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 *

171 related articles for article (PubMed ID: 31799319)

  • 1. Novel frameshift mutation causes early termination of the thyroxine-binding globulin protein and complete thyroxine-binding globulin deficiency in a Chinese family: A case report.
    Dang PP; Xiao WW; Shan ZY; Xi Y; Wang RR; Yu XH; Teng WP; Teng XC
    World J Clin Cases; 2019 Nov; 7(22):3887-3894. PubMed ID: 31799319
    [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. Two novel mutations in the gene encoding thyroxine-binding globulin (TBG) as a cause of complete TBG deficiency in Taiwan.
    Su CC; Wu YC; Chiu CY; Won JG; Jap TS
    Clin Endocrinol (Oxf); 2003 Apr; 58(4):409-14. PubMed ID: 12641622
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Two Novel Mutations in the Serpina7 Gene Are Associated with Complete Deficiency of Thyroxine-Binding Globulin.
    Moeller LC; Appiagyei-Dankah Y; Köhler B; Biebermann H; Janssen OE; Führer D
    Eur Thyroid J; 2015 Sep; 4(Suppl 1):108-12. PubMed ID: 26601081
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel mutation causing complete deficiency of thyroxine binding globulin.
    Ueta Y; Mitani Y; Yoshida A; Taniguchi S; Mori A; Hattori K; Hisatome I; Manabe I; Takeda K; Sato R; Ahmmed GU; Tsuboi M; Ohtahara A; Hiroe K; Tanaka Y; Shigemasa C
    Clin Endocrinol (Oxf); 1997 Jul; 47(1):1-5. PubMed ID: 9302363
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Gene screening in Japanese families with complete deficiency of thyroxine-binding globulin demonstrates that a nucleotide deletion at codon 352 may be a race specific mutation.
    Takeda K; Iyota K; Mori Y; Tamura Y; Suehiro T; Kubo Y; Refetoff S; Hashimoto K
    Clin Endocrinol (Oxf); 1994 Feb; 40(2):221-6. PubMed ID: 8137521
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Complete deficiency of thyroxine-binding globulin (TBG-CD Buffalo) caused by a new nonsense mutation in the thyroxine-binding globulin gene.
    Carvalho GA; Weiss RE; Vladutiu AO; Refetoff S
    Thyroid; 1998 Feb; 8(2):161-5. PubMed ID: 9510125
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Complete thyroxine-binding globulin (TBG) deficiency produced by a mutation in acceptor splice site causing frameshift and early termination of translation (TBG-Kankakee).
    Carvalho GA; Weiss RE; Refetoff S
    J Clin Endocrinol Metab; 1998 Oct; 83(10):3604-8. PubMed ID: 9768672
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. A NOVEL MUTATION CAUSING COMPLETE THYROID BINDING GLOBULIN DEFICIENCY (TBG-CD MIA) IN A MALE WITH COEXISTING GRAVES DISEASE.
    Berger HR; Creech MK; Hannoush Z; Watanabe Y; Kargi A; Weiss RE
    AACE Clin Case Rep; 2017; 3(2):e134-e139. PubMed ID: 28553659
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Nucleotide deletion resulting in frameshift as a possible cause of complete thyroxine-binding globulin deficiency in six Japanese families.
    Yamamori I; Mori Y; Seo H; Hirooka Y; Imamura S; Miura Y; Matsui N; Oiso Y
    J Clin Endocrinol Metab; 1991 Aug; 73(2):262-7. PubMed ID: 1906892
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. C-terminal amino acid alteration rather than late termination causes complete deficiency of thyroxine-binding globulin CD-NeuIsenburg.
    Moeller LC; Fingerhut A; Lahner H; Grasberger H; Weimer B; Happ J; Mann K; Janssen OE
    J Clin Endocrinol Metab; 2006 Aug; 91(8):3215-8. PubMed ID: 16735497
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Thyroxine-binding globulin variant (TBG-Kumamoto): identification of a point mutation and genotype analysis of its family.
    Shirotani T; Kishikawa H; Wake N; Miyamura N; Hashimoto Y; Motoyoshi S; Yamaguchi K; Shichiri M
    Endocrinol Jpn; 1992 Dec; 39(6):577-84. PubMed ID: 1294376
    [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 9.