thyroxine has been researched along with Chromosome Deletion in 8 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.
Chromosome Deletion: Actual loss of portion of a chromosome.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The liver dysfunction was associated with hypothyroidism that resolved with thyroid hormone treatment." | 5.38 | Hypothyroidism and levothyroxine-responsive liver dysfunction in a patient with ring chromosome 18 syndrome. ( Hara, T; Ihara, K; Ishimura, M; Ohga, S; Ohkubo, K, 2012) |
| "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) |
| "The liver dysfunction was associated with hypothyroidism that resolved with thyroid hormone treatment." | 1.38 | Hypothyroidism and levothyroxine-responsive liver dysfunction in a patient with ring chromosome 18 syndrome. ( Hara, T; Ihara, K; Ishimura, M; Ohga, S; Ohkubo, K, 2012) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (25.00) | 18.7374 |
| 1990's | 3 (37.50) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 3 (37.50) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Thompson, MD | 1 |
| Henry, RK | 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 |
| Ohkubo, K | 1 |
| Ihara, K | 1 |
| Ohga, S | 1 |
| Ishimura, M | 1 |
| Hara, T | 1 |
| Jones, KL | 1 |
| Carey, DE | 1 |
| Andler, W | 1 |
| Heüveldop, A | 1 |
| Polichronidou, T | 1 |
| Ono, S | 1 |
| Schwartz, ID | 1 |
| Mueller, OT | 1 |
| Root, AW | 1 |
| Usala, SJ | 1 |
| Bercu, BB | 1 |
| Yamamori, I | 1 |
| Mori, Y | 1 |
| Seo, H | 1 |
| Hirooka, Y | 1 |
| Imamura, S | 1 |
| Miura, Y | 1 |
| Matsui, N | 1 |
| Oiso, Y | 1 |
| Medeiros-Neto, G | 1 |
| Targovnik, H | 1 |
| Knobel, M | 1 |
| Propato, F | 1 |
| Varela, V | 1 |
| Alkmin, M | 1 |
| Barbosa, S | 1 |
| Wajchenberg, BL | 1 |
8 other studies available for thyroxine and Chromosome Deletion
| Article | Year |
|---|---|
Myxedema Coma Secondary to Central Hypothyroidism: A Rare but Real Cause of Altered Mental Status in Pediatrics.
Topics: Agenesis of Corpus Callosum; Cerebral Cortex; Child; Chromosome Deletion; Chromosomes, Human, Pair 1 | 2017 |
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 |
Hypothyroidism and levothyroxine-responsive liver dysfunction in a patient with ring chromosome 18 syndrome.
Topics: Child; Child, Preschool; Chromosome Deletion; Chromosome Disorders; Chromosomes, Human, Pair 18; Hep | 2012 |
Brief clinical report: Graves disease in a patient with the del(18p) syndrome.
Topics: Adolescent; Autoimmune Diseases; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; | 1982 |
[Endocrinologic disorders in deletion of chromosome 18].
Topics: Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 18; Dwarfism, Pituitary; Female; Gro | 1992 |
Homozygosity for a dominant negative thyroid hormone receptor gene responsible for generalized resistance to thyroid hormone.
Topics: Adolescent; Adult; Cells, Cultured; Child, Preschool; Chromosome Deletion; DNA; DNA Restriction Enzy | 1991 |
Nucleotide deletion resulting in frameshift as a possible cause of complete thyroxine-binding globulin deficiency in six Japanese families.
Topics: Amino Acid Sequence; Base Sequence; Chromosome Deletion; DNA; Female; Frameshift Mutation; Humans; J | 1991 |
Qualitative and quantitative defects of thyroglobulin resulting in congenital goiter. Absence of gross gene deletion of coding sequences in the TG gene structure.
Topics: Adolescent; Adult; Blotting, Southern; Child; Child, Preschool; Chromatography, Gel; Chromosome Dele | 1989 |