وحيدة بيتا لهرمونات البروتين السكري (TSHB) أو هرمون تنشيط الغدة الدرقية، بيتا (بالإنجليزية: Thyroid stimulating hormone, beta) المعروف أيضا باسم TSHB، هو بروتين في البشر مُشفّر بالجينTSHB.[1][2]
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Miyoshi I, Kasai N, Hayashizaki Y (1994)، "[Structure and regulation of human thyroid-stimulating hormone (TSH) gene]"، Nippon Rinsho، 52 (4): 940–7، PMID8196184.
Borck G, Topaloglu AK, Korsch E, وآخرون (2004)، "Four new cases of congenital secondary hypothyroidism due to a splice site mutation in the thyrotropin-beta gene: phenotypic variability and founder effect"، J. Clin. Endocrinol. Metab.، 89 (8): 4136–41، doi:10.1210/jc.2004-0494، PMID15292359.
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Brumm H, Pfeufer A, Biebermann H, وآخرون (2002)، "Congenital central hypothyroidism due to homozygous thyrotropin beta 313 Delta T mutation is caused by a Founder effect"، J. Clin. Endocrinol. Metab.، 87 (10): 4811–6، doi:10.1210/jc.2002-020297، PMID12364478.
Benhadi N, Wiersinga WM, Reitsma JB, وآخرون (2009)، "Higher maternal TSH levels in pregnancy are associated with increased risk for miscarriage, fetal or neonatal death"، Eur. J. Endocrinol.، 160 (6): 985–91، doi:10.1530/EJE-08-0953، PMID19273570.
^Tatsumi K, Hayashizaki Y, Hiraoka Y, Miyai K, Matsubara K (ديسمبر 1988)، "The structure of the human thyrotropin beta-subunit gene"، Gene، 73 (2): 489–97، doi:10.1016/0378-1119(88)90513-6، PMID3243440.