Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
The TRH gene encodes thyrotropin releasing hormone, mutations of which cause hypothalamic hypothyreosis.
| Clinic | Method | Carrier testing |
| Turnaround | 5 days | |
| Specimen type | genomic DNA |
| Research | Method | Genomic sequencing of the entire coding region |
| Turnaround | 25 days | |
| Specimen type | genomic DNA |
| 1. |
Krashes MJ et al. (2014) An excitatory paraventricular nucleus to AgRP neuron circuit that drives hunger. 
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| 2. |
Yamada M et al. (1991) Assignment of human preprothyrotropin-releasing hormone (TRH) gene to chromosome 3.
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| 3. |
Yamada M et al. (1990) Cloning and structure of human genomic DNA and hypothalamic cDNA encoding human prepro thyrotropin-releasing hormone.
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| 4. |
Roller ML et al. (1995) Localization of the thyrotropin-releasing hormone gene, Trh, on mouse chromosome 6.
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| 5. |
Yamada M et al. (1999) Assignment of the thyrotropin-releasing hormone gene (TRH) to human chromosome 3q13.3-->q21 by in situ hybridization.
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| 6. |
Gáspár E et al. (2010) Thyrotropin releasing hormone (TRH): a new player in human hair-growth control.
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| 7. |
NCBI article NCBI 7200
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| 8. |
OMIM.ORG article Omim 613879
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| 9. |
Orphanet article Orphanet ID 120259
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| 10. |
Wikipedia article Wikipedia EN (Thyrotropin-releasing_hormone)
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