PubMed for id: 6906

Year	Number of Results
1977	1
1986	1
1988	1
1989	2
1990	2
1991	5
1992	2
1993	3
1995	3
1998	2
2000	2
2001	1
2002	4
2003	1
2004	2
2005	2
2007	1
2008	1
2009	2
2010	1
2011	2
2012	1
2013	5
2015	2
2016	1
2017	3
2018	1
2020	2
2021	4
2022	3
2024	0

1

Identification of Mutations in the Thyroxine-Binding Globulin (TBG) Gene in Patients with TBG Deficiency in Korea.

Heo J, Kim SM, Ryu HJ, Park H, Kim TH, Chung JH, Park HD, Kim SW. Heo J, et al. Endocrinol Metab (Seoul). 2022 Dec;37(6):870-878. doi: 10.3803/EnM.2022.1591. Epub 2022 Dec 7. Endocrinol Metab (Seoul). 2022. PMID: 36475360 Free PMC article.

2

Identification of a novel mutation in thyroxine-binding globulin (TBG) gene associated with TBG-deficiency and its effect on the thyroid function.

Gawandi S, Jothivel K, Kulkarni S. Gawandi S, et al. J Endocrinol Invest. 2022 Apr;45(4):731-739. doi: 10.1007/s40618-021-01697-z. Epub 2021 Nov 10. J Endocrinol Invest. 2022. PMID: 34761328

3

The decrease of T3 / T4 is not hypothyroidism - a new mutation of Serpina7 gene results in partial thyroglobulin deficiency.

Cao L, Lou X, Zhou L, Wu Y. Cao L, et al. Pharmazie. 2021 Sep 1;76(9):428-430. doi: 10.1691/ph.2021.1559. Pharmazie. 2021. PMID: 34481533

4

Compound hemizygous variants in SERPINA7 gene cause thyroxine-binding globulin deficiency.

Fang Y, Chen H, Chen Q, Wang C, Liang L. Fang Y, et al. Mol Genet Genomic Med. 2021 Feb;9(2):e1571. doi: 10.1002/mgg3.1571. Epub 2021 Feb 7. Mol Genet Genomic Med. 2021. PMID: 33554479 Free PMC article.

5

Partial thyroxine-binding globulin deficiency in a family with coding region mutations in the TBG gene.

Chen LD, Lu HJ, Gan YL, Pang SW, Zheng Q, Ye DM, Huang XY, Qi HN, Xu WB, Wen XZ, Li LH, Li L. Chen LD, et al. J Endocrinol Invest. 2020 Dec;43(12):1703-1710. doi: 10.1007/s40618-020-01245-1. Epub 2020 Apr 7. J Endocrinol Invest. 2020. PMID: 32266677

6

Thyroxine-binding globulin deficiency due to a novel SERPINA7 mutation: Clinical characterization, analysis of X-chromosome inactivation pattern and protein structural modeling.

Gomes-Lima CJ, Maciel AAFL, Andrade MO, Cunha VSD, Mazzeu JF, Bleicher L, Neves FAR, Lofrano-Porto A. Gomes-Lima CJ, et al. Gene. 2018 Aug 5;666:58-63. doi: 10.1016/j.gene.2018.05.018. Epub 2018 May 4. Gene. 2018. PMID: 29733970

7

A Novel Mutation in the TBG Gene Producing Partial Thyroxine-Binding Globulin Deficiency (Glencoe) Identified in 2 Families.

Pappa T, Moeller LC, Edidin DV, Pannain S, Refetoff S. Pappa T, et al. Eur Thyroid J. 2017 Jul;6(3):138-142. doi: 10.1159/000455097. Epub 2017 Feb 2. Eur Thyroid J. 2017. PMID: 28785540 Free PMC article.

8

Identification of thyroxine-binding globulin as a candidate plasma marker of chronic obstructive pulmonary disease.

Diao W, Shen N, Du Y, Sun X, Liu B, Xu M, He B. Diao W, et al. Int J Chron Obstruct Pulmon Dis. 2017 May 25;12:1549-1564. doi: 10.2147/COPD.S137806. eCollection 2017. Int J Chron Obstruct Pulmon Dis. 2017. PMID: 28579773 Free PMC article.

9

A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.

Ferrara AM, Pappa T, Fu J, Brown CD, Peterson A, Moeller LC, Wyne K, White KP, Pluzhnikov A, Trubetskoy V, Nobrega M, Weiss RE, Dumitrescu AM, Refetoff S. Ferrara AM, et al. J Clin Endocrinol Metab. 2015 Jan;100(1):E173-81. doi: 10.1210/jc.2014-3490. J Clin Endocrinol Metab. 2015. PMID: 25361180 Free PMC article.

10

The allosteric modulation of thyroxine-binding globulin affinity is entropy driven.

Petruk AA, Labanda MS, Alvarez RM, Marti MA. Petruk AA, et al. Biochim Biophys Acta. 2013 Jun;1830(6):3570-7. doi: 10.1016/j.bbagen.2013.02.023. Epub 2013 Mar 1. Biochim Biophys Acta. 2013. PMID: 23458682

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