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Thyroid Stimulating Hormone, beta (TSH beta) (Pituitary Marker) Recombinant Monoclonal Antibody (TSHb/7001R) (7252-RBM3-P0)
NR4A1 (Nur77) Mediates Thyrotropin-Releasing Hormone-Induced Stimulation of Transcription of the Thyrotropin β Gene: Analysis of TRH Knockout Mice | PLOS ONE
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IJMS | Free Full-Text | The Pathogenic TSH β-Subunit Variant C105Vfs114X Causes a Modified Signaling Profile at TSHR
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Changes in thyroid hormone levels and related gene expressions in embryo–larval zebrafish exposed to binary combinations of bifenthrin and acetochlor | SpringerLink
Thyrotropin (TSH)-Releasing Hormone-Responsive Elements in the Rat TSHP Gene Have Distinct Biological and Nuclear Protein- Bindi
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A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING
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The syndrome of central hypothyroidism and macroorchidism: IGSF1 controls TRHR and FSHB expression by differential modulation of pituitary TGFβ and Activin pathways | Scientific Reports
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IJMS | Free Full-Text | The Pathogenic TSH β-Subunit Variant C105Vfs114X Causes a Modified Signaling Profile at TSHR
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Figure 13. [The regulatory region of human TSHB gene (see text for details)]. - Endotext - NCBI Bookshelf
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Molecular spectrum of TSHβ subunit gene defects in central hypothyroidism in the UK and Ireland - Nicholas - 2017 - Clinical Endocrinology - Wiley Online Library
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Thyroid-Stimulating Hormone and Thyroid-Stimulating Hormone Receptor Structure-Function Relationships | Semantic Scholar
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Visor Redalyc - A RECURRENT MUTATION IN TSHB GENE UNDERLYING CENTRAL CONGENITAL HYPOTHYROIDISM UNDETECTABLE IN NEONATAL SCREENING
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TSHB R75G is a founder variant and prevalent cause of low or undetectable TSH in Indian Jews in: European Thyroid Journal Volume 11 Issue 1 (2022)
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