thyroxine has been researched along with Abnormalities, Autosome in 27 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 |
|---|---|---|
| "We have studied the largest kindred with familial dysalbuminemic hyperthyroxinemia (FDH) thus far reported, comprising thirty-three blood relations in four generations and three of their spouses." | 7.67 | A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin. ( Braverman, LE; Etzkorn, JR; Ingbar, SH; Rajatanavin, R; Yabu, Y; Yeo, PP, 1987) |
| "We have studied the largest kindred with familial dysalbuminemic hyperthyroxinemia (FDH) thus far reported, comprising thirty-three blood relations in four generations and three of their spouses." | 3.67 | A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin. ( Braverman, LE; Etzkorn, JR; Ingbar, SH; Rajatanavin, R; Yabu, Y; Yeo, PP, 1987) |
| " The affected family members were clinically euthyroid but all had goiters and markedly increased serum thyroid hormone levels: thyroxine (T4) = 21." | 3.66 | Familial thyroid hormone resistance. ( Barbato, AL; Brooks, MH; Collins, S; Garbincius, J; Hoffman, D; Neidballa, RG, 1981) |
| "Variably penetrant pituitary insufficiency, including this severe and atypical presentation, can be correlated with LHX4 insufficiency and highlights the role of LHX4 for pituitary development." | 1.38 | Panhypopituitarism presenting as life-threatening heart failure caused by an inherited microdeletion in 1q25 including LHX4. ( Bischof-Renner, A; Filges, I; Glanzmann, R; Günthard, J; Huber, AR; Miny, P; Potthoff, C; Röthlisberger, B; Schneider, J; Szinnai, G; Zumsteg, U, 2012) |
| "A case of the rare genetic trisomy 22 in a live calf is described." | 1.30 | A case of trisomy 22 in a live hereford calf. ( Christensen, K; Juul, L, 1999) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 19 (70.37) | 18.7374 |
| 1990's | 3 (11.11) | 18.2507 |
| 2000's | 1 (3.70) | 29.6817 |
| 2010's | 4 (14.81) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| da Silva, MA | 1 |
| Valgôde, FG | 1 |
| Gonzalez, JA | 1 |
| Yoriyaz, H | 1 |
| Guimarães, MI | 1 |
| Ribela, MT | 1 |
| Buchpiguel, CA | 1 |
| Bartolini, P | 1 |
| Okazaki, K | 1 |
| Kini, U | 1 |
| Hurst, JA | 1 |
| Byren, JC | 1 |
| Wall, SA | 1 |
| Johnson, D | 1 |
| Wilkie, AO | 1 |
| Kameda, G | 2 |
| Knauer-Fischer, S | 1 |
| Kaminsky, E | 1 |
| Mayatepek, E | 1 |
| Meissner, T | 1 |
| Filges, I | 1 |
| Bischof-Renner, A | 1 |
| Röthlisberger, B | 1 |
| Potthoff, C | 1 |
| Glanzmann, R | 1 |
| Günthard, J | 1 |
| Schneider, J | 1 |
| Huber, AR | 1 |
| Zumsteg, U | 1 |
| Miny, P | 1 |
| Szinnai, G | 1 |
| Sharghi, S | 1 |
| Haghpanah, V | 1 |
| Heshmat, R | 1 |
| Fard-Esfahani, A | 1 |
| Hadizadeh, H | 1 |
| Lashkari, A | 1 |
| Tabatabaei, O | 1 |
| Taheri, E | 1 |
| Motesaddi, M | 1 |
| Mojtahedi, A | 1 |
| Larijani, B | 1 |
| Bösze, P | 1 |
| Kóvacs, Z | 1 |
| Egyed, J | 1 |
| László, J | 1 |
| Szilágyi, G | 1 |
| Brooks, MH | 1 |
| Barbato, AL | 1 |
| Collins, S | 1 |
| Garbincius, J | 1 |
| Neidballa, RG | 1 |
| Hoffman, D | 1 |
| Penhaligon, J | 1 |
| Wellby, ML | 1 |
| Jones, KL | 1 |
| Carey, DE | 1 |
| Christensen, K | 1 |
| Juul, L | 1 |
