital goiter.
    Molecular endocrinology (Baltimore, Md.), 2008, Volume: 22, Issue:2

    Topics: Alkaloids; Amino Acid Substitution; Animals; Arginine; Biological Transport; Blotting, Western; Calnexin; Chlorocebus aethiops; COS Cells; Electrophoresis, Polyacrylamide Gel; Endoplasmic Reticulum; Endoplasmic Reticulum Chaperone BiP; Goiter; Golgi Apparatus; Heat-Shock Proteins; Humans; Immunoprecipitation; Leupeptins; Lysine; Mice; Molecular Chaperones; Mutation; Protein Binding; Protein Disulfide-Isomerases; Protein Folding; Signal Transduction; Thyroglobulin

2008
Expression of nitric oxide synthase isoforms in the thyroid gland: evidence for a role of nitric oxide in vascular control during goiter formation.
    Endocrinology, 1995, Volume: 136, Issue:12

    Topics: Animals; Arginine; Base Sequence; Endothelins; Gene Expression Regulation, Enzymologic; Goiter; Isoenzymes; Male; Molecular Sequence Data; NG-Nitroarginine Methyl Ester; Nitric Oxide; Nitric Oxide Synthase; Rats; Rats, Wistar; RNA, Messenger; Thyroid Gland

1995
Identification of a new thyroglobulin variant: a guanine-to-adenine transition resulting in the substitution of arginine 2510 by glutamine.
    Thyroid : official journal of the American Thyroid Association, 1997, Volume: 7, Issue:4

    Topics: Adenine; Alleles; Animals; Arginine; Cattle; Gene Frequency; Genetic Variation; Glutamine; Goiter; Guanine; Humans; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Rats; RNA-Directed DNA Polymerase; Thyroglobulin; Thyroid Gland

1997
Long-term audiological feature in Pendred syndrome caused by PDS mutation.
    Archives of otolaryngology--head & neck surgery, 2001, Volume: 127, Issue:6

    Topics: Adult; Arginine; Biological Transport; Carrier Proteins; Chromosomes, Human, Pair 7; Disease Progression; DNA Mutational Analysis; Evoked Potentials, Auditory, Brain Stem; Female; Goiter; Hearing Loss, Sensorineural; Histidine; Humans; Magnetic Resonance Imaging; Membrane Transport Proteins; Mutation, Missense; Sulfate Transporters; Syndrome; Time Factors; Vestibular Aqueduct

2001
Phenotypes associated with replacement of His by Arg in the Pendred syndrome gene.
    European journal of endocrinology, 2001, Volume: 145, Issue:6

    Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Arginine; Carrier Proteins; Child; Endolymphatic Duct; Endolymphatic Sac; Female; Goiter; Hearing Loss, Sensorineural; Heterozygote; Histidine; Homozygote; Humans; Iodides; Iodine; Magnetic Resonance Imaging; Male; Membrane Transport Proteins; Mutation; Mutation, Missense; Phenotype; RNA Splicing; Sequence Analysis, DNA; Sulfate Transporters; Syndrome; Thyroglobulin; Vestibular Aqueduct

2001