thyroxine has been researched along with Genetic Predisposition in 43 studies
Thyroxine: The major hormone derived from the thyroid gland. Thyroxine is synthesized via the iodination of tyrosines (MONOIODOTYROSINE) and the coupling of iodotyrosines (DIIODOTYROSINE) in the THYROGLOBULIN. Thyroxine is released from thyroglobulin by proteolysis and secreted into the blood. Thyroxine is peripherally deiodinated to form TRIIODOTHYRONINE which exerts a broad spectrum of stimulatory effects on cell metabolism.
thyroxine : An iodothyronine compound having iodo substituents at the 3-, 3'-, 5- and 5'-positions.
Excerpt | Relevance | Reference |
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" Administration of the mAbs KSAb1 (IgG2b) or KSAb2 (IgG2a), which have similar stimulating properties but different TSH-binding blocking activity, resulted in significantly elevated serum thyroxine (T(4)) levels and thyroid hyperplasia." | 7.74 | Chronic exposure in vivo to thyrotropin receptor stimulating monoclonal antibodies sustains high thyroxine levels and thyroid hyperplasia in thyroid autoimmunity-prone HLA-DRB1*0301 transgenic mice. ( Banga, JP; David, CS; Flynn, JC; Gilbert, JA; Kong, YC; Meroueh, C; Snower, DP, 2007) |
"A young man was diagnosed with hyperthyroidism 10 years prior to current presentation after a random health screening revealed an elevated free thyroxine (fT4) of 36." | 4.89 | Elevated free thyroxine and non-suppressed thyrotropin. ( Deepak, DS; Loh, TP; Mok, SF; Venkatesh, B, 2013) |
"Subclinical hypothyroidism (SH) is defined as an elevated thyroid stimulating hormone (TSH) in association with a normal total or free thyroxine (T4) or triiodothyronine (T3)." | 4.87 | Subclinical hypothyroidism in childhood. ( Cody, D; O'Grady, MJ, 2011) |
" He had seizures attacks and apnea from the second week of his life." | 3.78 | Early-onset severe obesity with ACTH deficiency and red hair in a boy: the POMC deficiency. ( Aldemir, O; Ozen, S, 2012) |
" Administration of the mAbs KSAb1 (IgG2b) or KSAb2 (IgG2a), which have similar stimulating properties but different TSH-binding blocking activity, resulted in significantly elevated serum thyroxine (T(4)) levels and thyroid hyperplasia." | 3.74 | Chronic exposure in vivo to thyrotropin receptor stimulating monoclonal antibodies sustains high thyroxine levels and thyroid hyperplasia in thyroid autoimmunity-prone HLA-DRB1*0301 transgenic mice. ( Banga, JP; David, CS; Flynn, JC; Gilbert, JA; Kong, YC; Meroueh, C; Snower, DP, 2007) |
" L-thyroxine replacement with suppressive dosage should be employed targeting chronic TSH suppression." | 2.44 | [Thyroid carcinoma in children and adolescents]. ( Calliari, LE; Kochi, C; Longui, CA; Marone, M; Monte, O; Scalisse, NM, 2007) |
