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triiodothyronine and Genetic Predisposition

triiodothyronine has been researched along with Genetic Predisposition in 17 studies

Triiodothyronine: A T3 thyroid hormone normally synthesized and secreted by the thyroid gland in much smaller quantities than thyroxine (T4). Most T3 is derived from peripheral monodeiodination of T4 at the 5' position of the outer ring of the iodothyronine nucleus. The hormone finally delivered and used by the tissues is mainly T3.
3,3',5-triiodo-L-thyronine : An iodothyronine compound having iodo substituents at the 3-, 3'- and 5-positions. Although some is produced in the thyroid, most of the 3,3',5-triiodo-L-thyronine in the body is generated by mono-deiodination of L-thyroxine in the peripheral tissues. Its metabolic activity is about 3 to 5 times that of L-thyroxine. The sodium salt is used in the treatment of hypothyroidism.

Research Excerpts

ExcerptRelevanceReference
"Thyrotoxic hypokalemic periodic paralysis (TPP) is characterized by acute attacks of weakness, hypokalemia, and thyrotoxicosis of various etiologies."1.36Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis. ( Bernstein, HS; Brown, RH; Cheah, JS; da Silva, MR; Donaldson, MR; Fontaine, B; Ho, SC; Jongjaroenprasert, W; Khoo, DH; Kung, AW; Liang, MC; Maciel, RM; Ptácek, LJ; Ryan, DP; Soong, TW, 2010)
"HLA alleles of 106 patients with Graves' disease were determined, and the frequency of HLA-B46 was found to be significantly increased."1.29Association of HLA-DPB1*0501 with early-onset Graves' disease in Japanese. ( Inoko, H; Onuma, H; Ota, M; Sugenoya, A, 1994)

Research

Studies (17)

TimeframeStudies, this research(%)All Research%
pre-19901 (5.88)18.7374
1990's1 (5.88)18.2507
2000's7 (41.18)29.6817
2010's7 (41.18)24.3611
2020's1 (5.88)2.80

