Compounds > histidine
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histidine and Goiter

histidine has been researched along with Goiter in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19903 (50.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)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
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
de Vijlder, JJ; Fokkens, RH; Gons, MH; Kok, K; van Dijk, JE1
Massin, JP; Savoie, F; Savoie, JC1
Bilstad, JM; Cahnmann, HJ; Ogawara, H1

Other Studies

6 other study(ies) available for histidine 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
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
Prenatal diagnosis of a thyroglobulin synthesis defect in goats.
    Acta endocrinologica, 1985, Volume: 110, Issue:1

    Topics: Animals; Chromatography, High Pressure Liquid; Female; Goats; Goiter; Histidine; Iodine; Mass Spectrometry; Molecular Weight; Pregnancy; Prenatal Diagnosis; Thyroglobulin

1985
Studies on mono- and diiodohistidine. II. Congenital goitrous hypothyroidism with thyroglobulin defect and iodohistidine-rich iodoalbumin production.
    The Journal of clinical investigation, 1973, Volume: 52, Issue:1

    Topics: Adult; Albumins; Albuminuria; Child; Chromatography, Gel; Electrophoresis, Polyacrylamide Gel; Female; Goiter; Histidine; Humans; Hypothyroidism; Immunodiffusion; Iodides; Iodoproteins; Male; Monoiodotyrosine; Peroxidases; Thyroglobulin; Thyroid Gland

1973
Iodoamino acid distribution in thyroglobulin iodinated in vivo and in vitro.
    Biochimica et biophysica acta, 1972, Feb-29, Volume: 257, Issue:2

    Topics: Animals; Cattle; Chemical Phenomena; Chemistry; Chromatography, Ion Exchange; Chromatography, Thin Layer; Goiter; Histidine; Humans; Iodides; Iodine; Iodine Isotopes; Monoiodotyrosine; Pronase; Rats; Thyroglobulin; Thyronines; Triiodothyronine

1972