"Genotyping was performed on 901 breast cancer patients and 3335 controls." | 1.48 | Thyroid-associated genetic polymorphisms in relation to breast cancer risk in the Malmö Diet and Cancer Study. ( Almgren, P; Borgquist, S; Brandt, J; Försti, A; Huss, L; Manjer, J; Melander, O, 2018) |
"Chronic autoimmune thyroiditis was diagnosed in her mother, subsequently." | 1.35 | [19-year-old patient with adrenal cortex insufficiency--only the tip of the iceberg. Polyendocrine autoimmune syndrome type II (Schmidt syndrome)]. ( Brändle, M; Kehl, O; Lipowsky, C; Schorl-Schweikardt, BA, 2008) |
"GC rats with genetic predisposition to catalepsy were characterized by decreased serum thyroxin content in comparison with Wistar rats." | 1.31 | Thyroid hormone deficiency determines predisposition to catalepsy in rats. ( Alekhina, TA; Barykina, NN; Chugui, VF; Ivanova, EA; Kolpakov, VG; Kulikov, AV; Maksyutova, AV, 2001) |
"HLA alleles of 106 patients with Graves' disease were determined, and the frequency of HLA-B46 was found to be significantly increased." | 1.29 | Association of HLA-DPB1*0501 with early-onset Graves' disease in Japanese. ( Inoko, H; Onuma, H; Ota, M; Sugenoya, A, 1994) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (4.65) | 18.2507 |
2000's | 14 (32.56) | 29.6817 |
2010's | 25 (58.14) | 24.3611 |
2020's | 2 (4.65) | 2.80 |
Authors | Studies |
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Li, GH | 1 |
Tang, CM | 1 |
Cheung, CL | 1 |
Ragusa, F | 1 |
Fallahi, P | 1 |
Elia, G | 1 |
Gonnella, D | 1 |
Paparo, SR | 1 |
Giusti, C | 1 |
Churilov, LP | 1 |
Ferrari, SM | 1 |
Antonelli, A | 1 |
Ellervik, C | 1 |
Mora, S | 1 |
Kuś, A | 1 |
Åsvold, B | 1 |
Marouli, E | 1 |
Deloukas, P | 1 |
Sterenborg, RBTM | 1 |
Teumer, A | 2 |
Burgess, S | 2 |
Sabater-Lleal, M | 1 |
Huffman, J | 1 |
Johnson, AD | 1 |
Trégouet, DA | 1 |
Smith, NL | 1 |
Medici, M | 2 |
DeVries, PS | 1 |
Chasman, DI | 1 |
Kjaergaard, AD | 1 |
Nielsen, TR | 1 |
Appel, EV | 1 |
Svendstrup, M | 1 |
Ohrt, JD | 1 |
Dahl, M | 1 |
Fonvig, CE | 1 |
Hollensted, M | 1 |
Have, CT | 1 |
Kadarmideen, HN | 1 |
Pedersen, O | 1 |
Hansen, T | 1 |
Holm, JC | 1 |
Grarup, N | 1 |
Moran, C | 1 |
Agostini, M | 1 |
McGowan, A | 1 |
Schoenmakers, E | 1 |
Fairall, L | 1 |
Lyons, G | 1 |
Rajanayagam, O | 1 |
Watson, L | 1 |
Offiah, A | 1 |
Barton, J | 1 |
Price, S | 1 |
Schwabe, J | 1 |
Chatterjee, K | 1 |
Szczepanek-Parulska, E | 1 |
Zybek-Kocik, A | 1 |
Wartofsky, L | 1 |
Ruchala, M | 1 |
P Katare, D | 1 |
Malik, S | 1 |
J Mani, R | 1 |
Ranjpour, M | 1 |
Jain, SK | 1 |
Brandt, J | 1 |
Borgquist, S | 1 |
Almgren, P | 1 |
Försti, A | 1 |
Huss, L | 1 |
Melander, O | 1 |
Manjer, J | 1 |
Stanilova, SA | 1 |
Gerenova, JB | 1 |
Miteva, LD | 1 |
Manolova, IM | 1 |
Kim, SH | 1 |
Liu, M | 1 |