Authors

AuthorsStudies
Romartinez-Alonso, B1
Agostini, M1
Jones, H1
McLellan, J1
Sood, DE1
Tomkinson, N1
Marelli, F1
Gentile, I1
Visser, WE1
Schoenmakers, E1
Fairall, L1
Privalsky, M1
Moran, C1
Persani, L1
Chatterjee, K1
Schwabe, JWR1
Nelson, PT1
Gal, Z1
Wang, WX1
Niedowicz, DM1
Artiushin, SC1
Wycoff, S1
Wei, A1
Jicha, GA1
Fardo, DW1
Luo, M1
Zhou, XH1
Zou, T1
Keyim, K1
Dong, LM1
Vaurs-Barrière, C1
Deville, M1
Sarret, C1
Giraud, G1
Des Portes, V1
Prats-Viñas, JM1
De Michele, G1
Dan, B1
Brady, AF1
Boespflug-Tanguy, O1
Touraine, R1
Gudmundsson, J1
Sulem, P1
Gudbjartsson, DF1
Jonasson, JG1
Sigurdsson, A1
Bergthorsson, JT1
He, H1
Blondal, T1
Geller, F1
Jakobsdottir, M1
Magnusdottir, DN1
Matthiasdottir, S1
Stacey, SN1
Skarphedinsson, OB1
Helgadottir, H1
Li, W1
Nagy, R1
Aguillo, E1
Faure, E1
Prats, E1
Saez, B1
Martinez, M1
Eyjolfsson, GI1
Bjornsdottir, US1
Holm, H1
Kristjansson, K1
Frigge, ML1
Kristvinsson, H1
Gulcher, JR1
Jonsson, T1
Rafnar, T1
Hjartarsson, H1
Mayordomo, JI1
de la Chapelle, A1
Hrafnkelsson, J1
Thorsteinsdottir, U1
Kong, A1
Stefansson, K1
Daroszewski, J1
Pawlak, E1
Karabon, L1
Frydecka, I1
Jonkisz, A1
Slowik, M1
Bolanowski, M1
Ryan, DP1
da Silva, MR1
Soong, TW1
Fontaine, B1
Donaldson, MR1
Kung, AW1
Jongjaroenprasert, W1
Liang, MC1
Khoo, DH1
Cheah, JS1
Ho, SC1
Bernstein, HS1
Maciel, RM1
Brown, RH1
Ptácek, LJ1
Rooke, JA1
Houdijk, JG1
McIlvaney, K1
Ashworth, CJ1
Dwyer, CM1
Meulenbelt, I2
Bos, SD1
Chapman, K1
van der Breggen, R2
Houwing-Duistermaat, JJ2
Kremer, D2
Kloppenburg, M2
Carr, A1
Tsezou, A1
González, A1
Loughlin, J2
Slagboom, PE2
Everaert, N1
Willemsen, H1
Debonne, M1
Witters, A1
Kamers, B1
Darras, VM1
de Baerdemaeker, J1
Decuypere, E3
Bruggeman, V2
Zou, S1
Sang, Q1
Wang, H1
Feng, R1
Li, Q1
Zhao, X1
Xing, Q1
Jin, L1
He, L1
Wang, L1
FAENZI, C1
Shohet, RV1
Kisanuki, YY1
Zhao, XS1
Siddiquee, Z1
Franco, F1
Yanagisawa, M1
Hassanzadeh, M2
Gilanpour, H1
Charkhkar, S1
Buyse, J1
De Smit, L1
Tona, K1
Onagbesan, O1
Arckens, L1
Min, JL1
Bos, S1
Riyazi, N1
van der Wijk, HJ1
Kroon, HM1
Nakajima, M1
Ikegawa, S1
Uitterlinden, AG1
van Meurs, JB1
van der Deure, WM1
Visser, TJ1
Seymour, AB1
Lakenberg, N1
van Duijn, CM1
Onuma, H1
Ota, M1
Sugenoya, A1
Inoko, H1

Reviews

1 review available for triiodothyronine and Genetic Predisposition

ArticleYear
Meta-analyses of genes modulating intracellular T3 bio-availability reveal a possible role for the DIO3 gene in osteoarthritis susceptibility.
    Annals of the rheumatic diseases, 2011, Volume: 70, Issue:1

    Topics: Aged; Biological Availability; Female; Gene Frequency; Genetic Predisposition to Disease; Humans; Io

2011

Trials

1 trial available for triiodothyronine and Genetic Predisposition

ArticleYear
Differential effects of maternal undernutrition between days 1 and 90 of pregnancy on ewe and lamb performance and lamb parasitism in hill or lowland breeds.
    Journal of animal science, 2010, Volume: 88, Issue:12

    Topics: Animal Nutritional Physiological Phenomena; Animals; Breeding; Female; Genetic Predisposition to Dis

2010

Other Studies

15 other studies available for triiodothyronine and Genetic Predisposition

ArticleYear
Structure-Guided Approach to Relieving Transcriptional Repression in Resistance to Thyroid Hormone α.
    Molecular and cellular biology, 2022, 02-17, Volume: 42, Issue:2

    Topics: Animals; Co-Repressor Proteins; Gene Expression; Genetic Predisposition to Disease; Humans; Mutation

2022
TDP-43 proteinopathy in aging: Associations with risk-associated gene variants and with brain parenchymal thyroid hormone levels.
    Neurobiology of disease, 2019, Volume: 125

    Topics: Aged; Aged, 80 and over; Aging; Brain; Female; Genetic Predisposition to Disease; Humans; Male; Midd

2019
Type II deiodinase polymorphisms and serum thyroid hormone levels in patients with mild cognitive impairment.
    Genetics and molecular research : GMR, 2015, May-22, Volume: 14, Issue:2

    Topics: Adult; Cognitive Dysfunction; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; H

2015
Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects.
    Annals of neurology, 2009, Volume: 65, Issue:1