| Khan, F | 1 |
| Verma, RS | 1 |
| Dosik, H | 1 |
| Warman, J | 1 |
| Hasen, J | 1 |
| Bartalos, M | 1 |
| Nilsson, C | 1 |
| Hansson, A | 1 |
| Nilsson, G | 1 |
| Thorpe-Beeston, JG | 1 |
| Nicolaides, KH | 1 |
| Gosden, CM | 1 |
| McGregor, AM | 1 |
| Grodum, E | 1 |
| Kvetny, J | 1 |
| Bollerslev, J | 1 |
| Antipenko, EN | 2 |
| Timchenko, OI | 1 |
| Yeo, PP | 1 |
| Yabu, Y | 1 |
| Etzkorn, JR | 1 |
| Rajatanavin, R | 1 |
| Braverman, LE | 1 |
| Ingbar, SH | 1 |
| van Buul, PP | 1 |
| van Buul-Offers, SC | 1 |
| Lizarralde, G | 1 |
| Jones, B | 1 |
| Seal, US | 1 |
| Jones, JE | 1 |
| Luchsinger, U | 1 |
| Bühler, E | 1 |
| Méhes, K | 1 |
| Stalder, G | 1 |
| Burns, JK | 1 |
| Judin, GI | 1 |
| Chopra, IJ | 1 |
| Solomon, DH | 1 |
| Ho, RS | 1 |
| Nishikawa, M | 1 |
| Ito, S | 1 |
| Sano, K | 1 |
| Nishioeda, Y | 1 |
| Nasako, Y | 1 |
| Wu, C | 1 |
| al-Saadi, AA | 1 |
| Ling, RC | 1 |
| McKinnie, KL | 1 |
| Cross, HE | 1 |
| Hollander, CS | 1 |
| Rimoin, DL | 1 |
| McKusick, VA | 1 |
| Kitlak, W | 1 |
| Gebert, P | 1 |
1 review available for thyroxine and Abnormalities, Autosome
| Article | Year |
|---|---|
[Substantiation of the necessity and possibility of studying the genetic risk of low energy physical factors].
Topics: Animals; Chromosome Aberrations; Electromagnetic Phenomena; Humans; Mutation; Noise; Radiation Dosag | 1989 |
26 other studies available for thyroxine and Abnormalities, Autosome
| Article | Year |
|---|---|
Cytogenetic and dosimetric effects of (131)I in patients with differentiated thyroid carcinoma: comparison between stimulation with rhTSH and thyroid hormone withdrawal treatments.
Topics: Adult; Chromosome Aberrations; Dose-Response Relationship, Radiation; Humans; Iodine Radioisotopes; | 2016 |
Etiological heterogeneity and clinical characteristics of metopic synostosis: Evidence from a tertiary craniofacial unit.
Topics: Adolescent; Anticoagulants; Child; Child, Preschool; Chromosome Aberrations; Craniosynostoses; Enoxa | 2010 |
Detection of a mutation in the thyroid hormone receptor beta gene as a cause of pathological laboratory test results in an euthyreotic toddler.
Topics: Alleles; Chromosome Aberrations; Chromosomes, Human, Pair 3; Codon; DNA Mutational Analysis; Exons; | 2010 |
Panhypopituitarism presenting as life-threatening heart failure caused by an inherited microdeletion in 1q25 including LHX4.
Topics: Alleles; Chromosome Aberrations; Chromosome Deletion; Chromosomes, Human, Pair 1; Drug Therapy, Comb | 2012 |
Comparison of MRI findings with traditional criteria in diagnosis of Pendred syndrome.
Topics: Adolescent; Adult; Chromosome Aberrations; Female; Genes, Recessive; Genotype; Hearing Loss, Sensori | 2007 |
Thyrotrophin and prolactin responses to thyrotrophin-releasing hormone in patients with streak gonad syndrome.
Topics: Adolescent; Adult; Chromosome Aberrations; Female; Gonadal Dysgenesis; Humans; Male; Prolactin; Thyr | 1983 |
Familial thyroid hormone resistance.
Topics: Adolescent; Adult; Child; Chromosome Aberrations; Chromosome Disorders; Female; Genes, Dominant; Goi | 1981 |
Elevated serum thyroxine-binding globulin by X-chromosome transmission.