Jin, HS | 1 |
Park, S | 1 |
Nelson, PT | 1 |
Gal, Z | 1 |
Wang, WX | 1 |
Niedowicz, DM | 1 |
Artiushin, SC | 1 |
Wycoff, S | 1 |
Wei, A | 1 |
Jicha, GA | 1 |
Fardo, DW | 1 |
Larsson, SC | 1 |
Allara, E | 1 |
Mason, AM | 1 |
Michaëlsson, K | 1 |
Ozen, S | 1 |
Aldemir, O | 1 |
Bengtsson, C | 1 |
Padyukov, L | 1 |
Källberg, H | 1 |
Saevarsdottir, S | 1 |
Carvalho, A | 1 |
Hermanns, P | 1 |
Rodrigues, AL | 1 |
Sousa, I | 1 |
Anselmo, J | 1 |
Bikker, H | 1 |
Cabral, R | 1 |
Pereira-Duarte, C | 1 |
Mota-Vieira, L | 1 |
Pohlenz, J | 1 |
Mok, SF | 1 |
Loh, TP | 1 |
Venkatesh, B | 1 |
Deepak, DS | 1 |
Stevic, MS | 1 |
Stefanic, M | 1 |
Tokic, S | 1 |
Glavas-Obrovac, L | 1 |
Mihaljevic, S | 1 |
Karner, I | 1 |
Schultheiss, UT | 1 |
Li, Y | 1 |
Daya, N | 1 |
Chaker, L | 1 |
Homuth, G | 1 |
Uitterlinden, AG | 2 |
Nauck, M | 1 |
Hofman, A | 1 |
Selvin, E | 1 |
Völzke, H | 1 |
Peeters, RP | 3 |
Köttgen, A | 1 |
Zwaveling-Soonawala, N | 2 |
van Beijsterveldt, CE | 1 |
Mesfum, ET | 1 |
Wiedijk, B | 1 |
Oomen, P | 1 |
Finken, MJ | 1 |
Boomsma, DI | 1 |
van Trotsenburg, AS | 2 |
Luo, M | 1 |
Zhou, XH | 1 |
Zou, T | 1 |
Keyim, K | 1 |
Dong, LM | 1 |
Su, Y | 1 |
Wang, J | 1 |
Zhou, J | 1 |
Chen, Y | 1 |
Zhao, H | 1 |
Zeng, Y | 1 |
Lin, F | 1 |
Zhang, H | 1 |
Zhu, W | 1 |
Chen, H | 1 |
van Gucht, AL | 1 |
Meima, ME | 1 |
Visser, WE | 1 |
Fliers, E | 1 |
Wennink, JM | 1 |
Henny, C | 1 |
Visser, TJ | 2 |
Vaurs-Barrière, C | 1 |
Deville, M | 1 |
Sarret, C | 1 |
Giraud, G | 1 |
Des Portes, V | 1 |
Prats-Viñas, JM | 1 |
De Michele, G | 1 |
Dan, B | 1 |
Brady, AF | 1 |
Boespflug-Tanguy, O | 1 |
Touraine, R | 1 |
Gudmundsson, J | 1 |
Sulem, P | 1 |
Gudbjartsson, DF | 1 |
Jonasson, JG | 1 |
Sigurdsson, A | 1 |
Bergthorsson, JT | 1 |
He, H | 1 |
Blondal, T | 1 |
Geller, F | 1 |
Jakobsdottir, M | 1 |
Magnusdottir, DN | 1 |
Matthiasdottir, S | 1 |
Stacey, SN | 1 |
Skarphedinsson, OB | 1 |
Helgadottir, H | 1 |
Li, W | 1 |
Nagy, R | 1 |
Aguillo, E | 1 |
Faure, E | 1 |
Prats, E | 1 |
Saez, B | 1 |
Martinez, M | 1 |
Eyjolfsson, GI | 1 |
Bjornsdottir, US | 1 |
Holm, H | 1 |
Kristjansson, K | 1 |
Frigge, ML | 1 |
Kristvinsson, H | 1 |
Gulcher, JR | 1 |
Jonsson, T | 1 |
Rafnar, T | 1 |
Hjartarsson, H | 1 |
Mayordomo, JI | 1 |
de la Chapelle, A | 1 |
Hrafnkelsson, J | 1 |
Thorsteinsdottir, U | 1 |
Kong, A | 1 |
Stefansson, K | 1 |
Zubkov, EA | 1 |
Kulikov, AV | 3 |
Daroszewski, J | 1 |
Pawlak, E | 1 |
Karabon, L | 1 |
Frydecka, I | 1 |
Jonkisz, A | 1 |
Slowik, M | 1 |
Bolanowski, M | 1 |
O'Grady, MJ | 1 |
Cody, D | 1 |
Rooke, JA | 1 |
Houdijk, JG | 1 |
McIlvaney, K | 1 |
Ashworth, CJ | 1 |
Dwyer, CM | 1 |
Stoppa-Vaucher, S | 1 |
Van Vliet, G | 1 |
Deladoëy, J | 1 |
Everaert, N | 1 |
Willemsen, H | 1 |
Debonne, M | 1 |
Witters, A | 1 |
Kamers, B | 1 |