    Topics: Brain; Child; Disease Progression; DNA Mutational Analysis; Exons; Family Health; Follow-Up Studies;

2009
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.
    Nature genetics, 2009, Volume: 41, Issue:4

    Topics: Chromosome Mapping; Chromosomes, Human, Pair 4; Chromosomes, Human, Pair 9; DNA-Binding Proteins; Eu

2009
Soluble CTLA-4 receptor an immunological marker of Graves' disease and severity of ophthalmopathy is associated with CTLA-4 Jo31 and CT60 gene polymorphisms.
    European journal of endocrinology, 2009, Volume: 161, Issue:5

    Topics: Adolescent; Adult; Aged; Aged, 80 and over; Antigens, CD; Cohort Studies; CTLA-4 Antigen; DNA; Femal

2009
Mutations in potassium channel Kir2.6 cause susceptibility to thyrotoxic hypokalemic periodic paralysis.
    Cell, 2010, Jan-08, Volume: 140, Issue:1

    Topics: Amino Acid Sequence; Base Sequence; DNA Mutational Analysis; Electrophysiological Phenomena; Genetic

2010
Interaction between ascites susceptibility and CO(2) during the second half of incubation of two broiler lines: the effect on post-hatch development and ascites mortality.
    British poultry science, 2012, Volume: 53, Issue:2

    Topics: Animals; Ascites; Carbon Dioxide; Chick Embryo; Chickens; Corticosterone; Female; Genetic Predisposi

2012
Common genetic variation in CYP1B1 is associated with concentrations of T₄, FT₃ and FT₄ in the sera of polycystic ovary syndrome patients.
    Molecular biology reports, 2013, Volume: 40, Issue:4

    Topics: Adult; Aryl Hydrocarbon Hydroxylases; Cytochrome P-450 CYP1B1; Estrogens, Catechol; Female; Genetic

2013
[Influence of thyrotropic substances on the appearance and evolution of genetic susceptibility to audiogenic shock].
    Bollettino della Societa italiana di biologia sperimentale, 1961, Jul-15, Volume: 37

    Topics: Biological Evolution; Genetic Predisposition to Disease; Shock; Thyrotrophs; Triiodothyronine

1961
Mice with cardiomyocyte-specific disruption of the endothelin-1 gene are resistant to hyperthyroid cardiac hypertrophy.
    Proceedings of the National Academy of Sciences of the United States of America, 2004, Feb-17, Volume: 101, Issue:7

    Topics: Aging; Alleles; Animals; Cardiomegaly; Endothelin-1; Female; Gene Deletion; Genetic Predisposition t

2004
Anatomical parameters of cardiopulmonary system in three different lines of chickens: further evidence for involvement in ascites syndrome.
    Avian pathology : journal of the W.V.P.A, 2005, Volume: 34, Issue:3

    Topics: Aging; Animals; Ascites; Body Weight; Cardiovascular System; Chickens; Genetic Predisposition to Dis

2005
Comparison of three lines of broilers differing in ascites susceptibility or growth rate. 2. Egg weight loss, gas pressures, embryonic heat production, and physiological hormone levels.
    Poultry science, 2005, Volume: 84, Issue:9

    Topics: Animals; Ascites; Carbon Dioxide; Chick Embryo; Corticosterone; Genetic Predisposition to Disease; H

2005
Identification of DIO2 as a new susceptibility locus for symptomatic osteoarthritis.
    Human molecular genetics, 2008, Jun-15, Volume: 17, Issue:12

    Topics: Female; Genetic Predisposition to Disease; Genome, Human; Humans; Iodide Peroxidase; Iodothyronine D

2008
Association of HLA-DPB1*0501 with early-onset Graves' disease in Japanese.
    Human immunology, 1994, Volume: 39, Issue:3

    Topics: Adolescent; Adult; Disease Susceptibility; Female; Genetic Predisposition to Disease; Graves Disease

1994