These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 25361180)

  • 1. 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
    J Clin Endocrinol Metab; 2015 Jan; 100(1):E173-81. PubMed ID: 25361180
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    J Endocrinol Invest; 2020 Dec; 43(12):1703-1710. PubMed ID: 32266677
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Partial thyroxine binding globulin deficiency in test tube infants: report of cases and literature review].
    Fang YL; Wang CL; Liang L
    Zhonghua Er Ke Za Zhi; 2016 Jun; 54(6):428-32. PubMed ID: 27256229
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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
    Gene; 2018 Aug; 666():58-63. PubMed ID: 29733970
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    J Endocrinol Invest; 2022 Apr; 45(4):731-739. PubMed ID: 34761328
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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
    Endocrinol Metab (Seoul); 2022 Dec; 37(6):870-878. PubMed ID: 36475360
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    Eur Thyroid J; 2017 Jul; 6(3):138-142. PubMed ID: 28785540
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Coexistence of THRB and TBG gene mutations in a Turkish family.
    Ferrara AM; Cakir M; Henry PH; Refetoff S
    J Clin Endocrinol Metab; 2013 Jun; 98(6):E1148-51. PubMed ID: 23633200
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Novel mutation p.A64D in the Serpina7 gene as a cause of partial thyroxine-binding globulin deficiency associated with increases affinity in transthyretin by a known p.A109T mutation in the TTR gene.
    Sklate RT; Olcese MC; Maccallini GC; Sarmiento RG; Targovnik HM; Rivolta CM
    Horm Metab Res; 2014 Feb; 46(2):100-8. PubMed ID: 24356794
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Complete thyroxine-binding globulin (TBG) deficiency in two families without mutations in coding or promoter regions of the TBG genes: in vitro demonstration of exon skipping.
    Reutrakul S; Dumitrescu A; Macchia PE; Moll GW; Vierhapper H; Refetoff S
    J Clin Endocrinol Metab; 2002 Mar; 87(3):1045-51. PubMed ID: 11889160
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel variant in Serpina7 gene in a family with thyroxine-binding globulin deficiency.
    Domingues R; Font P; Sobrinho L; Bugalho MJ
    Endocrine; 2009 Aug; 36(1):83-6. PubMed ID: 19415532
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A new inherited abnormality of thyroxine-binding globulin (TBG-San Diego) with decreased affinity for thyroxine and triiodothyronine.
    Sarne DH; Refetoff S; Nelson JC; Linarelli LG
    J Clin Endocrinol Metab; 1989 Jan; 68(1):114-9. PubMed ID: 2491856
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Newborn Falsely Suspected of Congenital Hypothyroidism due to Mutated Thyroxine-Binding Globulin with Low Binding Affinity.
    Hengeveld RCC; Albersen M; Hadders MAH; Hellinga I; Bikker H; Heijboer AC; Paul van Trotsenburg AS; Hillebrand JJ; Boelen A; Zwaveling-Soonawala N
    Horm Res Paediatr; 2021; 94(1-2):76-80. PubMed ID: 34126618
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Inherited X chromosome linked thyroxine-binding globulin (TBG) deficiency in a homozygous female.
    Bigazzi M; Ronga R; Olivotti AL; Scarselli G; Refetoff S
    J Endocrinol Invest; 1980; 3(4):349-52. PubMed ID: 6162876
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of the thyroxine-binding globulin (TBG) gene in six unrelated families with complete TBG deficiency.
    Mori Y; Refetoff S; Flink IL; Charbonneau M; Murata Y; Seo H; Morkin E; Dussault JH
    J Clin Endocrinol Metab; 1988 Oct; 67(4):727-33. PubMed ID: 2901429
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Partial Thyroid Hormone-Binding Globulin Deficiency: A Case Report and Literature Review.
    Liu X; Li S; Xiong J; Chen D; Jiang C; Zeng L; Qiu Y; Xia BW
    Diabetes Metab Syndr Obes; 2023; 16():2225-2232. PubMed ID: 37525823
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Gene amplification as a cause of inherited thyroxine-binding globulin excess in two Japanese families.
    Mori Y; Miura Y; Takeuchi H; Igarashi Y; Sugiura J; Saito H; Oiso Y
    J Clin Endocrinol Metab; 1995 Dec; 80(12):3758-62. PubMed ID: 8530630
    [TBL] [Abstract][Full Text] [Related]  

  • 18. First report of inherited thyroxine-binding globulin deficiency in Iran caused by a known de novo mutation in SERPINA7.
    Soheilipour F; Fazilaty H; Jesmi F; Gahl WA; Behnam B
    Mol Genet Metab Rep; 2016 Sep; 8():13-6. PubMed ID: 27331012
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel mutation causing complete thyroxine-binding globulin deficiency (TBG-CD-Negev) among the Bedouins in southern Israel.
    Miura Y; Hershkovitz E; Inagaki A; Parvari R; Oiso Y; Phillip M
    J Clin Endocrinol Metab; 2000 Oct; 85(10):3687-9. PubMed ID: 11061524
    [TBL] [Abstract][Full Text] [Related]  

  • 20. TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature.
    Mannavola D; Vannucchi G; Fugazzola L; Cirello V; Campi I; Radetti G; Persani L; Refetoff S; Beck-Peccoz P
    J Mol Med (Berl); 2006 Oct; 84(10):864-71. PubMed ID: 16947003
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.