Darras, VM | 1 |
de Baerdemaeker, J | 1 |
Decuypere, E | 3 |
Bruggeman, V | 2 |
Zou, S | 1 |
Sang, Q | 1 |
Wang, H | 1 |
Feng, R | 1 |
Li, Q | 1 |
Zhao, X | 1 |
Xing, Q | 1 |
Jin, L | 1 |
He, L | 1 |
Wang, L | 1 |
Hassanzadeh, M | 2 |
Gilanpour, H | 1 |
Charkhkar, S | 1 |
Buyse, J | 1 |
De Smit, L | 1 |
Tona, K | 1 |
Onagbesan, O | 1 |
Arckens, L | 1 |
Seetharamaiah, GS | 1 |
Land, KJ | 1 |
van der Deure, WM | 1 |
van den Beld, AW | 1 |
van Toor, H | 1 |
Lamberts, SW | 1 |
Janssen, JA | 1 |
Flynn, JC | 1 |
Gilbert, JA | 1 |
Meroueh, C | 1 |
Snower, DP | 1 |
David, CS | 1 |
Kong, YC | 1 |
Banga, JP | 1 |
Monte, O | 1 |
Calliari, LE | 1 |
Kochi, C | 1 |
Scalisse, NM | 1 |
Marone, M | 1 |
Longui, CA | 1 |
Santos, RB | 1 |
Melo, TG | 1 |
Assumpção, LV | 1 |
Lipowsky, C | 1 |
Schorl-Schweikardt, BA | 1 |
Kehl, O | 1 |
Brändle, M | 1 |
Onuma, H | 1 |
Ota, M | 1 |
Sugenoya, A | 1 |
Inoko, H | 1 |
Heward, JM | 1 |
Allahabadia, A | 1 |
Armitage, M | 1 |
Hattersley, A | 1 |
Dodson, PM | 1 |
Macleod, K | 1 |
Carr-Smith, J | 1 |
Daykin, J | 1 |
Daly, A | 1 |
Sheppard, MC | 1 |
Holder, RL | 1 |
Barnett, AH | 1 |
Franklyn, JA | 1 |
Gough, SC | 1 |
Barykina, NN | 2 |
Chugui, VF | 1 |
Alekhina, TA | 2 |
Kolpakov, VG | 2 |
Ivanova, EA | 1 |
Maksyutova, AV | 1 |
Chuguy, VF | 1 |
Maksiutova, AV | 1 |
7 reviews available for thyroxine and Genetic Predisposition
Article | Year |
---|---|
Hashimotos' thyroiditis: Epidemiology, pathogenesis, clinic and therapy.
Topics: Genetic Predisposition to Disease; Hashimoto Disease; Hormone Replacement Therapy; Humans; Hypothyro | 2019 |
Thyroid Hemiagenesis: Incidence, Clinical Significance, and Genetic Background.
Topics: Animals; DNA-Binding Proteins; Female; Genetic Background; Genetic Predisposition to Disease; Humans | 2017 |
Thyroid Function and Dysfunction in Relation to 16 Cardiovascular Diseases.
Topics: Atrial Fibrillation; Cardiovascular Diseases; Databases, Factual; Genetic Predisposition to Disease; | 2019 |
Elevated free thyroxine and non-suppressed thyrotropin.
Topics: Adult; Carbimazole; Drug Resistance; Follow-Up Studies; Genetic Predisposition to Disease; Humans; H | 2013 |
Subclinical hypothyroidism in childhood.
Topics: Child; Child, Preschool; Down Syndrome; Genetic Predisposition to Disease; Hormone Replacement Thera | 2011 |
[Thyroid carcinoma in children and adolescents].
Topics: Adolescent; Carcinoma, Papillary; Child; Female; Genetic Predisposition to Disease; Humans; Iodine R | 2007 |
[Familial nommedullary thyroid cancer].
Topics: Adenocarcinoma, Follicular; Age Factors; Carcinoma, Papillary; Early Diagnosis; Female; Genetic Pred | 2007 |
1 trial available for thyroxine and Genetic Predisposition
Article | Year |
---|---|
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.