Topics: Adult; Chromosome Aberrations; Female; Genetic Linkage; Humans; Hyperthyroidism; Pedigree; Sex Chrom | 1982 |
Brief clinical report: Graves disease in a patient with the del(18p) syndrome.
Topics: Adolescent; Autoimmune Diseases; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; | 1982 |
A case of trisomy 22 in a live hereford calf.
Topics: Animals; Aorta; Cattle; Chromosome Aberrations; Chromosome Banding; Clitoris; Esotropia; Female; Thy | 1999 |
Primary amenorrhea in a black female with duplication and inversion of the secondary constriction regions of chromosome 9.
Topics: Adult; Amenorrhea; Androgens; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 6-12 | 1978 |
Dyshormonogenetic goitrous hypothyroidism in a patient with short arm deletion of E18 chromosome.
Topics: Adolescent; Adult; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Chromosome | 1975 |
Influence of thyroid hormones on satellite association in man and the origin of chromosome abnormalities.
Topics: Adult; Cells, Cultured; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Chr | 1975 |
Thyroid function in fetuses with chromosomal abnormalities.
Topics: Chromosome Aberrations; Chromosome Disorders; Fetal Blood; Fetal Diseases; Gestational Age; Humans; | 1991 |
Decreased thyroid hormone-stimulated oxygen consumption and glucose uptake in mononuclear blood cells from patients with autosomal dominant osteopetrosis type I.
Topics: Adult; Aged; Blood Glucose; Cells, Cultured; Chromosome Aberrations; Chromosome Disorders; Female; G | 1991 |
A four generation study of familial dysalbuminemic hyperthyroxinemia: diagnosis in the presence of an acquired excess of thyroxine-binding globulin.
Topics: Aged; Blood Protein Disorders; Chromosome Aberrations; Chromosome Disorders; Contraceptives, Oral; F | 1987 |
Effects of hormone treatment on chromosomal radiosensitivity of somatic and germ cells of Snell's dwarf mice.
Topics: Animals; Cell Nucleus; Chromosome Aberrations; Dwarfism, Pituitary; Erythropoiesis; Growth Hormone; | 1988 |
Goitrous cretinism with chromosomal aberration and defect in thyroglobulin synthesis.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Chromatography, Gel; Chromosome Aberrations; Chromosome | 1966 |
[Satellite associations in autosomal and gonosomal chromosome abnormalities and in hypothyreosis].
Topics: Adolescent; Adult; Child; Child, Preschool; Chromosome Aberrations; Cytogenetics; Down Syndrome; Fem | 1969 |
Proceedings: Examination of chromosomes following addition of hormones to human leucocyte cultures.
Topics: Cells, Cultured; Chromosome Aberrations; Chromosomes; Dehydroepiandrosterone; Estriol; Follicle Stim | 1974 |
Post-irradiation restoration of somatic cell chromosomes in mammals. The influence of thyroxine on the frequency of chromosome aberrations in liver cells of rats.
Topics: Animals; Chromosome Aberrations; Dose-Response Relationship, Radiation; Hepatectomy; Liver; Liver Re | 1972 |
Competitive ligand-binding assay for measurement of thyronine-binding globulin (TBG).
Topics: Animals; Binding Sites; Cattle; Chromosome Aberrations; Chromosome Disorders; Dogs; Female; Graves D | 1972 |
A case of familial cystathioninuria with goiter and some anomalies.
Topics: Abnormalities, Multiple; Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Animals; Chr | 1970 |
Some biochemical and cytogenetic properties of rat thyroid tumors.
Topics: Amino Acids; Aneuploidy; Animals; Chromosome Aberrations; Iodine; Iodine Isotopes; Karyotyping; Mono | 1971 |
Familial agoitrous cretinism accompanied by musclar hypertrophy.
Topics: Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Congenital Hypothyroidism; Fe | 1968 |
[Clinical and chromosomal studies in a congenital hypothyroidism caused by thyroxin synthesis disorders and middle ear hearing disorders (Pendred- or goiter-deafness syndrome)].
Topics: Adult; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Deafness; Female; Goit | 1968 |