Topics: Animal Nutritional Physiological Phenomena; Animals; Breeding; Female; Genetic Predisposition to Dis | 2010 |
35 other studies available for thyroxine and Genetic Predisposition
Article | Year |
---|---|
COVID-19 and Thyroid Function: A Bi-Directional Two-Sample Mendelian Randomization Study.
Topics: COVID-19; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Hyperthyroidism; | 2022 |
Effects of Thyroid Function on Hemostasis, Coagulation, and Fibrinolysis: A Mendelian Randomization Study.
Topics: Autoantibodies; Biomarkers; Blood Coagulation; Blood Coagulation Factors; Blood Coagulation Tests; C | 2021 |
A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents.
Topics: Adolescent; Adult; Age Factors; Body Mass Index; Child; Child, Preschool; Denmark; Female; Genetic L | 2017 |
Contrasting Phenotypes in Resistance to Thyroid Hormone Alpha Correlate with Divergent Properties of Thyroid Hormone Receptor α1 Mutant Proteins.
Topics: Adolescent; Genetic Predisposition to Disease; Genotype; Humans; Male; Mutation; Phenotype; Symptom | 2017 |
Novel mutations in transthyretin gene associated with hepatocellular carcinoma.
Topics: 2-Acetylaminofluorene; Amino Acid Sequence; Animals; Apolipoprotein A-I; Biomarkers, Tumor; Carcinom | 2018 |
Thyroid-associated genetic polymorphisms in relation to breast cancer risk in the Malmö Diet and Cancer Study.
Topics: Adult; Aged; Autoantibodies; Breast Neoplasms; Case-Control Studies; Female; Genetic Predisposition | 2018 |
The Role of Transforming Growth Factor-β1 Gene Polymorphism and Its Serum Levels in Hashimoto's Thyroiditis.
Topics: Biomarkers; Enzyme-Linked Immunosorbent Assay; Female; Genetic Markers; Genetic Predisposition to Di | 2018 |
High Genetic Risk Scores of ASIC2, MACROD2, CHRM3, and C2orf83 Genetic Variants Associated with Polycystic Ovary Syndrome Impair Insulin Sensitivity and Interact with Energy Intake in Korean Women.
Topics: Acid Sensing Ion Channels; Adult; Blood Glucose; Body Mass Index; C-Reactive Protein; Cohort Studies | 2019 |
TDP-43 proteinopathy in aging: Associations with risk-associated gene variants and with brain parenchymal thyroid hormone levels.
Topics: Aged; Aged, 80 and over; Aging; Brain; Female; Genetic Predisposition to Disease; Humans; Male; Midd | 2019 |
Early-onset severe obesity with ACTH deficiency and red hair in a boy: the POMC deficiency.
Topics: Adrenal Insufficiency; Adrenocorticotropic Hormone; Anti-Inflammatory Agents; Apnea; Caloric Restric | 2012 |
Thyroxin substitution and the risk of developing rheumatoid arthritis; results from the Swedish population-based EIRA study.
Topics: Adolescent; Adult; Aged; Arthritis, Rheumatoid; Autoantibodies; Case-Control Studies; Female; Geneti | 2014 |
A new PAX8 mutation causing congenital hypothyroidism in three generations of a family is associated with abnormalities in the urogenital tract.
Topics: Adult; Child, Preschool; Congenital Hypothyroidism; DNA Mutational Analysis; Genetic Predisposition | 2013 |
Pilot study of variants of the IL-23R and STAT3 genes reveals no association with Hashimoto's thyroiditis in the Croatian population.
Topics: Adult; Amino Acid Substitution; Case-Control Studies; Cohort Studies; Croatia; Female; Follow-Up Stu | 2014 |
A genetic risk score for thyroid peroxidase antibodies associates with clinical thyroid disease in community-based populations.
Topics: Female; Genetic Predisposition to Disease; Genome-Wide Association Study; Humans; Iodide Peroxidase; | 2015 |
Fetal Environment Is a Major Determinant of the Neonatal Blood Thyroxine Level: Results of a Large Dutch Twin Study.
Topics: Diseases in Twins; Environment; Female; Fetal Development; Genetic Predisposition to Disease; Humans | 2015 |
Type II deiodinase polymorphisms and serum thyroid hormone levels in patients with mild cognitive impairment.
Topics: Adult; Cognitive Dysfunction; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; H | 2015 |
[Association of thyroperoxidase gene polymorphisms with dyshormonogenesis in congenital hypothyroidism].
Topics: Alleles; Autoantigens; Base Sequence; Child, Preschool; Congenital Hypothyroidism; Female; Gene Freq | 2015 |
Resistance to Thyroid Hormone Alpha in an 18-Month-Old Girl: Clinical, Therapeutic, and Molecular Characteristics.
Topics: Cell Line; Child Development; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Hu | 2016 |
Pelizaeus-Merzbacher-Like disease presentation of MCT8 mutated male subjects.
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.
Topics: Chromosome Mapping; Chromosomes, Human, Pair 4; Chromosomes, Human, Pair 9; DNA-Binding Proteins; Eu | 2009 |
Effect of thyroxin on behavior of mice with inherited difference in predisposition to catalepsy.
Topics: Animals; Antidepressive Agents; Behavior, Animal; Catalepsy; Genetic Predisposition to Disease; Male | 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.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Antigens, CD; Cohort Studies; CTLA-4 Antigen; DNA; Femal | 2009 |
Variation by ethnicity in the prevalence of congenital hypothyroidism due to thyroid dysgenesis.
Topics: Age Factors; Case-Control Studies; Congenital Hypothyroidism; Ethnicity; Genetic Predisposition to D | 2011 |
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.
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.
Topics: Adult; Aryl Hydrocarbon Hydroxylases; Cytochrome P-450 CYP1B1; Estrogens, Catechol; Female; Genetic | 2013 |
Anatomical parameters of cardiopulmonary system in three different lines of chickens: further evidence for involvement in ascites syndrome.
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.
Topics: Animals; Ascites; Carbon Dioxide; Chick Embryo; Corticosterone; Genetic Predisposition to Disease; H | 2005 |
Differential Susceptibility of BALB/c and BALB/cBy mice to Graves' hyperthyroidism.
Topics: Adenoviridae; Animals; Cytokines; Disease Models, Animal; Enzyme-Linked Immunosorbent Assay; Genetic | 2006 |
The Asp727Glu polymorphism in the TSH receptor is associated with insulin resistance in healthy elderly men.
Topics: Age Factors; Aged; Analysis of Variance; Biomarkers; Blood Glucose; Body Composition; Gene Frequency | 2007 |
Chronic exposure in vivo to thyrotropin receptor stimulating monoclonal antibodies sustains high thyroxine levels and thyroid hyperplasia in thyroid autoimmunity-prone HLA-DRB1*0301 transgenic mice.
Topics: Animals; Antibodies, Monoclonal; Autoimmunity; Drug Administration Schedule; Female; Genetic Predisp | 2007 |
[19-year-old patient with adrenal cortex insufficiency--only the tip of the iceberg. Polyendocrine autoimmune syndrome type II (Schmidt syndrome)].
Topics: Addison Disease; Adrenocorticotropic Hormone; Adult; Cortisone; Diagnosis, Differential; Drug Therap | 2008 |
Association of HLA-DPB1*0501 with early-onset Graves' disease in Japanese.
Topics: Adolescent; Adult; Disease Susceptibility; Female; Genetic Predisposition to Disease; Graves Disease | 1994 |
The development of Graves' disease and the CTLA-4 gene on chromosome 2q33.
Topics: Abatacept; Alanine; Alleles; Antigens, CD; Antigens, Differentiation; Case-Control Studies; Chromoso | 1999 |
Thyroid hormone deficiency determines predisposition to catalepsy in rats.
Topics: Animals; Catalepsy; Genetic Predisposition to Disease; Genotype; Humans; Male; Rats; Rats, Wistar; T | 2001 |
Effects of thyroid hormone deficiency on behavior in rat strains with different predisposition to catalepsy.
Topics: Analysis of Variance; Animals; Behavior, Animal; Catalepsy; Genetic Predisposition to Disease; Locom | 2002 |